Suppr超能文献

脑腱性黄瘤病在德系犹太人中高发。

Cerebrotendinous Xanthomatosis occurs at high frequency in Ashkenazi Jews.

作者信息

Hanson Jennifer, Bonnen Penelope E

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

出版信息

Mol Genet Metab. 2025 Mar;144(3):109041. doi: 10.1016/j.ymgme.2025.109041. Epub 2025 Jan 22.

Abstract

Cerebrotendinous Xanthomatosis (CTX) is a treatable, inborn error of bile acids metabolism caused by pathogenic variants in CYP27A1. CTX is a multi-organ system disorder that progresses over decades. Clinical features include cerebellar dysfunction, pyramidal tract dysfunction, cognitive deficits and decline, peripheral neuropathy, chronic diarrhea, bilateral cataracts, and tendon xanthomas. Treatment is effective when started early, but diagnostic delays often result in individuals not being diagnosed until after the window of highest treatment efficacy. CTX is documented to occur in most global populations, however, no CTX-causing genetic variants have been reported in Ashkenazi Jews. We conducted a systematic review of every case of CTX reported in a person identified as Jewish and the specific CYP27A1 variants present. We also leveraged the Israeli Medical Genetics Database and the population genetics data resource gnomAD to identify CTX-causing alleles in Ashkenazi Jews. We found that there are three pathogenic CYP27A1 variants in the Ashkenazi Jewish population segregating at an appreciable frequency, with a gene carrier rate of 0.002 based on the gnomAD Ashkenazi Jewish data. One pathogenic variant appears only in the Ashkenazi Jewish group in gnomAD, which contains genetic data from across the globe. We compared the carrier frequency for CTX to the carrier frequencies for diseases that are commonly included in carrier screening for Ashkenazi Jews. These results show that CTX occurs in Ashkenazi Jews, and that both Sephardi and Ashkenazi Jews may benefit from newborn and carrier screening for CTX.

摘要

脑腱黄瘤病(CTX)是一种由CYP27A1基因的致病变异引起的可治疗的先天性胆汁酸代谢紊乱疾病。CTX是一种多器官系统疾病,病程长达数十年。临床特征包括小脑功能障碍、锥体束功能障碍、认知缺陷与衰退、周围神经病变、慢性腹泻、双侧白内障和肌腱黄瘤。早期开始治疗有效,但诊断延迟往往导致个体直到错过最高治疗疗效期才被确诊。文献记载CTX在全球大多数人群中都有发生,然而,在阿什肯纳兹犹太人中尚未报告过导致CTX的基因变异。我们对每一例被认定为犹太人的CTX病例以及所存在的特定CYP27A1变异进行了系统综述。我们还利用以色列医学遗传学数据库和群体遗传学数据资源gnomAD来识别阿什肯纳兹犹太人中导致CTX的等位基因。我们发现,在阿什肯纳兹犹太人群体中有三种致病性CYP27A1变异以可观的频率分离,根据gnomAD阿什肯纳兹犹太人的数据,基因携带率为0.002。在包含全球遗传数据的gnomAD中,有一种致病变异仅出现在阿什肯纳兹犹太人群体中。我们将CTX的携带者频率与阿什肯纳兹犹太人携带者筛查中通常包含的疾病的携带者频率进行了比较。这些结果表明,CTX在阿什肯纳兹犹太人中存在,并且西班牙裔犹太人和阿什肯纳兹犹太人都可能从CTX的新生儿筛查和携带者筛查中受益。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验