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Association of HLA-DRB1∗09:01 with tIgE levels among African-ancestry individuals with asthma.
Vince, Nicolas; Limou, Sophie; Daya, Michelle; Morii, Wataru; Rafaels, Nicholas; Geffard, Estelle; Douillard, Venceslas; Walencik, Alexandre; Boorgula, Meher Preethi; Chavan, Sameer; Vergara, Candelaria; Ortega, Victor E; Wilson, James G; Lange, Leslie A; Watson, Harold; Nicolae, Dan L; Meyers, Deborah A; Hansel, Nadia N; Ford, Jean G; Faruque, Mezbah U; Bleecker, Eugene R; Campbell, Monica; Beaty, Terri H; Ruczinski, Ingo; Mathias, Rasika A; Taub, Margaret A; Ober, Carole; Noguchi, Emiko; Barnes, Kathleen C; Torgerson, Dara; Gourraud, Pierre-Antoine.
Afiliação
  • Vince N; Université de Nantes, Centrale Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, Nantes, France.
  • Limou S; Université de Nantes, Centrale Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, Nantes, France; Ecole Centrale de Nantes, Nantes, France.
  • Daya M; Department of Medicine, University of Colorado Denver, Aurora, Colo.
  • Morii W; Department of Medical Genetics, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
  • Rafaels N; Department of Medicine, University of Colorado Denver, Aurora, Colo.
  • Geffard E; Université de Nantes, Centrale Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, Nantes, France.
  • Douillard V; Université de Nantes, Centrale Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, Nantes, France.
  • Walencik A; Université de Nantes, Centrale Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, Nantes, France.
  • Boorgula MP; Department of Medicine, University of Colorado Denver, Aurora, Colo.
  • Chavan S; Department of Medicine, University of Colorado Denver, Aurora, Colo.
  • Vergara C; Department of Medicine, Johns Hopkins University, Baltimore, Md.
  • Ortega VE; Department of Internal Medicine, Section on Pulmonary, Critical Care, Allergy and Immunologic Diseases, Center for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC.
  • Wilson JG; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Miss.
  • Lange LA; Department of Medicine, University of Colorado Denver, Aurora, Colo.
  • Watson H; Faculty of Medical Sciences Cave Hill Campus, The University of the West Indies, Bridgetown, Barbados.
  • Nicolae DL; Department of Medicine, University of Chicago, Chicago, Ill.
  • Meyers DA; Department of Medicine, University of Arizona College of Medicine, Tucson, Ariz.
  • Hansel NN; Department of Medicine, Johns Hopkins University, Baltimore, Md.
  • Ford JG; Department of Medicine, Einstein Medical Center, Philadelphia, Pa.
  • Faruque MU; National Human Genome Center, Howard University College of Medicine, Washington, DC.
  • Bleecker ER; Department of Medicine, University of Arizona College of Medicine, Tucson, Ariz.
  • Campbell M; Department of Medicine, University of Colorado Denver, Aurora, Colo.
  • Beaty TH; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Md.
  • Ruczinski I; Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Md.
  • Mathias RA; Department of Medicine, Johns Hopkins University, Baltimore, Md; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Md.
  • Taub MA; Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Md.
  • Ober C; Department of Human Genetics, University of Chicago, Chicago, Ill.
  • Noguchi E; Department of Medical Genetics, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
  • Barnes KC; Department of Medicine, University of Colorado Denver, Aurora, Colo.
  • Torgerson D; McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada.
  • Gourraud PA; Université de Nantes, Centrale Nantes, CHU Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, Nantes, France. Electronic address: pierre-antoine.gourraud@univ-nantes.fr.
J Allergy Clin Immunol ; 146(1): 147-155, 2020 07.
Article em En | MEDLINE | ID: mdl-31981624
ABSTRACT

BACKGROUND:

Asthma is a complex chronic inflammatory disease of the airways. Association studies between HLA and asthma were first reported in the 1970s, and yet, the precise role of HLA alleles in asthma is not fully understood. Numerous genome-wide association studies were recently conducted on asthma, but were always limited to simple genetic markers (single nucleotide polymorphisms) and not complex HLA gene polymorphisms (alleles/haplotypes), therefore not capturing the biological relevance of this complex locus for asthma pathogenesis.

OBJECTIVE:

To run the first HLA-centric association study with asthma and specific asthma-related phenotypes in a large cohort of African-ancestry individuals.

METHODS:

We collected high-density genomics data for the Consortium on Asthma among African-ancestry Populations in the Americas (N = 4993) participants. Using computer-intensive machine-learning attribute bagging methods to infer HLA alleles, and Easy-HLA to infer HLA 5-gene haplotypes, we conducted a high-throughput HLA-centric association study of asthma susceptibility and total serum IgE (tIgE) levels in subjects with and without asthma.

RESULTS:

Among the 1607 individuals with asthma, 972 had available tIgE levels, with a mean tIgE level of 198.7 IU/mL. We could not identify any association with asthma susceptibility. However, we showed that HLA-DRB1∗0901 was associated with increased tIgE levels (P = 8.5 × 10-4; weighted effect size, 0.51 [0.15-0.87]).

CONCLUSIONS:

We identified for the first time an HLA allele associated with tIgE levels in African-ancestry individuals with asthma. Our report emphasizes that by leveraging powerful computational machine-learning methods, specific/extreme phenotypes, and population diversity, we can explore HLA gene polymorphisms in depth and reveal the full extent of complex disease associations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Negro ou Afro-Americano / Imunoglobulina E / Polimorfismo de Nucleotídeo Único / Alelos / Cadeias HLA-DRB1 Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Negro ou Afro-Americano / Imunoglobulina E / Polimorfismo de Nucleotídeo Único / Alelos / Cadeias HLA-DRB1 Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França