PytheasDB:罕见儿科消化系统疾病临床数据的开放获取图形数据库。

IF 1.1 Q2 MEDICINE, GENERAL & INTERNAL
Alice Percheron, Paul Guerry, Alexandre Fabre
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引用次数: 0

摘要

在过去的几十年里,基因检测的进步推动了罕见遗传病的诊断和报告的持续增加,但尚未开发出一种工具来汇总已发表的分子和表型数据,尽管如此,这项任务对于优化患者护理至关重要。在这篇文章中,我们介绍了PytheasDB,一个罕见消化系统疾病患者已发表临床数据的在线数据库。在撰写本文时(2024年8月),该数据库包含来自172篇文章的833例进行性家族性肝内胆汁淤积或trichoho肝肠综合征患者的数据。用户可以比较所包括疾病的表型、性别比例、生存曲线、首次出现症状的年龄和近亲比率。PytheasDB是有史以来第一个提供文献中罕见消化系统疾病病例报告汇总临床数据的在线资源。该数据库目前正在扩展,以覆盖超罕见的儿科消化系统疾病,并定期更新,以优化这些疾病的研究和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PytheasDB: An open-access graphical database of clinical data on rare pediatric digestive diseases.

Advances in genetic testing over the past decades are driving a continuing increase in the diagnosis and reporting of rare genetic diseases, but no tool has yet been developed to aggregate published molecular and phenotypic data, a task that is nevertheless essential to optimize patient care. In this article, we present PytheasDB, an online database of published clinical data from patients with rare digestive diseases. At the time of writing (August 2024), the database contains data from 833 patients with progressive familial intrahepatic cholestasis or trichohepatoenteric syndrome, collected from 172 articles. Users can compare the phenotypic profiles, sex ratios, survival curves, ages at first symptoms, and consanguinity rates of the included diseases. PytheasDB is the first ever online resource providing access to aggregated clinical data from case reports of rare digestive diseases in the literature. The database is currently being expanded to cover ultra-rare pediatric digestive diseases with regular updates to optimize the study and treatment of these diseases.

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来源期刊
Intractable & rare diseases research
Intractable & rare diseases research MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
0.00%
发文量
29
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