早期诊断、疾病变异和护理质量对枫糖尿症神经认知结果的影响:一项荟萃分析。

IF 6.6 1区 医学 Q1 GENETICS & HEREDITY Genetics in Medicine Pub Date : 2024-10-17 DOI:10.1016/j.gim.2024.101303
Svenja Scharre, Katharina Mengler, Elena Schnabel, Oya Kuseyri Hübschmann, Ali Tunç Tuncel, Georg Friedrich Hoffmann Gf, Sven F Garbade, Ulrike Mütze, Stefan Kölker
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引用次数: 0

摘要

目的:枫糖尿症(MSUD)是一种罕见的遗传性代谢疾病,其特点是反复出现代谢失代偿、神经认知障碍和预期寿命有限。本荟萃分析旨在评估新生儿筛查(NBS)的早期诊断对幸存者死亡率和神经认知结果的影响,同时考虑到国家医疗保健系统的质量:方法:根据 PRISMA-P 进行系统文献检索。方法:根据 PRISMA-P 进行系统性文献检索,采用荟萃分析方法分析对结果参数的影响,并重新分析个体参与者的数据:结果:共纳入 33 项研究,报告了 1141 名 MSUD 患者。与变异型 MSUD 相比,典型 MSUD 患者的表型更为严重,表现为死亡率更高(17.1% 对 0%),智商中位数更低(90 对 104;PC 结论:NBS 是治疗 MSUD 的先决条件:NBS是改善MSUD患者预后的先决条件;然而,健康效益关键取决于国家医疗保健系统的质量。
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Impact of early diagnosis, disease variant, and quality of care on the neurocognitive outcome in maple syrup urine disease: a meta-analysis.

Purpose: Maple syrup urine disease (MSUD) is a rare inherited metabolic disease characterised by recurrent metabolic decompensations, neurocognitive impairment, and limited life expectancy. This meta-analysis aims to evaluate the impact of early diagnosis by newborn screening (NBS) on mortality and neurocognitive outcome in survivors, taking into account the quality of national healthcare systems.

Methods: Systematic literature search was performed according to PRISMA-P. Effects on outcome parameters were analysed using meta-analytical measures and re-analysis of individual participant data.

Results: Thirty-three studies were included, reporting on 1141 individuals with MSUD. Participants with classic MSUD presented a more severe phenotype compared to variant MSUD as demonstrated by higher mortality rate (17.1% versus 0%), and lower median IQ (90 versus 104; P<.001, linear mixed model). NBS was associated with improved cognition (mean IQ: 95 versus 82; P=.014, random effects model), and decreased mortality (3% versus 14.6%; P=.028, Kaplan-Meier estimates) compared to individuals identified after onset of symptoms, in trend even after exclusion of individuals with variant MSUD. Quality of national healthcare systems correlated with survival (P=.025, meta-regression) and permanent neurological symptoms (P=.031, meta-regression).

Conclusion: NBS is a prerequisite to improved outcome in individuals with MSUD; however, health benefit critically depends on the quality of the national healthcare systems.

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来源期刊
Genetics in Medicine
Genetics in Medicine 医学-遗传学
CiteScore
15.20
自引率
6.80%
发文量
857
审稿时长
1.3 weeks
期刊介绍: Genetics in Medicine (GIM) is the official journal of the American College of Medical Genetics and Genomics. The journal''s mission is to enhance the knowledge, understanding, and practice of medical genetics and genomics through publications in clinical and laboratory genetics and genomics, including ethical, legal, and social issues as well as public health. GIM encourages research that combats racism, includes diverse populations and is written by authors from diverse and underrepresented backgrounds.
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