Title
Diarrhea and reduced levels of antiretroviral drugs: Improvement with glutamine or alanyl-glutamine in a randomized controlled trial in northeast Brazil
Date Issued
15 June 2004
Access level
open access
Resource Type
journal article
Author(s)
Bushen O.Y.
Davenport J.A.
Lima A.B.
Piscitelli S.C.
Uzgiris A.J.
Silva T.M.J.
Leite R.
Dillingham R.A.
Girao A.
Lima A.A.M.
Guerrant R.L.
Abstract
The effects of therapy with glutamine and alanyl-glutamine on diarrhea and antiretroviral drug levels in patients with acquired immune deficiency syndrome (AIDS) were examined in a randomized, double-blinded, placebo-controlled study in northeast Brazil. Patients with AIDS and with diarrhea and/or wasting were randomized into 4 groups to determine the efficacy of glutamine or high- or low-dose alanyl-glutamine given for 7 days, compared with isonitrogenous glycine given to control subjects. All patients in whom baseline antiretroviral drug levels were determined had low levels 2 h after dosing. Gastrointestinal symptom scores improved with receipt of high-dose alanyl-glutamine (P<.05) or glutamine (P<.01). Antiretroviral drug levels increased in patients given alanyl-glutamine (P = .02) or glutamine (P = .03) by 113% (P = .02) and 14% (P = .01), respectively. Antiretroviral drug resistance mutations were common in all groups. The dose-related efficacy of alanyl-glutamine and glutamine in treating diarrhea and in increasing antiretroviral drug levels shows that these supplements may help to improve therapy for patients with AIDS who have diarrhea and/or wasting in developing, tropical areas.
Start page
1764
End page
1770
Volume
38
Issue
12
Language
English
OCDE Knowledge area
Enfermedades infecciosas
Gastroenterología, Hepatología
DOI
Scopus EID
2-s2.0-2942656778
PubMed ID
Source
Clinical Infectious Diseases
ISSN of the container
10584838
Sponsor(s)
Financial support. This study was supported in part by the University of Virginia Deans Geographic Medicine Scholarship (to J.A.D.), by Baxter Healthcare (Baxter-08012001), and by a National Institutes of Health (NIH) International Collaboration in Infectious Disease Research grant (grant no. 5 U01 AI 26512-14). O.Y.B. and R.A.D. were supported by an NIH training grant (grant no. 2 T32 AI 07046), and M.K. was supported by an NIH training grant (grant no. T 32 AI 107496-06) to the University of Virginia Beirne B. Carter Center for Immunology Research.
Sources of information:
Directorio de Producción Científica
Scopus