Association between IL1B rs16944 polymorphism and the risk of idiopathic inflammatory myopathies

Introduction: rs16944 polymorphism and the risk of developing IIMs. Methods: rs16944 polymorphism was analyzed. Myositis-specific autoantibodies (MSAs), myositis-associated autoantibodies (MAAs), and antinuclear antibodies (ANAs) were determined. Results: = 0.0044, respectively). Also, a significant association could be observed with DM, polymyositis (PM), DM+PM, juvenile DM, amyopathic DM, antisynthetase syndrome (ASyS), and cancer-associated myositis (CAM). Enzyme levels of CPK presented significant differences in our IIMs patients. The rs16944 polymorphism is significantly associated with various clinicopathological characteristics. Conclusion: rs16944 CC (codominant and dominant models) and CCTT (overdominant) genotypes and the IIMs phenotype (OR = 4.6136, 3.4232, and 3.5387, respectively).

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Publication Details

Journal
Frontiers in Immunology
Published
2026-04-01
DOI
https://doi.org/10.3389/fimmu.2026.1697044
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
Field-Weighted Citation Impact
0.00

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article

Association between IL1B rs16944 polymorphism and the risk of idiopathic inflammatory myopathies

Lilia Andrade-Ortega, Mónica Vázquez-Del Mercado, Irene Mendoza-Lujambio, Karina Lamadrid-Gámez et al.
Frontiers in Immunology
Inflammatory Myopathies and Dermatomyositis
article

Association between IL1B rs16944 polymorphism and the risk of idiopathic inflammatory myopathies

Lilia Andrade-Ortega, Mónica Vázquez-Del Mercado, Irene Mendoza-Lujambio, Karina Lamadrid-Gámez, Daniel Pérez-Covarrubias, Celso Pérez-Rostro, Ignacio García-De la Torre
article en

Abstract

Introduction: rs16944 polymorphism and the risk of developing IIMs. Methods: rs16944 polymorphism was analyzed. Myositis-specific autoantibodies (MSAs), myositis-associated autoantibodies (MAAs), and antinuclear antibodies (ANAs) were determined. Results: = 0.0044, respectively). Also, a significant association could be observed with DM, polymyositis (PM), DM+PM, juvenile DM, amyopathic DM, antisynthetase syndrome (ASyS), and cancer-associated myositis (CAM). Enzyme levels of CPK presented significant differences in our IIMs patients. The rs16944 polymorphism is significantly associated with various clinicopathological characteristics. Conclusion: rs16944 CC (codominant and dominant models) and CCTT (overdominant) genotypes and the IIMs phenotype (OR = 4.6136, 3.4232, and 3.5387, respectively).

Frontiers in ImmunologyVol. 17
Universidad de Guadalajara (MX), Secretaría de Salud de Jalisco (MX), Hospital Civil de Guadalajara (MX), Instituto Politécnico Nacional (MX), Institute for Social Security and Services for State Workers (MX), Centro de Estudios Científicos (CL)
Instituto Politécnico Nacional
Good health and well-being
Openalex Percentile: Top 33%
Inflammatory Myopathies and Dermatomyositis
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