C9orf72重复序列与神经变性疾病相关的元分析。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Journal of neurogenetics Pub Date : 2024-03-01 Epub Date: 2024-05-20 DOI:10.1080/01677063.2024.2343672
Pingfei Jin, Yong Li, Yao Li
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引用次数: 0

摘要

对 9 号染色体开放阅读框 72 (C9orf72) GGGGCC (G4C2) 与神经退行性疾病(NDs)(包括阿尔茨海默病(AD)、帕金森病(PD)、多系统萎缩(MSA)、进行性核上性麻痹(PSP)和皮质基底变性(CBD))之间的关系进行荟萃分析。我们检索了 EMBASE、PubMed、Web of Science 和 Cochrane 数据库。共纳入 27 项病例对照研究,包括 7202 例 AD、5856 例 PD、644 例 MSA、439 例 PSP 和 477 例 CBD 病例。该研究表明,C9orf72 重复扩增(>30)与 AD、MSA、PSP 和 CBD 相关(AD:OR = 4.88,95% CI = 2.71-8.78;MSA:OR=6.98,95% CI=1.48-33.01;PSP:OR=10.04,95% CI=2.72-37.10;CBD:或 = 28.04,95% CI = 10.17-77.31)。C9orf72 中间重复扩展(20-30)与 AD 和 MSA 无关(AD:OR = 1.16,95% CI = 0.39-3.45;MSA:OR = 5.65,95% CI = 0.69-46.19),而 C9orf72 中间重复扩展(20-30)与 AD 和 MSA 无关(AD:OR = 1.16,95% CI = 0.39-3.45;MSA:OR = 5.65,95% CI = 0.69-46.19)。19),而C9orf72重复扩增(>30)与PD风险无关(OR = 1.51,95% CI = 0.55-4.17),C9orf72中间重复扩增(20-30)确实与PD有关(OR = 2.43,95% CI = 1.20-4.9)。由于致病性扩增的数量不同,C9orf72 G4C2重复扩增在各种ND中的病理机制也不同。测量C9orf72 G4C2重复序列的数量可能有助于对各种ND进行早期鉴别诊断。
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Meta-analysis of the association between C9orf72 repeats and neurodegeneration diseases.

To conduct a meta-analysis investigating the relationship between the chromosome 9 open reading frame 72 (C9orf72) GGGGCC (G4C2) and neurodegenerative diseases (NDs), including Alzheimer's disease (AD), Parkinson's disease (PD), multiple system atrophy (MSA), progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD). We searched the EMBASE, PubMed, Web of Science, and Cochrane databases. Twenty-seven case-control studies were included, comprising 7202 AD, 5856 PD, 644 MSA, 439 PSP, and 477 CBD cases. This study demonstrated that C9orf72 repeat expansions (>30) were associated with AD, MSA, PSP, and CBD (AD: OR = 4.88, 95% CI = 2.71-8.78; MSA: OR = 6.98, 95% CI = 1.48-33.01; PSP: OR =10.04, 95% CI = 2.72-37.10; CBD: OR = 28.04, 95% CI = 10.17-77.31). C9orf72 intermediate repeat expansions (20-30) were not associated with AD and MSA (AD: OR = 1.16, 95% CI = 0.39-3.45; MSA: OR = 5.65, 95% CI = 0.69-46.19), while C9orf72 repeat expansions (>30) were not associated with the risk of PD (OR = 1.51, 95% CI = 0.55-4.17), C9orf72 intermediate repeat expansions (20-30) were indeed associated with PD (OR = 2.43, 95% CI = 1.20-4.9). The pathological mechanism of C9orf72 G4C2 repeat expansions differs across various NDs due to the varying number of pathogenic expansions. Measuring the number of C9orf72 G4C2 repeats may be useful in the early-stage differential diagnosis of various NDs.

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来源期刊
Journal of neurogenetics
Journal of neurogenetics 医学-神经科学
CiteScore
4.40
自引率
0.00%
发文量
13
审稿时长
>12 weeks
期刊介绍: The Journal is appropriate for papers on behavioral, biochemical, or cellular aspects of neural function, plasticity, aging or disease. In addition to analyses in the traditional genetic-model organisms, C. elegans, Drosophila, mouse and the zebrafish, the Journal encourages submission of neurogenetic investigations performed in organisms not easily amenable to experimental genetics. Such investigations might, for instance, describe behavioral differences deriving from genetic variation within a species, or report human disease studies that provide exceptional insights into biological mechanisms
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