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东亚人群中血清尿酸与代谢及心血管风险的孟德尔随机化研究。

A Mendelian randomization study of serum uric acid in metabolic and cardiovascular risk in East Asian populations.

作者信息

Li Jianing, Li Yanan, Zhang Shuang, Shi He

机构信息

Heilongjiang University of Traditional Chinese Medicine, Harbin, China.

Jiahe Clinic, Jinan, Shandong Province, China.

出版信息

Medicine (Baltimore). 2025 Sep 5;104(36):e44135. doi: 10.1097/MD.0000000000044135.

DOI:10.1097/MD.0000000000044135
PMID:40922357
Abstract

Serum uric acid (SUA) levels are linked to increased disease vulnerability and higher recurrence rates; however, the exact causal relationships are elusive. Despite the prevalent hyperuricemia in East Asian populations, comprehensive research on the intricate association between SUA levels and disease is lacking. To address this, a study utilizing a 2-sample Mendelian randomization (MR) approach was conducted in East Asian populations. This study utilized MR to explore the correlation between SUA levels and various disorders, employing data from genome-wide association studies and multiple independent single-nucleotide polymorphism. Multiple single-nucleotide polymorphisms were applied to assess the causal relationship between SUA and other diseases. Methodologies encompassed inverse-variance weighting, MR-Egger regression, and weighted median analysis. This study revealed that SUA increases the risk of coronary artery disease (β = 0.197 mm, 95% CI: 0.084-0.31 mm, P = .001) but decreases the risk of rheumatoid arthritis (β = -0.172 mm, 95% CI: -0.302 to -0.043 mm, P = .009). It also increases diastolic blood pressure, serum creatinine, eosinophil count, relative wall thickness, posterior wall thickness, and interventricular septum thickness and decreases high-density lipoprotein cholesterol and the estimated glomerular filtration rate. These findings suggest that SUA may be a potential risk factor for certain diseases. Research indicates a strong correlation between SUA and illnesses, particularly metabolism and rheumatoid arthritis, in East Asians. This study underscores the necessity of monitoring SUA levels to prevent further illnesses and prompt action to address the growing burden of SUA in the East Asian populations.

摘要

血清尿酸(SUA)水平与疾病易感性增加和复发率升高有关;然而,确切的因果关系尚不清楚。尽管东亚人群中高尿酸血症普遍存在,但缺乏关于SUA水平与疾病之间复杂关联的全面研究。为了解决这一问题,在东亚人群中进行了一项采用双样本孟德尔随机化(MR)方法的研究。本研究利用MR,采用全基因组关联研究数据和多个独立单核苷酸多态性,探索SUA水平与各种疾病之间的相关性。应用多个单核苷酸多态性来评估SUA与其他疾病之间的因果关系。方法包括逆方差加权、MR-Egger回归和加权中位数分析。本研究表明,SUA会增加冠状动脉疾病的风险(β = 0.197 mm,95%CI:0.084 - 0.31 mm,P = .001),但会降低类风湿性关节炎的风险(β = -0.172 mm,95%CI:-0.302至-0.043 mm,P = .009)。它还会增加舒张压、血清肌酐、嗜酸性粒细胞计数、相对壁厚、后壁厚度和室间隔厚度,并降低高密度脂蛋白胆固醇和估计肾小球滤过率。这些发现表明,SUA可能是某些疾病的潜在危险因素。研究表明,在东亚人群中,SUA与疾病,尤其是代谢和类风湿性关节炎之间存在密切关联。本研究强调了监测SUA水平以预防进一步疾病的必要性,并促使采取行动应对东亚人群中不断增加的SUA负担。

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Front Genet. 2024 Dec 2;15:1449205. doi: 10.3389/fgene.2024.1449205. eCollection 2024.
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Causal relationship between serum uric acid and cardiovascular disease: A Mendelian randomization study.血清尿酸与心血管疾病之间的因果关系:一项孟德尔随机化研究。
Int J Cardiol Heart Vasc. 2024 Jun 29;54:101453. doi: 10.1016/j.ijcha.2024.101453. eCollection 2024 Oct.
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Dysbiosis of gut microbiota is associated with pathogenesis of peptic ulcer diseases through inflammatory proteins: A Mendelian randomization study.
肠道微生物群落失调通过炎症蛋白与消化性溃疡疾病的发病机制相关:一项基于孟德尔随机化的研究。
Medicine (Baltimore). 2024 Sep 27;103(39):e39814. doi: 10.1097/MD.0000000000039814.
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Comprehensive analysis of therapeutic strategies for Gouty nephropathy: Insights from clinical trials.痛风性肾病治疗策略的综合分析:来自临床试验的见解
Pharmacol Res. 2024 Sep;207:107319. doi: 10.1016/j.phrs.2024.107319. Epub 2024 Jul 18.
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Uric acid and evaluate the coronary vascular stenosis gensini score correlation research and in gender differences.尿酸与冠状动脉血管狭窄程度 Gensini 评分的相关性研究及性别差异。
BMC Cardiovasc Disord. 2023 Nov 8;23(1):546. doi: 10.1186/s12872-023-03581-5.
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Ethnic disparities in bidirectional causal effects between serum uric acid concentrations and kidney function: -ethnic Mendelian randomization study.血清尿酸浓度与肾功能之间双向因果效应的种族差异:种族孟德尔随机化研究
Heliyon. 2023 Oct 19;9(11):e21108. doi: 10.1016/j.heliyon.2023.e21108. eCollection 2023 Nov.
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