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国家出生缺陷预防研究

The National Birth Defects Prevention Study.

作者信息

Yoon P W, Rasmussen S A, Lynberg M C, Moore C A, Anderka M, Carmichael S L, Costa P, Druschel C, Hobbs C A, Romitti P A, Langlois P H, Edmonds L D

机构信息

National Center for Environmental Health, Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia 30341-3724, USA.

出版信息

Public Health Rep. 2001;116 Suppl 1(Suppl 1):32-40. doi: 10.1093/phr/116.S1.32.

Abstract

The National Birth Defects Prevention Study was designed to identify infants with major birth defects and evaluate genetic and environmental factors associated with the occurrence of birth defects. The ongoing case-control study covers an annual birth population of 482,000 and includes cases identified from birth defect surveillance registries in eight states. Infants used as controls are randomly selected from birth certificates or birth hospital records. Mothers of case and control infants are interviewed and parents are asked to collect buccal cells from themselves and their infants for DNA testing. Information gathered from the interviews and the DNA specimens will be used to study independent genetic and environmental factors and gene-environment interactions for a broad range of birth defects. As of December 2000, 7,470 cases and 3,821 controls had been ascertained in the eight states. Interviews had been completed with 70% of the eligible case and control mothers, buccal cell collection had begun in all of the study sites, and researchers were developing analysis plans for the compiled data. This study is the largest and broadest collaborative effort ever conducted among the nation's leading birth defect researchers. The unprecedented statistical power that will result from this study will enable scientists to study the epidemiology of some rare birth defects for the first time. The compiled interview data and banked DNA of approximately 35 categories of birth defects will facilitate future research as new hypotheses and improved technologies emerge.

摘要

国家出生缺陷预防研究旨在识别患有主要出生缺陷的婴儿,并评估与出生缺陷发生相关的遗传和环境因素。正在进行的病例对照研究涵盖了每年48.2万的出生人口,并包括从八个州的出生缺陷监测登记处识别出的病例。用作对照的婴儿是从出生证明或出生医院记录中随机选取的。对病例组和对照组婴儿的母亲进行访谈,并要求父母采集他们自己和婴儿的颊细胞用于DNA检测。从访谈和DNA样本中收集的信息将用于研究广泛出生缺陷的独立遗传和环境因素以及基因-环境相互作用。截至2000年12月,在这八个州已确定了7470例病例和3821例对照。已对70%符合条件的病例组和对照组母亲完成了访谈,所有研究地点均已开始采集颊细胞,研究人员正在为汇总数据制定分析计划。这项研究是美国主要出生缺陷研究人员有史以来规模最大、范围最广的合作努力。这项研究将产生前所未有的统计效力,使科学家能够首次研究一些罕见出生缺陷的流行病学。随着新假设和改进技术的出现,大约35类出生缺陷的汇总访谈数据和储存的DNA将促进未来的研究。

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