G. Soardo et al., CHANGES IN BLOOD LIPID-COMPOSITION AND RESPONSE TO INTERFERON TREATMENT IN CHRONIC HEPATITIS-C, Journal of interferon & cytokine research, 15(8), 1995, pp. 705-712
To assess whether the initial status of lipid metabolism in patients w
ith chronic viral hepatitis might correlate with outcome of therapy, 5
2 patients (32 males and 20 female) with chronic hepatitis C were stud
ied: 44 were treated with human recombinant interferon-alpha(2b) (3 MU
three times per week for up to 12 months), and 8 served as controls.
At baseline, sera were tested for total and HDL cholesterol, HDL(2), H
DL(3), apolipoprotein A-I, apolipoprotein B, interferon-alpha, tumor n
ecrosis factor, and interleukin-6. Changes in blood lipids were evalua
ted after 3, 30, and 90 days of treatment. HDL cholesterol, apolipopro
tein A-I, and HDL(3) decreased by 9.4-11.4% within 4 weeks of starting
interferon treatment, but this effect was sustained only in patients
with a primary response to interferon. On multivariate analysis, a pri
mary response to interferon correlated with higher apolipoprotein A-I
and lower (<2.23 pg/ml) interleukin-6 levels (p < 0.005 for both). In
contrast, a sustained response was significantly more common in patien
ts with low (less than or equal to 13.3 pg/ml) serum interferon-cw and
lower interleukin-6 at baseline but did not correlate with any of the
blood lipids. Thus, in chronic hepatitis C, interferon treatment indu
ces specific changes in blood lipids. The concentration of apolipoprot
ein A-I at baseline is a strong predictor of primary response to treat
ment, and the likelihood of a sustained response seems to be reflected
by lower cytokine activation.