骨骼健康与骨质疏松症 资料

本页面由机器翻译,尚未经临床医生审核。英文版本为权威版本。

您的感受

骨质疏松症意味着您的骨骼失去了部分强度。在骨折发生之前,它通常完全没有症状。如果骨折是在轻微绊倒或轻微碰撞后发生的,就称为脆性骨折。常见部位是腕部、髋部和脊柱的骨骼。

如果您脊柱的某块骨骼变得脆弱,您可能会在该处感到疼痛。当您从椅子上站起、提起物品或扭转身体时,疼痛常会加剧。休息和平躺可能会缓解疼痛。有些人发现,清晨刚起床时或站立一段时间后疼痛更明显。腕部骨折会让倒水壶、端起沉重的锅或提购物袋变得困难。脊柱骨折会让弯腰穿鞋或起床变得不舒服。

还有一点值得了解。许多以这种方式发生骨折的人从未被告知自己患有骨质疏松症。骨折得到了治疗,但潜在的骨骼脆弱却未被诊断,也未得到治疗。这一空白很重要,因为治疗骨骼脆弱可将再次骨折的几率降低多达 50%,并将死亡率降低多达 30%。

体重较高与较低的风险相关。体质指数每升高 1 个单位,骨质疏松症风险降低 9%。体质指数(BMI)是衡量体重相对于身高的指标。

如果您患有骨质疏松症,同时又需要进行肩部手术,现有证据可以让您放心一些。骨密度降低的人在接受关节镜(微创)肩袖修复术后仍然恢复良好,这种手术是外科医生通过小切口修复撕裂的肩部肌腱。总体并发症发生率较低,骨质疏松症并不是排除该手术的理由。

您的外科医生可以为您安排骨密度扫描,并与您讨论治疗方案。

实际发生了什么

骨骼是活组织。您的身体在不断分解旧骨,并生成新骨来替代它。大约从中年开始,生成新骨的速度会放缓。被清除的骨量多于被替代的骨量,剩下的骨骼变得更薄、密度更低。

可以把骨骼想象成墙壁内部的木质框架。健康的骨骼有粗壮的支柱,彼此紧密排列。患骨质疏松症时,这些支柱会变细,有些甚至完全消失。框架仍然能撑起墙壁,但储备能力减少了。这就是为什么一次轻微的绊倒或碰撞就足以导致腕部、髋部或脊柱骨骼骨折,也是为什么脊柱骨折后的疼痛会在您站立、提物或扭转身体时加剧。

这其中还有第二部分值得了解。骨折本身得到了治疗,但其背后的骨骼脆弱却常常未被诊断,也未得到治疗。

预期情况

骨质疏松症本身是悄无声息的。它不会酸痛或跳痛,也不会时好时坏。大多数人在骨折之前毫无感觉。这就是为什么脆性骨折往往是第一个信号,也是为什么其背后的骨骼脆弱如此容易被忽视。

预后取决于接下来发生什么。如果骨折得到了治疗,但骨骼脆弱没有得到处理,您仍有再次骨折的风险,通常发生在腕部、髋部或脊柱。这是实事求是的情况:治疗潜在的问题会改变您未来多年的状况。

要做到这一点,首先需要诊断。骨密度扫描可以测量您骨骼的强度。您的外科医生可以为您安排扫描,并与您讨论治疗方案。增强骨骼强度的药物作用方式各不相同。有些先促进新骨生成,然后维持住新骨。另一些则减缓骨骼的分解。按这个顺序使用时,它们构成了一种针对高风险人群的公认治疗方案。也有一些较老的选择,但它们的效果不如现代药物,通常仅用于无法使用一线治疗的人群。

骨折后的恢复是一个单独的过程。腕部骨折或脊柱骨折需要数周到数月而不是数天才能恢复,在活动能力和力量逐步恢复的过程中,您的物理治疗师可以为您提供指导。如果您之后因肌腱撕裂需要进行肩部手术,骨密度降低并不会对情况造成太大改变。骨骼较脆弱的人在关节镜(微创)肩袖修复术后两年仍然恢复良好,这种手术是外科医生通过小切口修复肌腱。术后前三个月的并发症发生率总体较低,不过在这段时间内,骨质疏松症患者出现的内科问题比没有骨质疏松症的人略多。

实事求是的结论是:骨质疏松症不会自行好转,但它可以被发现、测量和治疗。只要管理得当,就能降低您再次骨折的几率。


Evidence & references

This is the clinical evidence summary written for health professionals. It is technical, and it lists the research this page was built from. You do not need to read it to understand your treatment or to make a decision about it.

Overview

  • A bone density-based aging model approach may facilitate and support the development of precision medicine strategies in osteoporosis prevention and management [1].
  • There is evidence of a care gap between the occurrence of a fragility fracture and the diagnosis and treatment of osteoporosis in Canada [2].
  • Investigators must select an osteoporotic fracture model that best reflects the clinical problem being studied and the underlying pathophysiology of the osteoporosis in the target patient group [3].
  • Current online health information on osteoporosis often fails to meet basic standards of evidence-based health information, highlighting the urgent need to improve quality to support informed decision-making [4].
  • Each 1-unit increase in body mass index was associated with a 9% reduction in osteoporosis risk based on a dose-response analysis of nine studies [5].
  • Sequential anabolic-to-anti-resorptive therapy may inform treatment guidelines for high-risk postmenopausal populations [6].
  • The book "Radiology of Osteoporosis" summarises the thoroughly researched topic of osteoporosis in a scientific approach [7].
  • Current evidence suggests that the efficacy of acupuncture in improving the symptoms of primary osteoporosis is encouraging for its use in clinical practice as a physical intervention [8].
  • Findings regarding osteoporosis in long-term hospitalized patients with muscular dystrophy may help inform strategies for osteoporotic treatment and nutritional care in this patient population [9].
  • There is no perfect model for osteoporosis, but a variety of models are appropriate for answering specific questions [10].
  • Randomized controlled trials have demonstrated that treatment of osteoporosis in patients with fragility fractures can reduce the risk of subsequent fractures by up to 50% and mortality rates by up to 30% [11].
  • Machine learning application to hand radiographs represents a possible step toward more accessible, cost-effective, automated diagnosis and therefore earlier treatment of osteoporosis/osteopenia [12].
  • Intranasal salmon calcitonin is less effective than bisphosphonates and modern anabolic agents for increasing bone mineral density and reducing fracture risk [13].
  • Intranasal salmon calcitonin use is best reserved for patients who cannot take first-line therapies due to contraindications, intolerance, or personal preference [13].
  • A fracture risk prediction model was successfully developed and validated for patients newly diagnosed with osteoporosis based on routine blood test markers [14].
  • A nomogram with an online dynamic calculator could facilitate the early prediction, diagnosis, and treatment of osteoporosis, contributing to the bone health of the elderly population and promoting the development of public health [15].
  • Patients with decreased bone mineral density can still achieve excellent 2-year outcomes following arthroscopic rotator cuff repair [16].
  • Low rates of osteoporotic pharmacotherapy were seen in patients who had femoral neck fractures despite established guidelines [19].
  • Patients with osteoporosis may experience a higher incidence of medical complications within the 90-day global period than nonosteoporotic patients following rotator cuff repair [21].
  • Overall rates of complication were low and osteoporosis should not be considered a contraindication to arthroscopic rotator cuff repair [22].
  • The standard Fragility Index is advocated for dichotomous data and the Continuous Fragility Index for continuous outcomes, recognizing the distinct valuable insights each metric offers [37].

How It Works

Risk Prediction and Screening

  • A bone density-based aging model approach may facilitate the development of precision medicine strategies in osteoporosis prevention and management [1].
  • Each 1-unit increase in BMI is associated with a 9% reduction in osteoporosis risk based on a dose-response analysis of nine studies [5].
  • A fracture risk prediction model for patients newly diagnosed with osteoporosis was successfully developed and validated using routine blood test markers [14].
  • A nomogram with an online dynamic calculator could facilitate the early prediction, diagnosis, and treatment of osteoporosis [15].
  • Current machine learning-based prediction models for postmenopausal osteoporosis without fractures demonstrate good discriminative ability but are characterized by a high risk of bias, a lack of calibration performance evaluation, and insufficient validation of clinical utility [18].
  • Machine learning application to hand radiographs represents a possible step toward more accessible, cost-effective, automated diagnosis and earlier treatment of osteoporosis or osteopenia [12].

Pathophysiology and Mechanisms

  • The gut microbiota–metabolite–bone network may be involved in the skeletal effects of leptin, providing mechanistic insights and potential therapeutic strategies for osteoporosis management [23].
  • Macrophage polarization-related genes with potential causal roles in osteoporosis were identified in a multi-omics Mendelian randomization study, though findings are exploratory and require validation in bone marrow-specific and functional studies [30].
  • MiR-137 promotes TLR4/NF-κB pathway activity through targeting KDM4A, which inhibits osteogenic differentiation of human bone marrow mesenchymal stem cells and aggravates osteoporosis [31].
  • Obesity-associated dyslipidemia drives bone mineral density loss partly through inflammation-mediated pathways, with key inflammatory cytokines significantly mediating lipid metabolism's impact on bone health [32].

Treatment and Management

  • Intranasal salmon calcitonin is less effective than bisphosphonates and modern anabolic agents for increasing bone mineral density and reducing fracture risk, and its use is best reserved for patients who cannot take first-line therapies due to contraindications, intolerance, or personal preference [13].
  • The efficacy of acupuncture in improving the symptoms of primary osteoporosis is encouraging for its use in clinical practice as a physical intervention [8].
  • Natural traditional Chinese medicine products provide a theoretical and experimental basis for the development of new drugs and the improvement of osteoporosis management [24].
  • A randomized controlled trial on the timing optimization of teriparatide dosing is expected to provide insights into optimizing administration timing to enhance bone formation and reduce fracture risk [17].
  • Key recommendations for people with osteoporosis include undertaking resistance and impact exercise to maximise bone strength, activities to improve strength and balance to reduce falls, and spinal extension exercise to improve posture and potentially reduce risk of falls and vertebral fractures [20].

Fracture Healing and Surgical Outcomes

  • There is promising experimental and clinical evidence for possible enhancement of the bone repair process via administration of systemic agents [25].
  • The use of bone mineral density measurements preoperatively to identify osteoporosis as a possible risk factor of nonunion has no clinical value [26].
  • In humans, de novo use of bisphosphonate therapy after fracture does not appear to have a significant effect on fracture healing [27].
  • Patients who received PTH (1–84) injections accelerated radiographic and clinical fracture healing to 7.8 weeks when compared to patients who received no treatment at 12.6 weeks [28].

Care Gaps and Information Quality

What the Evidence Shows

Risk Factors and Prediction

  • Each 1-unit increase in BMI is associated with a 9% reduction in osteoporosis risk [5].
  • A nomogram with an online dynamic calculator for predicting osteoporosis could facilitate early prediction, diagnosis, and treatment of the condition [15].
  • Mendelian randomization results show significant associations for Type 2 Diabetes on femoral neck and total body BMD, and HbA1c on heel BMD [38].

Diagnosis and Screening

  • Current online health information on osteoporosis often fails to meet basic standards of evidence-based health information [4].

Treatment and Management

  • Intranasal salmon calcitonin is less effective than bisphosphonates and modern anabolic agents for increasing BMD and reducing fracture risk, and its use is best reserved for patients who cannot take first-line therapies due to contraindications, intolerance, or personal preference [13].
  • Acupuncture efficacy in improving the symptoms of primary osteoporosis is encouraging for its use in clinical practice as a physical intervention [8].
  • Jintiange capsules are a good choice for patients with osteoporosis in terms of relieving pain, improving BMD, improving activity function, improving gait, and preventing fracture [34].
  • Genetically modified stem cell therapy is a safe and effective method that can significantly improve BMD and BV/TV in animal models of osteoporosis [36].
  • The gut microbiota–metabolite–bone network may be involved in the skeletal effects of leptin, providing novel mechanistic insights and potential therapeutic strategies for osteoporosis management [23].
  • A randomized controlled trial on teriparatide dosing timing is expected to provide insights into optimizing administration to enhance bone formation and reduce fracture risk in osteoporosis [17].

Fracture Healing and Surgical Outcomes

  • Patients who received PTH (1–84) injections accelerated radiographic and clinical fracture healing to 7.8 weeks compared to 12.6 weeks in patients who received no treatment [28].
  • There is some promising experimental and clinical evidence for possible enhancement of the bone repair process via administration of systemic agents [25].
  • Osteoporosis should not be considered a contraindication to arthroscopic rotator cuff repair, as overall rates of complication were low [22].
  • In osteopenic and osteoporotic patients undergoing total joint arthroplasty, rates of 2- and 5-year postoperative complications were low and similar among patients who used perioperative proton pump inhibitors and those who did not [29].
  • Continuous bone cement and standardized treatment for osteoporosis were guarantees of good clinical outcomes for percutaneous vertebroplasty, with injected bone cement >5.5 ml potentially being a guarantee [33].

Care Gaps and Guidelines

  • Despite established guidelines, low rates of osteoporotic pharmacotherapy were seen in patients who had femoral neck fractures [19].

Research Models

Practical Considerations

Risk Prediction and Screening

  • Each 1-unit increase in body mass index is associated with a 9% reduction in osteoporosis risk [5].
  • The prevalence of osteoporosis among postmenopausal women hospitalized for fractures in China is 76.9% [35].
  • Prolonged menopause, vertebral fractures, and recent fracture history are key risk profiles for osteoporosis in postmenopausal women hospitalized for fractures [35].

Diagnostic and Information Quality

  • There is a care gap between the occurrence of a fragility fracture and the diagnosis and treatment of osteoporosis in Canada [2].
  • Despite established guidelines, low rates of osteoporotic pharmacotherapy are observed in patients who have femoral neck fractures [19].

Pharmacological Management

  • The use of intranasal salmon calcitonin is best reserved for patients who cannot take first-line therapies due to contraindications, intolerance, or personal preference [13].
  • A randomized controlled trial is expected to provide insights into optimizing teriparatide administration timing to enhance bone formation and reduce fracture risk [17].

Non-Pharmacological and Adjunctive Interventions

  • People with osteoporosis should undertake resistance and impact exercise to maximize bone strength [20].
  • People with osteoporosis should undertake activities to improve strength and balance to reduce falls [20].
  • People with osteoporosis should undertake spinal extension exercise to improve posture and potentially reduce the risk of falls and vertebral fractures [20].

Surgical Considerations

  • Patients with decreased bone mineral density can achieve excellent 2-year outcomes following arthroscopic rotator cuff repair [16].
  • Overall rates of complication are low and osteoporosis should not be considered a contraindication to arthroscopic rotator cuff repair [22].
  • The use of preoperative bone mineral density measurements to identify osteoporosis as a possible risk factor for nonunion has no clinical value [26].
  • In osteopenic and osteoporotic patients undergoing total joint arthroplasty, rates of 2- and 5-year postoperative complications are low and similar among patients who used proton pump inhibitors perioperatively and those who did not [29].

Research Methodology

Key Evidence

  • [L3] This approach may facilitate and support the development of precision medicine strategies in osteoporosis prevention and management. [1] (10.1186/s12891-025-09298-0)
  • [L4] There is evidence of a care gap between the occurrence of a fragility fracture and the diagnosis and treatment of osteoporosis in Canada. [2] (10.1186/1471-2474-5-11)
  • [L5] Investigators must select a model that best reflects the clinical problem being studied, and the underlying pathophysiology of the osteoporosis in the target patient group. [3] (10.1016/s0020-1383(16)30004-3)
  • [Paper] Current OHI on osteoporosis often fails to meet basic standards of EBHI, highlighting the urgent need to improve the quality to support informed decision-making. [4] (10.1186/s12891-026-09711-2)
  • [L1] Based on our dose–response analysis of nine studies, each 1-unit increase in BMI was associated with a 9% reduction in osteoporosis risk. [5] (10.1186/s12891-026-09675-3)
  • [L1] This sequential anabolic-to-anti-resorptive therapy may inform treatment guidelines for high-risk postmenopausal populations. [6] (10.1186/s13018-025-06040-3)
  • [Paper] The book summarises the thoroughly researched topic of osteoporosis in a scientific approach. [7] (10.1016/s0020-1383(03)00201-8)
  • [L1] The current evidence suggests that the efficacy of acupuncture in improving the symptoms of primary osteoporosis is encouraging for its use in clinical practice as a physical intervention. [8] (10.1186/s13018-025-05513-9)
  • [L4] These findings may help inform strategies for osteoporotic treatment and nutritional care in this patient population. [9] (10.1186/s12891-026-10045-2)
  • [Paper] However, there is no perfect model for osteoporosis, but a variety of models appropriate for answering specific questions. [10] (10.1016/s0020-1383(16)30002-x)
  • [Paper] Randomized controlled trials have demonstrated that treatment of osteoporosis in patients with fragility fractures can reduce the risk of subsequent fractures by up to 50% and mortality rates by up to 30%. [11] (10.1016/s0020-1383(16)30014-6)
  • [L2] The findings represent a possible step toward more accessible, cost-effective, automated diagnosis and therefore earlier treatment of osteoporosis/osteopenia. [12] (10.1016/j.jhsa.2024.09.008)
  • [Paper] IN-CAL is less effective than bisphosphonates and modern anabolic agents for increasing BMD and reducing fracture risk; accordingly, its use is best reserved for patients who cannot take first-line therapies due to contraindications, intolerance, or personal preference. [13] (10.2106/jbjs.rvw.26.00021)
  • [L3] We successfully developed and validated a fracture risk prediction model for patients newly diagnosed with osteoporosis. [14] (10.1186/s12891-026-09768-z)
  • [L3] Ultimately, this tool could facilitate the early prediction, diagnosis, and treatment of osteoporosis, thus contributing to the bone health of the elderly population and promoting the development of public health. [15] (10.1186/s12891-026-09920-9)
  • [L3] Patients with decreased bone mineral density can still achieve excellent 2-year outcomes. [16] (10.1016/j.jse.2025.02.011)
  • [L2] This trial is expected to provide crucial insights into optimizing teriparatide administration timing, potentially guiding personalized dosing strategies to enhance bone formation and reduce fracture risk in osteoporosis. [17] (10.1186/s13018-025-06083-6)
  • [L1] Current machine learning-based prediction models for postmenopausal osteoporosis without fractures demonstrate good discriminative ability but are generally characterized by a high risk of bias, a notable lack of calibration performance evaluation, and insufficient validation of clinical utility. [18] (10.1186/s12891-025-09385-2)
  • [L3] Despite established guidelines, low rates of osteoporotic pharmacotherapy were seen in patients who had femoral neck fractures. [19] (10.1016/j.arth.2025.07.028)
  • [L5] Key recommendations are that people with osteoporosis should undertake (1) resistance and impact exercise to maximise bone strength; (2) activities to improve strength and balance to reduce falls; (3) spinal extension exercise to improve posture and potentially reduce risk of falls and vertebral fractures. [20] (10.1136/bjsports-2021-104634)
  • [L3] In addition, patients with osteoporosis may experience a higher incidence of medical complications within the 90-day global period than nonosteoporotic patient. [21] (10.1016/j.xrrt.2026.100723)
  • [L3] Overall rates of complication were low and osteoporosis should not be considered a contraindication to arthroscopic RCR. [22] (10.1016/j.jseint.2026.101678)
  • [Paper] These findings suggest that the gut microbiota–metabolite–bone network may be involved in the skeletal effects of leptin, providing novel mechanistic insights and potential therapeutic strategies for osteoporosis management. [23] (10.1186/s12891-026-09950-3)
  • [L4] This paper summarises recent research progress on natural TCM products in preventing and treating osteoporosis and provides a theoretical and experimental basis for the development of new drugs and the improvement of osteoporosis management. [24] (10.1186/s13018-025-05879-w)
  • [Paper] There is some promising experimental and clinical evidence for possible enhancement of the bone repair process via administration of systemic agents. [25] (10.1016/s0020-1383(16)30003-1)
  • [L3] These results indicate that the use of BMD measurements preoperatively to identify osteoporosis as a possible risk factor of nonunion has no clinical value. [26] (10.1016/s0020-1383(11)70106-1)
  • [L4] In humans, de novo use of bisphosphonate therapy after fracture does not appear to have a significant effect on fracture healing. [27] (10.1016/s0020-1383(16)30015-8)
  • [Paper] Patients who received the PTH (1–84) injections accelerated radiographic and clinical fracture healing (7.8 weeks) when compared to patients who received no treatment (12.6 weeks). [28] (10.1016/s0020-1383(16)30009-2)
  • [L3] In osteopenic and osteoporotic patients undergoing TJA, rates of 2- and 5-year postoperative complications were low and similar among patients who used PPIs perioperatively and those who did not. [29] (10.1016/j.arth.2025.07.067)
  • [Paper] These findings are exploratory and hypothesis-generating and require validation in bone marrow-specific and functional studies. [30] (10.1186/s13018-026-06905-1)
  • [Paper] This mechanism inhibits osteogenic differentiation of human bone marrow mesenchymal stem cells and aggravates osteoporosis. [31] (10.1186/s13018-023-03918-y)
  • [L4] Obesity-associated dyslipidemia drives BMD loss partly through inflammation-mediated pathways, with key inflammatory cytokines significantly mediating lipid metabolism's impact on bone health. [32] (10.1186/s12891-026-09576-5)
  • [L3] Continuous bone cement and standardized treatment for osteoporosis were guarantees of good clinical outcomes for PVP, and injected bone cement >5.5 ml might be a guarantee. [33] (10.1186/s12891-024-08153-y)
  • [L1] In terms of relieving pain, improving BMD, improving activity function, and improving gait and preventing fracture, JTG is a good choice for patients with osteoporosis (OP). [34] (10.1186/s12891-025-08694-w)
  • [L4] This study reveals an alarmingly high prevalence (76.9%) of osteoporosis among postmenopausal women hospitalized for fractures in China, identifying prolonged menopause, vertebral fractures, and recent fracture history as key risk profiles. [35] (10.1186/s12891-026-09517-2)
  • [L1] Genetically modified stem cell therapy is a safe and effective method that can significantly improve the BMD and BV/TV in animal models of osteoporosis. [36] (10.1186/s12891-025-08507-0)
  • [Paper] We advocate for the complementary use of both the standard Fragility Index (FI) for dichotomous data and the Continuous Fragility Index (CFI) for continuous outcomes, recognizing the distinct valuable insights each metric offers. [37] (10.1177/23259671251409149)
  • [Paper] The results show varying associations across different BMD sites (femoral neck, lumbar spine, heel, total body) and methods (IVW, MR-Egger, Weighted median), with some significant associations found for T2D on femoral neck and total body BMD, and HbA1c on heel BMD. [38] (10.1186/s12891-024-07430-0)

References

[1] Unveiling risk factors and predicting osteoporosis through bone density based aging model: a community-based cohort in Guangdong, China. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-09298-0

[2] The osteoporosis care gap in Canada. BMC Musculoskeletal Disorders. 2004. DOI: 10.1186/1471-2474-5-11

[3] Main differences in osteoporotic fracture models: which should I use?. Injury. 2016. DOI: 10.1016/s0020-1383(16)30004-3

[4] Mapping the quality of information on osteoporosis: a cross-sectional analysis of online health information. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-09711-2

[5] The association between body mass index and osteoporosis, with consideration of sex differences: a systematic review and dose-response meta-analysis. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-09675-3

[6] Effectiveness of anabolic and anti-resorptive agents for preventing postmenopausal osteoporosis fractures: a systematic review and network meta-analysis. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-06040-3

[7] Radiology of Osteoporosis. Injury. 2004. DOI: 10.1016/s0020-1383(03)00201-8

[8] Efficacy of acupuncture for primary osteoporosis: a systematic review and meta-analysis of randomized controlled trials. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-05513-9

[9] Osteoporosis in long-term hospitalized patients with muscular dystrophy: a retrospective cross-sectional study. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-10045-2

[10] Can we induce osteoporosis in animals comparable to the human situation?. Injury. 2016. DOI: 10.1016/s0020-1383(16)30002-x

[11] Medical management of osteoporosis and the surgeons' role. Injury. 2016. DOI: 10.1016/s0020-1383(16)30014-6

[12] Application of Machine Learning to Osteoporosis and Osteopenia Screening Using Hand Radiographs. The Journal of Hand Surgery. 2025. DOI: 10.1016/j.jhsa.2024.09.008

[13] Revisiting Intranasal Salmon Calcitonin: Historical Osteoporosis Evidence and a Potential Role in Acute Orthopaedic Pain Management. JBJS Reviews. 2026. DOI: 10.2106/jbjs.rvw.26.00021

[14] SuperLearner approach for predicting imminent risk of fracture in older Chinese patients with newly diagnosed osteoporosis based on their routine blood test markers. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-09768-z

[15] A nomogram with online dynamic calculator for predicting osteoporosis: development and validation based on NHANES. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-09920-9

[16] 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

[17] Timing optimization of teriparatide dosing for postmenopausal osteoporosis: a randomized controlled trial. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-06083-6

[18] Risk prediction models for postmenopausal osteoporosis: a systematic review and meta-analysis study. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-025-09385-2

[19] A Missed Opportunity? Osteoporosis Treatment Following Femoral Neck Fractures: Reducing the Risk of Secondary Hip Fracture. The Journal of Arthroplasty. 2026. DOI: 10.1016/j.arth.2025.07.028

[20] Strong, steady and straight: UK consensus statement on physical activity and exercise for osteoporosis. British Journal of Sports Medicine. 2022. DOI: 10.1136/bjsports-2021-104634

[21] Impact of osteoporosis on post-operative outcomes following rotator cuff repair. JSES Reviews, Reports, and Techniques. 2026. DOI: 10.1016/j.xrrt.2026.100723

[22] Osteoporosis is a risk factor for complications and reoperations at 1 and 3 years after arthroscopic rotator cuff repair. JSES International. 2026. DOI: 10.1016/j.jseint.2026.101678

[23] Role and mechanism of leptin in improving osteoporosis via the “gut–bone axis”. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-09950-3

[24] Natural traditional Chinese medicine products: emerging therapeutic targets for the treatment of osteoporosis. Journal of Orthopaedic Surgery and Research. 2025. DOI: 10.1186/s13018-025-05879-w

[25] Fracture repair: general aspects and influence of osteoporosis and anti-osteoporosis treatment. Injury. 2016. DOI: 10.1016/s0020-1383(16)30003-1

[26] A89 Osteoporosis is not a risk factor for the development of nonunion: a cohort nested case-control study. Injury. 2011. DOI: 10.1016/s0020-1383(11)70106-1

[27] How do bisphosphonates affect fracture healing?. Injury. 2016. DOI: 10.1016/s0020-1383(16)30015-8

[28] Use of teriparatide in osteoporotic fracture patients. Injury. 2016. DOI: 10.1016/s0020-1383(16)30009-2

[29] Effects of Perioperative Proton Pump Inhibitor Use on Outcomes of Total Joint Arthroplasty Patients Who Have Osteoporosis and Osteopenia. The Journal of Arthroplasty. 2026. DOI: 10.1016/j.arth.2025.07.067

[30] Macrophage polarization-related genes with potential causal roles in osteoporosis: a multi-omics Mendelian randomization study. Journal of Orthopaedic Surgery and Research. 2026. DOI: 10.1186/s13018-026-06905-1

[31] MiR-137 promotes TLR4/NF-κB pathway activity through targeting KDM4A, inhibits osteogenic differentiation of human bone marrow mesenchymal stem cells and aggravates osteoporosis. Journal of Orthopaedic Surgery and Research. 2023. DOI: 10.1186/s13018-023-03918-y

[32] Perioperative inflammatory cytokines nursing screening test indicate the link between dysregulated lipid metabolism and reduced bone mineral density in obese osteoporosis patients: a retrospective study. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-09576-5

[33] Continuity and volume of bone cement and anti osteoporosis treatment were guarantee of good clinical outcomes for percutaneous vertebroplasty: a multicenter study. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-024-08153-y

[34] The effect of Jintiange capsules on pain in patients with primary osteoporosis: a systematic review and meta-analysis. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-08694-w

[35] How prevalent is osteoporosis in a high-risk subgroup? A multicenter study of postmenopausal women hospitalized for fractures in China. BMC Musculoskeletal Disorders. 2026. DOI: 10.1186/s12891-026-09517-2

[36] Genetically modified stem cells for osteoporosis: a systematic review and meta-analysis of preclinical studies. BMC Musculoskeletal Disorders. 2025. DOI: 10.1186/s12891-025-08507-0

[37] Fragility of Assumptions: Response. Orthopaedic Journal of Sports Medicine. 2026. DOI: 10.1177/23259671251409149

[38] Diabetes and osteoporosis: a two-sample mendelian randomization study. BMC Musculoskeletal Disorders. 2024. DOI: 10.1186/s12891-024-07430-0