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基因中的中间重复序列扩增作为西班牙人群肌萎缩侧索硬化症和额颞叶痴呆的一个风险因素。

Intermediate Repeat Expansion in the Gene as a Risk Factor in the ALS and FTD Spanish Population.

作者信息

Borrego-Hernández Daniel, Vázquez-Costa Juan Francisco, Domínguez-Rubio Raúl, Expósito-Blázquez Laura, Aller Elena, Padró-Miquel Ariadna, García-Casanova Pilar, Colomina María J, Martín-Arriscado Cristina, Osta Rosario, Cordero-Vázquez Pilar, Esteban-Pérez Jesús, Povedano-Panadés Mónica, García-Redondo Alberto

机构信息

ALS Research Laboratory Unit, Department of Neurology, Hospital Universitario 12 de Octubre, 28041 Madrid, Spain.

Neuromuscular Unit, ERN-NMD Group, Department of Neurology, Hospital Universitario y Politécnico La Fe, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.

出版信息

Biomedicines. 2024 Feb 2;12(2):356. doi: 10.3390/biomedicines12020356.

Abstract

Intermediate CAG expansions in the gene ataxin-2 () are a known risk factor for ALS, but little is known about their role in FTD risk. Moreover, their contribution to the risk and phenotype of patients might vary in populations with different genetic backgrounds. The aim of this study was to assess the relationship of intermediate CAG expansions in with the risk and phenotype of ALS and FTD in the Spanish population. Repeat-primed PCR was performed in 620 ALS and 137 FTD patients in three referral centers in Spain to determine the exact number of CAG repeats. In our cohort, ≥27 CAG repeats in were associated with a higher risk of developing ALS (odds ratio [OR] = 2.666 [1.471-4.882]; = 0.0013) but not FTD (odds ratio [OR] = 1.446 [0.558-3.574]; = 0.44). Moreover, ALS patients with ≥27 CAG repeats in showed a shorter survival rate compared to those with <27 repeats (hazard ratio [HR] 1.74 [1.18, 2.56], = 0.005), more frequent limb onset (odds ratio [OR] = 2.34 [1.093-4.936]; = 0.028) and a family history of ALS (odds ratio [OR] = 2.538 [1.375-4.634]; = 0.002). Intermediate CAG expansions of ≥27 repeats in are associated with ALS risk but not with FTD in the Spanish population. ALS patients carrying an intermediate expansion in show more frequent limb onset but a worse prognosis than those without expansions. In patients carrying expansions, the intermediate expansion might increase the penetrance and modify the phenotype.

摘要

ataxin-2()基因中的中间CAG重复序列扩增是肌萎缩侧索硬化症(ALS)的已知危险因素,但对其在额颞叶痴呆(FTD)风险中的作用知之甚少。此外,它们对不同遗传背景人群患者的风险和表型的影响可能有所不同。本研究的目的是评估西班牙人群中ataxin-2基因中间CAG重复序列扩增与ALS和FTD的风险及表型之间的关系。在西班牙三个转诊中心的620例ALS患者和137例FTD患者中进行了重复引物PCR,以确定CAG重复的确切数目。在我们的队列中,ataxin-2基因中≥27个CAG重复序列与发生ALS的较高风险相关(比值比[OR]=2.666[1.471-4.882];P=0.0013),但与FTD无关(比值比[OR]=1.446[0.558-3.574];P=0.44)。此外,ataxin-2基因中具有≥27个CAG重复序列的ALS患者与重复序列<27个的患者相比,生存率较低(风险比[HR]1.74[1.18,2.56],P=0.005),肢体起病更频繁(比值比[OR]=2.34[1.093-4.936];P=0.028),且有ALS家族史(比值比[OR]=2.538[1.375-4.634];P=0.002)。在西班牙人群中,ataxin-2基因中≥27个重复序列的中间CAG扩增与ALS风险相关,但与FTD无关。携带ataxin-2基因中间扩增的ALS患者肢体起病更频繁,但预后比未扩增的患者更差。在携带ataxin-2基因扩增的患者中,中间扩增可能会增加外显率并改变表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9dc/10886453/1f4e130f36e5/biomedicines-12-00356-g001.jpg

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