We aimed to identify an expression profile of lncRNAs potentially related to treatment response in Psoriatic arthritis (PsA) patients, to be used as potential genomic biomarkers predictors of drug treatment effectiveness. In addition, we evaluated a possible association between lncRNAs genetic variants and the response to therapy using the clinical parameter of Disease Activity Index. For the expression study, we collected 48 treated PsA patients, monitoring the treatment response for 12 months. We initially used PCR Array and, then, we validated the results with qRT-PCR. We also retrospectively genotyped 163 treated PsA patients. Firstly, we observed a significant difference in the expression level between Responder and non-Responder patients, of 4 lncRNAs in the group of PsA patients treated with TNFi and of 3 lncRNAs in the group of patients treated with IL17i. Then, we confirmed a significant decrease of MEG3 expression in non-Responder patients compared to Responders, also considering separately the single groups of patients treated with TNFi and IL17i. In addition, our results seem to highlight a potential dose-dependent effect of rs941576 (MEG3) variant allele on Disease Activity Index. Our study suggests a possible role of the lncRNA MEG3 in the treatment response to biological drugs.

De Benedittis, G., D'Antonio, A., Latini, A., Morgante, C., Conigliaro, P., Triggianese, P., et al. (2024). Study of lncRNAs expression profile in the response to biological drugs in Psoriatic Arthritis: MEG3 could be a potential genomic biomarker of therapy efficacy. INTERNATIONAL IMMUNOPHARMACOLOGY, 134, 1-6 [10.1016/j.intimp.2024.112239].

Study of lncRNAs expression profile in the response to biological drugs in Psoriatic Arthritis: MEG3 could be a potential genomic biomarker of therapy efficacy

De Benedittis, Giada;D'Antonio, Arianna;Latini, Andrea;Morgante, Chiara;Conigliaro, Paola;Triggianese, Paola;Bergamini, Alberto;Novelli, Giuseppe;Ciccacci, Cinzia;Chimenti, Maria Sole;Borgiani, Paola
2024-06-15

Abstract

We aimed to identify an expression profile of lncRNAs potentially related to treatment response in Psoriatic arthritis (PsA) patients, to be used as potential genomic biomarkers predictors of drug treatment effectiveness. In addition, we evaluated a possible association between lncRNAs genetic variants and the response to therapy using the clinical parameter of Disease Activity Index. For the expression study, we collected 48 treated PsA patients, monitoring the treatment response for 12 months. We initially used PCR Array and, then, we validated the results with qRT-PCR. We also retrospectively genotyped 163 treated PsA patients. Firstly, we observed a significant difference in the expression level between Responder and non-Responder patients, of 4 lncRNAs in the group of PsA patients treated with TNFi and of 3 lncRNAs in the group of patients treated with IL17i. Then, we confirmed a significant decrease of MEG3 expression in non-Responder patients compared to Responders, also considering separately the single groups of patients treated with TNFi and IL17i. In addition, our results seem to highlight a potential dose-dependent effect of rs941576 (MEG3) variant allele on Disease Activity Index. Our study suggests a possible role of the lncRNA MEG3 in the treatment response to biological drugs.
15-giu-2024
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/16
English
MEG3
Personalised medicine
Psoriatic arthritis
Treatment response
lncRNAs
De Benedittis, G., D'Antonio, A., Latini, A., Morgante, C., Conigliaro, P., Triggianese, P., et al. (2024). Study of lncRNAs expression profile in the response to biological drugs in Psoriatic Arthritis: MEG3 could be a potential genomic biomarker of therapy efficacy. INTERNATIONAL IMMUNOPHARMACOLOGY, 134, 1-6 [10.1016/j.intimp.2024.112239].
De Benedittis, G; D'Antonio, A; Latini, A; Morgante, C; Conigliaro, P; Triggianese, P; Bergamini, A; Novelli, G; Ciccacci, C; Chimenti, Ms; Borgiani, ...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/378184
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