Prevalence of non-organ-specific autoantibodies and chronic liver disease in the general population: a nested case-control study of the Dionysos cohort
M. Lenzi et al., Prevalence of non-organ-specific autoantibodies and chronic liver disease in the general population: a nested case-control study of the Dionysos cohort, GUT, 45(3), 1999, pp. 435-441
Background-Several retrospective and prospective studies report an increase
d prevalence of non-organ-specific autoantibodies (NOSAs) in patients with
hepatitis C virus (HCV) related chronic liver disease (CLD). Some of the da
ta so far available are controversial and the true prevalence of NOSAs in t
he general population is still not known.
Aim-To explore the prevalence of NOSAs, their relation to different HCV gen
otypes, and the presence and severity of CLD in the general population of N
orthern Italy.
Patients-All 226 anti-HCV positive and 87 hepatitis B surface antigen (HBsA
g) positive patients of the Dionysos cohort study were analysed and compare
d with sex and age matched cases (226) negative for both anti-HCV antibody
and HBsAg selected from the same cohort.
Methods-Sera tested for the presence of NOSAs (anti-nuclear antibody (ANA),
anti-smooth muscle antibody (SIMA), and anti-liver/kidney microsomes type
1 antibody (LKM1)) were screened by indirect immunofluorescence at a 1:40 s
erum dilution. HCV RNA and HCV genotypes were also determined by nested pol
ymerase chain reaction (PCR) of the 5' non-coding region and by PCR amplifi
cation of the core region with type specific primers.
Results-The overall prevalence of NOSA reactivity was significantly higher
in anti-HCV positive subjects than in both normal and pathological controls
(25% upsilon 6% and 7% respectively, p<0.05). ANA, SMA, and LKM1 occurred
in 16, 10, and 1.3% of cases respectively. No specific association between
NOSAs and a specific HCV genotype was found. NOSAs were found more often as
sociated with more than one genotype (35.7%) and with untypable genotypes (
34.6%), although the association was not statistically significant. NOSAs w
ere associated with HCV RNA and CLD but not with the presence of cirrhosis
and/or hepatocellular carcinoma. On univariate analysis, NOSA reactivity wa
s independently associated with abnormal alanine aminotransferase (p<0.01)
and gamma-glutamyltranspeptidase levels (p<0.05). The risk for the presence
of NOSAs was 5.1 times higher in anti-HCV subjects than in controls.
Conclusions-In the general population the prevalence of NOSAs is higher in
anti-HCV positive subjects than in normal or disease controls. Moreover NOS
As are associated with CLD and with a more active disease in terms of alani
ne aminotransferase activity.