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African Journal of Biochemistry Research Vol.
1 (6), 090-094, November 2007
ISSN 1996-0778
© 2007 Academic Journals
Full Length Research Paper
Lavudine therapy and
hepatotoxicity as seen in a Nigerian tertiary antiretroviral treatment
centre
Akande A.A1*, Olaosebikan O.F1, Jimoh A.K1,
Abdulazeez1, Olawumi H.O2
1Department of Chemical Pathology and Immunology, University
of Ilorin Teaching Hospital, PMB 1459, Ilorin, Kwara State, Nigeria.
2Department of Hematology and Blood transfusion Services,
University of Ilorin Teaching Hospital, PMB 1459, Ilorin, Kwara State,
Nigeria.
*Corresponding author. E-mail:
yinkaakande@yahoo.com.
Accepted 28 September, 2007
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Hepatic toxicity is a common
complication of anti-retroviral treatment in HIV patients, usually
indicated or heralded by the elevation of liver transaminases measured
in the blood. There had been reported evidence of hepatic toxicity in
all the three currently approved classes of anti-retroviral drugs.
However, its severity in some cases may warrant stoppage of the
treatment. This study assessed the hepato-toxicity among HIV patients on
antiretroviral therapy with lavudine in a drug treatment centre in
Nigeria. Liver function test (LFT) results of patients treated with
lavudine (lamivudne, stavudine and nevirapine) antiretroviral drug was
collated and analyzed initially as baseline data and later over a period
of three months after treatment with lavudine for liver enzymes
assessment. Sixty three (63) subjects in all were analyzed, 28 males and
35 females (M: F = 0.8:1). The results showed that there was a
non-significant (p>0.45) decrease in the serum transaminases and
alkaline phosphatase of the pretreatment LFT compared with the LFT after
three months of treatment with lavudine. The levels of serum total
protein and albumin showed a concomitant but non-significant (p>0.20)
decrease over the same period. Antiretroviral treatment with lavudine
may be associated with hepatic enzymes induction but not toxicity at
least in the short run, however hepatic function test should be
monitored every month for the first three months after starting a new
drug regimen and followed by once in six month subsequently for a year.
Key words: Lavudine,
hepatotoxicity, treatment centre, HIV /AIDS patient.
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