4.5 Article

Current status of use of high throughput nucleotide sequencing in rheumatology

Journal

RMD OPEN
Volume 7, Issue 1, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/rmdopen-2020-001324

Keywords

lupus erythematosus; systemic; arthritis; rheumatoid; osteoarthritis; dermatomyositis; familial mediterranean fever

Categories

Funding

  1. Mainz Research School of Translational Biomedicine (TransMed)

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Through analyzing literature data and public HTS data, it is found that rheumatoid arthritis, systemic lupus erythematosus, and osteoarthritis are among the most studied rheumatic diseases using HTS assays. RNA-Seq assays are widely used for biomarker identification, but standardization of clinical data collection for patients is needed.
Objective Here, we assess the usage of high throughput sequencing (HTS) in rheumatic research and the availability of public HTS data of rheumatic samples. Methods We performed a semiautomated literature review on PubMed, consisting of an R-script and manual curation as well as a manual search on the Sequence Read Archive for public available HTS data. Results Of the 699 identified articles, rheumatoid arthritis (n=182 publications, 26%), systemic lupus erythematous (n=161, 23%) and osteoarthritis (n=152, 22%) are among the rheumatic diseases with the most reported use of HTS assays. The most represented assay is RNA-Seq (n=457, 65%) for the identification of biomarkers in blood or synovial tissue. We also find, that the quality of accompanying clinical characterisation of the sequenced patients differs dramatically and we propose a minimal set of clinical data necessary to accompany rheumatological-relevant HTS data. Conclusion HTS allows the analysis of a broad spectrum of molecular features in many samples at the same time. It offers enormous potential in novel personalised diagnosis and treatment strategies for patients with rheumatic diseases. Being established in cancer research and in the field of Mendelian diseases, rheumatic diseases are about to become the third disease domain for HTS, especially the RNA-Seq assay. However, we need to start a discussion about reporting of clinical characterisation accompany rheumatological-relevant HTS data to make clinical meaningful use of this data.

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