OUP accepted manuscript

医学 血压 危险系数 内科学 前瞻性队列研究 优势比 孟德尔随机化 心脏病学 舒张期 肾癌 肾细胞癌 置信区间 肿瘤科 遗传变异 化学 基因型 基因 生物化学
作者
Karine Alcala,Daniela Mariosa,Karl Smith-Byrne,Dariush Nasrollahzadeh Nesheli,Robert Carreras‐Torres,Eva Ardanaz Aicua,Nicola P. Bondonno,Catalina Bonet,Mattias Brunström,Bas Bueno‐de‐Mesquita,María‐Dolores Chirlaque,Sofia Christakoudi,Alicia K. Heath,Rudolf Kaaks,Verena Katzke,Vittorio Krogh,Börje Ljungberg,Richard M Martin,Anne M. May,Olle Melander,Domenico Palli,Miguel Rodríguez‐Barranco,Carlotta Sacerdote,Tanja Stocks,Anne Tjønneland,Ruth C. Travis,Roel Vermeulen,Stephen J. Chanock,Mark P. Purdue,Elisabete Weiderpass,David C. Müller,Paul Brennan,Mattias Johansson
出处
期刊:International Journal of Epidemiology [Oxford University Press]
被引量:1
标识
DOI:10.1093/ije/dyac042
摘要

The relation between blood pressure and kidney cancer risk is well established but complex and different study designs have reported discrepant findings on the relative importance of diastolic blood pressure (DBP) and systolic blood pressure (SBP). In this study, we sought to describe the temporal relation between diastolic and SBP with renal cell carcinoma (RCC) risk in detail.Our study involved two prospective cohorts: the European Prospective Investigation into Cancer and Nutrition study and UK Biobank, including >700 000 participants and 1692 incident RCC cases. Risk analyses were conducted using flexible parametric survival models for DBP and SBP both separately as well as with mutuality adjustment and then adjustment for extended risk factors. We also carried out univariable and multivariable Mendelian randomization (MR) analyses (DBP: ninstruments = 251, SBP: ninstruments = 213) to complement the analyses of measured DBP and SBP.In the univariable analysis, we observed clear positive associations with RCC risk for both diastolic and SBP when measured ≥5 years before diagnosis and suggestive evidence for a stronger risk association in the year leading up to diagnosis. In mutually adjusted analysis, the long-term risk association of DBP remained, with a hazard ratio (HR) per standard deviation increment 10 years before diagnosis (HR10y) of 1.20 (95% CI: 1.10-1.30), whereas the association of SBP was attenuated (HR10y: 1.00, 95% CI: 0.91-1.10). In the complementary multivariable MR analysis, we observed an odds ratio for a 1-SD increment (ORsd) of 1.34 (95% CI: 1.08-1.67) for genetically predicted DBP and 0.70 (95% CI: 0.56-0.88) for genetically predicted SBP.The results of this observational and MR study are consistent with an important role of DBP in RCC aetiology. The relation between SBP and RCC risk was less clear but does not appear to be independent of DBP.
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