Association between metabolic syndrome and kidney cancer risk: a prospective cohort study

被引:0
|
作者
Wang, Lin [1 ]
Du, Han [1 ]
Sheng, Chao [1 ]
Dai, Hongji [1 ]
Chen, Kexin [1 ]
机构
[1] Tianjin Med Univ, Canc Inst & Hosp, Natl Clin Res Ctr Canc,Dept Epidemiol & Biostat,Mi, Key Lab Prevent & Control Human Major Dis,Key Lab, Tianjin 300060, Peoples R China
关键词
Metabolic syndrome; Renal cancer; Hypertension; Central obesity; Dyslipidemia; Polygenic risk score; RENAL-CELL CANCER; INSULIN-RESISTANCE; OBESITY; PATHOPHYSIOLOGY; HYPERTENSION; POPULATION; COMPONENTS; DISEASE;
D O I
10.1186/s12944-024-02138-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background Kidney cancer has become known as a metabolic disease. However, there is limited evidence linking metabolic syndrome (MetS) with kidney cancer risk. This study aimed to investigate the association between MetS and its components and the risk of kidney cancer. Methods UK Biobank data was used in this study. MetS was defined as having three or more metabolic abnormalities, while pre-MetS was defined as the presence of one or two metabolic abnormalities. Hazard ratios (HRs) and 95% confidence intervals (CIs) for kidney cancer risk by MetS category were calculated using multivariable Cox proportional hazards models. Subgroup analyses were conducted for age, sex, BMI, smoking status and drinking status. The joint effects of MetS and genetic factors on kidney cancer risk were also analyzed. Results This study included 355,678 participants without cancer at recruitment. During a median follow-up of 11 years, 1203 participants developed kidney cancer. Compared to the metabolically healthy group, participants with pre-MetS (HR= 1.36, 95% CI: 1.06-1.74) or MetS (HR= 1. 70, 95% CI: 1.30-2.23) had a significantly greater risk of kidney cancer. This risk increased with the increasing number of MetS components (P for trend < 0.001). The combination of hypertension, dyslipidemia and central obesity contributed to the highest risk of kidney cancer (HR= 3.03, 95% CI: 1.91-4.80). Compared with participants with non-MetS and low genetic risk, those with MetS and high genetic risk had the highest risk of kidney cancer (HR= 1. 74, 95% CI: 1.41-2.14). Conclusions Both pre-MetS and MetS status were positively associated with kidney cancer risk. The risk associated with kidney cancer varied by combinations of MetS components. These findings may offer novel perspectives on the aetiology of kidney cancer and assist in designing primary prevention strategies.
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页数:11
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