Impact of Newborn Screening on Survival and Developmental Outcome in Classic Isovaleric Aciduria: A Meta-Analysis

IF 3.8 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Anna T. Reischl-Hajiabadi, Sven F. Garbade, Florian Gleich, Elena Schnabel-Besson, Roland Posset, Matthias Zielonka, Georg F. Hoffmann, Stefan Kölker, Ulrike Mütze
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Abstract

Classic isovaleric aciduria (cIVA) is a rare inherited metabolic disorder characterized by recurrent life-threatening metabolic decompensations and neurocognitive impairment in untreated patients. This meta-analysis aims to assess the impact of early diagnosis by newborn screening (NBS) on mortality and neurocognitive outcome. A systematic literature search for articles published until 2022 was conducted following PRISMA protocol guidelines. We investigated effects on clinical outcomes and survival, analyzing outcome parameters using meta-analytical measures and estimating effect sizes with a random-effects model. Overall, 20 studies were included, reporting on 240 individuals with cIVA. Individuals identified by NBS presented with a lower frequency of neurological symptoms (13.0% vs. 44.9%; p = 0.0040) and developmental delay (6.1% vs. 51.2%; p < 0.0001), and had a lower mortality rate (1.1% vs. 10.9%; p = 0.0320). The quality of healthcare systems did not have a measurable impact on neurocognitive outcome and mortality. Despite the beneficial effect of NBS on clinical outcome and mortality, it could not reliably prevent the manifestation of neonatal decompensation in all individuals with cIVA identified by NBS. Early diagnosis through NBS is essential for the timely initiation of therapy and for improving outcomes and survival rates in individuals with cIVA.

Abstract Image

新生儿筛查对典型异戊酸尿患者生存和发育结局的影响:一项荟萃分析
经典异戊酸尿(cIVA)是一种罕见的遗传性代谢疾病,其特征是未经治疗的患者会出现复发性危及生命的代谢失代偿和神经认知障碍。本荟萃分析旨在评估新生儿筛查(NBS)早期诊断对死亡率和神经认知结果的影响。按照PRISMA协议指南,对2022年之前发表的文章进行了系统的文献检索。我们调查了对临床结果和生存的影响,使用荟萃分析方法分析了结果参数,并使用随机效应模型估计了效应大小。总共纳入了20项研究,报告了240名cIVA患者。NBS鉴定的个体表现出较低的神经症状频率(13.0%对44.9%,p = 0.0040)和发育迟缓(6.1%对51.2%,p < 0.0001),死亡率较低(1.1%对10.9%,p = 0.0320)。医疗保健系统的质量对神经认知结果和死亡率没有可测量的影响。尽管NBS对临床结果和死亡率有有益的影响,但它并不能可靠地预防所有经NBS鉴定的cIVA患者的新生儿失代偿表现。通过NBS进行早期诊断对于及时开始治疗以及改善cIVA患者的预后和生存率至关重要。
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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
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