使用孟德尔随机化方法研究眩晕可改变的危险因素

IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY
Xingzhi Guo, Chen Hou, Peng Tang, Xin Zhang, Ning Gou, Li Chong, Peng Liu, Rui Li
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引用次数: 0

摘要

背景:眩晕是一种非常普遍的症状,有广泛的原因和不良后果。虽然眩晕的常见危险因素已经确定,但它们与眩晕的因果关系仍不完全清楚。因此,确定与眩晕有因果关系的可改变因素对于预防眩晕至关重要。方法:采用一项全面的孟德尔随机化研究,在40多种遗传预测的可改变危险因素中调查眩晕的因果关系,这些因素被分类为生活方式特征、血液参数和代谢合并症。这项研究使用了来自deCODE和FinnGen联盟的两种不同的眩晕汇总统计数据。使用反方差加权方法计算估计,并通过替代方法进行验证。结果:基因预测较高的受教育程度与眩晕风险降低显著相关(解码:优势比(OR) = 0.757, 95% CI = 0.697-0.822, pFDR[错误发现率]<;0.001;FinnGen: OR = 0.796, 95%CI = 0.703-0.901, pFDR = 0.007),而基因预测的长时间看电视与眩晕风险增加显著相关(deCODE: OR = 1.193, 95%CI = 1.076-1.323, pFDR = 0.011;FinnGen: OR = 1.269, 95%CI = 1.085 ~ 1.483, pFDR = 0.030)。此外,基因预测的谷丙转氨酶(ALT)水平升高与眩晕的风险呈正相关。基因预测增加的体力活动与降低眩晕风险有相关性,而较高的甘油三酯、体重指数(BMI)和舒张压(DBP)与眩晕风险增加有相关性(praw <;0.05)。结论:我们的研究结果表明,基因预测的教育水平和体育活动的增加与眩晕风险的降低有关,而ALT和甘油三酯水平、电视观看时间、BMI和DBP水平的升高与眩晕风险呈正相关。因此,调整这些因素将降低眩晕的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Insights Into Modifiable Risk Factors of Vertigo Using the Mendelian Randomization Approach

Insights Into Modifiable Risk Factors of Vertigo Using the Mendelian Randomization Approach

Background: Vertigo is a highly prevalent symptom with wide-ranging causes and adverse consequences. While common risk factors for vertigo have been identified, their causal relationship with vertigo remains not fully known. Thus, identifying the modifiable factors causally related to vertigo is crucial for preventing vertigo.

Methods: A comprehensive Mendelian randomization study was employed to investigate the causal effects of vertigo among more than 40 genetically predicted modifiable risk factors, categorized into lifestyle traits, blood parameters, and metabolic comorbidities. This study used two different vertigo summary statistics from the deCODE and FinnGen consortia. Estimates were calculated using the inverse-variance weighted method and validated through alternative approaches.

Results: The results indicated that genetically predicted higher educational level was significantly associated with a decreased risk of vertigo (deCODE: odds ratio (OR) = 0.757, 95% CI = 0.697–0.822, pFDR[false discover rate] < 0.001; FinnGen: OR = 0.796, 95%CI = 0.703–0.901, pFDR = 0.007), while genetically predicted longer television watching was significantly associated with an increased risk of vertigo (deCODE: OR = 1.193, 95%CI = 1.076–1.323, pFDR = 0.011; FinnGen: OR = 1.269, 95%CI = 1.085–1.483, pFDR = 0.030). Additionally, genetically predicted elevated levels of alanine transaminase (ALT) were positively associated with the risk of vertigo. Genetically predicted increased physical activity was suggestively related to a reduced risk of vertigo, while higher triglyceride, body mass index (BMI), and diastolic blood pressure (DBP) were suggestively associated with an increased risk of vertigo (praw < 0.05).

Conclusions: Our findings indicate that genetically predicted increased educational levels and physical activity were associated with a decreased risk of vertigo, while higher levels of ALT and triglycerides, television watching time, BMI, and DBP were positively associated with the risk of vertigo. Thus, modifying these factors would decrease the risk of vertigo.

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来源期刊
Acta Neurologica Scandinavica
Acta Neurologica Scandinavica 医学-临床神经学
CiteScore
6.70
自引率
2.90%
发文量
161
审稿时长
4-8 weeks
期刊介绍: Acta Neurologica Scandinavica aims to publish manuscripts of a high scientific quality representing original clinical, diagnostic or experimental work in neuroscience. The journal''s scope is to act as an international forum for the dissemination of information advancing the science or practice of this subject area. Papers in English will be welcomed, especially those which bring new knowledge and observations from the application of therapies or techniques in the combating of a broad spectrum of neurological disease and neurodegenerative disorders. Relevant articles on the basic neurosciences will be published where they extend present understanding of such disorders. Priority will be given to review of topical subjects. Papers requiring rapid publication because of their significance and timeliness will be included as ''Clinical commentaries'' not exceeding two printed pages, as will ''Clinical commentaries'' of sufficient general interest. Debate within the speciality is encouraged in the form of ''Letters to the editor''. All submitted manuscripts falling within the overall scope of the journal will be assessed by suitably qualified referees.
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