Metabolic syndrome and risk of kidney cancer in the United States.

IF 5.1 2区 医学 Q1 ONCOLOGY
Cancer Pub Date : 2026-05-01 DOI:10.1002/cncr.70435
Minji Jung, Xiaoyu Wang, Sun Y Jeon, Rebecca E Graff, Zhengyi Deng, Kevin L'Espérance, Mingyi Li, Marvin E Langston, Benjamin I Chung
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引用次数: 0

Abstract

Background: Metabolic dysregulation may contribute to kidney cancer development through shared biological mechanisms and/or as an independent risk factor. However, evidence on this association in the US population remains limited.

Objective: This study identifies associations between metabolic syndrome (MetS) and kidney cancer risk in the United States.

Methods: This case-control study using administrative claims data from the MarketScan database (2007-2022) identified adult kidney cancer cases and 1:10 frequency-matched controls by age, index year, sex, insurance duration, and region. Metabolic exposures (obesity, hypertension, diabetes, and dyslipidemia) were assessed using diagnoses and prescriptions, with binary classification (MetS: ≥3 conditions; non-MetS: <3). Secondary analyses examined pre-MetS (1-2 conditions), metabolically healthy, dose-response relationships, combinations of conditions, and interaction between obesity and MetS. Multivariable logistic regression models were used to estimate odds ratios (ORs) and 95% confidence intervals (CIs).

Results: A total of 48,587 kidney cancer cases and 480,714 controls were included. MetS was associated with an increased risk of kidney cancer compared with non-MetS (OR, 1.43; 95% CI, 1.39-1.47). MetS (OR, 1.83; 95% CI, 1.77-1.88) and pre-MetS (OR, 1.47; 95% CI, 1.44-1.50) were associated with a higher risk compared with metabolically healthy. Each additional condition was associated with a 22% increase in the odds (95% CI, 1.21-1.23). Multiple conditions had higher odds than a single condition. Metabolically healthy obesity (OR, 1.48) and metabolically unhealthy obesity (OR, 1.77) showed stronger associations than metabolically healthy nonobesity.

Conclusion: MetS was associated with an increased risk of kidney cancer, highlighting the importance of overall metabolic health in its prevention.

代谢综合征和肾癌的风险在美国。
背景:代谢失调可能通过共同的生物学机制和/或作为一个独立的危险因素促进肾癌的发展。然而,这种关联在美国人群中的证据仍然有限。目的:本研究在美国确定代谢综合征(MetS)与肾癌风险之间的关系。方法:本病例对照研究使用来自MarketScan数据库(2007-2022)的行政索赔数据,根据年龄、指标年、性别、保险期限和地区确定成人肾癌病例和1:10频率匹配的对照组。使用诊断和处方评估代谢暴露(肥胖、高血压、糖尿病和血脂异常),并采用二元分类(MetS:≥3种情况;非MetS:结果:共纳入48,587例肾癌病例和480,714例对照。与非MetS相比,MetS与肾癌风险增加相关(OR, 1.43; 95% CI, 1.39-1.47)。与代谢健康的人相比,met (OR, 1.83; 95% CI, 1.77-1.88)和met前(OR, 1.47; 95% CI, 1.44-1.50)与更高的风险相关。每增加一种疾病,患病几率增加22% (95% CI, 1.21-1.23)。多种情况下比单一情况下的几率更高。代谢健康型肥胖(OR, 1.48)和代谢不健康型肥胖(OR, 1.77)比代谢健康型非肥胖表现出更强的相关性。结论:MetS与肾癌风险增加相关,强调了整体代谢健康在预防肾癌中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer
Cancer 医学-肿瘤学
CiteScore
13.10
自引率
3.20%
发文量
480
审稿时长
2-3 weeks
期刊介绍: The CANCER site is a full-text, electronic implementation of CANCER, an Interdisciplinary International Journal of the American Cancer Society, and CANCER CYTOPATHOLOGY, a Journal of the American Cancer Society. CANCER publishes interdisciplinary oncologic information according to, but not limited to, the following disease sites and disciplines: blood/bone marrow; breast disease; endocrine disorders; epidemiology; gastrointestinal tract; genitourinary disease; gynecologic oncology; head and neck disease; hepatobiliary tract; integrated medicine; lung disease; medical oncology; neuro-oncology; pathology radiation oncology; translational research
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