TY - JOUR KW - Toll-like receptor (TLR) KW - Erythema nodosum leprosum (ENL) KW - leprosy KW - Prednisone KW - Thalidomide AU - Maciel-Fiuza M AU - Costa P AU - Kowalski TW AU - Schüler-Faccini L AU - Bonamigo RR AU - Vetoratto R AU - Eidt LM AU - de Moraes P AU - Silveira M AU - Camargo L AU - Callegari-Jacques S AU - Castro S AU - Sales Luiz Vianna F AB -

Erythema nodosum leprosum (ENL) is an inflammatory complication caused by a dysregulated immune response to . Some Toll-like receptors (TLRs) have been identified as capable of recognizing antigens from , triggering a wide antimicrobial and inflammatory response. Genetic polymorphisms in these receptors could influence in the appearance of ENL as well as in its treatment. Thus, the objective of this work was to evaluate the association of genetic variants of genes with the response to treatment of ENL with thalidomide and prednisone. A total of 162 ENL patients were recruited from different regions of Brazil and clinical information was collected from their medical records. Genomic DNA was isolated from blood and saliva samples and genetic variants in (rs4833095), (rs3804099), (rs1927914), and (rs5743810) genes were genotyped by TaqMan real-time PCR system. In order to evaluate the variants' association with the dose of the medications used during the treatment, we applied the Generalized Estimating Equations (GEE) analysis. In the present sample, 123 (75.9%) patients were men and 86 (53.1%) were in treatment for leprosy during the ENL episode. We found an association between polymorphisms in /rs4833095, /rs3804099, /rs1927914, and /rs5783810 with the dose variation of thalidomide in a time-dependent manner, i.e., the association with the genetic variant and the dose of the drug was different depending on the moment of the treatment evaluated. In addition, we identified that the association of polymorphisms in /rs4833095, /rs3804099, and /rs5783810 with the dose variation of prednisone also were time-dependent. Despite these associations, in all the interactions found, the influence of genetic variants on dose variation was not clinically relevant for therapeutic changes. The results obtained in this study show that TLRs polymorphism might play a role in the response to ENL treatment, however, in this context, they could not be considered as useful biomarkers in the clinical setting due small differences in medication doses. A larger sample size with patients with a more genetic profile is fundamental in order to estimate the association of genetic variants with the treatment of ENL and their clinical significance.

BT - Frontiers in medicine C1 -

https://www.ncbi.nlm.nih.gov/pubmed/35141236

DA - 01/2021 DO - 10.3389/fmed.2021.713143 J2 - Front Med (Lausanne) LA - eng N2 -

Erythema nodosum leprosum (ENL) is an inflammatory complication caused by a dysregulated immune response to . Some Toll-like receptors (TLRs) have been identified as capable of recognizing antigens from , triggering a wide antimicrobial and inflammatory response. Genetic polymorphisms in these receptors could influence in the appearance of ENL as well as in its treatment. Thus, the objective of this work was to evaluate the association of genetic variants of genes with the response to treatment of ENL with thalidomide and prednisone. A total of 162 ENL patients were recruited from different regions of Brazil and clinical information was collected from their medical records. Genomic DNA was isolated from blood and saliva samples and genetic variants in (rs4833095), (rs3804099), (rs1927914), and (rs5743810) genes were genotyped by TaqMan real-time PCR system. In order to evaluate the variants' association with the dose of the medications used during the treatment, we applied the Generalized Estimating Equations (GEE) analysis. In the present sample, 123 (75.9%) patients were men and 86 (53.1%) were in treatment for leprosy during the ENL episode. We found an association between polymorphisms in /rs4833095, /rs3804099, /rs1927914, and /rs5783810 with the dose variation of thalidomide in a time-dependent manner, i.e., the association with the genetic variant and the dose of the drug was different depending on the moment of the treatment evaluated. In addition, we identified that the association of polymorphisms in /rs4833095, /rs3804099, and /rs5783810 with the dose variation of prednisone also were time-dependent. Despite these associations, in all the interactions found, the influence of genetic variants on dose variation was not clinically relevant for therapeutic changes. The results obtained in this study show that TLRs polymorphism might play a role in the response to ENL treatment, however, in this context, they could not be considered as useful biomarkers in the clinical setting due small differences in medication doses. A larger sample size with patients with a more genetic profile is fundamental in order to estimate the association of genetic variants with the treatment of ENL and their clinical significance.

PY - 2021 EP - 713143 T2 - Frontiers in medicine TI - Evaluation of Polymorphisms in Toll-Like Receptor Genes as Biomarkers of the Response to Treatment of Erythema Nodosum Leprosum. UR - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819000/pdf/fmed-08-713143.pdf VL - 8 SN - 2296-858X ER -