Alcohol Intake and Bone Microarchitecture Deterioration in Older Men: The Prospective Structure of Aging Men's Bones (STRAMBO) Study.

Q2 Medicine
Journal of Bone Metabolism Pub Date : 2026-08-01 Epub Date: 2026-08-31 DOI:10.11005/jbm.25.989
Pawel Szulc, Danielle E Whittier, Steven K Boyd, Roland Chapurlat
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Abstract

Background: Data on the link between alcohol intake and prospectively assessed changes in areal bone mineral density (aBMD) are scarce. Our aim was to assess the association of alcohol intake with bone loss and microarchitectural decline prospectively assessed in older men.

Methods: In 818 men aged 60 to 87 years, bone microarchitecture was assessed at the distal radius and distal tibia (XtremeCT; Scanco Medical). Areal aBMD was assessed by dual energy X-ray absorptiometry (Hologic Inc.). Both were assessed at baseline, then after 4 and 8 years. Linear mixed models were adjusted for age, body mass index, bioavailable 17β-estradiol, osteoprotegerin, parathyroid hormone, Creactive protein and for grip strength (radius) or for the lower limb physical function score (tibia).

Results: At baseline, aBMD and bone microarchitecture measures did not differ across the classes of alcohol intake. During the follow-up, aBMD decrease did not vary differently across the classes of alcohol intake. Men drinking 16 to 112 g alcohol per week had the slowest bone microarchitecture decline (reference group). At the distal radius, trabecular BMD (Tb.BMD) and number (Tb.N) decreased faster in men consuming <16 g/week and in men drinking >224 g/week vs. the reference group. At the distal tibia, cortical thickness (Ct.Thd), cortical area (Ct.Ar), reaction force, and failure load decreased faster in men consuming <16 g/week and in men drinking >224 g/week versus the reference group.

Conclusions: Moderate alcohol intake is associated with slower bone decline. Very low and higher alcohol intake were associated with faster bone microarchitecture deterioration in older men when assessed prospectively.

老年男性饮酒与骨微结构恶化:老年男性骨骼前瞻性结构(STRAMBO)研究
背景:关于酒精摄入与前瞻性评估的面骨矿物质密度(aBMD)变化之间关系的数据很少。我们的目的是评估酒精摄入与老年男性骨质流失和微结构下降的相关性。方法:对818名60 - 87岁男性进行桡骨远端和胫骨远端骨微结构评估(XtremeCT; Scanco Medical)。采用双能x线吸收仪(Hologic Inc.)评估面积aBMD。在基线时进行评估,然后在4年和8年后进行评估。对线性混合模型进行年龄、体重指数、生物利用度17β-雌二醇、骨保护素、甲状旁腺激素、活性蛋白以及握力(半径)或下肢身体功能评分(胫骨)调整。结果:在基线时,aBMD和骨微结构测量在不同酒精摄入类别之间没有差异。在随访期间,aBMD的下降在不同的酒精摄入类别中没有差异。每周饮酒16至112克的男性骨骼微结构下降最慢(参照组)。在桡骨远端,与对照组相比,每周摄入224 g的男性骨小梁骨密度(tbd)和骨密度(tbn)下降更快。在胫骨远端,皮质厚度(Ct。Thd),皮质面积(Ct。与对照组相比,服用224 g/周的男性的Ar)、反作用力和失效负荷下降更快。结论:适量饮酒与减缓骨质衰退有关。在前瞻性评估中,极低和较高的酒精摄入量与老年男性骨微结构恶化的速度有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bone Metabolism
Journal of Bone Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
3.70
自引率
0.00%
发文量
23
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