首页> 外文OA文献 >The Italian Twin Project: From the personal identification number to a national Twin Registry
【2h】

The Italian Twin Project: From the personal identification number to a national Twin Registry

机译:意大利双胞胎项目:从个人身份证号码到国家双胞胎注册中心

摘要

he unique opportunity given by the "fiscal code", an alphanumeric identification with demographic information on any single person residing in Italy, introduced in 1976 by the Ministry of Finance, allowed a database of all potential Italian twins to be created. This database contains up to now name, surname, date and place of birth and home address of about 1,300,000 "possible twins". Even thought we estimated an excess of 40% of pseudo-twins, this still is the world's largest twin population ever collected. The database of possible twins is currently used in population-based studies on multiple sclerosis, Alzheimer's disease, celiac disease, and type 1 diabetes. A system is currently being developed for linking the database with data from mortality and cancer registries. In 2001, the Italian Government, through the Ministry of Health, financed a broad national research program on twin studies, including the establishment of a national twin registry. Among all the possible twins, a sample of 500,000 individuals are going to be contacted and we expect to enrol around 120,000 real twin pairs in a formal Twin Registry. According to available financial resources, a sub sample of the enrolled population will be asked to donate DNA. A biological bank from twins will be then implemented, guaranteeing information on future etiological questions regarding genetic and modifiable factors for physical impairment and disability, cancers, cardiovascular diseases and other age related chronic illnesses.
机译:财政部于1976年推出了由“财政代码”提供的独特机会,“财政代码”是居住在意大利的任何单身人士的字母数字识别人口统计信息,从而可以创建所有潜在意大利双胞胎的数据库。该数据库包含到目前为止的姓名,姓氏,出生日期和地点以及大约1,300,000个“可能的双胞胎”的家庭住址。即使以为我们估计有超过40%的假双胞胎,这仍然是世界上有史以来最大的双胞胎种群。目前,可能的双胞胎数据库被用于基于人群的多发性硬化症,阿尔茨海默氏病,腹腔疾病和1型糖尿病研究。当前正在开发一种系统,用于将数据库与死亡率和癌症登记处的数据链接起来。 2001年,意大利政府通过卫生部资助了一项广泛的关于双胞胎研究的国家研究计划,包括建立了一个国家双胞胎注册中心。在所有可能的双胞胎中,将与500,000个人进行联系,我们预计将在正式的Twin Registry中注册大约120,000个真正的双胞胎。根据可用的财务资源,将要求已登记人群的子样本捐赠DNA。然后将建立一个由双胞胎组成的生物库,以保证有关将来的病因学问题的信息,这些问题涉及身体和残障,癌症,心血管疾病和其他与年龄有关的慢性病的遗传和可修改因素。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号