TY - JOUR
T1 - INTERLEUKIN 6 PROMOTER
POLYMORPHISMS INFLUENCE THE OUTCOME OF CHRONIC HEPATITIS C
AU - CUSSIGH, A
AU - FALLETI, E
AU - FABRIS, C
AU - BITETTO, D
AU - CMET, S
AU - FONTANINI, E
AU - BIGNULIN, S
AU - FORNASIERE, E
AU - FUMOLO, E
AU - MINISINI, Rosalba
AU - PIRISI, Mario
AU - TONIUTTO, P.
N1 - Funding Information:
Acknowledgments This study is supported in part by grants from the “Ricerca Sanitaria Finalizzata” Program, Regione Piemonte, Italy and Fondazione CRUP Udine, Italy
PY - 2011
Y1 - 2011
N2 - Host genetic variation may affect the outcome of chronic viral hepatitides, favoring viral clearance and/or modulating the inflammatory response to persistent infection. Our aims were to assess whether interleukin 6 (IL-6) promoter polymorphisms are associated with chronic hepatitis C virus (HCV) infection and to clarify the role of IL-6 haplotypes in facilitating progressive disease. The study included 424 Italian patients (233 males, median age 53 years) affected by HCV chronic infection. IL6 -1363, -597, -572, -174, and +2954 polymorphic loci were assayed by means of restriction fragment length polymorphism. Three hundred forty-four healthy Italian blood donors (245 males, median age 50 years) served as controls. Comparing patients and controls analysis of molecular variance was highly significant (p∈<∈0.0001); at a locus by locus approach, the frequencies of minor alleles in the -1363 (p∈<∈0.02), -597 (p∈<∈0.02), and -174 (p∈<∈0.01) polymorphisms were confirmed to be less represented in patients than in controls. Carrying the wild-type G allele at the -597 and -174 loci identified an unfavorable haplotype; carrying the minor allele in one/both loci identified an indifferent/favorable haplotype. Male patients carrying two unfavorable haplotypes had the highest adjusted mean∈±∈standard error Ishak staging score (3.56∈±∈0.19), while females carrying one or no unfavorable haplotypes had the lowest (2. 69∈±∈0.21); the remaining patients had an intermediate value (3.12∈±∈0.13, p∈<∈0.01). In conclusion, IL-6 promoter polymorphisms influence the development of chronic HCV infection. With the permissive effect of male gender, haplotypes represented by the wild-type allele for -597 and -174 loci appear to favor a worse evolution of the disease.
AB - Host genetic variation may affect the outcome of chronic viral hepatitides, favoring viral clearance and/or modulating the inflammatory response to persistent infection. Our aims were to assess whether interleukin 6 (IL-6) promoter polymorphisms are associated with chronic hepatitis C virus (HCV) infection and to clarify the role of IL-6 haplotypes in facilitating progressive disease. The study included 424 Italian patients (233 males, median age 53 years) affected by HCV chronic infection. IL6 -1363, -597, -572, -174, and +2954 polymorphic loci were assayed by means of restriction fragment length polymorphism. Three hundred forty-four healthy Italian blood donors (245 males, median age 50 years) served as controls. Comparing patients and controls analysis of molecular variance was highly significant (p∈<∈0.0001); at a locus by locus approach, the frequencies of minor alleles in the -1363 (p∈<∈0.02), -597 (p∈<∈0.02), and -174 (p∈<∈0.01) polymorphisms were confirmed to be less represented in patients than in controls. Carrying the wild-type G allele at the -597 and -174 loci identified an unfavorable haplotype; carrying the minor allele in one/both loci identified an indifferent/favorable haplotype. Male patients carrying two unfavorable haplotypes had the highest adjusted mean∈±∈standard error Ishak staging score (3.56∈±∈0.19), while females carrying one or no unfavorable haplotypes had the lowest (2. 69∈±∈0.21); the remaining patients had an intermediate value (3.12∈±∈0.13, p∈<∈0.01). In conclusion, IL-6 promoter polymorphisms influence the development of chronic HCV infection. With the permissive effect of male gender, haplotypes represented by the wild-type allele for -597 and -174 loci appear to favor a worse evolution of the disease.
UR - https://iris.uniupo.it/handle/11579/16130
U2 - 10.1007/s00251-010-0491-7
DO - 10.1007/s00251-010-0491-7
M3 - Article
SN - 0093-7711
VL - 63
SP - 33
EP - 41
JO - Immunogenetics
JF - Immunogenetics
ER -