Aldoori Joanna, Zulyniak Michael A, Toogood Giles J, Hull Mark A
Leeds Institute of Medical Research, University of Leeds, St James's University Hospital, Leeds, United Kingdom.
Food, Nutrition and Health, University of British Columbia, Vancouver, Canada.
Cancer Epidemiol Biomarkers Prev. 2025 Mar 3;34(3):394-404. doi: 10.1158/1055-9965.EPI-24-1154.
The relationship between omega-3 polyunsaturated fatty acid (n-3 PUFA) intake and colorectal cancer risk is unclear. Blood n-3 PUFA concentration is a biomarker of dietary n-3 PUFA intake. We examined the relationship between plasma n-3 PUFA concentrations and colorectal cancer risk in UK Biobank (UKBB) participants.
We analyzed the relationship between tertiles (T) of plasma total n-3 PUFAs and n-3 PUFA docosahexaenoic acid (DHA) levels, and overall colorectal cancer (also stratified by tumor location and sex) risk. Cox proportional hazards regression models were adjusted for clinical covariates. Nonlinearity was tested by restricted cubic splines.
There were 2,602 incident colorectal cancer cases in 234,598 UKBB participants with baseline plasma fatty acid data (mean follow-up 13.4 years). There was an inverse association between the plasma total n-3 PUFA level [T2 HR = 0.88 (95% confidence interval, 0.80-0.97) compared with the T1 reference; T3 = 0.91 (0.83-1.00)], as well as the plasma DHA concentration [T2 = 0.89 (0.80-0.98); T3 = 0.91 (0.82-1.00)], and colorectal cancer risk. The relationship was nonlinear [P for nonlinearity = 0.14 (total n-3 PUFAs) and 0.008 (DHA)], with a plateau effect at the highest n-3 PUFA concentrations. The relationship was more pronounced for proximal colon cancer [T2 = 0.82 (0.69-0.97); T3 = 0.76 (0.64-0.90) for DHA] and was evident for males [T2 = 0.84 (0.74-0.95); T3 = 0.89 (0.78-1.00)], but not for females.
Higher plasma n-3 PUFAs are associated with reduced colorectal cancer risk in the UKBB.
Nonlinearity, as well as tumor site and sex specificities, of the inverse relationship between plasma n-3 PUFA levels and colorectal cancer risk, if confirmed in other diverse populations, has significant implications for nutritional prevention guidelines.
ω-3多不饱和脂肪酸(n-3 PUFA)摄入量与结直肠癌风险之间的关系尚不清楚。血液中n-3 PUFA浓度是膳食n-3 PUFA摄入量的生物标志物。我们在英国生物银行(UKBB)参与者中研究了血浆n-3 PUFA浓度与结直肠癌风险之间的关系。
我们分析了血浆总n-3 PUFAs三分位数(T)和n-3 PUFA二十二碳六烯酸(DHA)水平与总体结直肠癌(也按肿瘤位置和性别分层)风险之间的关系。Cox比例风险回归模型针对临床协变量进行了调整。通过受限立方样条检验非线性。
在234,598名有基线血浆脂肪酸数据的UKBB参与者中,有2602例结直肠癌新发病例(平均随访13.4年)。血浆总n-3 PUFA水平[T2风险比(HR)=0.88(95%置信区间,0.80 - 0.97),与T1参考值相比;T3 = 0.91(0.83 - 1.00)]以及血浆DHA浓度[T2 = 0.89(0.80 - 0.98);T3 = 0.91(0.82 - 1.00)]与结直肠癌风险呈负相关。这种关系是非线性的[非线性P值=0.14(总n-3 PUFAs)和0.008(DHA)],在n-3 PUFA浓度最高时存在平台效应。这种关系在近端结肠癌中更为明显[DHA的T2 = 0.82(0.69 - 0.97);T3 = 0.76(0.64 - 0.90)],在男性中也很明显[T2 = 0.84(0.74 - 0.95);T3 = 0.89(0.78 - 1.00)],但在女性中不明显。
在UKBB中,较高的血浆n-3 PUFAs与降低结直肠癌风险相关。
如果在其他不同人群中得到证实,血浆n-3 PUFA水平与结直肠癌风险之间的负相关关系的非线性以及肿瘤部位和性别特异性,对营养预防指南具有重要意义。