首页> 外文期刊>Chinese Medical Journal >PRELIMINARY REPORT ON THE RESULTS OF NUTRITION PREVENTION TRIALS OF CANCER AND OTHER COMMON DISEASES AMONG RESIDENTS IN LINXIAN, CHINA
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PRELIMINARY REPORT ON THE RESULTS OF NUTRITION PREVENTION TRIALS OF CANCER AND OTHER COMMON DISEASES AMONG RESIDENTS IN LINXIAN, CHINA

机译:临县居民癌症及其他常见疾病的营养预防试验结果初报

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摘要

To examine whether vitamin / mineral supplementation may lower mortality and incidence for human cancer and mortality from other diseases as well as to provide the scientific basis and feasible approach for human cancer prevention and control, from 1982 to 1991 scientists from China and USA conducted two randomized, double-blind, placebo-controlled nutrition intervention trials in Linxian, China, where the mortality rates of esophageal and gastric cardia cancer are among the highest in the world and there is suspicion that the population's chronic deficiencies of multiple nutrients are etiologically involved. In the first trial, the Dysplasia trial, 3318 individuals with a cytological diagnosis of esophageal dysplasia received daily 26 vitamin / mineral supplements or placebo for 6 years. The second trial, the General Population Trial, involved 29584 individuals and used a one—half replicate of a 2~4 fractional factorial design that randomized to 8 groups for testing the effects of daily supplementation of 4 different vitamin / mineral combinations and placebo for a period of 5.25 years. Compliance assessed by monthly pill counts and quarterly monitoring of biochemical assays indicated that the participant compliance was excellent. As endpoints of the trials, incident cancers and deaths were identified through all medical facilities in local areas, supplemented by special endoscopy and cytology examinations, and confirmed by 3—level review groups.
机译:为了研究维生素/矿物质补充剂是否可以降低人类癌症的死亡率和发病率以及其他疾病的死亡率,并为人类癌症的预防和控制提供科学依据和可行的方法,从1982年到1991年,中美两国科学家进行了两次随机分组,是在中国临县进行的一项双盲,安慰剂对照的营养干预试验,该地区的食管癌和gastric门癌死亡率是世界上最高的,并且有可能是人群长期缺乏多种营养素的病因。在第一个试验(发育异常试验)中,有3318位经细胞学诊断为食管发育异常的个体每天接受26种维生素/矿物质补充剂或安慰剂治疗6年。第二项试验是“一般人群试验”,涉及29584名个体,并使用了2〜4个分数阶乘设计的一半重复样本,将其随机分为8个组,以测试每日补充4种不同的维生素/矿物质组合和安慰剂的效果。期限为5.25年。通过每月药丸计数和生化测定的季度监测评估的依从性表明参与者的依从性非常好。作为试验的终点,通过当地的所有医疗机构识别出事件性癌症和死亡,并辅以专门的内窥镜检查和细胞学检查,并由三级审查小组确认。

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