Association of an IGHV3-66 gene variant with Kawasaki disease
In a meta-analysis of three GWAS for susceptibility to Kawasaki disease (KD) conducted in Japan, Korea, and Taiwan and follow-up studies with a total of 11,265 subjects (3428 cases and 7837 controls), a significantly associated SNV in the immunoglobulin heavy variable gene ( IGHV ) cluster in 14q33....
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Published in | Journal of human genetics Vol. 66; no. 5; pp. 475 - 489 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Singapore
Springer Singapore
01.05.2021
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1434-5161 1435-232X 1435-232X |
DOI | 10.1038/s10038-020-00864-z |
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Summary: | In a meta-analysis of three GWAS for susceptibility to Kawasaki disease (KD) conducted in Japan, Korea, and Taiwan and follow-up studies with a total of 11,265 subjects (3428 cases and 7837 controls), a significantly associated SNV in the
immunoglobulin heavy variable
gene (
IGHV
) cluster in 14q33.32 was identified (rs4774175; OR = 1.20,
P
= 6.0 × 10
−9
). Investigation of nonsynonymous SNVs of the
IGHV
cluster in 9335 Japanese subjects identified the C allele of rs6423677, located in
IGHV3-66
, as the most significant reproducible association (OR = 1.25,
P
= 6.8 × 10
−10
in 3603 cases and 5731 controls). We observed highly skewed allelic usage of
IGHV3-66
, wherein the rs6423677 A allele was nearly abolished in the transcripts in peripheral blood mononuclear cells of both KD patients and healthy adults. Association of the high-expression allele with KD strongly indicates some active roles of B-cells or endogenous immunoglobulins in the disease pathogenesis. Considering that significant association of SNVs in the
IGHV
region with disease susceptibility was previously known only for rheumatic heart disease (RHD), a complication of acute rheumatic fever (ARF), these observations suggest that common B-cell related mechanisms may mediate the symptomology of KD and ARF as well as RHD. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1434-5161 1435-232X 1435-232X |
DOI: | 10.1038/s10038-020-00864-z |