Frontiers in Oncology (Jun 2022)

Association Between Metabolic Syndrome and Risk of Renal Cell Cancer: A Meta-Analysis

  • Wurong Du,
  • Kaibo Guo,
  • Kaibo Guo,
  • Huimin Jin,
  • Leitao Sun,
  • Leitao Sun,
  • Shanming Ruan,
  • Shanming Ruan,
  • Qiaoling Song,
  • Qiaoling Song

DOI
https://doi.org/10.3389/fonc.2022.928619
Journal volume & issue
Vol. 12

Abstract

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BackgroundMetabolic syndrome (MetS) has been related to increased risks of a variety of cancers. However, the association between MetS and the risk of renal cell cancer (RCC) remains not fully determined. This meta-analysis was conducted to investigate whether MetS is independently associated with the risk of RCC in adults.MethodsRelevant observational studies were obtained by searching PubMed, Embase, Cochrane’s Library, and Web of Science databases. Study characteristics and outcome data were extracted independently by two authors. The random-effect model was used for meta-analysis considering the possible influence of between-study heterogeneity. Predefined subgroup analyses were used to evaluate the possible influences of study characteristics on the outcome.ResultsEight studies involving 10,601,006 participants contributed to the meta-analysis. Results showed that MetS was independently associated with a higher risk of RCC in adult population (risk ratio [RR]: 1.62, 95% confidence interval [CI]: 1.41 to 1.87, p<0.001; I2 = 85%). Subgroup analyses showed consistent association in men (RR: 1.52, 95% CI: 1.23 to 1.89, p<0.001) and in women (RR: 1.71, 95% CI: 1.28 to 2.27, p<0.001), in Asians (RR: 1.51, 95% CI: 1.25 to 1.83, p<0.001) and in Caucasians (RR: 1.76, 95% CI: 1.46 to 2.12, p<0.001), and in community derived (RR: 1.56, 95% CI: 1.34 to 1.82, p<0.001) and non-community derived population (RR: 1.87, 95% CI: 1.71 to 2.04, p<0.001). Differences in study design or quality score also did not significantly affect the association (p for subgroup difference both >0.05).ConclusionsMetS may be independently associated with RCC in adult population.

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