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Association of single-nucleotide polymorphisms in JAK3, STAT4, and STAT6 with new cardiovascular events in incident dialysis patients.

Authors :
Sperati CJ
Parekh RS
Berthier-Schaad Y
Jaar BG
Plantinga L
Fink N
Powe NR
Smith MW
Coresh J
Kao WH
Sperati, C John
Parekh, Rulan S
Berthier-Schaad, Yvette
Jaar, Bernard G
Plantinga, Laura
Fink, Nancy
Powe, Neil R
Smith, Michael W
Coresh, Josef
Kao, W H Linda
Source :
American Journal of Kidney Diseases; May2009, Vol. 53 Issue 5, p845-855, 11p
Publication Year :
2009

Abstract

<bold>Background: </bold>Increasing evidence supports a role for cell-mediated immunity in the pathogenesis of cardiovascular disease. Single-nucleotide polymorphisms (SNPs) in JAK3, STAT4, and STAT6 of the Janus kinase-signal transducer and activator of transcription (Jak-Stat) signal transduction pathway were examined for association with time to new cardiovascular events in incident dialysis patients from the Choices for Healthy Outcomes in Caring for End-Stage Renal Disease Study.<bold>Study Design: </bold>Prospective cohort study.<bold>Setting& Participants: </bold>764 white (n = 518) and black (n = 246) participants from 79 dialysis centers.<bold>Predictor: </bold>SNPs in JAK3, STAT4, and STAT6 selected using a pairwise approach to identify a maximally informative set of tag SNPs for populations of European and African descent.<bold>Outcomes& Measurements: </bold>Cox proportional hazards models were used to estimate unadjusted and multivariable-adjusted hazard ratios (HRs) for incident cardiovascular disease events after dialysis therapy initiation associated with each race-specific SNP.<bold>Results: </bold>2 European tag SNPs (rs3212780 and rs3213409) in JAK3 were associated with new cardiovascular disease events in white patients with unadjusted HRs of 1.92 (P < 0.001) and 1.82 (P = 0.07), respectively. One dual-tag SNP (rs3212752) in JAK3 was associated with new cardiovascular events in white patients with an unadjusted HR of 2.09 (P < 0.001) and in black patients with an HR of 2.07 (P = 0.007). SNP rs3213409 codes for a valine to isoleucine change at amino acid 722, a potentially functional mutation. SNPs in STAT4 and STAT6 were not associated with cardiovascular events after the initiation of dialysis therapy.<bold>Limitations: </bold>This study does not provide direct evidence for the mechanism of increased risk. Replication in independent cohorts is necessary.<bold>Conclusions: </bold>Genetic polymorphisms in the Jak-Stat signaling pathway are associated with an increased risk of new cardiovascular events in incident dialysis patients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02726386
Volume :
53
Issue :
5
Database :
Supplemental Index
Journal :
American Journal of Kidney Diseases
Publication Type :
Academic Journal
Accession number :
105514741
Full Text :
https://doi.org/10.1053/j.ajkd.2008.12.025