心功能磁共振成像与衰弱指数的因果关系:一项孟德尔随机研究。

IF 3.7 Q2 GENETICS & HEREDITY Phenomics (Cham, Switzerland) Pub Date : 2022-09-29 eCollection Date: 2022-12-01 DOI:10.1007/s43657-022-00072-z
Hui Zhang, Meng Hao, Zixin Hu, Yi Li, Xiaoxi Hu, Xiaoyan Jiang, Zuyun Liu, Xuehui Sun, Xiaofeng Wang
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引用次数: 0

摘要

由于传统观察性研究易受混杂因素和反向因果关系的影响,心功能与虚弱之间的因果关系尚不清楚。我们的目的是研究心功能是否对虚弱有因果影响。在这项研究中,一项双样本孟德尔随机化(MR)研究使用与心功能相关的遗传变异作为工具变量,通过磁共振成像表型进行评估。通过磁共振成像(包括七种心功能表型)和脆弱指数(FI)获得与心功能相关的遗传变异,这些变异来自两个大型全基因组关联研究。每个遗传工具的MR估计值使用逆方差加权(IVW)、加权中位数和MR - egger回归方法进行组合。我们发现,在Bonferroni校正后的IVW MR分析中,遗传决定的卒中体积(β - 0.13, 95% CI - 0.16至- 0.10,p = 1.39E-6)的增加,而不是其他心脏表型,与较低的FI相关。多效性或反向因果关系引起的潜在偏倚的敏感性分析显示了类似的结果(例如,MR-Egger截距检验的截距[SE], - 0.008 [0.011], p = 0.47)。遗漏分析表明,这种关联不是由单核苷酸多态性驱动的。遗传变异之间没有发现异质性的证据(例如,MR-Egger: Q统计量= 14.4,p = 0.156)。总之,我们提供的证据表明,改善心功能有助于降低FI。这些发现支持了增强心脏功能可能是预防虚弱的有效策略的假设。补充资料:在线版本包含补充资料,下载地址:10.1007/s43657-022-00072-z。
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Causal Association of Cardiac Function by Magnetic Resonance Imaging with Frailty Index: A Mendelian Randomization Study.

Owing to the susceptibility of conventional observational studies to confounding factors and reverse causation, the causal association between cardiac function and frailty is unclear. We aimed to investigate whether cardiac function has causal effects on frailty. In this study, a two-sample Mendelian randomization (MR) study was conducted using genetic variants associated with cardiac function assessed by magnetic resonance imaging phenotypes as instrumental variables. Genetic variants associated with cardiac function by magnetic resonance imaging (including seven cardiac function phenotypes) and the frailty index (FI) were obtained from two large genome-wide association studies. MR estimates from each genetic instrument were combined using inverse variance weighted (IVW), weighted median, and MR‒Egger regression methods. We found that the increase in genetically determined stroke volume (beta - 0.13, 95% CI - 0.16 to - 0.10, p = 1.39E-6), rather than other cardiac phenotypes, was associated with lower FI in MR analysis of IVW after Bonferroni correction. Sensitivity analyses examining potential bias caused by pleiotropy or reverse causality revealed similar findings (e.g., intercept [SE], - 0.008 [0.011], p = 0.47 by MR‒Egger intercept test). The leave-one-out analysis indicated that the association was not driven by single nucleotide polymorphisms. No evidence of heterogeneity was found among the genetic variants (e.g., MR‒Egger: Q statistic = 14.4, p = 0.156). In conclusion, we provided evidence that improved cardiac function could contribute to reducing FI. These findings support the hypothesis that enhancing cardiac function could be an effective prevention strategy for frailty.

Supplementary information: The online version contains supplementary material available at 10.1007/s43657-022-00072-z.

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