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Published in: Clinical Rheumatology 9/2021

Open Access 01-09-2021 | Sarcoidosis | Original Paper

Whole genome sequencing identifies variants associated with sarcoidosis in a family with a high prevalence of sarcoidosis

Authors: Daan Fritz, Bart Ferwerda, Matthijs C. Brouwer, Diederik van de Beek

Published in: Clinical Rheumatology | Issue 9/2021

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Abstract

Objective

We studied genetic risk factors associated with sarcoidosis within a family with a high prevalence of this disease.

Methods

We studied 41 members of a family with a high rate of sarcoidosis, including an index patient with treatment-resistant neurosarcoidosis. Whole genome sequencing was performed for six affected family members and variations associated with loss of function were filtered out as candidate genes. Findings were validated by using amplicon sequencing within all 41 family members with DNA available and candidate genes were screened on absence and presence within the sarcoidosis affected and non-affected.

Results

Family members (n = 61) from 5 generations were available for participation including 13 subjects diagnosed with sarcoidosis (20%). Analyses identified 36 candidate variants within 34 candidate genes. Variations within three of these genes (JAK2, BACH2, and NCF1) previously have been associated with autoimmune diseases.

Conclusions

We identified 34 genes with a possible role in the etiology of sarcoidosis, including JAK2. Our results may suggest evaluation of JAK inhibitors in treatment-resistant sarcoidosis.
Key Points
• JAK2 has a potential role in the etiology of sarcoidosis and is a potential therapeutic target.
• We identified 33 additional candidate genes of which BACH2 and NCF1 have been previously associated with autoimmune disease.
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Metadata
Title
Whole genome sequencing identifies variants associated with sarcoidosis in a family with a high prevalence of sarcoidosis
Authors
Daan Fritz
Bart Ferwerda
Matthijs C. Brouwer
Diederik van de Beek
Publication date
01-09-2021
Publisher
Springer International Publishing
Published in
Clinical Rheumatology / Issue 9/2021
Print ISSN: 0770-3198
Electronic ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-021-05684-w

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