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评估衰弱指数对前庭疾病的因果效应:一项两样本孟德尔随机化研究。

Estimating the causal effect of frailty index on vestibular disorders: A two-sample Mendelian randomization.

作者信息

Xiao Gui, Wang Hu, Hu Jiaji, Liu Li, Zhang Tingting, Zhou Mengjia, Li Xingxing, Qin Chunxiang

机构信息

Department of Health Management, The Third Xiangya Hospital, Central South University, Changsha, China.

Xiangya School of Nursing, Central South University, Changsha, China.

出版信息

Front Neurosci. 2022 Aug 24;16:990682. doi: 10.3389/fnins.2022.990682. eCollection 2022.

Abstract

BACKGROUND

Frailty index and vestibular disorders appear to be associated in observational studies, but causality of the association remains unclear.

METHODS

A two-sample Mendelian randomization (MR) study was implemented to explore the causal relationship between the frailty index and vestibular disorders in individuals of European descent. A genome-wide association study (GWAS) of frailty index was used as the exposure ( = 175, 226), whereas the GWAS of vestibular disorders was the outcome ( = 462,933). MR Steiger filtering method was conducted to investigate the causal effect of the frailty index on vestibular disorders. An inverse variance weighted (IVW) approach was used as the essential approach to examine the causality. Additionally, the MR-Egger methods, the simple mode analysis, the weighted median analysis, and the weighted mode analysis were used as supplementary methods. The MR-PRESSO analysis, the MR-Egger intercept analysis, and Cochran's Q statistical analysis also were used to detect the possible heterogeneity as well as directional pleiotropy. To evaluate this association, the odds ratio (OR) with 95% confidence intervals (CIs) was used. All statistical analyses were performed in R. The STROBE-MR checklist for the reporting of MR studies was used in this study.

RESULTS

In total, 14 single nucleotide polymorphisms (SNPs) were identified as effective instrumental variables (IVs) in the two sample MR analyses. The significant causal effect of the frailty index on vestibular disorders was demonstrated by IVW method [OR 1.008 (95% CI 1.003, 1.013), = 0.001]. Results from the various sensitivity analysis were consistent. The "leave-one-out" analysis indicated that our results were robust even without a single SNP. According to the MR-Egger intercept test [intercept = -0.000151, SE = 0.011, = 0.544], genetic pleiotropy did not affect the results. No heterogeneity was detected by Cochran's Q test. Results of MR Steiger directionality test indicated the accuracy of our estimate of the potential causal direction (Steiger < 0.001).

CONCLUSION

The MR study suggested that genetically predicted frailty index may be associated with an increased risk of vestibular disorders. Notably, considering the limitations of this study, the causal effects between frailty index and vestibular disorders need further investigation. These results support the importance of effectively managing frailty which may minimize vestibular disorders and improve the quality of life for those with vestibular disorders.

摘要

背景

在观察性研究中,衰弱指数与前庭疾病似乎存在关联,但这种关联的因果关系仍不明确。

方法

开展了一项两样本孟德尔随机化(MR)研究,以探讨欧洲血统个体中衰弱指数与前庭疾病之间的因果关系。将衰弱指数的全基因组关联研究(GWAS)用作暴露因素(n = 175,226),而将前庭疾病的GWAS作为结局(n = 462,933)。采用MR Steiger过滤方法来研究衰弱指数对前庭疾病的因果效应。采用逆方差加权(IVW)方法作为检验因果关系的主要方法。此外,还采用MR-Egger方法、简单模式分析、加权中位数分析和加权模式分析作为补充方法。MR-PRESSO分析、MR-Egger截距分析和 Cochr an Q统计分析也用于检测可能的异质性以及定向多效性。为评估这种关联,使用了具有95%置信区间(CI)的比值比(OR)。所有统计分析均在R中进行。本研究采用了用于报告MR研究的STROBE-MR清单。

结果

在两样本MR分析中,总共鉴定出14个单核苷酸多态性(SNP)作为有效的工具变量(IV)。IVW方法证实了衰弱指数对前庭疾病具有显著的因果效应[OR 1.008(95%CI 1.003, 1.013),P = 0.001]。各种敏感性分析的结果一致。“留一法”分析表明,即使没有单个SNP,我们的结果也很稳健。根据MR-Egger截距检验[截距 = -0.000151,SE = 0.011,P = 0.544],基因多效性并未影响结果。 Cochr an Q检验未检测到异质性。MR Steiger方向性检验的结果表明我们对潜在因果方向估计的准确性(Steiger P < 0.001)。

结论

MR研究表明,基因预测的衰弱指数可能与前庭疾病风险增加有关。值得注意的是,考虑到本研究的局限性,衰弱指数与前庭疾病之间的因果效应需要进一步研究。这些结果支持了有效管理衰弱的重要性,这可能会最大限度地减少前庭疾病,并改善前庭疾病患者的生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6e2/9448900/9878c8897810/fnins-16-990682-g0001.jpg

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