Skip to content

Bone Density & Osteoporosis

Systemic bone fragility and microarchitectural decay — T-score diagnostics, vertebral compression fracture risk, and implications for spinal stability.

Overview

Osteoporosis is a systemic skeletal disorder characterized by decreased bone mineral density, significantly increasing the risk of fragility fractures. Fracture prevention remains the primary efficacy endpoint in medical management [4]. While national guidelines recommend densitometry for diagnosis [2], a substantial proportion of patients with subsequent contralateral proximal femoral fractures were neither screened nor formally treated [5]. Consequently, identifying high-risk individuals is critical to effectively deploy the expanding array of osteoporosis therapies [3].

Screening strategies extend beyond traditional densitometry. Circulating markers of bone turnover may identify patients at risk for low bone mineral density long before standard screening thresholds, though prospective validation is required before widespread clinical adoption [6]. Adult children of patients with proximal femur fractures constitute a high-risk demographic, with nearly half meeting treatment thresholds [56]. In pediatric populations, the effectiveness of regular screening for low bone mineral density risk factors in children with idiopathic scoliosis requires further investigation to prevent osteoporosis [12].

Bone health directly influences surgical outcomes and perioperative risk. Osteoporosis exacerbates complications in total knee arthroplasty, advocating for routine screening, preoperative optimization, and enhanced postoperative surveillance to mitigate risks and improve implant durability [29]. Management in spine surgery is challenging but can yield pain relief, deformity correction, and improved function through appropriate patient selection, medical optimization, and surgical technique [30]. Conversely, patients with decreased bone mineral density can still achieve excellent 2-year outcomes following arthroscopic rotator cuff repair [9]. Therapeutic interventions such as denosumab result in higher spine bone mineral density in selected postmenopausal women [27]. Clinical practice regarding bisphosphonate prescribing and treatment decision-making varies significantly among providers [57].

Anatomy & Pathophysiology

Osseous

Bone density and its relation to the development of acromial stress fracture following reverse total shoulder arthroplasty do not predictably decrease with age or osteoporosis diagnosis [23]. Mechanical bone properties of vertebral cancellous bone can be modelled with high accuracy in the investigated bone density range based on quantitative computed tomography [39]. Data from individual spinal segments measured using Hounsfield units of computed tomography may be helpful to comprehensively evaluate the status of the spine and to design a better preoperative plan before instrumentation [69].

The L2‒L4 lumbar spine segment may substantially increase in bone mineral density with whole-body vibration training, whereas the L1‒L4 lumbar spine segment and total hip region have a negligible effect [63]. Participation in one or more high-impact sports in adulthood is associated with larger vertebral size, and thus increased vertebral strength, among middle-aged women [74]. Due to the unique microarchitecture of the cervical vertebrae, fractures occur much later in this region than in the thoracic or lumbar spine [44]. Acute multiple osteoporotic vertebral compression fractures are an accelerated form of osteoporotic vertebral compression fracture cascades, showing similar anatomical distribution and distribution pattern of osteoporotic vertebral compression fractures in the spine [70].

Ligamentous & Disc

Endplate thickness and bone density significantly influence biomechanical stability after anterior cervical discectomy and fusion, highlighting the importance of preserving endplate integrity and evaluating bone quality to mitigate the risk of postoperative subsidence [79]. Osteoporosis leads to the deterioration of biomechanical characteristics in the adjacent segment disc after percutaneous transforaminal endoscopic discectomy, which may result in an increase in the incidence of adjacent segment disease [52]. The co-morbidity of intervertebral disc degeneration and osteoporosis is driven by a synergistic network of biomechanical coupling and molecular pathways, including inflammatory factors, senescence signaling, and immunometabolic reprogramming [72].

Classification

Osteoporosis is a common bone disorder with increasing incidence [1]. It is a condition of bone mass loss often associated with cellular activity alterations rather than obvious biochemical defects [7]. Current clinical management focuses excessively on the diagnosis of osteoporosis, neglecting previous stages of low bone mineral density such as osteopenia, bone quality, and bone tissue structure [8]. The identification of high-risk patients is important to effectively use the growing number of available osteoporosis therapies [3]. Proper recognition of the etiology of osteoporosis is an essential step in improving bone health and preventing further bone loss [18].

Trabecular Pattern Analysis: Femoral trabecular patterns are of little help in establishing the diagnosis or severity of osteoporosis [10]. The femoral trabecular scoring system as described by Singh and associates is of little or no help in establishing the diagnosis or the severity of osteoporosis [58]. Conversely, trabecular patterns can be utilized as a roentgenographic scale for the diagnosis and grading of osteoporosis [11].

Bone Density Indices: Trabecular bone density of the peripheral skeleton is a reliable index of postmenopausal osteoporosis [43]. Osteoporotic patients can be distinguished from those with age-related bone loss based on the magnitude of the decrease in trabecular bone density [43]. Distal radius bone mineral density has the potential to be integrated into future osteoporosis classification systems [17].

Advanced Imaging Models: A three-classification predictive model combining deep learning-based automatic segmentation of the proximal femur and radiomics-based bone status classification on low-dose abdominal CT images can be used for the opportunistic detection of osteoporosis [61]. Specific characteristics of vertebral fractures in elderly men, including the number of fractures, fracture type, and degree of compression, are associated with low bone mineral density and osteoporosis [64].

Other Considerations: The evidence highlights a tension between traditional radiographic scoring systems and emerging quantitative or AI-driven classification methods. While Singh’s system and general femoral trabecular patterns are deemed of little diagnostic help, other trabecular pattern analyses and peripheral density metrics remain clinically relevant.

Clinical Presentation

Osteoporosis is a common bone disorder with increasing incidence [1]. It is a condition of bone mass loss often associated with cellular activity alterations rather than obvious biochemical defects [7]. The condition is prevalent among specific demographics, including Palestinian people above 50 years old [22]. However, disparities in incidence, awareness, diagnosis, treatment, and outcomes exist across racial and ethnic lines, with minority women often underdiagnosed and undertreated [35].

Clinical management currently focuses excessively on the diagnosis of osteoporosis, neglecting previous stages of low bone mineral density, such as osteopenia, bone quality, and bone tissue structure [8]. A high proportion of women diagnosed with osteoporosis had been evaluated by densitometry, in agreement with national guidelines [2]. Conversely, most patients with subsequent contralateral proximal femoral fracture were not screened or formally treated for osteoporosis [5]. Proper recognition of the etiology of osteoporosis is an essential step in improving bone health and preventing further bone loss [18].

Imaging and Screening Modalities

Trabecular Patterns: These are of little help in establishing the diagnosis or severity of osteoporosis [10]. Alternatively, trabecular patterns can be utilized as a roentgenographic scale for the diagnosis and grading of osteoporosis [11].

CT-Based Opportunistic Screening: Vertebral HU value and the pectoral muscle index based on chest CT can be used to opportunistically screen for osteoporosis [13]. This opportunistic screening approach allows early prevention of osteoporotic fractures via timely screening of individuals at high risk without requiring additional radiation [13]. Hounsfield unit measurements on CT scans are useful for identifying osteoporosis and predicting complications in patients undergoing spinal surgery [20]. Based on CT at the third lumbar spine level, the skeletal muscle index and psoas muscle index can predict osteoporosis [21].

Lumbar Degenerative Disease Parameters: Combinations of two imaging parameters can improve bone mineral density assessment in patients with lumbar degenerative diseases [19]. Parameters at the single-segment level are recommended to assist in the diagnosis of osteoporosis due to easier measurement and same diagnostic performance [19]. Specific metrics such as VFI, SFI, and VSR do not help clinicians to diagnose osteoporosis well [21].

Pediatric Considerations: Regular screening for low bone mineral density risk factors in children with idiopathic scoliosis needs to be investigated to prevent osteoporosis [12].

Physical and Laboratory Assessment

Mechanical Characteristics: Mechanical characteristics do not predictably decrease with age or osteoporosis diagnosis [23].

Muscle Metrics: Findings regarding the association between muscle strength and mass and bone mineral density may have profound implications for public health regarding osteopenia and osteoporosis prevention, early diagnosis, and treatment [36].

Biomarkers: Prospective validation is necessary before recommending widespread clinical use of circulating markers of bone turnover to identify patients at risk for developing low bone mineral density long before traditional screening [6].

Investigations

Plain radiography: Osteoporosis is characterized by bone mass loss and cellular activity alterations rather than obvious biochemical defects [7]. While trabecular patterns of the upper end of the femur can serve as a roentgenographic scale for diagnosis and grading [11], general trabecular patterns are of little help in establishing the diagnosis or severity of osteoporosis [10]. Vertebral fracture indices (VFI), subchondral fracture index (SFI), and vertebral shape ratio (VSR) do not help clinicians diagnose osteoporosis effectively [21].

MRI: Average cortical bone thickness measurements obtained from shoulder MRI correlate with DXA and appear effective in differentiating patients with normal and abnormal BMD [73]. Radionucleotide bone scanning and MRI are helpful in diagnosing regional migratory osteoporosis [60].

CT: Hounsfield unit (HU) measurements on CT scans are useful for identifying osteoporosis and predicting complications in patients undergoing spinal surgery [20]. Vertebral HU value and the pectoral muscle index based on chest CT can be used to opportunistically screen for osteoporosis without requiring additional radiation [13]. Known 2D radiographic and novel 3D measurements of bone density can be reproducibly measured from CT scans and show moderately strong correlation [66]. For patients with lumbar degenerative diseases, parameters at the single-segment level are recommended to assist in diagnosis, offering the same diagnostic performance with easier measurement [19]. Diffusion tensor imaging (DTI) with a cutoff of 1.6 may help prompt clinicians to initiate workup and manage underlying osteoporosis [82].

Other Considerations: A high proportion of women diagnosed with osteoporosis had been evaluated by densitometry, aligning with national guidelines [2]. However, most patients who sustained subsequent contralateral proximal femoral fractures were not screened or formally treated for osteoporosis [5]. Current clinical management focuses excessively on osteoporosis diagnosis, neglecting previous stages such as osteopenia, bone quality, and bone tissue structure [8]. Improved osteoporosis workup and intervention are needed among patients who have sustained low-energy vertebral compression fractures [16]. Distal radius bone mineral density has the potential to be integrated into future osteoporosis classification systems for patients with a history of fragility fracture [17]. Patients with decreased bone mineral density can still achieve excellent 2-year outcomes after arthroscopic rotator cuff repair [9]. In AS patients not using antiosteoporotic therapy, spine trabecular bone density evaluated by QCT decreased over 10-year follow-up and was not related to baseline radiological severity of spine involvement [77]. Denosumab results in higher spine BMD in selected women with postmenopausal osteoporosis [27].

Treatment

Non-Operative

Osteoporosis management rests on early recognition, medical therapy, and fracture prevention [1]. Fracture prevention serves as the primary efficacy endpoint in medical management [4]. Identifying high-risk patients is critical to effectively deploying the expanding array of osteoporosis therapies [3]. More than one in two patients with clinical vertebral or non-vertebral fractures and BMD-osteoporosis have correctable secondary contributors [32]. Circulating bone turnover markers may identify patients at risk for low BMD long before traditional screening, though prospective validation is needed before widespread clinical adoption [6]. For children with idiopathic scoliosis, the effectiveness of regular screening for low BMD risk factors to prevent osteoporosis requires further investigation [12]. Non-NOF fragility fractures receive less attention for assessment and treatment than NOF fractures [65]. Bisphosphonate therapy reduces fracture risk but does not reduce overall mortality risk [42].

Operative

Indications: Management of osteoporosis in spine surgery is challenging but can yield pain relief, deformity correction, and improved function through appropriate patient selection, medical optimization, and surgical techniques [30]. Active treatment for lumbar spinal stenosis (LSS) with potent osteoporosis therapy is indicated to increase BMD in patients with both conditions [45]. Conventional instrumentation combined with complete osteoporosis treatment improves surgical outcomes in LSS patients with osteoporosis [71]. Lower limb deformity correction techniques are likely contraindicated in osteogenesis imperfecta patients with significant bone fragility or ongoing fractures [54].

Surgical Approach / Technique: Good immediate stability can be achieved after surgery regardless of the cage type used in osteoporotic patients [83]. Short-term anabolic agent administration followed by sequential therapy may effectively enhance bone health and reduce subsequent fracture risk in osteoporotic hip fractures [80].

Implant Selection: Patient-reported and clinical outcomes for osteoporotic patients on teriparatide are comparable to those with normal BMD undergoing long spinal fusion [46].

Adjuncts: Teriparatide treatment combined with denosumab alone effectively improves spine BMD [15]. The combination of calcitriol and bisphosphonates demonstrates superior clinical efficacy and safety in postmenopausal osteoporosis, reducing pain and disability while enhancing bone metabolism, immune function, BMD, and daily living ability [37]. Both denosumab and alendronate effectively improve BMD in postmenopausal breast cancer patients with aromatase inhibitor-associated osteoporosis [40]. Twelve months of alendronate treatment increases BMD at axial and appendicular skeletons in postmenopausal women with established osteoporosis [41]. Bisphosphonate treatment improves health-related quality of life (HRQoL) in men with osteopenia/osteoporosis [47]. Denosumab shows promising efficacy in maintaining bone health and preventing joint damage in rheumatoid arthritis patients with coexisting osteoporosis [48]. Traditional Chinese Exercise (TCE) significantly affects postmenopausal osteoporosis and serves as a non-pharmacological treatment option [75]. The efficacy of risedronate against bone resorption remains disputed in medium- or long-term follow-up due to declining trends and safety challenges, necessitating larger, longer clinical trials focusing on clinically relevant endpoints [14].

Complications

Osteoporosis: Osteoporosis is a common bone disorder with increasing incidence [1]. It is a condition of bone mass loss often associated with cellular activity alterations rather than obvious biochemical defects [7]. Osteopenia and osteoporosis are conditions often associated with cellular activity alterations rather than obvious biochemical defects [7]. Osteoporosis is common among Palestinian people above 50 years old [22]. A negative calcium balance of as little as fifty milligrams a day over twenty years may produce significant osteoporosis [33]. More than one in two patients presenting with a clinical vertebral or non-vertebral fracture and BMD-osteoporosis have secondary contributors to osteoporosis, most of which were correctable [32].

Screening and Diagnosis: The identification of high-risk patients is important to effectively use the growing number of available osteoporosis therapies [3]. Vertebral HU value and the pectoral muscle index based on chest CT can be used to opportunistically screen for osteoporosis without requiring additional radiation [13]. Prospective validation is necessary before recommending widespread clinical use of circulating markers of bone turnover to identify patients at risk for developing low bone mineral density long before traditional screening would ostensibly take place [6]. Current clinical management focuses excessively on the diagnosis of osteoporosis, neglecting previous stages of low bone mineral density, such as osteopenia, bone quality, and bone tissue structure [8].

Treatment Gaps and Outcomes: Most patients with subsequent contralateral proximal femoral fracture were not screened or formally treated for osteoporosis [5]. Osteoporosis is undertreated after low-energy vertebral compression fractures [16]. Health Related Quality of Life was low in osteoporosis and unaffected by bone specific treatment [25].

Pharmacologic Management: The efficacy of risedronate against bone resorption remains disputed in medium or long-term follow-up due to declining trends and potential safety challenges, necessitating future larger clinical trials with longer duration focusing on clinically relevant endpoints [14]. Short-term teriparatide administration followed by denosumab alone was effective only in improving spine BMD [15]. Long term treatment with pamidronate iv has a comparable effect on BMD as oral bisphosphates [24]. BMD is preserved at the lumbar spine and total hip following discontinuation of bisphosphonate for a short period following long-term treatment, although a gradual loss occurs at the femoral neck [26]. Medication history and age-specific gender differences must be considered in bone turnover and metabolic clinical research [28].

Fracture Healing and Natural History: The study clarified the natural history of the progression pattern of vertebral deformities in radiographic prevalent vertebral fractures in elderly individuals [31]. The current evidence indicates that the beneficial effects of anti-osteoporosis treatment exceed any concerns about possible adverse consequences on fracture healing in most circumstances [49].

Recovery

Light activity (weeks): Evidence does not provide specific week ranges for light activity or desk work return in the context of osteoporosis management or fracture recovery.

Full activity (months): Evidence does not provide specific month ranges for full activity, manual work, or strength return.

Complete recovery / outcome plateau (months): Patients with decreased bone mineral density can achieve excellent 2-year outcomes after arthroscopic rotator cuff repair [9]. Health-related quality of life was low in osteoporosis and unaffected by bone-specific treatment in a 10-year follow-up study [25].

Rehabilitation protocol: Evidence does not specify PT phasing, immobilisation duration, or weight-bearing progression for osteoporosis-related conditions.

Functional milestones: Evidence does not provide validated PROM trajectories or outcome-measure benchmarks.

Other Considerations: Osteoporosis is a common bone disorder with increasing incidence [1]. Early recognition, medical management, and fracture prevention are main pillars of osteoporosis treatment [1]. Fracture prevention is the key efficacy end point in the medical management of osteoporosis [4]. Circulating markers of bone turnover may identify patients at risk for developing low bone mineral density long before traditional screening [6], although prospective validation is necessary before recommending widespread clinical use of these markers for early risk identification [6].

The efficacy of risedronate against bone resorption remains disputed in medium or long-term follow-up due to declining trends and potential safety challenges [14], necessitating future clinical trials to evaluate risedronate efficacy with longer duration and clinically relevant endpoints [14]. Short-term teriparatide administration followed by denosumab alone was effective only in improving spine BMD in patients with osteoporotic hip fracture [15]. Osteoporosis is undertreated after low-energy vertebral compression fractures, indicating a need for improved workup and intervention [16]. Intravenous pamidronate is a good alternative for patients with gastrointestinal side effects or contraindications for oral bisphosphonates [24], and long-term treatment with intravenous pamidronate has a comparable effect on BMD as oral bisphosphonates [24].

BMD is preserved at the lumbar spine and total hip following short-term discontinuation of bisphosphonates after long-term treatment [26], whereas a gradual loss of BMD occurs at the femoral neck following discontinuation of bisphosphonates after long-term treatment [26]. Medication history and age-specific gender differences must be considered in bone turnover and metabolic clinical research [28]. Osteoporosis exacerbates perioperative complications in total knee arthroplasty [29], and routine osteoporosis screening, preoperative optimization of bone health, and enhanced postoperative surveillance are advocated to mitigate risks and improve long-term implant durability in total knee arthroplasty [29]. Preoperative screening and management of osteoporosis may be important for optimizing long-term outcomes in patients requiring multilevel cervical fusion [62].

The study clarified the natural history of the progression pattern of vertebral deformities in radiographic prevalent vertebral fractures in elderly individuals [31]. A negative calcium balance of as little as fifty milligrams a day over twenty years may produce significant osteoporosis [33]. Some osteoporotic patients retain calcium on high intake, but retention may disappear over time [33]. Low trabecular bone density at the site of the hip was associated with the duration of disease progression and degree of hip involvement in ankylosing spondylitis patients [84]. In chronically treated osteoporotic patients, 95% have a bone turnover in the premenopausal range [85]. The burden of screening for markers of bone health and subsequent treatment in at-risk elderly patients with proximal femur fractures has increased over time [86]. Bone metabolism factors were associated with poor prognosis of osteoporosis in the elderly [88]. Reductions in bone mineral density were observed in some postmenopausal women previously tolerant of brand alendronate who switched to generic alendronate [89].

Key Evidence

  • [L3] A high proportion of women diagnosed with osteoporosis had been evaluated by densitometry, in agreement with national guidelines. (10.1186/1471-2474-12-7)
  • [L4] The identification of high-risk patients is important to effectively use the growing number of available osteoporosis therapies. (10.1186/1471-2474-3-22)
  • [L4] Most of these patients were not screened or formally treated for osteoporosis. (10.1186/s13018-023-03621-y)
  • [L2] Although prospective validation is necessary before recommending widespread clinical use, this information may be used to identify patients at risk for developing low bone mineral density long before traditional screening would ostensibly take place. (10.1016/j.jhsa.2021.02.019)
  • [L5] This article defines osteopenia and osteoporosis, discusses their pathophysiology, clinical manifestations, diagnostic modalities, and current therapeutic modes, emphasizing that osteoporosis is a condition of bone mass loss often associated with cellular activity alterations rather than obvious biochemical defects. (10.2106/jbjs.l.01168)
  • [L5] The study concludes that current clinical management focuses excessively on the diagnosis of osteoporosis, neglecting previous stages of low bone mineral density, such as osteopenia, bone quality, and bone tissue structure. (10.1186/s12891-025-08997-y)
  • [L3] Patients with decreased bone mineral density can still achieve excellent 2-year outcomes. (10.1016/j.jse.2025.02.011)
  • [L3] Thus, these trabecular patterns are of little help in establishing the diagnosis or severity of osteoporosis. (10.2106/00004623-197254070-00011)
  • [L4] These patterns can be utilized as a roentgenographic scale for the diagnosis and grading of osteoporosis. (10.2106/00004623-197052030-00005)
  • [L4] To prevent osteoporosis, the effectiveness of regular screening for low BMD risk factors in children with IS needs to be investigated. (10.1186/s12891-023-06157-8)
  • [L3] This approach allows the early prevention of osteoporotic fractures via the timely screening of individuals at high risk of osteoporosis without requiring additional radiation. (10.1186/s13018-024-04825-6)
  • [Letter] The efficacy of risedronate against bone resorption remains disputed in medium or long-term follow-up due to declining trends and potential safety challenges, necessitating future larger clinical trials with longer duration focusing on clinically relevant endpoints. (10.1186/s13018-022-03118-0)
  • [L3] Short-term teriparatide administration followed by denosumab alone was effective only in improving spine BMD. (10.1186/s12891-020-03771-8)
  • [L4] Our study demonstrates the additional need for improved osteoporosis workup and intervention among patients who have sustained VCFs. (10.5435/jaaos-d-20-01132)
  • [L3] Consequently, it has the potential to be integrated into future osteoporosis classification systems. (10.1186/s12891-025-09431-z)
  • [L4] Proper recognition of the etiology of osteoporosis is an essential step in improving bone health and preventing further bone loss. (10.3390/jcm11092382)
  • [L3] Considering the same diagnostic performance but easier measurement, parameters at the single-segment level were recommended to assist in the diagnosis of osteoporosis. (10.1186/s12891-023-06888-8)
  • [L5] This review serves as an update to diagnosis, management, and treatment of patients with osteoporosis undergoing spinal surgery, highlighting new anabolic pharmacologic options and the utility of Hounsfield unit measurements on CT scans for identifying osteoporosis and predicting complications. (10.5435/jaaos-d-24-00311)
  • [L3] In addition, VFI, SFI, and VSR do not help clinicians to diagnose osteoporosis well. (10.1186/s12891-022-05887-5)
  • [L4] Osteoporosis is common among Palestinian people above 50 years old. (10.1186/1471-2474-14-284)
  • [L3] These mechanical characteristics also do not predictably decrease with age or osteoporosis diagnosis. (10.1177/1758573220949992)
  • [L3] Long term treatment with pamidronate iv has a comparable effect on BMD as oral bisphosphonates. (10.1186/1471-2474-10-86)
  • [L3] Health Related Quality of Life was low in osteoporosis and unaffected by bone specific treatment. (10.1186/s12891-022-05987-2)
  • [L3] BMD is preserved at the lumbar spine and total hip following discontinuation of bisphosphonate for a short period following long-term treatment, although a gradual loss occurs at the femoral neck. (10.1186/1471-2474-8-3)
  • [L1] Denosumab results in higher spine BMD in selected women with postmenopausal osteoporosis. (10.1186/s13018-021-02678-x)
  • [L4] Medication history and age-specific gender differences must be considered in bone turnover and metabolic clinical research. (10.1186/s12891-020-03610-w)
  • [L3] These findings advocate for routine osteoporosis screening, optimization of bone health preoperatively, and enhanced postoperative surveillance to mitigate risks and improve long-term implant durability. (10.1186/s13018-025-06340-8)
  • [L5] Management of osteoporosis in patients undergoing spine surgery is challenging, but with appropriate patient selection, medical optimization, and surgical techniques, these patients can experience pain relief, deformity correction, and improved function. (10.5435/jaaos-d-14-00042)
  • [L2] This study clarified the natural history of the progression pattern of vertebral deformities in radiographic prevalent vertebral fractures in elderly individuals. (10.1186/s12891-024-07254-y)
  • [L3] More than one in two patients presenting with a clinical vertebral or non-vertebral fracture and BMD-osteoporosis have secondary contributors to osteoporosis, most of which were correctable. (10.1186/1471-2474-9-109)
  • [L4] Disparities in incidence, awareness, diagnosis, treatment, and outcomes of osteoporosis exist across racial and ethnic lines, with minority women often underdiagnosed and undertreated. (10.5435/00124635-200700001-00008)
  • [L4] These findings may have profound implications for public health regarding osteopenia and osteoporosis prevention, early diagnosis, and treatment. (10.1186/s13018-023-03877-4)
  • [L3] The combination of calcitriol and bisphosphonates demonstrates superior clinical efficacy and safety in treating postmenopausal osteoporosis, effectively reducing pain and disability, enhancing bone metabolism and immune function, and improving bone mineral density and daily living ability. (10.1186/s13018-025-05714-2)
  • [L5] The mechanical bone properties of vertebral cancellous bone could be modelled with high accuracy in the investigated bone density range. (10.1186/s12891-021-04571-4)
  • [L3] Both therapeutic regimens effectively improved BMD in the study population. (10.1186/s12891-025-09280-w)
  • [L2] 12 months Alendronate treatment was effective to increase BMD at both axial and appendicular skeletons in postmenopausal women with established osteoporosis. (10.1186/1749-799x-2-9)
  • [L1] Based on our comprehensive meta-analysis, there is high-quality evidence suggesting that bisphosphonate therapy for patients with osteoporosis does not reduce the overall risk of mortality despite its effectiveness in reducing the risk of fractures. (10.1097/corr.0000000000003204)
  • [L3] Trabecular bone density of the peripheral skeleton is a reliable index of postmenopausal osteoporosis, and osteoporotic patients can be distinguished from those with age-related bone loss based on the magnitude of the decrease in trabecular bone density. (10.2106/00004623-198466070-00007)
  • [L5] Due to the unique microarchitecture of the cervical vertebrae, fractures occur much later in this region than they do in the thoracic or lumbar spine. (10.1186/s13018-022-03105-5)
  • [L3] Active treatment for LSS with more potent treatment for osteoporosis should be taken to increase BMD for patients with osteoporosis and LSS. (10.1186/s12891-021-04273-x)
  • [L3] Moreover, patient-reported and clinical outcomes for osteoporotic patients on teriparatide were not different from those for patients with normal BMD. (10.2106/jbjs.23.00272)
  • [L2] Bisphosphonates treatment is beneficial to improve HRQoL of osteopenia/osteoporosis men. (10.1186/s12891-023-06397-8)
  • [L1] Denosumab demonstrates promising efficacy in maintaining bone health and preventing joint damage in rheumatoid arthritis patients with coexisting osteoporosis. (10.1186/s12891-025-08688-8)
  • [L5] The current evidence indicates that the beneficial effects of anti-osteoporosis treatment exceed any concerns about possible adverse consequences on fracture healing in most circumstances. (10.1016/j.injury.2018.04.016)
  • [L5] Osteoporosis leads to the deterioration of biomechanical characteristics in the adjacent segment disc after PTED; this variation may also result in an increase in the incidence of ASD. (10.1186/s13018-019-1166-1)
  • [L4] The technique is probably contraindicated in patients who have a greater degree of fragility of the bones and in those who continue to sustain fractures. (10.2106/00004623-199602000-00008)
  • [L4] Adult children of patients with proximal femur fractures represent a high-risk group for osteoporosis, with nearly half meeting treatment thresholds. (10.1186/s12891-025-09378-1)
  • [L4] Approaches to making treatment decisions and supporting patients when prescribing bisphosphonates for osteoporosis vary in practice. (10.1186/s12891-023-06865-1)
  • [L5] Radionucleotide bone scanning and MRI were helpful in the diagnosis of regional migratory osteoporosis, and all patients recovered with conservative treatment. (10.1007/s00402-003-0557-1)
  • [L4] A three-classification predictive model combining a deep learning-based automatic segmentation of the proximal femur and a radiomics-based bone status classification on LDCT images can be used for the opportunistic detection of osteoporosis. (10.1186/s12891-025-08631-x)
  • [L3] These data indicate that preoperative screening and management of osteoporosis may be important for optimizing long-term outcomes in patients who require multilevel CF. (10.5435/jaaos-d-22-00361)
  • [L1] The L2‒L4 lumbar spine segment may substantially increase, whereas the L1‒L4 lumbar spine segment and total hip region have negligible effect. (10.1186/s12891-026-09504-7)
  • [L3] Specific characteristics of vertebral fractures in elderly men, including the number of fractures, fracture type, and degree of compression, are associated with low bone mineral density and osteoporosis. (10.1302/0301-620x.97b8.35032)
  • [L4] Non-NOF fragility fractures received less attention for osteoporosis assessment and treatment compared to NOF fractures. (10.1186/s13018-023-04266-7)
  • [L2] This study has demonstrated that known 2D radiographic and novel 3D measurements of bone density can reproducibly be measured from CT scans and have moderately strong correlation. (10.1016/j.jseint.2021.07.015)
  • [L4] These data from the individual spinal segments may be helpful to comprehensively evaluate the status of the spine and to design a better preoperative plan before instrumentation. (10.1186/s12891-024-07324-1)
  • [L3] amOVCF are an accelerated form of OVCFcs showing similar anatomical distribution and distribution pattern of OVCF in the spine. (10.1186/s13018-024-05337-z)
  • [L3] The use of conventional instrumentation along with complete treatment of osteoporosis can help improve the clinical outcome of surgery in these patients. (10.1186/s13018-023-03935-x)
  • [L5] The co-morbidity of intervertebral disc degeneration and osteoporosis is driven by a synergistic network of biomechanical coupling and molecular pathways, including inflammatory factors, senescence signaling, and immunometabolic reprogramming. (10.1186/s13018-025-06075-6)
  • [L3] Average cortical bone thickness measurements obtained from shoulder MRI are correlated with DXA and appear effective in differentiating patients with normal and abnormal BMD, potentially guiding further diagnostic assessments. (10.1177/17585732241279090)
  • [L2] Participation in one or more high-impact sports in adulthood is associated with larger vertebral size, and thus increased vertebral strength, among middle-aged women. (10.1186/s12891-017-1794-8)
  • [L1] TCE has a significant effect on postmenopausal patients with osteoporosis and can be used as a non-pharmacological treatment. (10.1186/s13018-024-05288-5)
  • [L3] In AS patients who were not using antiosteoporotic therapy spine trabecular bone density evaluated by QCT decreased over 10-year follow-up and was not related to baseline radiological severity of spine involvement. (10.1186/1471-2474-12-121)
  • [L5] Endplate thickness and bone density significantly influence biomechanical stability after ACDF, highlighting the importance of preserving endplate integrity and evaluating bone quality to mitigate the risk of postoperative subsidence. (10.1186/s12891-025-09255-x)
  • [L3] This treatment approach may be an effective strategy to enhance bone health and potentially reduce subsequent fracture risk in this high-risk population. (10.1186/s13018-025-06084-5)
  • [L3] DTI with a cutoff of 1.6 may help prompt clinicians to initiate workup and thus manage underlying osteoporosis. (10.1016/j.jse.2024.05.018)
  • [L5] For people with osteoporosis, no matter what type of cage is used, good immediate stability can be achieved after surgery. (10.1186/s12891-024-07221-7)
  • [L3] The low trabecular bone density at the site of the hip was associated with the duration of disease progression and degree of hip involvement. (10.1186/s12891-021-04912-3)
  • [L3] In chronically treated patients, 95% have a bone turnover in the premenopausal range. (10.1186/1471-2474-12-167)
  • [L3] The burden of screening for markers of bone health and subsequent treatment in at-risk patients has increased over time. (10.1186/s13018-025-06202-3)
  • [L3] Bone metabolism factors were associated with poor prognosis of osteoporosis in the elderly. (10.1186/s12891-024-07560-5)
  • [L3] In addition, reductions in bone mineral density were observed in some patients who had stable BMDs before January 2006. (10.1186/1471-2474-11-68)

See Also

References

[1] Chapter 6 Osteoporosis and Pathologic Bone. 2021.

[2] Management of osteoporosis and associated quality of life in post menopausal women. BMC Musculoskeletal Disorders. 2011. DOI: 10.1186/1471-2474-12-7

[3] The association between iliocostal distance and the number of vertebral and non-vertebral fractures in women and men registered in the Canadian Database For Osteoporosis and Osteopenia (CANDOO). BMC Musculoskeletal Disorders. 2002. DOI: 10.1186/1471-2474-3-22

[4] FREDERICK M. AZAR EDITOR, VOL. 58. 2008.

[5] Characteristics of subsequent contralateral proximal femoral fracture: more convenient access is needed to treat osteoporosis. Journal of Orthopaedic Surgery and Research. 2023. DOI: 10.1186/s13018-023-03621-y

[6] Longitudinal Analysis of Circulating Markers of Bone Turnover Across Multiple Decades in Osteoporotic Women. The Journal of Hand Surgery. 2022. DOI: 10.1016/j.jhsa.2021.02.019

[7] Early or Continued Osteoporosis Treatment During Nonvertebral Fracture-Healing: No Harm Done. Journal of Bone and Joint Surgery. 2012. DOI: 10.2106/jbjs.l.01168

[8] Multidisciplinary consensus on the management of patients with osteopenia and fracture risk in Spain. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-08997-y

[9] No difference in 2-year outcomes of arthroscopic rotator cuff repair in patients with osteoporosis. Journal of Shoulder and Elbow Surgery. 2025. DOI: 10.1016/j.jse.2025.02.011

[10] Femoral Trabecular Patterns and Bone Mineral Content. The Journal of Bone & Joint Surgery. 1972. DOI: 10.2106/00004623-197254070-00011

[11] Changes in Trabecular Pattern of the Upper End of the Femur as an Index of Osteoporosis. The Journal of Bone & Joint Surgery. 1970. DOI: 10.2106/00004623-197052030-00005

[12] Risk factors associated with low bone mineral density in children with idiopathic scoliosis: a scoping review. BMC Musculoskeletal Disorders. 2023. DOI: 10.1186/s12891-023-06157-8

[13] Vertebral HU value and the pectoral muscle index based on chest CT can be used to opportunistically screen for osteoporosis. Journal of Orthopaedic Surgery and Research. 2024. DOI: 10.1186/s13018-024-04825-6

[14] Comment on “The efficiency of risedronate in reducing bone resorption after total hip arthroplasty: a meta-analysis of randomized control trials at a minimum of 6 months’ follow-up”. Journal of Orthopaedic Surgery and Research. 2022. DOI: 10.1186/s13018-022-03118-0

[15] The impact of sequential therapy from short-term teriparatide to denosumab compared with denosumab alone in patients with osteoporotic hip fracture: a 1-year follow-up study. BMC Musculoskeletal Disorders. 2020. DOI: 10.1186/s12891-020-03771-8

[16] Osteoporosis Is Undertreated After Low-energy Vertebral Compression Fractures. Journal of the American Academy of Orthopaedic Surgeons. 2021. DOI: 10.5435/jaaos-d-20-01132

[17] The added value of distal radius bone mineral density for the diagnosis of osteoporosis in patients with a history of fragility fracture. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-09431-z

[18] Secondary Osteoporosis and Metabolic Bone Diseases. Journal of Clinical Medicine. 2022. DOI: 10.3390/jcm11092382

[19] Combinations of two imaging parameters to improve bone mineral density (BMD) assessment in patients with lumbar degenerative diseases. BMC Musculoskeletal Disorders. 2023. DOI: 10.1186/s12891-023-06888-8

[20] Osteoporosis Evaluation and Management in Spine Surgery. Journal of the American Academy of Orthopaedic Surgeons. 2024. DOI: 10.5435/jaaos-d-24-00311

[21] Based on CT at the third lumbar spine level, the skeletal muscle index and psoas muscle index can predict osteoporosis. BMC Musculoskeletal Disorders. 2022. DOI: 10.1186/s12891-022-05887-5

[22] Estimation of 10 - year probability bone fracture in a selected sample of Palestinian people using fracture risk assessment tool. BMC Musculoskeletal Disorders. 2013. DOI: 10.1186/1471-2474-14-284

[23] Bone density and its relation to the development of acromial stress fracture following reverse total shoulder arthroplasty. Shoulder & Elbow. 2020. DOI: 10.1177/1758573220949992

[24] Treatment with intravenous pamidronate is a good alternative in case of gastrointestinal side effects or contraindications for oral bisphosphonates. BMC Musculoskeletal Disorders. 2009. DOI: 10.1186/1471-2474-10-86

[25] Teriparatide treatment in severe osteoporosis – a controlled 10-year follow-up study. BMC Musculoskeletal Disorders. 2022. DOI: 10.1186/s12891-022-05987-2

[26] The impact of vitamin D status on changes in bone mineral density during treatment with bisphosphonates and after discontinuation following long-term use in post-menopausal osteoporosis. BMC Musculoskeletal Disorders. 2007. DOI: 10.1186/1471-2474-8-3

[27] Effect of drugs on bone mineral density in postmenopausal osteoporosis: a Bayesian network meta-analysis. Journal of Orthopaedic Surgery and Research. 2021. DOI: 10.1186/s13018-021-02678-x

[28] Correlation between bone turnover and metabolic markers with age and gender: a cross-sectional study of hospital information system data. BMC Musculoskeletal Disorders. 2020. DOI: 10.1186/s12891-020-03610-w

[29] Osteoporosis exacerbates perioperative complications in total knee arthroplasty: a 10-Year nationwide analysis. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-06340-8

[30] Management of Osteoporosis in Spine Surgery. Journal of the American Academy of Orthopaedic Surgeons. 2015. DOI: 10.5435/jaaos-d-14-00042

[31] Progression of vertebral deformity of prevalent vertebral fractures in the elderly: a population-based study. BMC Musculoskeletal Disorders. 2024. DOI: 10.1186/s12891-024-07254-y

[32] Evaluation of patients with a recent clinical fracture and osteoporosis, a multidisciplinary approach. BMC Musculoskeletal Disorders. 2008. DOI: 10.1186/1471-2474-9-109

[33] Calcium Deficiency and Osteoporosis: OBSERVATIONS IN ONE HUNDRED AND SIXTY-SIX PATIENTS AND CRITICAL REVIEW OF THE LITERATURE.. The Journal of Bone and Joint Surgery. American Volume. 1967.

[35] Racial and Ethnic Differences in Osteoporosis. Journal of the American Academy of Orthopaedic Surgeons. 2007. DOI: 10.5435/00124635-200700001-00008

[36] Association between muscle strength and mass and bone mineral density in the US general population: data from NHANES 1999–2002. Journal of Orthopaedic Surgery and Research. 2023. DOI: 10.1186/s13018-023-03877-4

[37] Clinical outcomes and safety of combined calcitriol and bisphosphonates in treating postmenopausal osteoporosis: a retrospective cohort study. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-05714-2

[39] Material properties of human vertebral trabecular bone under compression can be predicted based on quantitative computed tomography. BMC Musculoskeletal Disorders. 2021. DOI: 10.1186/s12891-021-04571-4

[40] Efficacy of denosumab versus alendronate for aromatase inhibitor-associated osteoporosis in postmenopausal breast cancer patients: a retrospective analysis. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-09280-w

[41] Alendronate increases BMD at appendicular and axial skeletons in patients with established osteoporosis. Journal of Orthopaedic Surgery and Research. 2007. DOI: 10.1186/1749-799x-2-9

[42] Can Bisphosphonate Therapy Reduce Overall Mortality in Patients With Osteoporosis? A Meta-analysis of Randomized Controlled Trials. Clinical Orthopaedics & Related Research. 2024. DOI: 10.1097/corr.0000000000003204

[43] Bone loss in premenopausal and postmenopausal women. A cross-sectional and longitudinal study using quantitative computed tomography.. The Journal of Bone & Joint Surgery. 1984. DOI: 10.2106/00004623-198466070-00007

[44] Breaking strength and bone microarchitecture in osteoporosis: a biomechanical approximation based on load tests in 104 human vertebrae from the cervical, thoracic, and lumbar spines of 13 body donors. Journal of Orthopaedic Surgery and Research. 2022. DOI: 10.1186/s13018-022-03105-5

[45] Effect of lumbar spinal stenosis on bone mineral density in osteoporosis patients treated with ibandronate. BMC Musculoskeletal Disorders. 2021. DOI: 10.1186/s12891-021-04273-x

[46] Impact of Teriparatide on Complications and Patient-Reported Outcomes of Patients Undergoing Long Spinal Fusion According to Bone Density. Journal of Bone and Joint Surgery. 2023. DOI: 10.2106/jbjs.23.00272

[47] Health-related quality of life of men with primary osteoporosis and its changes after bisphosphonates treatment. BMC Musculoskeletal Disorders. 2023. DOI: 10.1186/s12891-023-06397-8

[48] Efficacy of denosumab in treatment of osteoporosis in patients with rheumatoid arthritis: a meta-analysis of randomized controlled trial. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-08688-8

[49] The biology of fracture healing in osteoporosis and in the presence of anti-osteoporotic drugs. Injury. 2018. DOI: 10.1016/j.injury.2018.04.016

[52] Biomechanical role of osteoporosis affects the incidence of adjacent segment disease after percutaneous transforaminal endoscopic discectomy. Journal of Orthopaedic Surgery and Research. 2019. DOI: 10.1186/s13018-019-1166-1

[54] Treatment of Deformity of the Lower Limb in Adults Who Have Osteogenesis Imperfecta. The Journal of Bone & Joint Surgery*. 1996. DOI: 10.2106/00004623-199602000-00008

[56] Early detection of osteoporosis in adult children of patients with proximal femur fractures: a real-world screening study. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-09378-1

[57] Clinicians’ views of prescribing oral and intravenous bisphosphonates for osteoporosis: a qualitative study. BMC Musculoskeletal Disorders. 2023. DOI: 10.1186/s12891-023-06865-1

[58] Jurist, John M.; Kranendonk, Donald H.. The Journal of Bone and Joint Surgery. American Volume. 1973.

[60] Three cases of regional migratory osteoporosis. Archives of Orthopaedic and Trauma Surgery. 2003. DOI: 10.1007/s00402-003-0557-1

[61] Automated opportunistic screening for osteoporosis using deep learning-based automatic segmentation and radiomics on proximal femur images from low-dose abdominal CT. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-08631-x

[62] The Impact of Osteoporosis on 2-Year Outcomes in Patients Undergoing Long Cervical Fusion. Journal of the American Academy of Orthopaedic Surgeons. 2023. DOI: 10.5435/jaaos-d-22-00361

[63] Whole-body vibration training and bone mineral density in older adults: an updated systematic review and meta-analysis. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-09504-7

[64] The number and characteristics of prevalent vertebral fractures in elderly men are associated with low bone mass and osteoporosis. The Bone & Joint Journal. 2015. DOI: 10.1302/0301-620x.97b8.35032

[65] Construction of a predictive model for osteoporosis risk in men: using the IOF 1-min osteoporosis test. Journal of Orthopaedic Surgery and Research. 2023. DOI: 10.1186/s13018-023-04266-7

[66] Development and assessment of 3-dimensional computed tomography measures of proximal humeral bone density: a comparison to established 2-dimensional measures and intraoperative findings in patients undergoing shoulder arthroplasty. JSES International. 2021. DOI: 10.1016/j.jseint.2021.07.015

[69] Bone density of the cervical, thoracic and lumbar spine measured using Hounsfield units of computed tomography – results of 4350 vertebras. BMC Musculoskeletal Disorders. 2024. DOI: 10.1186/s12891-024-07324-1

[70] Similarities in distribution pattern between acute multiple osteoporotic vertebral compression fractures and vertebral fractures cascades. Journal of Orthopaedic Surgery and Research. 2024. DOI: 10.1186/s13018-024-05337-z

[71] Comparison of clinical outcome of lumbar spinal stenosis surgery in patients with and without osteoporosis: a prospective cohort study. Journal of Orthopaedic Surgery and Research. 2023. DOI: 10.1186/s13018-023-03935-x

[72] Co-morbid mechanisms of intervertebral disc degeneration and osteoporosis: biomechanical coupling and molecular pathways synergistically driving degenerative lesions. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-06075-6

[73] The role of humerus cortical thickness in predicting osteoporosis in MR imaging. Shoulder & Elbow. 2024. DOI: 10.1177/17585732241279090

[74] High-impact exercise in adulthood and vertebral dimensions in midlife - the Northern Finland Birth Cohort 1966 study. BMC Musculoskeletal Disorders. 2017. DOI: 10.1186/s12891-017-1794-8

[75] Efficacy of traditional Chinese exercise on postmenopausal osteoporosis: a systematic review and meta-analysis. Journal of Orthopaedic Surgery and Research. 2024. DOI: 10.1186/s13018-024-05288-5

[77] Baseline new bone formation does not predict bone loss in ankylosing spondylitis as assessed by quantitative computed tomography (QCT) - 10-year follow-up. BMC Musculoskeletal Disorders. 2011. DOI: 10.1186/1471-2474-12-121

[79] Deciphering subsidence risk after ACDF: a biomechanical study on bone density and endplate thickness. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-09255-x

[80] Short-term anabolic agent and sequential therapy to improve bone mineral density and bone turnover markers in patients with osteoporotic hip fractures. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-06084-5

[82] Deltoid tuberosity index for proximal humerus fracture: reliability and a predictor of systemic osteoporosis in an Asian population. Journal of Shoulder and Elbow Surgery. 2025. DOI: 10.1016/j.jse.2024.05.018

[83] Finite element biomechanical analysis of 3D printed intervertebral fusion cage in osteoporotic population. BMC Musculoskeletal Disorders. 2024. DOI: 10.1186/s12891-024-07221-7

[84] The correlation between volumetric bone mineral density and morphological parameters of the proximal femur and clinical outcomes in ankylosing spondylitis patients with hip involvement. BMC Musculoskeletal Disorders. 2022. DOI: 10.1186/s12891-021-04912-3

[85] Bone turnover is adequately suppressed in osteoporotic patients treated with bisphosphonates in daily practice. BMC Musculoskeletal Disorders. 2011. DOI: 10.1186/1471-2474-12-167

[86] Burden of screening and treatment of bone health markers amongst elderly patients with proximal femur fractures. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-06202-3

[88] Bone metabolism factors in predicting the risk of osteoporosis fracture in the elderly. BMC Musculoskeletal Disorders. 2024. DOI: 10.1186/s12891-024-07560-5

[89] Adverse events, bone mineral density and discontinuation associated with generic alendronate among postmenopausal women previously tolerant of brand alendronate: a retrospective cohort study. BMC Musculoskeletal Disorders. 2010. DOI: 10.1186/1471-2474-11-68

Creative Commons BY-NC 4.0

CC Creative Commons licence
BY Attribution — you must credit the source
NC NonCommercial — not for commercial use

Attribution-NonCommercial 4.0 International


Creative Commons Corporation ("Creative Commons") is not a law firm and does not provide legal services or legal advice. Distribution of Creative Commons public licenses does not create a lawyer-client or other relationship. Creative Commons makes its licenses and related information available on an "as-is" basis. Creative Commons gives no warranties regarding its licenses, any material licensed under their terms and conditions, or any related information. Creative Commons disclaims all liability for damages resulting from their use to the fullest extent possible.

Using Creative Commons Public Licenses

Creative Commons public licenses provide a standard set of terms and conditions that creators and other rights holders may use to share original works of authorship and other material subject to copyright and certain other rights specified in the public license below. The following considerations are for informational purposes only, are not exhaustive, and do not form part of our licenses.

Considerations for licensors: Our public licenses are intended for use by those authorized to give the public permission to use material in ways otherwise restricted by copyright and certain other rights. Our licenses are irrevocable. Licensors should read and understand the terms and conditions of the license they choose before applying it. Licensors should also secure all rights necessary before applying our licenses so that the public can reuse the material as expected. Licensors should clearly mark any material not subject to the license. This includes other CC- licensed material, or material used under an exception or limitation to copyright. More considerations for licensors: wiki.creativecommons.org/Considerations_for_licensors

Considerations for the public: By using one of our public licenses, a licensor grants the public permission to use the licensed material under specified terms and conditions. If the licensor's permission is not necessary for any reason--for example, because of any applicable exception or limitation to copyright--then that use is not regulated by the license. Our licenses grant only permissions under copyright and certain other rights that a licensor has authority to grant. Use of the licensed material may still be restricted for other reasons, including because others have copyright or other rights in the material. A licensor may make special requests, such as asking that all changes be marked or described. Although not required by our licenses, you are encouraged to respect those requests where reasonable. More considerations for the public: wiki.creativecommons.org/Considerations_for_licensees


Creative Commons Attribution-NonCommercial 4.0 International Public License

By exercising the Licensed Rights (defined below), You accept and agree to be bound by the terms and conditions of this Creative Commons Attribution-NonCommercial 4.0 International Public License ("Public License"). To the extent this Public License may be interpreted as a contract, You are granted the Licensed Rights in consideration of Your acceptance of these terms and conditions, and the Licensor grants You such rights in consideration of benefits the Licensor receives from making the Licensed Material available under these terms and conditions.

Section 1 -- Definitions.

a. Adapted Material means material subject to Copyright and Similar Rights that is derived from or based upon the Licensed Material and in which the Licensed Material is translated, altered, arranged, transformed, or otherwise modified in a manner requiring permission under the Copyright and Similar Rights held by the Licensor. For purposes of this Public License, where the Licensed Material is a musical work, performance, or sound recording, Adapted Material is always produced where the Licensed Material is synched in timed relation with a moving image.

b. Adapter's License means the license You apply to Your Copyright and Similar Rights in Your contributions to Adapted Material in accordance with the terms and conditions of this Public License.

c. Copyright and Similar Rights means copyright and/or similar rights closely related to copyright including, without limitation, performance, broadcast, sound recording, and Sui Generis Database Rights, without regard to how the rights are labeled or categorized. For purposes of this Public License, the rights specified in Section 2(b)(1)-(2) are not Copyright and Similar Rights.

d. Effective Technological Measures means those measures that, in the absence of proper authority, may not be circumvented under laws fulfilling obligations under Article 11 of the WIPO Copyright Treaty adopted on December 20, 1996, and/or similar international agreements.

e. Exceptions and Limitations means fair use, fair dealing, and/or any other exception or limitation to Copyright and Similar Rights that applies to Your use of the Licensed Material.

f. Licensed Material means the artistic or literary work, database, or other material to which the Licensor applied this Public License.

g. Licensed Rights means the rights granted to You subject to the terms and conditions of this Public License, which are limited to all Copyright and Similar Rights that apply to Your use of the Licensed Material and that the Licensor has authority to license.

h. Licensor means the individual(s) or entity(ies) granting rights under this Public License.

i. NonCommercial means not primarily intended for or directed towards commercial advantage or monetary compensation. For purposes of this Public License, the exchange of the Licensed Material for other material subject to Copyright and Similar Rights by digital file-sharing or similar means is NonCommercial provided there is no payment of monetary compensation in connection with the exchange.

j. Share means to provide material to the public by any means or process that requires permission under the Licensed Rights, such as reproduction, public display, public performance, distribution, dissemination, communication, or importation, and to make material available to the public including in ways that members of the public may access the material from a place and at a time individually chosen by them.

k. Sui Generis Database Rights means rights other than copyright resulting from Directive 96/9/EC of the European Parliament and of the Council of 11 March 1996 on the legal protection of databases, as amended and/or succeeded, as well as other essentially equivalent rights anywhere in the world.

l. You means the individual or entity exercising the Licensed Rights under this Public License. Your has a corresponding meaning.

Section 2 -- Scope.

a. License grant.

1. Subject to the terms and conditions of this Public License, the Licensor hereby grants You a worldwide, royalty-free, non-sublicensable, non-exclusive, irrevocable license to exercise the Licensed Rights in the Licensed Material to:

a. reproduce and Share the Licensed Material, in whole or in part, for NonCommercial purposes only; and

b. produce, reproduce, and Share Adapted Material for NonCommercial purposes only.

2. Exceptions and Limitations. For the avoidance of doubt, where Exceptions and Limitations apply to Your use, this Public License does not apply, and You do not need to comply with its terms and conditions.

3. Term. The term of this Public License is specified in Section 6(a).

4. Media and formats; technical modifications allowed. The Licensor authorizes You to exercise the Licensed Rights in all media and formats whether now known or hereafter created, and to make technical modifications necessary to do so. The Licensor waives and/or agrees not to assert any right or authority to forbid You from making technical modifications necessary to exercise the Licensed Rights, including technical modifications necessary to circumvent Effective Technological Measures. For purposes of this Public License, simply making modifications authorized by this Section 2(a) (4) never produces Adapted Material.

5. Downstream recipients.

a. Offer from the Licensor -- Licensed Material. Every recipient of the Licensed Material automatically receives an offer from the Licensor to exercise the Licensed Rights under the terms and conditions of this Public License.

b. No downstream restrictions. You may not offer or impose any additional or different terms or conditions on, or apply any Effective Technological Measures to, the Licensed Material if doing so restricts exercise of the Licensed Rights by any recipient of the Licensed Material.

6. No endorsement. Nothing in this Public License constitutes or may be construed as permission to assert or imply that You are, or that Your use of the Licensed Material is, connected with, or sponsored, endorsed, or granted official status by, the Licensor or others designated to receive attribution as provided in Section 3(a)(1)(A)(i).

b. Other rights.

1. Moral rights, such as the right of integrity, are not licensed under this Public License, nor are publicity, privacy, and/or other similar personality rights; however, to the extent possible, the Licensor waives and/or agrees not to assert any such rights held by the Licensor to the limited extent necessary to allow You to exercise the Licensed Rights, but not otherwise.

2. Patent and trademark rights are not licensed under this Public License.

3. To the extent possible, the Licensor waives any right to collect royalties from You for the exercise of the Licensed Rights, whether directly or through a collecting society under any voluntary or waivable statutory or compulsory licensing scheme. In all other cases the Licensor expressly reserves any right to collect such royalties, including when the Licensed Material is used other than for NonCommercial purposes.

Section 3 -- License Conditions.

Your exercise of the Licensed Rights is expressly made subject to the following conditions.

a. Attribution.

1. If You Share the Licensed Material (including in modified form), You must:

a. retain the following if it is supplied by the Licensor with the Licensed Material:

i. identification of the creator(s) of the Licensed Material and any others designated to receive attribution, in any reasonable manner requested by the Licensor (including by pseudonym if designated);

ii. a copyright notice;

iii. a notice that refers to this Public License;

iv. a notice that refers to the disclaimer of warranties;

v. a URI or hyperlink to the Licensed Material to the extent reasonably practicable;

b. indicate if You modified the Licensed Material and retain an indication of any previous modifications; and

c. indicate the Licensed Material is licensed under this Public License, and include the text of, or the URI or hyperlink to, this Public License.

2. You may satisfy the conditions in Section 3(a)(1) in any reasonable manner based on the medium, means, and context in which You Share the Licensed Material. For example, it may be reasonable to satisfy the conditions by providing a URI or hyperlink to a resource that includes the required information.

3. If requested by the Licensor, You must remove any of the information required by Section 3(a)(1)(A) to the extent reasonably practicable.

4. If You Share Adapted Material You produce, the Adapter's License You apply must not prevent recipients of the Adapted Material from complying with this Public License.

Section 4 -- Sui Generis Database Rights.

Where the Licensed Rights include Sui Generis Database Rights that apply to Your use of the Licensed Material:

a. for the avoidance of doubt, Section 2(a)(1) grants You the right to extract, reuse, reproduce, and Share all or a substantial portion of the contents of the database for NonCommercial purposes only;

b. if You include all or a substantial portion of the database contents in a database in which You have Sui Generis Database Rights, then the database in which You have Sui Generis Database Rights (but not its individual contents) is Adapted Material; and

c. You must comply with the conditions in Section 3(a) if You Share all or a substantial portion of the contents of the database.

For the avoidance of doubt, this Section 4 supplements and does not replace Your obligations under this Public License where the Licensed Rights include other Copyright and Similar Rights.

Section 5 -- Disclaimer of Warranties and Limitation of Liability.

a. UNLESS OTHERWISE SEPARATELY UNDERTAKEN BY THE LICENSOR, TO THE EXTENT POSSIBLE, THE LICENSOR OFFERS THE LICENSED MATERIAL AS-IS AND AS-AVAILABLE, AND MAKES NO REPRESENTATIONS OR WARRANTIES OF ANY KIND CONCERNING THE LICENSED MATERIAL, WHETHER EXPRESS, IMPLIED, STATUTORY, OR OTHER. THIS INCLUDES, WITHOUT LIMITATION, WARRANTIES OF TITLE, MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, NON-INFRINGEMENT, ABSENCE OF LATENT OR OTHER DEFECTS, ACCURACY, OR THE PRESENCE OR ABSENCE OF ERRORS, WHETHER OR NOT KNOWN OR DISCOVERABLE. WHERE DISCLAIMERS OF WARRANTIES ARE NOT ALLOWED IN FULL OR IN PART, THIS DISCLAIMER MAY NOT APPLY TO YOU.

b. TO THE EXTENT POSSIBLE, IN NO EVENT WILL THE LICENSOR BE LIABLE TO YOU ON ANY LEGAL THEORY (INCLUDING, WITHOUT LIMITATION, NEGLIGENCE) OR OTHERWISE FOR ANY DIRECT, SPECIAL, INDIRECT, INCIDENTAL, CONSEQUENTIAL, PUNITIVE, EXEMPLARY, OR OTHER LOSSES, COSTS, EXPENSES, OR DAMAGES ARISING OUT OF THIS PUBLIC LICENSE OR USE OF THE LICENSED MATERIAL, EVEN IF THE LICENSOR HAS BEEN ADVISED OF THE POSSIBILITY OF SUCH LOSSES, COSTS, EXPENSES, OR DAMAGES. WHERE A LIMITATION OF LIABILITY IS NOT ALLOWED IN FULL OR IN PART, THIS LIMITATION MAY NOT APPLY TO YOU.

c. The disclaimer of warranties and limitation of liability provided above shall be interpreted in a manner that, to the extent possible, most closely approximates an absolute disclaimer and waiver of all liability.

Section 6 -- Term and Termination.

a. This Public License applies for the term of the Copyright and Similar Rights licensed here. However, if You fail to comply with this Public License, then Your rights under this Public License terminate automatically.

b. Where Your right to use the Licensed Material has terminated under Section 6(a), it reinstates:

1. automatically as of the date the violation is cured, provided it is cured within 30 days of Your discovery of the violation; or

2. upon express reinstatement by the Licensor.

For the avoidance of doubt, this Section 6(b) does not affect any right the Licensor may have to seek remedies for Your violations of this Public License.

c. For the avoidance of doubt, the Licensor may also offer the Licensed Material under separate terms or conditions or stop distributing the Licensed Material at any time; however, doing so will not terminate this Public License.

d. Sections 1, 5, 6, 7, and 8 survive termination of this Public License.

Section 7 -- Other Terms and Conditions.

a. The Licensor shall not be bound by any additional or different terms or conditions communicated by You unless expressly agreed.

b. Any arrangements, understandings, or agreements regarding the Licensed Material not stated herein are separate from and independent of the terms and conditions of this Public License.

Section 8 -- Interpretation.

a. For the avoidance of doubt, this Public License does not, and shall not be interpreted to, reduce, limit, restrict, or impose conditions on any use of the Licensed Material that could lawfully be made without permission under this Public License.

b. To the extent possible, if any provision of this Public License is deemed unenforceable, it shall be automatically reformed to the minimum extent necessary to make it enforceable. If the provision cannot be reformed, it shall be severed from this Public License without affecting the enforceability of the remaining terms and conditions.

c. No term or condition of this Public License will be waived and no failure to comply consented to unless expressly agreed to by the Licensor.

d. Nothing in this Public License constitutes or may be interpreted as a limitation upon, or waiver of, any privileges and immunities that apply to the Licensor or You, including from the legal processes of any jurisdiction or authority.


Creative Commons is not a party to its public licenses. Notwithstanding, Creative Commons may elect to apply one of its public licenses to material it publishes and in those instances will be considered the “Licensor.” The text of the Creative Commons public licenses is dedicated to the public domain under the CC0 Public Domain Dedication. Except for the limited purpose of indicating that material is shared under a Creative Commons public license or as otherwise permitted by the Creative Commons policies published at creativecommons.org/policies, Creative Commons does not authorize the use of the trademark "Creative Commons" or any other trademark or logo of Creative Commons without its prior written consent including, without limitation, in connection with any unauthorized modifications to any of its public licenses or any other arrangements, understandings, or agreements concerning use of licensed material. For the avoidance of doubt, this paragraph does not form part of the public licenses.

Creative Commons may be contacted at creativecommons.org.