INVESTIGADORES
FRECHTEL Gustavo Daniel
artículos
Título:
- 174 G>C IL-6 polymorphism and primary iron overload in male patients.
Autor/es:
TETZLAFF WF1,2, MEROÑO T3,4, BOTTA EE3,4,5, MARTÍN ME3,4, SORROCHE PB6, BOERO LE3,4, CASTRO M4,7, FRECHTEL GD8, REY J4,7, DARUICH J9, CERRONE GE8,10, BRITES F3,4,5.
Revista:
ANNALS OF HEMATOLOGY
Editorial:
SPRINGER
Referencias:
Lugar: Berlin; Año: 2018
ISSN:
0939-5555
Resumen:
Primary iron overload (IO) is commonly associated with mutations in the hereditary hemochromatosis gene (HFE). Nonetheless, other genetic variants may influence the development of IO beyond HFE mutations. There is a single nucleotide polymorphism (SNP) at - 174 G>C of the interleukin (IL)-6 gene which might be associated with primary IO. Our aim was to study the association between the SNP - 174 G>C gene promoter of IL-6 and primary IO in middle-aged male patients. We studied 37 men with primary IO diagnosed by liver histology. Controls were age-matched male volunteers (n = 37). HFE mutations and the SNP - 174 G>C gene promoter of IL-6 were evaluated by PCR-RFLP. Logistic regression was used to evaluate the association between primary IO and SNP - 174 G>C gene promoter of IL-6. Patients and control subjects were in Hardy-Weinberg equilibrium for the SNP - 174 G>C gene promoter of IL-6 (p = 0.17). Significantly different genotype frequencies were observed between patients (43% CC, 43% CG, and 14% GG) and control subjects (10% CC, 41% CG, and 49% GG) (OR = 4.09, 95% CI = 2.06-8.13; p C gene promoter of IL-6 (OR = 6.3, 95% CI = 1.9-21.4; p C gene promoter of IL-6 can be proposed as one of the gene variants influencing iron accumulation in male adults with HFE mutations. Studies in larger cohorts are warranted.