Migliaretti G, Aimaretti G, Borraccino A, Bellone J, Vannelli S, Angeli A, Benso L, Bona G, Camanni F, de Sanctis C, Ravaglia A, Cavallo F
Department of Public Health and Microbiology, University of Turin, Turin, Italy.
J Endocrinol Invest. 2006 May;29(5):438-42. doi: 10.1007/BF03344127.
The aim of this study is to estimate the annual incidence and prevalence rate of the GH treatment exposure in patients under the age of 18 treated for hypopituitarism or isolated GH deficiency (GHD) in Piedmont, during the period January 1, 2002 to December 31, 2004.
The selection criteria for recombinant human GH (rhGH) treatment in childhood were approved by the Ministry of Health in Italy in the yr 1998. The present analysis is based on data from the Registry of subjects receiving GH therapy (GH Registry) made up of the 918 pediatric patients (age <18 yr) with a diagnosis of GHD (excluding Prader-Willi and Turner syndromes and other conditions), diagnosed in the period January 1, 2002 - December 31, 2004. The case series has been described as regards the number of cases per year of diagnosis; the prevalence and incidence rates, calculated per 10,000 (per ten thousand) inhabitants, are given for each year of the study period.
The prevalence rate increases slightly from 8.62 per thousand in 2002 to 9.44 per thousand in 2004 and the incidence rates estimated were 2.49 per ten thousand, 1.86 per ten thousand and 1.97 per ten thousand in the yr 2002, 2003 and 2004, respectively.
The Piedmont GH Registry represents the first database available in Italy and could set an example for the other Italian regions as well.
本研究旨在估算2002年1月1日至2004年12月31日期间,意大利皮埃蒙特地区18岁以下因垂体功能减退或孤立性生长激素缺乏(GHD)接受生长激素(GH)治疗的患者中,GH治疗暴露的年发病率和患病率。
1998年意大利卫生部批准了儿童期重组人生长激素(rhGH)治疗的选择标准。本分析基于生长激素治疗登记处(GH登记处)的数据,该登记处由2002年1月1日至2004年12月31日期间诊断为GHD(不包括普拉德-威利综合征、特纳综合征和其他病症)的918名儿科患者(年龄<18岁)组成。已按每年诊断的病例数描述了病例系列;给出了研究期间各年每10000(万)居民计算的患病率和发病率。
患病率从2002年的千分之8.62略有上升至2004年的千分之9.44,估计发病率在2002年、2003年和2004年分别为万分之2.49、万分之1.86和万分之1.97。
皮埃蒙特GH登记处是意大利首个可用的数据库,也可为其他意大利地区树立榜样。