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Mol Genet Genomic Med ; 9(4): e1648, 2021 04.
Artigo em Inglês | MEDLINE | ID: mdl-33687153

RESUMO

BACKGROUND: Lupus nephritis is a common complication of systemic lupus erythematosus (SLE, OMIM #15200) in the Asian population and a main contributor to mortality and morbidity. In this study, we evaluate the variants on three genes STAT4, CDKN1A, and IRF5 and their association with lupus nephritis. METHOD: One hundred fifty-two SLE patients with confirmed lupus nephritis (through biopsy) and 76 healthy controls were recruited. Genotyping of SNPs on three gene STAT4, CDKN1A, and IRF5, phenotypic, and laboratory assessment were performed; renal biopsy and classification were carried out for the patient group. RESULTS: Carriers of rs7582694 C alleles on STAT4 have higher risk of lupus nephritis (OR 2.0; 95% CI [1.14, 3.19]; p = 0.015), at higher risk of hematuria and higher serum level of dsDNA antibodies compared to controls (p < 0.05) and were more likely to have nephrotic histopathology grading of class III or higher. No association was observed for CDKN1A; and no variation was observed for the IRF5 gene in both the study and control group. CONCLUSION: This study investigates the relationship between STAT4, CDKN1A, and IRF5 gene and SLE in a Vietnamese patient population. Patients with the C allele (STAT4) in rs7582694 were associated with a more severe disease phenotype.


Assuntos
Inibidor de Quinase Dependente de Ciclina p21/genética , Fatores Reguladores de Interferon/genética , Nefrite Lúpica/genética , Polimorfismo de Nucleotídeo Único , Fator de Transcrição STAT4/genética , Adulto , Feminino , Humanos , Rim/patologia , Nefrite Lúpica/classificação , Nefrite Lúpica/patologia , Masculino , Vietnã
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