Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.

IF 1.1 4区 生物学 Medizinische Genetik Pub Date : 2022-05-07 eCollection Date: 2022-04-01 DOI:10.1515/medgen-2022-2115
Veronika Sanin, Raphael Schmieder, Sara Ates, Lea Dewi Schlieben, Jens Wiehler, Ruoyu Sun, Manuela Decker, Michaela Sander, Stefan Holdenrieder, Florian Kohlmayer, Anna Friedmann, Volker Mall, Therese Feiler, Arne Dreßler, Tim M Strom, Holger Prokisch, Thomas Meitinger, Moritz von Scheidt, Wolfgang Koenig, Georg Leipold, Heribert Schunkert
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Abstract

Familial hypercholesterolemia (FH) is the most frequent monogenic disorder (prevalence 1:250) in the general population. Early diagnosis during childhood enables pre-emptive treatment, thus reducing the risk of severe atherosclerotic manifestations later in life. Nonetheless, FH screening programs are scarce. VRONI offers all children aged 5-14 years in Bavaria a FH screening in the context of regular pediatric visits. LDL-cholesterol (LDL-C) is measured centrally, followed by genetic analysis for FH if exceeding the age-specific 95th percentile (130 mg/dl, 3.34 mmol/l). Children with FH pathogenic variants are treated by specialized pediatricians and offered a FH-focused training course by a qualified training center. Reverse cascade screening is recommended for all first-degree relatives. VRONI aims to prove the feasibility of a population-based FH screening in children and to lay the foundation for a nationwide screening program.

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为早期诊断和治疗家族性高胆固醇血症而对儿童进行的人群筛查:VRONI 研究的设计。
家族性高胆固醇血症(FH)是普通人群中最常见的单基因疾病(发病率为 1:250)。儿童期的早期诊断可使患者得到先期治疗,从而降低日后出现严重动脉粥样硬化表现的风险。然而,FH 筛查项目却很少。在巴伐利亚州,VRONI 为所有 5-14 岁的儿童在定期儿科就诊时提供 FH 筛查。对低密度脂蛋白胆固醇(LDL-C)进行集中测量,如果超过特定年龄的第 95 百分位数(130 毫克/分升,3.34 毫摩尔/升),则进行 FH 基因分析。有 FH 致病变异的儿童由专业儿科医生治疗,并由合格的培训中心提供以 FH 为重点的培训课程。建议对所有一级亲属进行逆向级联筛查。VRONI 的目的是证明基于人群的儿童 FH 筛查的可行性,并为在全国范围内开展筛查计划奠定基础。
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来源期刊
Medizinische Genetik
Medizinische Genetik GENETICS & HEREDITY-
自引率
9.10%
发文量
48
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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