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HLA-DQA1*05 Allele Carriage and Anti-TNF Therapy Persistence in Inflammatory Bowel Disease.
Doherty, Jayne; Ryan, Anthony W; Quinn, Emma; Conroy, Judith; Dolan, Jackie; Corcoran, Roisin; Hara, Fintan O; Cullen, Garret; Sheridan, Juliette; Bailey, Yvonne; Dunne, Cara; Hartery, Karen; McNamara, Deirdre; Doherty, Glen A; Kevans, David.
Afiliación
  • Doherty J; Gastroenterology Department, St James's Hospital, Dublin, Ireland.
  • Ryan AW; Department of Gastroenterology, Tallaght University Hospital, Dublin, Ireland.
  • Quinn E; INITIative IBD Research Network, Dublin, Ireland.
  • Conroy J; Genuity Science (Ireland) Limited, Dublin, Ireland.
  • Dolan J; Genuity Science (Ireland) Limited, Dublin, Ireland.
  • Corcoran R; Genuity Science (Ireland) Limited, Dublin, Ireland.
  • Hara FO; Genuity Science (Ireland) Limited, Dublin, Ireland.
  • Cullen G; Gastroenterology Department, St James's Hospital, Dublin, Ireland.
  • Sheridan J; Trinity Academic Gastroenterology Group, School of Medicine, Trinity College Dublin, Ireland.
  • Bailey Y; Department of Gastroenterology, Tallaght University Hospital, Dublin, Ireland.
  • Dunne C; Department of Gastroenterology, St Vincent's University Hospital, Dublin, Ireland.
  • Hartery K; School of Medicine, University College Dublin, Ireland.
  • McNamara D; INITIative IBD Research Network, Dublin, Ireland.
  • Doherty GA; Department of Gastroenterology, St Vincent's University Hospital, Dublin, Ireland.
  • Kevans D; School of Medicine, University College Dublin, Ireland.
Inflamm Bowel Dis ; 2024 Jun 27.
Article en En | MEDLINE | ID: mdl-38937958
ABSTRACT

INTRODUCTION:

Carriage of the HLA-DQA1*05 allele is associated with development of antidrug antibodies (ADAs) to antitumor necrosis factor (anti-TNF) therapy in patients with Crohn's disease. However, ADA is not uniformly associated with treatment failure. We aimed to determine the impact of carriage of HLA-DQA1*05 allele on outcome of biologic therapy evaluated by drug persistence.

METHODS:

A multicenter, retrospective study of 877 patients with inflammatory bowel disease (IBD) treated with anti-TNF therapy with HLA-DQA1*05 genotypes were generated by imputation from whole genome sequence using the HIBAG package, in R. Primary end point was anti-TNF therapy persistence, (time to therapy failure), segregated by HLA-DQA1*05 allele genotype and development of a risk score to predict anti-TNF therapy failure, incorporating HLA-DQA1*05 allele genotype status (LORisk score).

RESULTS:

In all, 877 patients receiving anti-TNF therapy were included in our study; 543 (62%) had no copy, 281 (32%) one copy, and 53 (6%) 2 copies of HLA-DQA1*05 allele. Mean time to anti-TNF therapy failure in patients with 2 copies of HLA-DQA1*05 allele was significantly shorter compared with patients with 0 or 1 copy at 700 days' follow-up 418 vs 541 vs 513 days, respectively (P = .012). Factors independently associated with time to anti-TNF therapy failure included carriage of HLA-DQA1*05 allele (hazard ratio [HR], 1.2, P = .02; female gender HR, 1.6, P < .001; UC phenotype HR, 1.4, P = .009; and anti-TNF therapy type [infliximab], HR, 1.5, P = .002). The LORisk score was significantly associated with shorter time to anti-TNF therapy failure (P < .001).

CONCLUSIONS:

Carriage of 2 HLA-DQA1*05 alleles is associated with less favorable outcomes for patients receiving anti-TNF therapy with shorter time to therapy failure. HLA-DQA1*05 genotype status in conjunction with clinical factors may aid in therapy selection in patients with IBD.
Our study found carriage of 2 copies of the HLA-DQA1*05 allele is associated with a less favorable response to anti-TNF therapy with shorter time to therapy failure. HLA-DQA1*05 genotype status in conjunction with clinical factors may aid in therapy selection in IBD patients.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Inflamm Bowel Dis Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Inflamm Bowel Dis Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article