新生儿筛查的二级策略——潜力和局限性

IF 0.8 4区 生物学 Q4 GENETICS & HEREDITY Medizinische Genetik Pub Date : 2022-05-07 eCollection Date: 2022-04-01 DOI:10.1515/medgen-2022-2117
Gwendolyn Gramer, Georg F Hoffmann
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引用次数: 0

摘要

摘要新生儿筛查(NBS)是一种公共卫生措施,用于识别出生后第一天内患有可治疗疾病的儿童,并允许进行症状前治疗。这是世界上许多国家最成功的二级医疗预防措施,也是公共卫生计划的一部分。在NBS中应用第二层策略可以提高特异性,并连续获得更高的阳性预测值。第二层策略可以包括对靶向疾病的特定生物标志物的分析,或者可以基于分子遗传分析。提高NBS的质量,例如通过二级策略,对于保持家庭对NBS的高度接受至关重要——尤其是在越来越多的目标疾病被连续纳入NBS计划的情况下。
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Second-tier strategies in newborn screening - potential and limitations.

Newborn screening (NBS) is a public health measure to identify children with treatable disorders within the first days of life allowing presymptomatic treatment. It is the most successful measure of secondary medical prevention and part of public health programs in many countries worldwide. Application of second-tier strategies in NBS allows for increased specificity and consecutively a higher positive predictive value. Second-tier strategies can include analysis of specific biomarkers for a target disorder or may be based on molecular genetic analyses. Improving the quality of NBS, for example by second-tier strategies, is of utmost importance to maintain the high acceptance of NBS by families - especially as an increasing number of target disorders is being consecutively included into NBS programs.

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来源期刊
Medizinische Genetik
Medizinische Genetik Medicine-Genetics (clinical)
CiteScore
1.40
自引率
9.10%
发文量
48
审稿时长
>12 weeks
期刊介绍: medizinischegenetik is a scientific journal that is owned and published by the German Society of Human Genetics e.V. since 1989. The journal was founded by Prof. Jan Murken, München. Self-published until 2006, from 2007-2019 published at Springer Verlag and since 2020 at De Gruyter. medizinischegenetik serves education and training among colleagues, the interdisciplinary exchange of knowledge in all areas of human genetics in clinics, practice, research and teaching. Each issue of the quarterly journal deals with a focus that provides a comprehensive overview of current developments in specific clinical pictures, technical developments and therapeutic approaches. All reviews are written in English language. The journal thus creates a platform for the international exchange of knowledge and increased awareness of German research activities in the scientific community. In addition, medizinischegenetik contains information on activities in its own subject in the German-language section. This includes conference reports, association announcements, personnel matters, statements and guidelines. With health policy questions, historical retrospectives and comments on current developments, the profession takes a stand on human genetic issues in Germany, Austria and Switzerland.
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