Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/212227
Title: Association study of human leukocyte antigen variants and idiopathic pulmonary fibrosis
Author: Guillén Guió, Beatriz
Paynton, Megan L.
Allen, Richard J.
Chin, Daniel P. W.
Donoghue, Lauren J.
Stockwell, Amy
Leavy, Olivia C.
Hernández Beeftink, Tamara
Reynolds, Carl
Cullinan, Paul
Martínez, Fernando
Booth, Helen L.
Fahy, William A.
Hall, Ian P.
Hart, Simon P.
Hill, Mike R.
Hirani, Nik
Hubbard, Richard B.
Mcanulty, Robin J.
Millar, Ann B.
Navaratnam, Vidya
Oballa, Eunice
Parfrey, Helen
Saini, Gauri
Sayers, Ian
Tobin, Martin D.
Whyte, Moira K. B.
Adegunsoye, Ayodeji
Kaminski, Naftali
Ma, Shwu-Fan
Strek, Mary E.
Zhang, Yingze
Fingerlin, Tasha E.
Molina Molina, María
Neighbors, Margaret
Sheng, X. Rebecca
Oldham, Justin M.
Maher, Toby M.
Molyneaux, Philip L.
Flores, Carlos
Noth, Imre
Schwartz, David A.
Yaspan, Brian L.
Jenkins, R. Gisli
Wain, Louise V.
Hollox, Edward J.
Keywords: Fibrosi pulmonar
Antígens CD
Pulmonary fibrosis
CD antigens
Issue Date: 21-Dec-2023
Publisher: European Respiratory Society (ERS)
Abstract: Introduction Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial pneumonia marked by progressive lung fibrosis and a poor prognosis. Recent studies have highlighted the potential role of infection in the pathogenesis of IPF, and a prior association of the HLA-DQB1 gene with idiopathic fibrotic interstitial pneumonia (including IPF) has been reported. Owing to the important role that the human leukocyte antigen (HLA) region plays in the immune response, here we evaluated if HLA genetic variation was associated specifically with IPF risk. Methods We performed a meta-analysis of associations of the HLA region with IPF risk in individuals of European ancestry from seven independent case-control studies of IPF (comprising 5159 cases and 27 459 controls, including a prior study of fibrotic interstitial pneumonia). Single nucleotide polymorphisms, classical HLA alleles and amino acids were analysed and signals meeting a region-wide association threshold of p<4.5x10-4 and a posterior probability of replication >90% were considered significant. We sought to replicate the previously reported HLA-DQB1 association in the subset of studies independent of the original report. Results The meta-analysis of all seven studies identified four significant independent single nucleotide polymorphisms associated with IPF risk. However, none met the posterior probability for replication criterion. The HLA-DQB1 association was not replicated in the independent IPF studies. Conclusion Variation in the HLA region was not consistently associated with risk in studies of IPF. However, this does not preclude the possibility that other genomic regions linked to the immune response may be involved in the aetiology of IPF.
Note: Reproducció del document publicat a: https://doi.org/10.1183/23120541.00553-2023
It is part of: ERJ Open Research, 2023, vol. 10, num. 1
URI: https://hdl.handle.net/2445/212227
Related resource: https://doi.org/10.1183/23120541.00553-2023
ISSN: 2312-0541
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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