Butterworth C E, Hatch K D, Gore H, Mueller H, Krumdieck C L
Am J Clin Nutr. 1982 Jan;35(1):73-82. doi: 10.1093/ajcn/35.1.73.
Forty-seven young women with mild or moderate dysplasia of the uterine cervix (cervical intraepithelial neoplasia) diagnosed by cervical smears, received oral supplements of folic acid, 10 mg, or a placebo (ascorbic acid, 10 mg) daily for 3 months under double-blind conditions. All had used a combination-type oral contraceptive agent for at least 6 months and continued it while returning monthly for follow-up examinations. All smears and a biopsy obtained at the end of the trial period were classified by a single observer without knowledge of treatment status using an arbitrary scoring system (1 normal, 2 mild, 3 moderate, 4 severe, 5 carcinoma in situe). Mean biopsy scores from folate supplemented subjects were significantly better than in folate-unsupplemented subjects (2.28 versus 2.92, respectively; p less than 0.05). Final versus initial cytology scores were also significantly better in supplemented subjects (1.95 versus 2.32, respectively; p less than 0.05), unchanged in patients receiving the placebo (2.27 versus 2.30, respectively). Before treatment the mean red cell folate concentration was lower among oral contraceptive agent users than nonusers (189 versus 269 ng/ml, respectively; p less than 0.01) and even lower among users with dysplasia (161 versus 269 ng/ml, respectively; p less than 0.001). Morphological features of megaloblastosis were associated with dysplasia and also improved in folate supplemented subjects. These studies indicate that either a reversible, localized derangement in folate metabolism may sometimes be misdiagnosed as cervical dysplasia, or else such a derangement is an integral component of the dysplastic process that may be arrested or in some cases reversed by oral folic acid supplementation.
47名经宫颈涂片诊断为轻度或中度子宫颈发育异常(宫颈上皮内瘤变)的年轻女性,在双盲条件下,每日口服补充10毫克叶酸或安慰剂(10毫克抗坏血酸),持续3个月。所有受试者均使用复方口服避孕药至少6个月,并在每月复诊进行随访检查期间继续服用。试验期结束时,所有涂片及活检样本均由一名不知治疗情况的观察者,使用任意评分系统(1为正常,2为轻度,3为中度,4为重度,5为原位癌)进行分类。补充叶酸的受试者活检平均评分显著优于未补充叶酸的受试者(分别为2.28和2.92;p<0.05)。补充叶酸的受试者最终细胞学评分与初始评分相比也显著更好(分别为1.95和2.32;p<0.05),而接受安慰剂的患者评分无变化(分别为2.27和2.30)。治疗前,口服避孕药使用者的平均红细胞叶酸浓度低于未使用者(分别为189和269纳克/毫升;p<0.01),发育异常的使用者中更低(分别为161和269纳克/毫升;p<0.001)。巨幼细胞贫血的形态学特征与发育异常相关,在补充叶酸的受试者中也有所改善。这些研究表明, 叶酸代谢中可逆的局部紊乱有时可能被误诊为宫颈发育异常,或者这种紊乱是发育异常过程的一个组成部分,口服补充叶酸可能会阻止这种紊乱,在某些情况下甚至使其逆转。