Department of Biostatistics and Epidemiology, University of Massachusetts, Amherst, MA.
Channing Division of Network Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
Int J Cancer. 2019 Apr 15;144(8):1929-1940. doi: 10.1002/ijc.31934. Epub 2019 Jan 3.
Prior epidemiologic findings for plasma folate and B-vitamins and breast cancer risk are inconsistent and have not assessed the influence of folic acid fortification. Therefore, we examined the associations of plasma folate, B , pyridoxal 5'-phosphate (PLP), homocysteine, cysteine and cysteinylglycine with breast cancer risk, before and after fortification. We conducted a nested case-control study within the prospective Nurses' Health Study. In 1989-1990 (pre-fortification), 32,826 women donated a blood sample and 18,743 donated an additional blood sample in 2000-2001 (post-fortification). Between the first blood collection and 2006, 1874 incident breast cancer cases with at least one blood sample and 367 with two were 1:1 matched to controls. Conditional logistic regression was used to estimate relative risks (RR) and 95% confidence intervals (CI) adjusting for breast cancer risk factors. Overall, higher plasma folate, B , PLP, homocysteine, cysteine and cysteinylglycine levels were not associated with breast cancer risk. Associations did not vary by in situ/invasive, hormone receptor status, or tumor molecular subtype. Additionally, associations were null before and after fortification. For example, the RR (95% CI) for the highest versus lowest tertile of 1990 (pre-fortification) plasma folate with 1990-2000 follow-up was 0.93 (0.75-1.16) and for the 2000 plasma folate (post-fortification) with 2000-2006 follow-up the RR (95% CI) was 1.17 (0.79-1.74). Plasma folate, B , PLP, homocysteine, cysteine and cysteinylglycine were not significantly associated with breast cancer overall, before and after fortification, or with specific tumor molecular subtypes. However, long term associations (>8 years) after the implementation of fortification could not be examined.
先前关于血浆叶酸和 B 族维生素与乳腺癌风险的流行病学研究结果并不一致,并且没有评估叶酸强化的影响。因此,我们在强化之前和之后,研究了血浆叶酸、B 族维生素、吡哆醛 5'-磷酸(PLP)、同型半胱氨酸、半胱氨酸和半胱氨酰甘氨酸与乳腺癌风险之间的关系。我们在前瞻性护士健康研究中进行了一项巢式病例对照研究。1989-1990 年(强化前),32826 名女性捐献了一份血样,2000-2001 年(强化后),18743 名女性捐献了另一份血样。在第一次采血和 2006 年之间,至少有一份血样的 1874 例乳腺癌病例和有两份血样的 367 例病例与对照 1:1 匹配。使用条件逻辑回归来估计相对风险(RR)和 95%置信区间(CI),并调整乳腺癌风险因素。总体而言,较高的血浆叶酸、B 族维生素、PLP、同型半胱氨酸、半胱氨酸和半胱氨酰甘氨酸水平与乳腺癌风险无关。关联在原位/浸润性、激素受体状态或肿瘤分子亚型之间没有差异。此外,强化前后的关联均为阴性。例如,1990 年(强化前)血浆叶酸最高与最低三分位的 RR(95%CI)为 0.93(0.75-1.16),而 2000 年(强化后)血浆叶酸的 RR(95%CI)为 1.17(0.79-1.74),随访时间为 1990-2000 年。总体而言,在强化前后或特定的肿瘤分子亚型中,血浆叶酸、B 族维生素、PLP、同型半胱氨酸、半胱氨酸和半胱氨酰甘氨酸与乳腺癌均无显著关联。然而,无法检查强化实施后超过 8 年的长期关联。