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容量稀释而非隔离,更好地解释了肥胖人群维生素 D 水平低的原因。

Volumetric dilution, rather than sequestration best explains the low vitamin D status of obesity.

机构信息

Department of Medicine, Creighton University, Omaha, NE, USA.

出版信息

Obesity (Silver Spring). 2012 Jul;20(7):1444-8. doi: 10.1038/oby.2011.404. Epub 2012 Jan 19.

Abstract

Vitamin D status is known to be poor in obese individuals; there is no consensus as to the reason. Cross-sectional study of the relation between serum 25-hydroxyvitamin D (25(OH)D) concentration and body size in the baseline data from unsupplemented adults entering two study cohorts in our research unit, N = 686. Regression analyses of body size variables against serum 25(OH)D concentration, using both linear and hyperbolic models. The fit to a hyperbolic model of 25(OH)D against body weight completely removed the obesity-related component of inter-individual variability in serum 25(OH)D concentration. The hyperbolic fit using total body weight was significantly better than any linear model, and specifically better than any using BMI. Dilution of ingested or cutaneously synthesized vitamin D in the large fat mass of obese patients fully explains their typically low vitamin D status. There is no evidence for sequestration of supplemental or endogenous cholecalciferol. Vitamin D replacement therapy needs to be adjusted for body size if desired serum 25(OH)D concentrations are to be achieved.

摘要

维生素 D 状态在肥胖个体中已知较差;至于原因,尚无共识。对未补充成年人进入我们研究单位的两个研究队列的基线数据中血清 25-羟维生素 D(25(OH)D)浓度与体型之间关系的横断面研究,N = 686。使用线性和双曲线模型对体型变量与血清 25(OH)D 浓度进行回归分析。25(OH)D 与体重的双曲线模型拟合完全消除了血清 25(OH)D 浓度个体间变异性中与肥胖相关的成分。使用总体重的双曲线拟合明显优于任何线性模型,特别是优于任何使用 BMI 的模型。肥胖患者大量脂肪组织中摄入或皮肤合成的维生素 D 的稀释完全解释了他们通常较低的维生素 D 状态。没有证据表明补充或内源性胆钙化醇被隔离。如果需要达到理想的血清 25(OH)D 浓度,则需要根据体型调整维生素 D 替代治疗。

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