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骨质减少症:流行病学、诊断和治疗-事实和数字。

Osteosarcopenia: epidemiology, diagnosis, and treatment-facts and numbers.

机构信息

Department of Medicine, Western Health, Melbourne Medical School, University of Melbourne, Melbourne, Australia.

Australian Institute for Musculoskeletal Science (AIMSS), University of Melbourne and Western Health, Melbourne, Australia.

出版信息

J Cachexia Sarcopenia Muscle. 2020 Jun;11(3):609-618. doi: 10.1002/jcsm.12567. Epub 2020 Mar 22.

Abstract

BACKGROUND

Osteosarcopenia, the presence of osteopenia/osteoporosis and sarcopenia, is an emerging geriatric giant, which poses a serious global health burden.

METHODS AND RESULTS

The prevalence of osteosarcopenia ranges in community-dwelling older adults [5-37% (≥65 years)] with the highest rates observed in those with fractures (low-trauma fracture: ~46%; hip fracture: 17.1-96.3%). Among 2353 community-dwelling adults, risk factors associated with osteosarcopenia include older age [men: 14.3% (60-64 years) to 59.4% (≥75 years); women: 20.3% (60-64 years) to 48.3% (≥75 years), P < 0.05], physical inactivity [inverse relationship: 0.64, 95% confidence interval (CI) 0.46-0.88 (sexes combined)], low body mass index (inverse relationship: men: 0.84, 95% CI 0.81-0.88; women: 0.77, 95% CI 0.74-0.80), and higher fat mass (men: 1.46, 95% CI 1.11-1.92; women: 2.25, 95% CI 1.71-2.95). Among 148 geriatric inpatients, osteosarcopenic individuals demonstrate poorer nutritional status (mini-nutritional assessment scores: 8.50 ± 2.52 points, P < 0.001) vs. osteoporosis or sarcopenia alone, while among 253 older Australians, osteosarcopenia is associated with impaired balance and functional capacity [odds ratios (ORs): 2.56-7.19; P < 0.05] vs. non-osteosarcopenia. Osteosarcopenia also associates with falls (ORs: 2.83-3.63; P < 0.05), fractures (ORs: 3.86-4.38; P < 0.05), and earlier death [hazard ratio (1-year follow-up): 1.84, 95% CI; 0.69-4.92, P = 0.023] vs. non-osteosarcopenia.

CONCLUSIONS

This syndrome is expected to grow in age-related and disease-related states, a likely consequence of immunosenescence coinciding with increased sedentarism, obesity, and fat infiltration of muscle and bone. Evidence suggests the pathophysiology of osteosarcopenia includes genetic polymorphisms, reduced mechanical loading, and impaired endocrine functioning, as well as altered crosstalk between muscle, bone, and fat cells. Clinicians should screen for osteosarcopenia via imaging methods (i.e. dual-energy X-ray absorptiometry) to quantify muscle and bone mass, in addition to assessing muscle strength (i.e. grip strength) and functional capacity (i.e. gait speed). A comprehensive geriatric assessment, including medical history and risk factors, must also be undertaken. Treatment of this syndrome should include osteoporotic drugs [bone anabolics/antiresorptives (i.e. teriparatide, denosumab, bisphosphates)] where indicated, and progressive resistance and balance exercises (at least 2-3 times/week). To maximize musculoskeletal health, nutritional recommendations [protein (1.2-1.5 g/kg/day), vitamin D (800-1000 IU/day), calcium (1300 mg/day), and creatine (3-5 g/day)] must also be met. It is anticipated that diagnosis and treatment for osteosarcopenia will become part of routine healthcare in the future. However, further work is required to identify biomarkers, which, in turn, may increase diagnosis, risk stratification, and targeted treatments to improve health outcomes.

摘要

背景

骨量减少/骨质疏松症和肌少症并存的骨肌减少症是一种新兴的老年病巨人,它给全球健康带来了严重的负担。

方法和结果

社区居住的老年人中骨肌减少症的患病率为 5-37%(≥65 岁),骨折患者的患病率最高(低创伤性骨折:约 46%;髋部骨折:17.1-96.3%)。在 2353 名社区居住的成年人中,与骨肌减少症相关的危险因素包括年龄较大(男性:60-64 岁至 59.4%(≥75 岁);女性:60-64 岁至 48.3%(≥75 岁),P<0.05)、身体活动不足(反比关系:0.64,95%置信区间(CI)0.46-0.88(男女合并))、低体重指数(男性:0.84,95%CI 0.81-0.88;女性:0.77,95%CI 0.74-0.80)和更高的脂肪量(男性:1.46,95%CI 1.11-1.92;女性:2.25,95%CI 1.71-2.95)。在 148 名老年住院患者中,与骨质疏松症或肌少症单独存在相比,骨肌减少症患者表现出较差的营养状况(微型营养评估评分:8.50±2.52 分,P<0.001),而在 253 名澳大利亚老年人中,与非骨肌减少症相比,骨肌减少症与平衡和功能能力受损有关(比值比(ORs):2.56-7.19;P<0.05)。与非骨肌减少症相比,骨肌减少症还与跌倒(ORs:2.83-3.63;P<0.05)、骨折(ORs:3.86-4.38;P<0.05)和更早死亡(1 年随访时的风险比(HR):1.84,95%CI;0.69-4.92,P=0.023)相关。

结论

这种综合征预计会随着年龄相关和疾病相关状态的增长而增加,这可能是免疫衰老与增加的久坐不动、肥胖和肌肉和骨骼脂肪浸润同时发生的结果。证据表明,骨肌减少症的病理生理学包括遗传多态性、减少的机械负荷和内分泌功能障碍,以及肌肉、骨骼和脂肪细胞之间的异常相互作用。临床医生应通过影像学方法(即双能 X 射线吸收法)来筛查骨肌减少症,以定量肌肉和骨量,此外还应评估肌肉力量(即握力)和功能能力(即步态速度)。还必须进行全面的老年评估,包括病史和危险因素。这种综合征的治疗应包括骨质疏松症药物(骨合成代谢剂/抗吸收剂,如特立帕肽、地诺单抗、双磷酸盐),如果需要,还应进行渐进性阻力和平衡运动(至少每周 2-3 次)。为了最大限度地促进肌肉骨骼健康,还必须满足营养建议(蛋白质(1.2-1.5 g/kg/天)、维生素 D(800-1000 IU/天)、钙(1300 mg/天)和肌酸(3-5 g/天))。预计未来骨肌减少症的诊断和治疗将成为常规医疗保健的一部分。然而,需要进一步的工作来确定生物标志物,这反过来又可能增加诊断、风险分层和靶向治疗,以改善健康结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30aa/7296259/9984f95e1d3d/JCSM-11-609-g001.jpg

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