Evidence map›Paper›PMID 39044201›Full record

ArticleOrphanet journal of rare diseases2024

The Digital Atlas of Ancient Rare Diseases (DAARD) and its relevance for current research.

Julia Gresky, Melina Frotscher, Juliane Dorn, Kristina Scheelen-Nováček, Yannick Ahlbrecht, Tina Jakob, Toni Schönbuchner, José Canalejo, Benjamin Ducke, Emmanuele Petiti

Abstract readHistorical Article
In one paragraph

Article in Orphanet journal of rare diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Julia GreskyDivision of Natural Sciences, German Archaeological Institute, Berlin, Germany. Julia.gresky@dainst.de.ORCID 0000-0003-3493-2757
Melina FrotscherDivision of Natural Sciences, German Archaeological Institute, Berlin, Germany.
Juliane DornDivision of Natural Sciences, German Archaeological Institute, Berlin, Germany.
Kristina Scheelen-NováčekDivision of Natural Sciences, German Archaeological Institute, Berlin, Germany.
Yannick AhlbrechtDivision of Natural Sciences, German Archaeological Institute, Berlin, Germany.
Tina JakobDepartment of Archaeology, Durham University, Durham, UK.
Toni SchönbuchnerCuprit GbR, Leipzig, Germany.
José CanalejoCuprit GbR, Leipzig, Germany.
Benjamin DuckeCentral Research Services/IT, German Archaeological Institute, Berlin, Germany.
Emmanuele PetitiDivision of Natural Sciences, German Archaeological Institute, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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.

resultsThis 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.

conclusionsAs 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.

Indexed as

Rare DiseasesHumansMummiesAchondroplasiaArchaeologyDatabaseFAIR principleHistoryMedical collectionsPaleopathologyShort statureStunted growth

Identifiers

PMID39044201
PMCPMC11267669

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.