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魁北克尼曼-皮克 C 型病的估计患病率。

Estimated prevalence of Niemann-Pick type C disease in Quebec.

机构信息

Bioinformatics Program, Department of Biochemistry and Molecular Medicine, Université de Montréal, Montréal, QC, Canada.

CHUM Research Center, Tour Viger, 900 rue Saint-Denis, R, Montréal, QC, H2X 0A9, Canada.

出版信息

Sci Rep. 2021 Nov 19;11(1):22621. doi: 10.1038/s41598-021-01966-0.

Abstract

Niemann-Pick type C (NP-C) disease is an autosomal recessive disease caused by variants in the NPC1 or NPC2 genes. It has a large range of symptoms depending on age of onset, thus making it difficult to diagnose. In adults, symptoms appear mainly in the form of psychiatric problems. The prevalence varies from 0.35 to 2.2 per 100,000 births depending on the country. The aim of this study is to calculate the estimated prevalence of NP-C in Quebec to determine if it is underdiagnosed in this population. The CARTaGENE database is a unique database that regroups individuals between 40 and 69 years old from metropolitan regions of Quebec. RNA-sequencing data was available for 911 individuals and exome sequencing for 198 individuals. We used a bioinformatic pipeline on those individuals to extract the variants in the NPC1/2 genes. The prevalence in Quebec was estimated assuming Hardy-Weinberg Equilibrium. Two pathogenic variants were used. The variant p.Pro543Leu was found in three heterozygous individuals that share a common haplotype, which suggests a founder French-Canadian pathogenic variant. The variant p.Ile1061Thr was found in two heterozygous individuals. Both variants have previously been reported and are usually associated with infantile onset. The estimated prevalence calculated using those two variants is 0.61:100,000 births. This study represents the first estimate of NP-C in Quebec. The estimated prevalence for NP-C is likely underestimated due to misdiagnosis or missed cases. It is therefore important to diagnose all NP-C patients to initiate early treatment.

摘要

尼曼-皮克 C 型(NP-C)疾病是一种常染色体隐性疾病,由 NPC1 或 NPC2 基因的变异引起。它的症状范围广泛,取决于发病年龄,因此难以诊断。在成年人中,症状主要表现为精神问题。患病率因国家而异,在每 10 万出生儿中有 0.35 至 2.2 例。本研究旨在计算魁北克 NP-C 的估计患病率,以确定该人群是否存在诊断不足的情况。CARTaGENE 数据库是一个独特的数据库,汇集了来自魁北克大都市区 40 至 69 岁的个体。为 911 名个体提供了 RNA 测序数据,为 198 名个体提供了外显子组测序数据。我们使用这些个体的生物信息学管道提取 NPC1/2 基因中的变异。假设 Hardy-Weinberg 平衡,计算了魁北克的患病率。使用了两种致病性变异。p.Pro543Leu 变异在三个共享常见单倍型的杂合个体中发现,这表明存在一个法裔加拿大的致病变异。p.Ile1061Thr 变异在两个杂合个体中发现。这两种变异以前都有报道,通常与婴儿发病有关。使用这两种变异计算的估计患病率为 0.61:100,000 出生儿。本研究代表了魁北克首例 NP-C 的估计。由于误诊或漏诊,NP-C 的估计患病率可能被低估。因此,诊断所有 NP-C 患者并尽早开始治疗非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d85/8604933/581ba1378560/41598_2021_1966_Fig1_HTML.jpg

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