Weinstein S J, Ziegler R G, Frongillo E A, Colman N, Sauberlich H E, Brinton L A, Hamman R F, Levine R S, Mallin K, Stolley P D, Bisogni C A
Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
J Nutr. 2001 Jul;131(7):2040-8. doi: 10.1093/jn/131.7.2040.
Previous observational epidemiologic studies of folate and cervical cancer, as well as folate supplementation trials for cervical dysplasia, have produced mixed results. We examined the relationship between serum and RBC folate and incident invasive cervical cancer in a large, multicenter, community-based case-control study. Detailed in-person interviews were conducted, and blood was drawn at least 6 mo after completion of cancer treatment from 51% of cases and 68% of controls who were interviewed. Blood folate was measured with both microbiologic and radiobinding assays. Included in the final analyses were 183 cases and 540 controls. Logistic regression was used to control for all accepted risk factors, including age, sexual behavior, smoking, oral contraceptive use, Papanicolaou smear history and human papillomavirus (HPV)-16 serology. For all four folate measures, the geometric mean in cases was lower than in controls (e.g., 11.6 vs. 13.0 nmol/L, P < 0.01 for the serum radiobinding assay). Folate measures using microbiologic and radiobinding assays were correlated (serum: r = 0.90; RBC: r = 0.77). For serum folate, multivariate-adjusted odds ratios (OR) in the lowest vs. highest quartile were 1.3 [95% confidence interval (CI) = 0.8--2.9] and 1.6 (0.9--2.9), using the microbiologic and radiobinding assays, respectively. For RBC folate, comparable OR were 1.2 (0.6--2.2) and 1.5 (0.8--2.7). Similar risks were obtained when restricting analyses to subjects with a history of HPV infection. Thus, low serum and RBC folate were each moderately, but nonsignificantly, associated with increased invasive cervical cancer risk. These findings support a role for one-carbon metabolism in the etiology of cervical cancer.
先前关于叶酸与宫颈癌的观察性流行病学研究以及针对宫颈发育异常的叶酸补充试验结果不一。我们在一项大型、多中心、基于社区的病例对照研究中,考察了血清和红细胞叶酸水平与浸润性宫颈癌发病之间的关系。我们进行了详细的面对面访谈,并在癌症治疗结束至少6个月后,对51%的病例和68%接受访谈的对照者进行了采血。采用微生物学检测法和放射结合检测法测定血叶酸水平。最终分析纳入了183例病例和540例对照。采用逻辑回归分析对所有公认的风险因素进行校正,这些因素包括年龄、性行为、吸烟、口服避孕药使用情况、巴氏涂片检查史和人乳头瘤病毒(HPV)-16血清学检测结果。对于所有四项叶酸检测指标,病例组的几何均值均低于对照组(例如,血清放射结合检测法:11.6 vs. 13.0 nmol/L,P < 0.01)。采用微生物学检测法和放射结合检测法测得的叶酸水平具有相关性(血清:r = 0.90;红细胞:r = 0.77)。对于血清叶酸,最低四分位数与最高四分位数相比,多变量校正比值比(OR)分别为1.3 [95%置信区间(CI)= 0.8 - 2.9]和1.6(0.9 - 2.9),分别采用微生物学检测法和放射结合检测法。对于红细胞叶酸,相应的OR分别为1.2(0.6 - 2.2)和1.5(0.8 - 2.7)。将分析限定于有HPV感染史的受试者时,得到了类似的风险结果。因此,低血清和红细胞叶酸水平均与浸润性宫颈癌风险增加呈中度相关,但无统计学意义。这些发现支持了一碳代谢在宫颈癌病因学中的作用。