利塞膦酸钠或运动对更年期瘦体重的保护作用:随机对照试验的二次分析。

JCSM rapid communications Pub Date : 2022-07-01 Epub Date: 2022-03-09 DOI:10.1002/rco2.59
Laura E Flores, Kevin Kupzyk, Nancy Waltman, Kristen M Beavers, Laura Bilek
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引用次数: 0

摘要

背景:绝经过渡期的特点是荷尔蒙变化导致身体成分发生变化,如脂肪量增加和瘦肉量减少。负重和阻力运动有助于在更年期过渡期间保持瘦体重;然而,这种运动的吸收率很低。临床前研究表明,双膦酸盐也能有效防止瘦体重的减少。因此,我们试图研究双膦酸盐疗法是否能在绝经后的几年内减轻瘦体重的流失,并优于负重运动:方法:数据来自心脏地带骨质疏松症预防研究(NCT02186600),在该研究中,骨质疏松的绝经后妇女被随机分配到双膦酸盐(91 人)、负重/阻力运动(92 人)或对照组(93 人),为期一年。在基线、6 个月和 12 个月期间,对双能 X 射线吸收测定法(DXA)得出的身体成分测量结果(包括总瘦肉质量、总脂肪质量、瘦肉质量指数和瘦肉质量与脂肪质量比)进行确认。利塞膦酸盐和负重锻炼的依从性定义为服用剂量和参加锻炼次数的百分比。采用线性建模的意向治疗分析产生了对身体成分的治疗效果。结果:276 名女性(年龄:54.5 岁;83.3% 白种人;体重指数:25.7 kg/m2)被纳入分析。利塞膦酸盐和运动干预12个月的坚持率分别为89%和64%。在瘦体重方面观察到了组间时间交互作用,显示运动组(0.43±1.49 千克)和利塞膦酸钠组(0.31±1.68 千克)在 12 个月内增加的瘦体重明显高于对照组(-0.15±1.27 千克)。然而,在二次分析中控制体重变化后,对照组和利塞膦酸钠组的瘦体重变化差异变得不显著(P=0.059):结果表明,与对照组相比,口服利塞膦酸钠 12 个月和负重锻炼 12 个月可减少绝经过渡期的瘦体重减轻。利塞膦酸钠的瘦体重减少效应可能是由整体体重变化驱动的。
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Risedronate or Exercise for Lean Mass Preservation During Menopause: Secondary Analysis of a Randomized Controlled Trial.

Background: The menopause transition is marked by hormonal shifts leading to body composition changes, such as fat mass gain and lean mass loss. Weight-bearing and resistance exercise can help maintain lean mass during the menopause transition; however, uptake is low. Pre-clinical research points to bisphosphonates as also being effective in preventing loss of lean mass. Thus, we sought to investigate whether bisphosphonate therapy can mitigate loss of lean mass and outperform weight-bearing exercise in the years immediately following menopause.

Methods: Data come from the Heartland Osteoporosis Prevention Study (NCT02186600), where osteopenic, postmenopausal women were randomized to bisphosphonate (n=91), weight-bearing/resistance exercise (n=92), or control (n=93) conditions over a one-year period. Dual energy X-ray absorptiometry (DXA)-derived body composition measures (including total lean mass, total fat mass, lean mass index, and lean mass-to-fat mass ratio) were ascertained at baseline, six, and 12-months. Adherence to risedronate and weight-bearing exercise was defined as the percentage of dosages taken and exercise sessions attended. Intent-to-treat analysis using linear modeling was used to generate treatment effects on body composition. Secondary analysis utilized per-protocol analysis and included adjustment for weight change.

Results: 276 women (age: 54.5 years; 83.3% Caucasian; BMI: 25.7 kg/m2) were included in the analyses. 12-month adherence to the risedronate and exercise interventions was 89% and 64%, respectively. Group-by-time interactions were observed for lean mass, revealing exercise (0.43±1.49kg) and risedronate groups (0.31±1.68 kg) gained significantly more lean mass than control (-0.15±1.27 kg) over 12-months. However, after controlling for weight change in secondary analysis, the difference in lean mass change between control and risedronate became non-significant (p=0.059).

Conclusions: Results suggest both 12 months of oral risedronate and 12 months of weight-bearing exercise may diminish lean mass loss experienced during the menopause transition as compared to control. The lean mass sparing effect for risedronate may be driven by overall weight change.

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