4.7 Article

Genome-wide Association Study Implicates PARD3B-based AIDS Restriction

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 203, Issue 10, Pages 1491-1502

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jir046

Keywords

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Funding

  1. National Institutes of Health, National Cancer Institute, Center for Cancer Research
  2. National Cancer Institute, National Institutes of Health [HHSN26120080001E]
  3. National Institutes of Health, National Institute of Child Health and Human Development [1 R01 HD41224]
  4. Netherlands Organization for Scientific Research [9120.6046]

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Methods. European American HIV seroconverters (n = 755) were interrogated for single-nucleotide polymorphisms (SNPs) (n = 700,022) associated with progression to AIDS 1987 (Cox proportional hazards regression analysis, co-dominant model). Results. Association with slower progression was observed for SNPs in the gene PARD3B. One of these, rs11884476, reached genome-wide significance (relative hazard = 0.3; P =3. 370 x 10(-9)) after statistical correction for 700,022 SNPs and contributes 4.52% of the overall variance in AIDS progression in this study. Nine of the top-ranked SNPs define a PARD3B haplotype that also displays significant association with progression to AIDS (hazard ratio, 0.3; P = 3.220 x 10(-8)). One of these SNPs, rs10185378, is a predicted exonic splicing enhancer; significant alteration in the expression profile of PARD3B splicing transcripts was observed in B cell lines with alternate rs10185378 genotypes. This SNP was typed in European cohorts of rapid progressors and was found to be protective for AIDS 1993 definition (odds ratio, 0.43, P = .025). Conclusions. These observations suggest a potential unsuspected pathway of host genetic influence on the dynamics of AIDS progression.

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