首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Men with metabolic syndrome have lower bone mineral density but lower fracture risk--the MINOS study.
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Men with metabolic syndrome have lower bone mineral density but lower fracture risk--the MINOS study.

机译:MINOS研究显示,患有代谢综合征的男性的骨矿物质密度较低,但骨折风险较低。

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Data on the association of the metabolic syndrome (MetS) with bone mineral density (BMD) and fracture risk in men are inconsistent. We studied the association between MetS and bone status in 762 older men followed up for 10 years. After adjustment for age, body mass index, height, physical activity, smoking, alcohol intake, and serum 25-hydroxycholecalciferol D and 17beta-estradiol levels, men with MetS had lower BMD at the hip, whole body, and distal forearm (2.2% to 3.2%, 0.24 to 0.27 SD, p < .05 to .005). This difference was related to abdominal obesity (assessed by waist circumference, waist-hip ratio, or central fat mass) but not other MetS components. Men with MetS had lower bone mineral content (3.1% to 4.5%, 0.22 to 0.29 SD, p < .05 to 0.001), whereas differences in bone size were milder. Men with MetS had a lower incidence of vertebral and peripheral fractures (6.7% versus 12.0%, p < .05). After adjustment for confounders, MetS was associated with a lower fracture incidence [odds ratio (OR) = 0.33, 95% confidence interval (CI) 0.15-0.76, p < .01]. Among the MetS components, hypertriglyceridemia was most predictive of the lower fracture risk (OR = 0.25, 95%CI 0.10-0.62, p < .005). Lower fracture risk in men with MetS cannot be explained by differences in bone size, rate of bone turnover rate and bone loss, or history of falls or fractures. Thus older men with MetS have a lower BMD related to the abdominal obesity and a lower risk of fracture related to hypertriglyceridemia. MetS probably is not a meaningful concept in the context of bone metabolism. Analysis of its association with bone-related variables may obscure the pathophysiologic links of its components with bone status.
机译:男性的代谢综合征(MetS)与骨矿物质密度(BMD)和骨折风险之间的关联数据不一致。我们研究了762位年龄在10年以上的男性中MetS与骨骼状态之间的关系。调整年龄,体重指数,身高,体力活动,吸烟,饮酒和血清25-羟胆钙化固醇D和17β-雌二醇水平后,患有MetS的男性在臀部,全身和前臂远端的BMD较低(2.2%至3.2%,0.24至0.27 SD,p <.05至.005)。这种差异与腹部肥胖(通过腰围,腰臀比或中央脂肪量评估)有关,但与其他MetS组件无关。患有MetS的男性的骨矿物质含量较低(3.1%至4.5%,SD为0.22至0.29 SD,p <.05至0.001),而骨骼尺寸差异较小。患有MetS的男性椎骨和周围骨折的发生率较低(6.7%比12.0%,p <.05)。调整混杂因素后,MetS与较低的骨折发生率相关[比值比(OR)= 0.33,95%置信区间(CI)0.15-0.76,p <.01]。在MetS组件中,高甘油三酯血症最能预测较低的骨折风险(OR = 0.25,95%CI 0.10-0.62,p <.005)。患有MetS的男性较低的骨折风险无法用骨骼大小,骨周转率和骨质流失或跌倒或骨折史的差异来解释。因此,患有MetS的老年男性与腹部肥胖相关的BMD较低,而与高甘油三酯血症相关的骨折风险较低。在骨骼代谢方面,MetS可能不是一个有意义的概念。与骨骼相关变量的关联分析可能会掩盖其成分与骨骼状态的病理生理联系。

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