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Macrophage Migration Inhibitory Factor is not Associated with Sarcoidosis Susceptibility or Severity in Whites or Blacks
Macrophage migration inhibitory factor (MIF) is an inflammatory cytokine, and increased expression has been associated with the development and severity of multiple granulomatous, autoimmune diseases. However, association studies have been discordant in sarcoidosis. To evaluate associations between...
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Published in: | Sarcoidosis, vasculitis, and diffuse lung diseases vasculitis, and diffuse lung diseases, 2020-01, Vol.37 (3), p.e2020003-e2020003 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Macrophage migration inhibitory factor (MIF) is an inflammatory cytokine, and increased
expression has been associated with the development and severity of multiple granulomatous, autoimmune diseases. However,
association studies have been discordant in sarcoidosis.
To evaluate associations between macrophage migration inhibitory factor (
) promoter polymorphisms and sarcoidosis susceptibility and severity.
Three hundred and fifty one patients with sarcoidosis were recruited through the Genomic Research in Alpha-1 Antitrypsin Deficiency and Sarcoidosis (GRADS) study. Genomic DNA was isolated from serum, and the
173G/C SNP [
] and
-794 CATT
microsatellite repeat [
] were genotyped. Allelic frequencies were compared between cases and healthy controls and associations between
alleles and sarcoidosis severity were assessed.
The frequencies of the high expression -173C SNP and the low expression -794 CATT
containing genotypes in white and black sarcoidosis patients were the same as those of healthy controls. High expression
alleles were not associated with sarcoidosis severity. Associations between
alleles and extrapulmonary sarcoidosis phenotypes were limited by small sample sizes.
High expression
genotypes were not associated with the susceptibility to or severity of pulmonary sarcoidosis in a large North American cohort.
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ISSN: | 1124-0490 2532-179X |
DOI: | 10.36141/svdld.v37i3.9273 |