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New polymorphisms associated with response to anti-TNF drugs in patients with moderate-to-severe plaque psoriasis

Abstract

Anti-tumor necrosis factor (anti-TNF) drugs are effective against psoriasis, although 20–30% of patients are nonresponders. Few pharmacogenomic studies have been performed to predict the response to anti-TNF drugs in psoriasis. We studied 173 polymorphisms to establish an association with the response to anti-TNF drugs in patients with moderate-to-severe plaque psoriasis (N=144). We evaluated the response using PASI75 at 3, 6 and 12 months. The results of the multivariate analysis showed an association between polymorphisms in PGLYR4, ZNF816A, CTNNA2, IL12B, MAP3K1 and HLA-C genes and the response at 3 months. Besides, the results for polymorphisms in IL12B and MAP3K1 were replicated at 6 months. We also obtained significant results for IL12B polymorphism at 1 year. Moreover, polymorphisms in FCGR2A, HTR2A and CDKAL1 were significant at 6 months. This is the first study to show an association with these polymorphisms. However, these biomarkers should be validated in large-scale studies before implementation in clinical practice.

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Acknowledgements

This study was supported by Instituto de Salud Carlos III (FIS PI10/01740), Fundación Teófilo Hernando and AbbVie. RP-P has a grant from Universidad Autónoma de Madrid (FPI program 2013). We are grateful to Thomas O’Boyle for editorial assistance and Cristina Carazo for helping to set up the patient databases.

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Correspondence to F Abad-Santos.

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Competing interests

F Abad-Santos has been a consultant or investigator in clinical trials sponsored by the following pharmaceutical companies: Abbott, Alter, Chemo, Farmalíder, Ferrer, GlaxoSmithKline, Gilead, Janssen-Cilag, Kern, Normon, Novartis, Servier, Teva and Zambon. E Daudén has potential conflicts of interest (advisory board member, consultant, grants, research support, participation in clinical trials, honoraria for speaking and research support) with the following pharmaceutical companies: AbbVie (Abbott), Amgen, Janssen-Cilag, Leo Pharma, Novartis, Pfizer, MSD and Celgene. P de la Cueva has conflicts of interest (advisory board member, consultant, grants, research support, participation in clinical trials, honoraria for speaking and/or research support) with the following pharmaceutical companies: AbbVie (Abbott), Astellas, Janssen-Cilag, Leo Pharma, Novartis, Pfizer, MSD, Gebro, Isdin and Lilly. JL López-Estebaranz has conflicts of interest (advisory board member, speaker or participation in clinical trials) with AbbVie, Amgen, Pfizer, MSD, Janssen-Cilag, Lilly and Celgene. O Baniandrés has conflicts of interest (participation in clinical trials and honoraria for speaking) with the following pharmaceutical companies: AbbVie (Abbott), Janssen-Cilag, Leo Pharma, Pfizer and MSD.

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Prieto-Pérez, R., Solano-López, G., Cabaleiro, T. et al. New polymorphisms associated with response to anti-TNF drugs in patients with moderate-to-severe plaque psoriasis. Pharmacogenomics J 18, 70–75 (2018). https://doi.org/10.1038/tpj.2016.64

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