古代罕见疾病数字图集(DAARD)及其对当前研究的意义。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Julia Gresky, Melina Frotscher, Juliane Dorn, Kristina Scheelen-Nováček, Yannick Ahlbrecht, Tina Jakob, Toni Schönbuchner, José Canalejo, Benjamin Ducke, Emmanuele Petiti
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引用次数: 0

摘要

背景:罕见病的历史大多不为人知。有关这一主题的研究主要集中在著名(历史)人物的个案和艺术(如图标)表现形式上。医学藏品中包括大量显示罕见疾病迹象的标本,但其中大部分都是相对较近时期的。不过,在木乃伊和考古发掘中发现的骨骼遗骸中也有罕见疾病的病例记录。然而,这些来自历史和考古背景的直接证据在学术讨论中主要是缺席的,在罕见疾病的医学研究中一般也不会参考:古代罕见疾病数字地图集》(DAARD: https://daard.dainst.org )解决了这一问题。该地图集是一个开放存取/开放数据数据库和网络制图工具,收集了全球所有历史和史前时期在骨骼和木乃伊中发现的各种罕见疾病的证据。该数据库易于搜索,可按诊断、遗骸保存程度、研究方法、收藏地点和出版物进行查询。在本手稿中,将以软骨发育不全和其他类型的发育迟缓为例,说明 DAARD 的设计和功能:DAARD作为一个开放的协作性资料库,可用于收集、绘制和查询自古以来有关个人的结构良好的医学数据,为研究开辟了新的途径。随着时间的推移,来自博物馆藏品和考古发掘等不同背景的新病例将会增加罕见病的数量。根据研究问题的不同,可以检索表型或遗传信息,以及选定时空间隔内罕见疾病的总体发生情况。此外,对于被诊断患有罕见疾病的人来说,这种方法可以帮助他们建立身份认同,并揭示他们可能没有意识到的病情的某个方面。因此,DAARD 有助于从长远角度了解罕见病,并为最新医学研究添砖加瓦。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Digital Atlas of Ancient Rare Diseases (DAARD) and its relevance for current research.

Background: The history of rare diseases is largely unknown. Research on this topic has focused on individual cases of prominent (historical) individuals and artistic (e.g., iconographic) representations. Medical collections include large numbers of specimens that exhibit signs of rare diseases, but most of them date to relatively recent periods. However, cases of rare diseases detected in mummies and skeletal remains derived from archaeological excavations have also been recorded. Nevertheless, this direct evidence from historical and archaeological contexts is mainly absent from academic discourse and generally not consulted in medical research on rare diseases.

Results: This desideratum is addressed by the Digital Atlas of Ancient Rare Diseases (DAARD: https://daard.dainst.org ), which is an open access/open data database and web-based mapping tool that collects evidence of different rare diseases found in skeletons and mummies globally and throughout all historic and prehistoric time periods. This easily searchable database allows queries by diagnosis, the preservation level of human remains, research methodology, place of curation and publications. In this manuscript, the design and functionality of the DAARD are illustrated using examples of achondroplasia and other types of stunted growth.

Conclusions: As an open, collaborative repository for collecting, mapping and querying well-structured medical data on individuals from ancient times, the DAARD opens new avenues of research. Over time, the number of rare diseases will increase through the addition of new cases from varied backgrounds such as museum collections and archaeological excavations. Depending on the research question, phenotypic or genetic information can be retrieved, as well as information on the general occurrence of a rare disease in selected space-time intervals. Furthermore, for individuals diagnosed with a rare disease, this approach can help them to build identity and reveal an aspect of their condition they might not have been aware of. Thus, the DAARD contributes to the understanding of rare diseases from a long-term perspective and adds to the latest medical research.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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