VAGAL SYSTEM IMPAIRMENT IN HUMAN IMMUNODEFICIENCY VIRUS-POSITIVE PATIENTS WITH CHRONIC HEPATITIS-C - DOES HEPATIC GLUTATHIONE DEFICIENCY HAVE A PATHOGENETIC ROLE
G. Barbaro et al., VAGAL SYSTEM IMPAIRMENT IN HUMAN IMMUNODEFICIENCY VIRUS-POSITIVE PATIENTS WITH CHRONIC HEPATITIS-C - DOES HEPATIC GLUTATHIONE DEFICIENCY HAVE A PATHOGENETIC ROLE, Scandinavian journal of gastroenterology, 32(12), 1997, pp. 1261-1266
Background: Both an autonomic impairment and a systemic depletion of r
educed glutathione (GSH) may be documented in patients with chronic li
ver diseases and in human immunodeficiency virus (HIV)-positive patien
ts. Methods: The coefficients of electrocardiographic R-R interval var
iation (CVc) were assessed in 125 patients with chronic hepatitis C (C
HC) (65 HIV-positive and 60 HIV-negative) and in 61 healthy controls.
The CVc values were correlated with hepatic (H-GSH), plasmatic (P-GSH)
, lymphocyte (L-GSH), and erythrocyte (E-GSH) concentrations of GSH an
d with erythrocyte malondialdehyde (MDA) levels. Results: Compared wit
h healthy controls, in CHC patients the concentrations of H-GSH, P-GSH
, L-GSH, and E-GSH were reduced, whereas MDA levels were increased wit
h a statistically significant difference (P < 0.001). CVc was signific
antly reduced in patients with CHC (especially in those who were HIV-p
ositive) and correlated significantly with the values of H-GSH, P-GSH,
L-GSH, E-GSH, and MDA (P < 0.001). Conclusions: A dysfunction of the
cardiac vagal system may be detected in patients with CHC (especially
in those who are HIV-positive); this abnormality may be related to a r
educed response to oxidative stress because of a systemic depletion of
GSH.