Jarvis David, Mitchell Jonathan S, Law Philip J, Palin Kimmo, Tuupanen Sari, Gylfe Alexandra, Hänninen Ulrika A, Cajuso Tatiana, Tanskanen Tomas, Kondelin Johanna, Kaasinen Eevi, Sarin Antti-Pekka, Kaprio Jaakko, Eriksson Johan G, Rissanen Harri, Knekt Paul, Pukkala Eero, Jousilahti Pekka, Salomaa Veikko, Ripatti Samuli, Palotie Aarno, Järvinen Heikki, Renkonen-Sinisalo Laura, Lepistö Anna, Böhm Jan, Meklin Jukka-Pekka, Al-Tassan Nada A, Palles Claire, Martin Lynn, Barclay Ella, Farrington Susan M, Timofeeva Maria N, Meyer Brian F, Wakil Salma M, Campbell Harry, Smith Christopher G, Idziaszczyk Shelley, Maughan Timothy S, Kaplan Richard, Kerr Rachel, Kerr David, Buchanan Daniel D, Win Aung K, Hopper John L, Jenkins Mark A, Lindor Noralane M, Newcomb Polly A, Gallinger Steve, Conti David, Schumacher Fred, Casey Graham, Taipale Jussi, Aaltonen Lauri A, Cheadle Jeremy P, Dunlop Malcolm G, Tomlinson Ian P, Houlston Richard S
Division of Genetics and Epidemiology, The Institute of Cancer Research, London SW7 3RP, UK.
Genome-Scale Biology Research Program, Research Programs Unit, University of Helsinki 00014, Helsinki, Finland.
Br J Cancer. 2016 Jul 12;115(2):266-72. doi: 10.1038/bjc.2016.188. Epub 2016 Jun 23.
Observational studies have associated adiposity with an increased risk of colorectal cancer (CRC). However, such studies do not establish a causal relationship. To minimise bias from confounding we performed a Mendelian randomisation (MR) analysis to examine the relationship between adiposity and CRC.
We used SNPs associated with adult body mass index (BMI), waist-hip ratio (WHR), childhood obesity and birth weight as instrumental variables in a MR analysis of 9254 CRC cases and 18 386 controls.
In the MR analysis, the odds ratios (ORs) of CRC risk per unit increase in BMI, WHR and childhood obesity were 1.23 (95% CI: 1.02-1.49, P=0.033), 1.59 (95% CI: 1.08-2.34, P=0.019) and 1.07 (95% CI: 1.03-1.13, P=0.018), respectively. There was no evidence for association between birth weight and CRC (OR=1.22, 95% CI: 0.89-1.67, P=0.22). Combining these data with a concurrent MR-based analysis for BMI and WHR with CRC risk (totalling to 18 190 cases, 27 617 controls) provided increased support, ORs for BMI and WHR were 1.26 (95% CI: 1.10-1.44, P=7.7 × 10(-4)) and 1.40 (95% CI: 1.14-1.72, P=1.2 × 10(-3)), respectively.
These data provide further evidence for a strong causal relationship between adiposity and the risk of developing CRC highlighting the urgent need for prevention and treatment of adiposity.
观察性研究表明肥胖与结直肠癌(CRC)风险增加有关。然而,此类研究并未确立因果关系。为尽量减少混杂因素造成的偏倚,我们进行了孟德尔随机化(MR)分析,以研究肥胖与结直肠癌之间的关系。
我们使用与成人身体质量指数(BMI)、腰臀比(WHR)、儿童肥胖和出生体重相关的单核苷酸多态性(SNPs)作为工具变量,对9254例结直肠癌病例和18386例对照进行MR分析。
在MR分析中,BMI、WHR和儿童肥胖每增加一个单位,结直肠癌风险的比值比(OR)分别为1.23(95%可信区间:1.02 - 1.49,P = 0.033)、1.59(95%可信区间:1.08 - 2.34,P = 0.019)和1.07(95%可信区间:1.03 - 1.13,P = 0.018)。没有证据表明出生体重与结直肠癌有关联(OR = 1.22,95%可信区间:0.89 - 1.67,P = 0.22)。将这些数据与同时进行的基于MR的BMI和WHR与结直肠癌风险分析(共18190例病例,27617例对照)相结合,提供了更多支持,BMI和WHR的OR分别为1.26(95%可信区间:1.10 - 1.44,P = 7.7×10⁻⁴)和1.40(95%可信区间:1.14 - 1.72,P = 1.2×10⁻³)。
这些数据进一步证明了肥胖与患结直肠癌风险之间存在强烈的因果关系,凸显了预防和治疗肥胖的迫切需求。