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Polymorphisms at phase I-metabolizing enzyme and hormone receptor loci influence the response to anti-TNF therapy in rheumatoid arthritis patients.
Canet, Luz M; Sánchez-Maldonado, Jose M; Cáliz, Rafael; Rodríguez-Ramos, Ana; Lupiañez, Carmen B; Canhão, Helena; Martínez-Bueno, Manuel; Escudero, Alejandro; Segura-Catena, Juana; Sorensen, Signe B; Hetland, Merete L; Soto-Pino, María José; Ferrer, Miguel A; García, Antonio; Glintborg, Bente; Filipescu, Ileana; Pérez-Pampin, Eva; González-Utrilla, Alfonso; Nevot, Miguel Ángel López; Conesa-Zamora, Pablo; Broeder, Alfons den; De Vita, Salvatore; Jacobsen, Sven Erik Hobe; Collantes-Estevez, Eduardo; Quartuccio, Luca; Canzian, Federico; Fonseca, João E; Coenen, Marieke J H; Andersen, Vibeke; Sainz, Juan.
Afiliación
  • Canet LM; Genomic Oncology Area, GENYO Centre for Genomics and Oncological Research, Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.
  • Sánchez-Maldonado JM; Genomic Oncology Area, GENYO Centre for Genomics and Oncological Research, Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.
  • Cáliz R; Genomic Oncology Area, GENYO Centre for Genomics and Oncological Research, Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.
  • Rodríguez-Ramos A; Rheumatology Department, Virgen de las Nieves University Hospital, Granada, Spain.
  • Lupiañez CB; Genomic Oncology Area, GENYO Centre for Genomics and Oncological Research, Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.
  • Canhão H; Genomic Oncology Area, GENYO Centre for Genomics and Oncological Research, Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.
  • Martínez-Bueno M; CEDOC, EpiDoC Unit, NOVA Medical School and National School of Public Health, Universidade Nova de Lisboa, Lisbon, Portugal.
  • Escudero A; Area of Genomic Medicine, GENYO Centre for Genomics and Oncological Research, Pfizer / University of Granada / Andalusian Regional Government, Granada, Spain.
  • Segura-Catena J; Rheumatology Department, Reina Sofía Hospital/IMIBIC/University of Córdoba, Córdoba, Spain.
  • Sorensen SB; Genomic Oncology Area, GENYO Centre for Genomics and Oncological Research, Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.
  • Hetland ML; The Danish Rheumatologic Biobank, the DANBIO Registry and Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • Soto-Pino MJ; Faculty of Health and Medical Sciences, Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Ferrer MA; The Danish Rheumatologic Biobank, the DANBIO Registry and Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • García A; Faculty of Health and Medical Sciences, Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Glintborg B; Rheumatology Department, Virgen de las Nieves University Hospital, Granada, Spain.
  • Filipescu I; Rheumatology Department, Virgen de las Nieves University Hospital, Granada, Spain.
  • Pérez-Pampin E; Rheumatology Department, Virgen de las Nieves University Hospital, Granada, Spain.
  • González-Utrilla A; The Danish Rheumatologic Biobank, the DANBIO Registry and Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • Nevot MÁL; Department of Rheumatology, Gentofte and Herlev Hospital, Copenhagen University Hospital, Copenhagen, Denmark.
  • Conesa-Zamora P; Rheumatology Department, University of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.
  • Broeder AD; Rheumatology Unit, University Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
  • De Vita S; Rheumatology Department, Virgen de las Nieves University Hospital, Granada, Spain.
  • Jacobsen SEH; Immunology Department, Virgen de las Nieves University Hospital, Granada, Spain.
  • Collantes-Estevez E; Clinical Analysis Department, Santa Lucía University Hospital, Cartagena, Spain.
  • Quartuccio L; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, The Netherlands.
  • Canzian F; Department of Medical and Biological Sciences, Clinic of Rheumatology, University of Udine, Udine, Italy.
  • Fonseca JE; The Danish Rheumatologic Biobank, the DANBIO Registry and Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • Coenen MJH; Faculty of Health and Medical Sciences, Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Andersen V; Rheumatology Department, Reina Sofía Hospital/IMIBIC/University of Córdoba, Córdoba, Spain.
  • Sainz J; Department of Medical and Biological Sciences, Clinic of Rheumatology, University of Udine, Udine, Italy.
Pharmacogenomics J ; 19(1): 83-96, 2019 02.
Article en En | MEDLINE | ID: mdl-30287909
The aim of this case-control study was to evaluate whether 47 single-nucleotide polymorphisms (SNPs) in steroid hormone-related genes are associated with the risk of RA and anti-TNF drug response. We conducted a case-control study in 3 European populations including 2936 RA patients and 2197 healthy controls. Of those, a total of 1985 RA patients were treated with anti-TNF blockers. The association of potentially interesting markers in the discovery population was validated through meta-analysis with data from DREAM and DANBIO registries. Although none of the selected variants had a relevant role in modulating RA risk, the meta-analysis of the linear regression data with those from the DREAM and DANBIO registries showed a significant correlation of the CYP3A4rs11773597 and CYP2C9rs1799853 variants with changes in DAS28 after the administration of anti-TNF drugs (P = 0.00074 and P = 0.006, respectively). An overall haplotype analysis also showed that the ESR2GGG haplotype significantly associated with a reduced chance of having poor response to anti-TNF drugs (P = 0.0009). Finally, a ROC curve analysis confirmed that a model built with eight steroid hormone-related variants significantly improved the ability to predict drug response compared with the reference model including demographic and clinical variables (AUC = 0.633 vs. AUC = 0.556; PLR_test = 1.52 × 10-6). These data together with those reporting that the CYP3A4 and ESR2 SNPs correlate with the expression of TRIM4 and ESR2 mRNAs in PBMCs (ranging from P = 1.98 × 10-6 to P = 2.0 × 10-35), and that the CYP2C9rs1799853 SNP modulates the efficiency of multiple drugs, suggest that steroid hormone-related genes may have a role in determining the response to anti-TNF drugs.KEY POINTS• Polymorphisms within the CYP3A4 and CYP2C9 loci correlate with changes in DAS28 after treatment with anti-TNF drugs.• A haplotype including eQTL SNPs within the ESR2 gene associates with better response to anti-TNF drugs.• A genetic model built with eight steroid hormone-related variants significantly improved the ability to predict drug response.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Artritis Reumatoide / Factor de Necrosis Tumoral alfa / Antirreumáticos / Polimorfismo de Nucleótido Simple / Fase I de la Desintoxicación Metabólica Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: Pharmacogenomics J Asunto de la revista: BIOLOGIA MOLECULAR / FARMACOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Artritis Reumatoide / Factor de Necrosis Tumoral alfa / Antirreumáticos / Polimorfismo de Nucleótido Simple / Fase I de la Desintoxicación Metabólica Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: Pharmacogenomics J Asunto de la revista: BIOLOGIA MOLECULAR / FARMACOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: España