Serum lipid profiles and risk of colorectal cancer: a prospective cohort study in the UK Biobank

被引:42
|
作者
Fang, Zhe [1 ]
He, Mingming [1 ,2 ]
Song, Mingyang [1 ,3 ,4 ,5 ,6 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Sun Yat Sen Univ, Canc Ctr, Collaborat Innovat Ctr Canc Med, Dept Med Oncol,State Key Lab Oncol South China, Guangzhou, Guangdong, Peoples R China
[3] Massachusetts Gen Hosp, Div Gastroenterol, Boston, MA 02114 USA
[4] Harvard Med Sch, Boston, MA 02115 USA
[5] Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[6] Massachusetts Gen Hosp, Clin & Translat Epidemiol Unit, Boston, MA 02114 USA
基金
英国医学研究理事会; 美国国家卫生研究院; 英国惠康基金;
关键词
PHYSICAL-ACTIVITY; COLON-CANCER; OBESITY; DYSLIPIDEMIA; METAANALYSIS; CHOLESTEROL; DISEASE; ADENOMA; WOMEN;
D O I
10.1038/s41416-020-01143-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background It remains unclear whether serum lipids influence colorectal cancer (CRC) risk. Methods We conducted a prospective cohort study of 380,087 adults aged 40-69 years in the UK Biobank. Serum high-density cholesterol, low-density cholesterol, total cholesterol, triglycerides, and apolipoprotein A and B were measured. We used Cox proportional hazard models to estimate the multivariable hazard ratios (HRs) of CRC according to one standard deviation (SD) increment in serum lipids. We conducted subgroup analysis by tumour anatomical subsites. Results During a median of 10.3 years of follow-up, we documented 2667 incident CRC cases. None of the lipid biomarkers was associated with the risk of CRC after adjusting for potential confounding factors, including body mass index and waist circumference. When assessed by cancer subsites, serum triglycerides was associated with an increased risk of cancer in the caecum and transverse colon, with the HR of 1.12 (95% CI, 1.00-1.25) and 1.29 (95% CI, 1.09-1.53), respectively; and apolipoprotein A was associated with a lower risk of hepatic flexure cancer (HR, 0.73, 95% CI, 0.56-0.96). Conclusions Serum lipid profiles were not associated with colorectal cancer risk after adjusting for obesity indicators. The potential subsite-specific effects of triglycerides and apolipoprotein A require further confirmation.
引用
收藏
页码:663 / 670
页数:8
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