Investigating causal relations between sleep traits and risk of breast cancer in women: mendelian randomisation study

医学 乳腺癌 多基因风险评分 孟德尔遗传 心理学 孟德尔随机化 内科学 临床心理学 肿瘤科 癌症 遗传学 生物 遗传变异 基因 单核苷酸多态性 基因型
作者
Rebecca C Richmond,Emma L Anderson,Hassan S. Dashti,Samuel E. Jones,Jacqueline M. Lane,Linn Beate Strand,Ben Brumpton,Martin K. Rutter,Andrew R. Wood,Kurt Straif,Caroline L Relton,Marcus R. Munafò,Timothy M. Frayling,Richard M Martin,Richa Saxena,Michael N. Weedon,Debbie A. Lawlor,George Davey Smith
出处
期刊:BMJ [BMJ]
卷期号:: l2327-l2327 被引量:79
标识
DOI:10.1136/bmj.l2327
摘要

To examine whether sleep traits have a causal effect on risk of breast cancer.Mendelian randomisation study.UK Biobank prospective cohort study and Breast Cancer Association Consortium (BCAC) case-control genome-wide association study.156 848 women in the multivariable regression and one sample mendelian randomisation (MR) analysis in UK Biobank (7784 with a breast cancer diagnosis) and 122 977 breast cancer cases and 105 974 controls from BCAC in the two sample MR analysis.Self reported chronotype (morning or evening preference), insomnia symptoms, and sleep duration in multivariable regression, and genetic variants robustly associated with these sleep traits.Breast cancer diagnosis.In multivariable regression analysis using UK Biobank data on breast cancer incidence, morning preference was inversely associated with breast cancer (hazard ratio 0.95, 95% confidence interval 0.93 to 0.98 per category increase), whereas there was little evidence for an association between sleep duration and insomnia symptoms. Using 341 single nucleotide polymorphisms (SNPs) associated with chronotype, 91 SNPs associated with sleep duration, and 57 SNPs associated with insomnia symptoms, one sample MR analysis in UK Biobank provided some supportive evidence for a protective effect of morning preference on breast cancer risk (0.85, 0.70, 1.03 per category increase) but imprecise estimates for sleep duration and insomnia symptoms. Two sample MR using data from BCAC supported findings for a protective effect of morning preference (inverse variance weighted odds ratio 0.88, 95% confidence interval 0.82 to 0.93 per category increase) and adverse effect of increased sleep duration (1.19, 1.02 to 1.39 per hour increase) on breast cancer risk (both oestrogen receptor positive and oestrogen receptor negative), whereas evidence for insomnia symptoms was inconsistent. Results were largely robust to sensitivity analyses accounting for horizontal pleiotropy.Findings showed consistent evidence for a protective effect of morning preference and suggestive evidence for an adverse effect of increased sleep duration on breast cancer risk.
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