Grandolfo M E, Sagliocca L, Stazi M A, Medda E, Olivieri A, Sorcini M
Laboratorio di Epidemiologia e Biostatistica, Instituto Superiore di Sanità, Roma.
Ann Ist Super Sanita. 1994;30(3):295-8.
The availability of a National Register of congenital hypothyroid infants allowed to perform descriptive studies on characteristics of the cases and the efficiency of the neonatal screening. Continuous and exhaustive recording of data concerning congenital hypothyroidism cases provided valuable epidemiological informations about congenital hypothyroidism in Italy. Moreover, the National Register allowed to develop a network of collaboration which can promote a population based case-control study. As the etiopathogenesis of congenital hypothyroidism has not been completely elucidated, performing of a case-control study can contribute to evidence the most important risk factors of congenital hypothyroidism and to improve the prevention also by prenatal diagnosis of this disease. Screening centers will be involved in the study and questionnaires of the National Register for congenital hypothyroidism will be used to record case and control informations. A biological bank concerning cases, controls and their parents, will be organized.
全国先天性甲状腺功能减退症婴儿登记册的建立,使得对病例特征和新生儿筛查效率进行描述性研究成为可能。对先天性甲状腺功能减退症病例数据的持续详尽记录,提供了有关意大利先天性甲状腺功能减退症的宝贵流行病学信息。此外,全国登记册有助于建立一个合作网络,从而推动基于人群的病例对照研究。由于先天性甲状腺功能减退症的病因尚未完全阐明,开展病例对照研究有助于找出先天性甲状腺功能减退症最重要的风险因素,并通过对该疾病的产前诊断来改进预防措施。筛查中心将参与这项研究,并使用先天性甲状腺功能减退症全国登记册的问卷来记录病例和对照信息。将建立一个涉及病例、对照及其父母的生物样本库。