Association of a Combined Body Mass Index and Regional Body Fat Percentage Metric With Fragility Fracture Risk: Evidence from a Large Observational Cohort

IF 9.4 1区 医学 Q1 GERIATRICS & GERONTOLOGY
Hamzah Amin, Michelle G. Swainson, Muhammed Aqib Khan, Marwan Bukhari
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Abstract

Background

Evidence suggests that high body fat and low muscle mass may increase the risk of fragility fractures. However, current fracture risk models, which largely rely on body mass index (BMI), may not fully capture these compositional factors. We recommend integrating additional body composition variables into fracture risk calculators to improve accuracy. Previously, we described partial body fat percentage (PBF%), a novel measure that is routinely available and calculated as the proportion of fat at the lumbar spine and hip during DXA scans. We hypothesize that a combined BMI and PBF% approach (BMI/PBF%) could be associated with fragility fracture.

Methods

Patients were referred to our DXA scanner between June 2004 and February 2024 and had combined lumbar spine and bilateral femoral scans. Patients were initially categorized by BMI (underweight, normal weight, overweight and obese) and then divided into tertiles of PBF%. Based on each patient's unique combination of BMI and PBF% tertile, they were stratified into 12 binary BMI/PBF% groups for analysis. Multivariable logistic regression models, reporting odds ratios (OR), with BMI/PBF% groups as the independent variables and fragility fractures as the dependent variable were fit, with all results adjusted for known fracture risk factors.

Results

We analysed 36 235 patients (83.4% female, 16.6% male), of whom 14 342 (39.5%) reported fragility fractures. The median (IQR) age was 67.7 (57.5–75.0) years, with a BMI of 26.4 (23.3–30.2) kg/m2 and PBF% of 30.6% (25.5% – 35.4%). In females, those in the lowest PBF% tertile had reduced odds of fragility fractures across all BMI categories (e.g., obese low PBF%: OR 0.70, 95% CI 0.64–0.78), whereas in males, this reduction was observed only amongst overweight and obese individuals (e.g., obese low PBF%: OR 0.71, 95% CI 0.57–0.88). No association was found for patients in the middle PBF% tertile across any BMI group. In contrast, females in the highest PBF% tertile exhibited increased odds of fractures across all BMI categories except underweight (e.g., obese high PBF%: OR 1.31, 95% CI 1.22–1.42), and a similar pattern was seen in males, but limited to the overweight and obese groups (e.g., obese high PBF%: OR 1.27, 95% CI 1.04–1.55).

Conclusion

High or low PBF% within BMI categories is associated with fragility fractures, challenging the traditional notion that high BMI protects against fractures. This study highlights the importance of body composition measures beyond BMI in fracture risk assessment.

综合体重指数和区域体脂百分比与脆性骨折风险的关联:来自大型观察队列的证据
背景证据表明,高体脂和低肌肉量可能会增加脆性骨折的风险。然而,目前的骨折风险模型主要依赖于身体质量指数(BMI),可能无法完全捕捉到这些组成因素。我们建议将额外的身体成分变量整合到骨折风险计算器中,以提高准确性。以前,我们描述了部分体脂百分比(PBF%),这是一种常规可用的新测量方法,并在DXA扫描期间计算腰椎和髋关节的脂肪比例。我们假设BMI和PBF%的联合方法(BMI/PBF%)可能与脆性骨折有关。方法患者于2004年6月至2024年2月接受DXA扫描,并进行腰椎和双侧股骨联合扫描。患者最初按BMI(体重过轻、体重正常、超重和肥胖)进行分类,然后按PBF%分成四分位数。根据每位患者BMI和PBF%的独特组合,将他们分为12个BMI/PBF%二元组进行分析。以BMI/PBF%组为自变量,脆性骨折为因变量,拟合报告优势比(OR)的多变量logistic回归模型,并根据已知骨折危险因素对所有结果进行调整。结果本组共分析36 235例患者(女性83.4%,男性16.6%),其中14 342例(39.5%)为脆性骨折。中位(IQR)年龄为67.7(57.5-75.0)岁,BMI为26.4 (23.3-30.2)kg/m2, PBF%为30.6%(25.5% - 35.4%)。在女性中,PBF百分比最低的个体在所有BMI类别中发生脆性骨折的几率都降低了(例如,肥胖低PBF%: OR 0.70, 95% CI 0.64-0.78),而在男性中,这种降低仅在超重和肥胖个体中观察到(例如,肥胖低PBF%: OR 0.71, 95% CI 0.57-0.88)。在任何BMI组中,均未发现中间PBF百分比的患者存在关联。相比之下,PBF百分比最高的女性在所有BMI类别中都表现出骨折的几率增加,除了体重不足(例如,肥胖高PBF%: OR 1.31, 95% CI 1.22-1.42),并且在男性中也出现了类似的模式,但仅限于超重和肥胖组(例如,肥胖高PBF%: OR 1.27, 95% CI 1.94 - 1.55)。结论BMI类别中PBF百分比的高低与脆性骨折有关,挑战了高BMI可预防骨折的传统观念。这项研究强调了身体成分测量在骨折风险评估中的重要性。
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来源期刊
Journal of Cachexia Sarcopenia and Muscle
Journal of Cachexia Sarcopenia and Muscle MEDICINE, GENERAL & INTERNAL-
CiteScore
13.30
自引率
12.40%
发文量
234
审稿时长
16 weeks
期刊介绍: The Journal of Cachexia, Sarcopenia and Muscle is a peer-reviewed international journal dedicated to publishing materials related to cachexia and sarcopenia, as well as body composition and its physiological and pathophysiological changes across the lifespan and in response to various illnesses from all fields of life sciences. The journal aims to provide a reliable resource for professionals interested in related research or involved in the clinical care of affected patients, such as those suffering from AIDS, cancer, chronic heart failure, chronic lung disease, liver cirrhosis, chronic kidney failure, rheumatoid arthritis, or sepsis.
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