Screening of Islet Autoantibodies for Children in the General Population: A Position Statement Endorsed by the European Society for Paediatric Endocrinology

医学 人口 1型糖尿病 儿科 糖尿病酮症酸中毒 糖尿病前期 新生儿筛查 入射(几何) 自身抗体 疾病 公共卫生 家庭医学 糖尿病 2型糖尿病 内科学 内分泌学 免疫学 环境卫生 护理部 物理 抗体 光学
作者
Francesco Chiarelli,Marian Rewers,Moshe Phillip
出处
期刊:Hormone Research in Paediatrics [S. Karger AG]
卷期号:95 (4): 393-396 被引量:6
标识
DOI:10.1159/000525824
摘要

<b><i>Background:</i></b> Type 1 diabetes (T1D) is the most frequent chronic autoimmune disease in childhood and adolescence, its incidence is increasing particularly in toddlers and preschool children, and up to 60% of young patients present with diabetic ketoacidosis (DKA), a severe and life-threatening complication. So far, the majority of screening efforts have been performed in the at-risk group, i.e., relatives of people with T1D; anyhow, around 90% of young patients who eventually develop T1D do not have a family history. <b><i>Summary:</i></b> Some studies in Europe and the USA have clearly shown that a public health screening of children (with positive autoantibodies) is effective in reducing the prevalence of DKA by more than 10 times, decreasing the rate of hospitalization and its costs, providing psychological, emotional, and social support to children and their families. In addition, several treatments and trials are available for children with stage 2 and stage 3 T1D. There is still room for improvement of sensitivity, specificity, positive and negative predictive value in a population screening program; anyhow, there is vivid debate on the opportunity for a screening program in the general population of children at risk for developing T1D. <b><i>Key Messages:</i></b> This paper, endorsed by the European Society for Paediatric Endocrinology (ESPE), discusses the issues of a screening program in the general population with the hope that uncertainties and difficulties in this field will be overcome by better screening methods, improved cost-effectiveness, reliable treatments for secondary prevention, and relevant delay in clinically evident T1D in children and adolescents.

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