Department of Clinical Biochemistry, Copenhagen University Hospital, Herlev and Gentofte Hospital, Borgmester Ib Juuls Vej 1, DK-2730, Herlev, Denmark.
The Copenhagen General Population Study, Copenhagen University Hospital, Herlev and Gentofte Hospital, Herlev, Denmark.
J Hematol Oncol. 2020 Sep 30;13(1):129. doi: 10.1186/s13045-020-00963-6.
Increasing evidence suggests that high-density lipoprotein (HDL) may play a role in cancer development. We tested the hypothesis that low HDL levels are associated with increased risk of cancer.
Individuals from two population-based cohorts, the Copenhagen General Population Study (2003-2015, N = 107 341), and the Copenhagen City Heart Study (1991-1994, N = 9387) were followed prospectively until end of 2016 to assess low plasma HDL cholesterol and apolipoprotein A1 as risk factors for cancer using Cox proportional hazard regression.
During up to 25 years follow-up, we observed 8748 cancers in the Copenhagen General Population Study and 2164 in the Copenhagen City Heart Study. In the Copenhagen General Population Study and compared to individuals with HDL cholesterol ≥ 2.0 mmol/L (≥ 77 mg/dL), multivariable adjusted hazard ratios (HRs) for any cancer were 1.13 (95% confidence interval 1.04-1.22) for individuals with HDL cholesterol of 1.5-1.99 mmol/L (58-77 mg/dL), 1.18 (1.08-1.30) for HDL cholesterol of 1.0-1.49 mmol/L (39-58 mg/dL), and 1.29 (1.12-1.48) for individuals with HDL cholesterol < 1.0 mmol/L (< 39 mg/dL). Correspondingly, compared to individuals with apolipoprotein A1 ≥ 190 mg/dL, HRs for any cancer were 1.06 (0.96-1.17) for individuals with apolipoprotein A1 of 160-189 mg/dL, 1.18 (1.07-1.30) for apolipoprotein A1 of 130-159 mg/dL, and 1.28 (1.13-1.46) for individuals with apolipoprotein A1 < 130 mg/dL. Among 27 cancer types, low HDL cholesterol and/or apolipoprotein A1 were associated with increased risk of multiple myeloma, myeloproliferative neoplasm, non-Hodgkin lymphoma, breast cancer, lung cancer, and nervous system cancer. Results were overall similar in women and men separately, and in the Copenhagen City Heart Study.
Low HDL levels were associated with increased risk of several cancers. Increased risk was most pronounced for hematological and nervous system cancer, and to a minor extent for breast and respiratory cancer.
越来越多的证据表明高密度脂蛋白(HDL)可能在癌症发展中发挥作用。我们检验了低 HDL 水平与癌症风险增加相关的假设。
本前瞻性研究纳入了两个基于人群的队列中的个体,哥本哈根普通人群研究(2003-2015 年,N=107341)和哥本哈根城市心脏研究(1991-1994 年,N=9387),直至 2016 年底,使用 Cox 比例风险回归评估低血浆 HDL 胆固醇和载脂蛋白 A1 作为癌症的风险因素。
在长达 25 年的随访期间,我们在哥本哈根普通人群研究中观察到 8748 例癌症,在哥本哈根城市心脏研究中观察到 2164 例癌症。在哥本哈根普通人群研究中,与 HDL 胆固醇≥2.0mmol/L(≥77mg/dL)的个体相比,HDL 胆固醇为 1.5-1.99mmol/L(58-77mg/dL)的个体、HDL 胆固醇为 1.0-1.49mmol/L(39-58mg/dL)的个体和 HDL 胆固醇<1.0mmol/L(<39mg/dL)的个体的多变量调整后的癌症风险比(HR)分别为 1.13(95%置信区间 1.04-1.22)、1.18(1.08-1.30)和 1.29(1.12-1.48)。相应地,与载脂蛋白 A1≥190mg/dL 的个体相比,载脂蛋白 A1 为 160-189mg/dL 的个体、载脂蛋白 A1 为 130-159mg/dL 的个体和载脂蛋白 A1<130mg/dL 的个体的癌症风险比(HR)分别为 1.06(0.96-1.17)、1.18(1.07-1.30)和 1.28(1.13-1.46)。在 27 种癌症类型中,低 HDL 胆固醇和/或载脂蛋白 A1 与多发性骨髓瘤、骨髓增生性肿瘤、非霍奇金淋巴瘤、乳腺癌、肺癌和神经系统癌症风险增加相关。在女性和男性中以及在哥本哈根城市心脏研究中,结果总体上相似。
低 HDL 水平与多种癌症风险增加相关。风险增加最明显的是血液系统和神经系统癌症,其次是乳腺癌和呼吸系统癌症。