Protective Role of the Interleukin 33 rs3939286 Gene Polymorphism in the Development of Subclinical Atherosclerosis in Rheumatoid Arthritis Patients
To determine whether the interleukin-33 (IL-33)-interleukin-1 receptor like 1 (IL-1RL1) signaling pathway is implicated in the risk of subclinical atherosclerosis in patients with rheumatoid arthritis (RA). A total of 576 Spanish RA patients from Northern Spain were genotyped for 6 well-known IL33-I...
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Published in | PloS one Vol. 10; no. 11; p. e0143153 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
16.11.2015
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | To determine whether the interleukin-33 (IL-33)-interleukin-1 receptor like 1 (IL-1RL1) signaling pathway is implicated in the risk of subclinical atherosclerosis in patients with rheumatoid arthritis (RA).
A total of 576 Spanish RA patients from Northern Spain were genotyped for 6 well-known IL33-IL1RL1 polymorphisms (IL33 rs3939286, IL33 rs7025417, IL33 rs7044343, IL1RL1 rs2058660, IL1RL1 rs2310173 and IL1RL1 rs13015714) by TaqMan genotyping assay. The presence of subclinical atherosclerosis was determined by the assessment of carotid intima-media thickness (cIMT) by carotid ultrasound (US).
RA patients carrying the TT genotype of the IL33 rs3939286 polymorphism had lower cIMT values than those homozygous for the CC genotype (mean ± standard deviation (SD): 0.71 ± 0.14 mm versus 0.76 ± 0.16 mm, respectively) while patients carrying the CT genotype had intermediate cIMT values (mean ± SD: 0.73 ± 0.17 mm). Moreover, RA patients carrying the mutant allele T of the IL33 rs3939286 polymorphism exhibited significantly lower cIMT values than those carrying the wild allele C (mean ± SD: 0.72 ± 0.16 mm versus 0.75 ± 0.18 mm respectively; p = 0.04). The association of both genotype and allele frequencies of IL33 rs3939286 and cIMT levels remained statistically significant after adjustment for sex, age at the time of US study, follow-up and center (p = 0.006 and p = 0.0023, respectively), evidencing that the potential effect conferred by IL33 rs3939286 may be independent of confounder factors. No association with other IL33-IL1RL1 genetic variants was observed.
In conclusion, our results may suggest a potential protective effect of the IL33 rs3939286 allele T in the risk of subclinical atherosclerosis in patients with RA. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: The authors have declared that no competing interests exist. MAGG and JM are joint senior authors on this work. Conceived and designed the experiments: FG RLM SRM MRV MGB BU JAMF VM TP RB JJAS MARH MDMS BTS IFA EV FDC SC AC CGJ JL JM MAGG. Performed the experiments: FG RLM SRM MRV MGB BU JAMF VM TP RB JJAS MARH MDMS BTS IFA EV FDC SC AC CGJ JL JM MAGG. Analyzed the data: FG RLM SRM MRV MGB BU JAMF VM TP RB JJAS MARH MDMS BTS IFA EV FDC SC AC CGJ JL JM MAGG. Contributed reagents/materials/analysis tools: FG RLM SRM MRV MGB BU JAMF VM TP RB JJAS MARH MDMS BTS IFA EV FDC SC AC CGJ JL JM MAGG. Wrote the paper: FG RLM SRM MRV MGB BU JAMF VM TP RB JJAS MARH MDMS BTS IFA EV FDC SC AC CGJ JL JM MAGG. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0143153 |