Title | Causal effects of gallstone disease on risk of gastrointestinal cancer in Chinese |
Authors | Pang, Yuanjie Lv, Jun Kartsonaki, Christiana Guo, Yu Yu, Canqing Chen, Yiping Yang, Ling Bian, Zheng Millwood, Iona Y. Walters, Robin G. Li, Xiaojun Zou, Ju Holmes, Michael V. Chen, Junshi Chen, Zhengming Li, Liming |
Affiliation | Peking Univ, Hlth Sci Ctr, Sch Publ Hlth, Dept Epidemiol & Biostat, Beijing, Peoples R China Peking Univ, Peking Univ Ctr Publ Hlth & Epidem Preparedness &, 38 Xueyuan Rd, Beijing 100191, Peoples R China Univ Oxford, Nuffield Dept Populat Hlth, Clin Trial Serv Unit, Big Data Inst Bldg,Roosevelt Dr, Oxford, England Univ Oxford, Nuffield Dept Populat Hlth, Epidemiol Studies Unit CTSU, Big Data Inst Bldg,Roosevelt Dr, Oxford, England Univ Oxford, Nuffield Dept Populat Hlth, Med Res Council Populat Hlth Res Unit MRC PHRU, Oxford, England Chinese Acad Med Sci, Beijing, Peoples R China Jili St Community Hlth Serv Ctr, Liuyang, Peoples R China Oxford Univ Hosp, Natl Inst Hlth Res Oxford Biomed Res Ctr, Oxford, England Natl Ctr Food Safety Risk Assessment, Beijing, Peoples R China Univ Oxford, Nuffield Dept Populat Hlth, Med Res Council Populat Hlth Res Unit MRC PHRU, Oxford, England |
Issue Date | Mar-2021 |
Publisher | BRITISH JOURNAL OF CANCER |
Abstract | Background Gallstone disease (GSD) is associated with a higher risk of gastrointestinal (GI) cancer. However, it is unclear whether the associations are causal. Methods The prospective China Kadoorie Biobank (CKB) recorded 17,598 cases of GI cancer among 510,137 participants without cancer at baseline during 10 years of follow-up. Cox regression was used to estimate hazard ratios (HRs) for specific cancer by GSD status and duration. Mendelian randomisation was conducted to assess the genetic associations of GSD with specific cancer. Results Overall 6% of participants had symptomatic GSD at baseline. Compared with those without GSD, individuals with symptomatic GSD had adjusted HRs of 1.13 (1.01-1.29) for colorectal, 2.01 (1.78-2.26) for liver, 3.70 (2.88-4.87) for gallbladder, 2.31 (1.78-3.07) for biliary tract, and 1.38 (1.18-1.74) for pancreatic cancer. Compared with participants without GSD, the risks of colorectal, liver, gallbladder, biliary tract, and pancreatic cancer were highest during 0 to <5 years following disease diagnosis. There was evidence of genetic associations of GSD with these cancers, with odds ratios per 1-SD genetic score of 1.08 (1.05-1.11) for colorectal, 1.22 (1.19-1.25) for liver, 1.56 (1.49-1.64) for gallbladder, 1.39 (1.31-1.46) for biliary tract, and 1.16 (1.10-1.22) for pancreatic cancer. When meta-analysing the genetic estimates in CKB and UK Biobank, there was evidence of causal associations of GSD with colon cancer, gallbladder and biliary tract cancer (GBTC), and total GI cancer (RR per 1-SD: 1.05 [0.99-1.11], 2.00 [1.91-2.09], and 1.09 [1.05-1.13]). Conclusions GSD was associated with higher risks of several GI cancers, warranting future studies on the underlying mechanisms. |
URI | http://hdl.handle.net/20.500.11897/611323 |
ISSN | 0007-0920 |
DOI | 10.1038/s41416-021-01325-w |
Indexed | SCI(E) |
Appears in Collections: | 医学部待认领 |