López-Rodríguez, Rosario
Perez-Pampin, Eva
Márquez, Ana
Blanco, Francisco J.
Joven, Beatriz
Carreira, Patricia
Ferrer, Miguel Angel
Caliz, Rafael
Valor, Lara
Narváez García, Francisco Javier
Canete, Juan D.
Ordóñez, María del Carmen
Manrique Arija, Sara
Vasilopoulos, Yiannis
Balsa, Alejandro
Pascual-Salcedo, Dora
Moreno-Ramos, Manuel J.
Alegre-Sancho, Juan José
Navarro Sarabia, Federico
Moreira, Virginia
Garcia Portales, Rosa
Raya, Enrique
Magro Checa, Cesar
Martín, Javier
Gomez Reino, Juan J.
Gonzalez, Antonio
2018-07-25T07:38:59Z
2018-07-25T07:38:59Z
2018-05-07
2018-07-24T11:41:17Z
Genetic biomarkers are sought to personalize treatment of patients with rheumatoid arthritis (RA), given their variable response to TNF inhibitors (TNFi). However, no genetic biomaker is yet sufficiently validated. Here, we report a validation study of 18 previously reported genetic biomarkers, including 11 from GWAS of response to TNFi. The validation was attempted in 581 patients with RA that had not been treated with biologic antirheumatic drugs previously. Their response to TNFi was evaluated at 3, 6 and 12 months in two ways: change in the DAS28 measure of disease activity, and according to the EULAR criteria for response to antirheumatic drugs. Association of these parameters with the genotypes, obtained by PCR amplification followed by single-base extension, was tested with regression analysis. These analyses were adjusted for baseline DAS28, sex, and the specific TNFi. However, none of the proposed biomarkers was validated, as none showed association with response to TNFi in our study, even at the time of assessment and with the outcome that showed the most significant result in previous studies. These negative results are notable because this was the first independent validation study for 12 of the biomarkers, and because they indicate that prudence is needed in the interpretation of the proposed biomarkers of response to TNFi even when they are supported by very low p values. The results also emphasize the requirement of independent replication for validation, and the need to search protocols that could increase reproducibility of the biomarkers of response to TNFi.
English
Artritis reumatoide; Marcadors bioquímics; Rheumatoid arthritis; Biochemical markers
Public Library Science
Reproducció del document publicat a: https://doi.org/10.1371/journal.pone.0196793
Plos One, 2018, Vol. 13, Issue 5
https://doi.org/10.1371/journal.pone.0196793
cc by (c) Lopez-Rodriguez, Rosario et al., 2018
http://creativecommons.org/licenses/by/3.0/es/