CLINICAL RESEARCH POSTER PRESENTATION ABSTRACTS
Please note: All posters will be displayed in Salons 10-12.

FRIDAY, 5:45-6:30 PM


Abrams DI, Couey P, Shade SB, Aweeka F, Stamets P.

Antihyperlipidemic effects of Pleurotus Ostreatus (oyster mushrooms) in HIV-infected individuals with antiretroviral-induced hypercholesterolemia: preliminary results.

Community Consortium, Positive Health Program, University of California, San Francisco dabrams@php.ucsf.edu

PURPOSE: Hyperlipidemia is a common complication of antiretroviral therapy in HIV disease, and prior studies indicate potential interactions between botanical agents and antiretrovirals. This study evaluates the short-term safety and potential efficacy of P. ostreatus for treatment of hypercholesterolemia in persons with HIV who are taking low-dose ritonavir and another protease inhibitor (PI).

METHODS: This is a single-arm, open-label, 8-week proof-of-concept pilot study to examine the effect of P. ostreatus in 20 HIV-positive patients taking a ritonavir-boosted protease inhibitor who have elevated non-HDL cholesterol (>160 mg/dl). Patients are given packets of freeze-dried P. ostreatus (15 gm/day) to be administered orally each day for the 8-week trial period. They are followed with lipid levels drawn every two weeks to assess efficacy. Safety assessments include a pharmacokinetic sub-study to determine if P. ostreatus alter the hepatic metabolism of the PIs, self-reported incidence of muscle aches, and measurement of liver and muscle enzymes. HMG CoA reductase inhibition activity following P. ostreatus ingestion will be measured.

RESULTS: Of the 10 participants who have completed the study, three had at least a 30-point decline in non-HDL cholesterol over the eight-week study. Overall, mean non-HDL cholesterol declined approximately 10%, from 213 +52 to 194 +51. We also observed a 25% decline in mean triglyceride level (from 288 +169 to 214 +102) and an 11% increase in HDL cholesterol (from 32 +9 to 35 +6). There was no evidence of substantial toxicity associated with oyster mushrooms. Mean AST declined slightly from 25 +9 to 23 +7, mean ALT increased slightly from 19 +8 to 20 +8 and mean creatine phosphokinase declined from 205 +169 to 159 +108.

CONCLUSIONS: There is some preliminary evidence of a small decline in non-HDL cholesterol and other metabolic parameters associated with the use of oyster mushrooms. In addition, there is no evidence of substantial toxicity associated with their use. Although these results are based on a small sample, they do warrant continued enrollment to the trial.

 

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