|
Prevalence
of Lipoatrophy and Mitochondrial DNA Content in HIV Patients Randomly
Allocated to Zidovudine- or Stavudine-based Therapy
The
results of several studies suggest that mitochondrial toxicity resulting
from mitochondrial DNA (mtDNA) depletion is involved in the pathogenesis
of lipodystrophy
in HIV patients on HAART.
In
this study researchers cross-sectionally assessed lipodystrophy
both clinically and radiographically in patients who, 4 years before,
had been enrolled in a randomized comparative trial of stavudine (Zerit)-
or zidovudine
(Retrovir)-based therapy.
mtDNA
content was measured in peripheral blood mononuclear cells (PBMCs)
and subcutaneous adipose tissue from the thigh and back.
Results
Twenty-eight
of the 45 patients enrolled in the original trial were included.
Despite comparable exposure to stavudine or zidovudine (51 and 50
months, respectively), lipoatrophy prevalence by intent-to-treat
analysis was significantly greater in stavudine recipients (82 vs
9%, P=0.0001).
Likewise,
those allocated to stavudine had significantly less peripheral fat.
In an analysis restricted to patients who had remained on randomly
allocated nucleoside
reverse transcriptase inhibitors (NRTIs), mtDNA in
PBMCs decreased after the start of treatment in both groups (P<0.0001)
(–73% for stavudine and –67% for zidovudine, P=0.11), resulting
in significantly lower levels in patients with lipoatrophy
(P=0.007).
The
mtDNA content in subcutaneous adipose tissue from the thigh, but
not from the back, was significantly lower in patients allocated
to stavudine compared to zidovudine (P=0.01).
mtDNA
in adipose tissue from either location did not differ significantly
between those with or without lipoatrophy.
Discussion
According
to the authors, this study objectively confirms that regimens containing
stavudine are associated with a greater risk of lipoatrophy than
those containing zidovudine.
mtDNA
in PBMCs markedly declined with both treatments and was lowest in
patients with lipoatrophy.
The
lack of difference in mtDNA in adipose tissue from patients with
as opposed to without lipoatrophy may have been masked by a relative
preponderance of stromal and vascular tissue in the subcutaneous
tissue samples from these patients, combined with compensatory mitochondrial
proliferation in remaining adipocytes.
“However,”
note the authors, “our findings may also suggest that the different
risk of lipoatrophy observed between NRTIs cannot solely be explained
by differences in mtDNA depletion directly at the level of peripheral
adipose tissue.”
08/16/04
Reference
Marc
van der Valk. Prevalence
of lipoatrophy and mitochondrial DNA content of blood and subcutaneous
fat in HIV-1-infected patients randomly allocated to zidovudine-
or stavudine-based therapy. Antiviral Therapy
9: 385-393. 2004.
|