Fernanda Morales Berstein, Jasmine Khouja, Mark Gormley, Elmira Ebrahimi, Shama Virani, James D McKay, Paul Brennan, Tom G Richardson, Caroline L Relton, George Davey Smith, M Carolina Borges, Tom Dudding, Rebecca C Richmond
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引用次数: 0
摘要
背景:肥胖与头颈癌(HNC)风险增加有关。尽管在吸烟者中,身体质量指数(BMI)与HNC风险呈负相关,但这可能是由于混淆。以前的孟德尔随机化(MR)研究不能完全排除肥胖和HNC之间的因果关系。因此,我们的目标是利用现有的最大的HNC全基因组关联研究(GWAS)来重新审视这一问题,该研究拥有HNC亚位点的更细粒度数据。方法:采用双样本MR框架评估BMI (N=806,834)、腰臀比(WHR; N=697,734)和腰围(N=462,166)对HNC (N=12,264例)及其亚位点风险的遗传预测影响。我们使用逆方差加权(IVW)磁共振和多敏感性分析,包括多变量磁共振(MVMR),探讨肥胖措施对HNC的直接影响,同时考虑吸烟行为(一个众所周知的HNC风险因素)。结果:在单变量MR中,较高的遗传预测BMI增加了总体HNC的风险(IVW OR = 1.17 / 1-SD高BMI, 95% CI 1.02-1.34)。然而,当吸烟被纳入MVMR模型时,IVW效应减弱(OR占综合吸烟指数= 0.96,每1-SD高BMI, 95% CI 0.80-1.15)。此外,我们没有发现遗传预测腰臀比(腰臀比每高1个标准差的IVW OR = 1.05, 95% CI 0.89-1.24)或腰围与HNC风险(IVW OR = 1.01每高1个标准差的腰围,95% CI 0.85-1.21)之间的联系。结论:我们的研究结果表明,肥胖在HNC风险中并不起主要作用。资助:FMB由威康信托基金分子、遗传和生命过程流行病学博士研究生资助(224982/Z/22/Z)。RCR由英国癌症研究基金(C18281/A29019)支持。MCB由布里斯托大学副校长奖学金,英国心脏基金会(AA/18/1/34219)和英国医学研究理事会(MC_UU_00032/5)支持。GDS在布里斯托尔大学MRC综合流行病学部门工作,该部门由医学研究理事会(MC_UU_00032/1)支持。CLR得到了医学研究理事会(MC_UU_00011/5)和英国癌症研究中心(C18281/A29019)项目资助(综合癌症流行病学项目)的支持。SV由EU Horizon 2020拨款(协议号825771)和NIDCR国家牙科和颅面健康研究所(R03DE030257)资助。JK所在的单位得到了布里斯托尔大学、英国癌症研究资助(C18281/A29019)和英国医学研究理事会(资助号:MC_UU_00032/7)的支持。
Reassessing the link between adiposity and head and neck cancer: a Mendelian randomization study.
Background: Adiposity has been associated with an increased risk of head and neck cancer (HNC). Although body mass index (BMI) has been inversely associated with HNC risk among smokers, this is likely due to confounding. Previous Mendelian randomization (MR) studies could not fully discount causality between adiposity and HNC. Hence, we aimed to revisit this using the largest genome-wide association study (GWAS) of HNC available, which has more granular data on HNC subsites.
Methods: We assessed the genetically predicted effects of BMI (N=806,834), waist-to-hip ratio (WHR; N=697,734) and waist circumference (N=462,166) on the risk of HNC (N=12,264 cases) and its subsites using a two-sample MR framework. We used inverse variance weighted (IVW) MR and multiple sensitivity analyses, including multivariable MR (MVMR), to explore the direct effects of the adiposity measures on HNC, while accounting for smoking behaviour (a well-known HNC risk factor).
Results: In univariable MR, higher genetically predicted BMI increased the risk of overall HNC (IVW OR = 1.17 per 1-SD higher BMI, 95% CI 1.02-1.34). However, the IVW effect was attenuated when smoking was included in the MVMR model (OR accounting for comprehensive smoking index = 0.96 per 1-SD higher BMI, 95% CI 0.80-1.15). Furthermore, we did not find a link between genetically predicted WHR (IVW OR = 1.05 per 1-SD higher WHR, 95% CI 0.89-1.24) or waist circumference and HNC risk (IVW OR = 1.01 per 1-SD higher waist circumference, 95% CI 0.85-1.21).
Conclusions: Our findings suggest that adiposity does not play a major role in HNC risk.
Funding: FMB was supported by a Wellcome Trust PhD studentship in Molecular, Genetic and Lifecourse Epidemiology (224982/Z/22/Z). RCR was supported by a Cancer Research UK grant (C18281/A29019). MCB is supported by a University of Bristol Vice Chancellor's Fellowship, the British Heart Foundation (AA/18/1/34219) and the UK Medical Research Council (MC_UU_00032/5). GDS works within the MRC Integrative Epidemiology Unit at the University of Bristol, which is supported by the Medical Research Council (MC_UU_00032/1). CLR was supported by the Medical Research Council (MC_UU_00011/5) and by a Cancer Research UK (C18281/A29019) programme grant (the Integrative Cancer Epidemiology Programme). SV was funded by an EU Horizon 2020 grant (agreement number 825771) and NIDCR National Institutes of Dental and Craniofacial Health (R03DE030257). JK works in a unit that receives support from the University of Bristol, a Cancer Research UK grant (C18281/A29019) and the UK Medical Research Council (grant number: MC_UU_00032/7).
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