Metabolic Syndrome and the Risk of Kidney Stones: Evidence from 487 860 UK Biobank Participants.

IF 5.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Clinical Endocrinology & Metabolism Pub Date : 2025-03-17 DOI:10.1210/clinem/dgae295
Minghui Liu, Meng Gao, Jian Wu, Zewu Zhu, Jiao Hu, Hequn Chen, Zhiyong Chen, Jinbo Chen
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Abstract

Context: While some studies have suggested an association between metabolic syndrome and kidney stones, the quality and level of evidence in these studies vary.

Objective: Whether some individual characteristics and clustering of metabolic syndrome traits increase the risk of kidney stones has not been examined in a large-scale prospective cohort.

Materials: We conducted a retrospective analysis of data from a prospective cohort of 487 860 UK Biobank participants who were free from kidney stones at baseline. The presence of metabolic syndrome was based on 5 criteria: abdominal obesity, high triglyceride levels, low high-density lipoprotein (HDL) cholesterol levels, high blood pressure (HBP), and type 2 diabetes mellitus (T2DM). Cox proportional hazards regression models were used to evaluate the association between metabolic syndrome and risk of kidney stones.

Results: After an average follow-up period of 12.6 years, a total of 5213 of the 487 860 participants included in the UK Biobank study developed kidney stones. The partial traits of metabolic syndrome, including waist circumference (hazard ratio [HR]: 1.15; 95% CI, 1.10-1.20), HDL cholesterol (0.66; 95% CI, 0.55-0.79), HBP (1.11; 95% CI, 1.03-1.19), and T2DM (1.14; 95% CI, 1.04-1.21), were independently associated with the occurrence of kidney stones. The clustering of metabolic syndrome is significantly associated with kidney stone formation, and as the number of metabolic syndrome traits increases, the risk of kidney stones gradually increases.

Conclusion: Metabolic syndrome is a significant and independent risk factor for the development of kidney stones. This association suggests that kidney stones may represent a systemic disorder influenced by the interplay of various metabolic risk factors.

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代谢综合征与肾结石风险:来自 487,860 名英国生物库参与者的大规模队列研究。
目的:虽然一些研究表明代谢综合征与肾结石之间存在关联,但这些研究的质量和证据水平参差不齐。在大规模的前瞻性队列中,还没有研究过代谢综合征的某些个体特征和聚集特征是否会增加肾结石的风险:我们对前瞻性队列中 487,860 名英国生物库参与者的数据进行了回顾性分析,这些参与者在基线时没有肾结石。代谢综合征的存在基于五个标准:腹部肥胖、甘油三酯水平高、高密度脂蛋白胆固醇水平低、高血压(HBP)和 2 型糖尿病(T2DM)。采用 Cox 比例危险回归模型评估代谢综合征与肾结石风险之间的关系:经过平均 12.6 年的随访,英国生物库研究的 487 860 名参与者中共有 5 213 人患上了肾结石。代谢综合征的部分特征,包括腰围(HR:1.15,95% CI:1.10-1.20)、高密度脂蛋白胆固醇(0.66,0.55-0.79)、HBP(1.11,1.03-1.19)和T2DM(1.14,1.04-1.21),与肾结石的发生独立相关。代谢综合征的聚集与肾结石的形成显著相关,随着代谢综合征特征数量的增加,肾结石的风险也逐渐增加:结论:代谢综合征是肾结石发生的一个重要且独立的风险因素。这种关联表明,肾结石可能是受各种代谢风险因素相互作用影响的一种全身性疾病。
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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
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