M. Deutsch et al., THYROID ABNORMALITIES IN CHRONIC VIRAL-HEPATITIS AND THEIR RELATIONSHIP TO INTERFERON-ALFA THERAPY, Hepatology, 26(1), 1997, pp. 206-210
The prevalence of antithyroid peroxidase antibodies (ATPO) and/or of t
hyroid dysfunction was studied in 422 patients with chronic viral hepa
titis C, B, and D. Baseline results were compared with those during an
d 6 months after interferon alfa (IFN-alpha) therapy. The overall prev
alence of ATPO among untreated patients was 14.1%, with no significant
differences between chronic hepatitis C, B, or D, as well as between
males and females. However, high ATPO titers (greater than or equal to
18 IU/mL) clustered significantly among females (8.7% vs, 3.4%; P = .
022), especially those with chronic hepatitis C (11.2% vs. 3.6%; P = .
036). Before treatment, 3.7% of the patients had thyroid dysfunction,
mostly hypothyroidism (3.5%), the latter increasing to 14.3% among pat
ients with ATPO titers greater than or equal to 18 IU/mL. IFN-alpha tr
eatment significantly increased overall thyroid dysfunction (9.7%; P =
.001) and hypothyroidism (7.8%; P = .01), particularly among patients
with high baseline ATPO (38.5%; P = .0002). Six months after stopping
IFN-alpha treatment, the prevalence of thyroid dysfunction was 8.0%,
still significantly higher than at baseline. By multivariate analysis,
the only predictor positively associated with pre- or on-treatment hy
pothyroidism was the baseline titer of the ATPO antibodies (relative r
isk [RR], 3.0 and 3.8 per each log titer increase, respectively). In c
onclusion, patients with chronic viral hepatitis on IFN-alpha treatmen
t exhibit an almost threefold increase of baseline thyroid dysfunction
, persisting long after the end of therapy. High ATPO titers, clusteri
ng among females, particularly those with hepatitis C, represent the o
nly predictor of pre- and on-treatment hypothyroidism by multivariate
analysis. Patients with chronic viral hepatitis, especially females, s
hould be tested for ATPO and thyroid function and monitored during and
posttreatment for free thyroxin (FT4) and thyroid-stimulating hormone
(TSH) levels.