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代谢有利的肥胖和骨密度:孟德尔随机化分析。

Metabolically favorable adiposity and bone mineral density: a Mendelian randomization analysis.

机构信息

School of Nutritional Sciences and Wellness, University of Arizona, Tucson, Arizona, USA.

Department of Health Promotion Sciences, University of Arizona, Tucson, Arizona, USA.

出版信息

Obesity (Silver Spring). 2023 Jan;31(1):267-278. doi: 10.1002/oby.23604. Epub 2022 Dec 10.

Abstract

OBJECTIVE

This analysis assessed the putative causal association between genetically predicted percent body fat and areal bone mineral density (aBMD) and, more specifically, the association between genetically predicted metabolically "favorable adiposity" (MFA) and aBMD at clinically relevant bone sites.

METHODS

Mendelian randomization was used to assess the relationship of MFA and percent body fat with whole-body, lumbar spine, femoral neck, and forearm aBMD. Sex-stratified and age-stratified exploratory analyses were conducted.

RESULTS

In all MR analyses, genetically predicted MFA was inversely associated with aBMD for the whole body (β = -0.053, p = 0.0002), lumbar spine (β = -0.075; p = 0.0001), femoral neck (β = -0.045; p = 0.008), and forearm (β = -0.115; p = 0.001). This negative relationship was strongest in older individuals and did not differ by sex. The relationship between genetically predicted percent body fat and aBMD was nonsignificant across all Mendelian randomization analyses. Several loci that were associated at a genome-wide significance level (p < 5 × 10 ) in opposite directions with body fat and aBMD measures were also identified.

CONCLUSIONS

This study did not support the hypothesis that MFA protects against low aBMD. Instead, it showed that MFA may result in lower aBMD. Further research is needed to understand how MFA affects aBMD and other components of bone health such as bone turnover, bone architecture, and osteoporotic fractures.

摘要

目的

本分析评估了遗传预测体脂百分比与面积骨密度(aBMD)之间的潜在因果关系,更具体地说,评估了遗传预测代谢“有利肥胖”(MFA)与临床相关骨部位的 aBMD 之间的关系。

方法

孟德尔随机化用于评估 MFA 和体脂百分比与全身、腰椎、股骨颈和前臂 aBMD 的关系。进行了性别分层和年龄分层的探索性分析。

结果

在所有 MR 分析中,遗传预测的 MFA 与全身(β=-0.053,p=0.0002)、腰椎(β=-0.075;p=0.0001)、股骨颈(β=-0.045;p=0.008)和前臂(β=-0.115;p=0.001)的 aBMD 呈负相关。这种负相关在年龄较大的个体中最强,且与性别无关。在所有孟德尔随机化分析中,遗传预测的体脂百分比与 aBMD 之间的关系均无统计学意义。还确定了一些与体脂肪和 aBMD 测量值呈相反方向的全基因组显著水平(p<5×10)相关的基因座。

结论

本研究不支持 MFA 可预防低 aBMD 的假说。相反,它表明 MFA 可能导致低 aBMD。需要进一步研究以了解 MFA 如何影响 aBMD 以及其他骨骼健康成分,如骨转换、骨结构和骨质疏松性骨折。

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