Universidad Peruana Cayetano Heredia

Pharmacokinetics of rifampin in peruvian tuberculosis patients with and without comorbid diabetes or HIV

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dc.contributor.author Requena-Méndez, A.
dc.contributor.author Davies, G.
dc.contributor.author Ardrey, A.
dc.contributor.author Jave, O.
dc.contributor.author López-Romero, S.L.
dc.contributor.author Ward, S.A.
dc.contributor.author Moore, David Alexander James
dc.date.accessioned 2022-01-18T19:26:53Z
dc.date.available 2022-01-18T19:26:53Z
dc.date.issued 2012
dc.identifier.uri https://hdl.handle.net/20.500.12866/10992
dc.description.abstract For drug-compliant patients, poor responses to tuberculosis (TB) treatment might be attributable to subtherapeutic drug concentrations. An impaired absorption of rifampin was previously reported for patients with diabetes mellitus (DM) or HIV. The objectives of this study were to determine whether TB drug pharmacokinetics differed in Peruvian TB patients withDMor HIV. In this cross-sectional study, TB patients, recruited from health centers in Lima, Peru, had blood samples taken at 2 and 6 h after directly observed TB drug ingestion, to determine plasma concentrations of rifampin. Of 105 patients, 50 had TB without a comorbidity, 26 had coexistent DM, and 29 had coexistent HIV. Unexpectedly, the overall median 2- and 6-h levels of rifampin were 1.6 and 3.2 mg/liter, respectively, and the time to the peak concentration was 6 h (slow absorber) instead of 2 h (fast absorber) for 61 patients (62.2%). The geometric mean peak concentration of drug in serum (C max) was significantly higher in fast absorbers than in slow absorbers (5.0 versus 3.8 mg/liter; P = 0.05). The rifampin C max was significantly lower in male patients than in female patients (3.3 versus 6.3 mg/liter; P < 0.001). Neither slow nor fast absorbers with comorbidities (DM or HIV) had significantly different Cmax results compared to those of TB patients without comorbidities. An analysis of variance regression analysis showed that female gender (P < 0.001) and the time to maximum concentration of drug in serum (T max) at 2 h (P =0.012) were independently correlated with increased exposure to rifampin. Most of this Peruvian study population exhibited rifampin pharmacokinetics different from those conventionally reported, with delayed absorption and low plasma concentrations, independent of the presence of an HIV or DM comorbidity. en_US
dc.language.iso eng
dc.publisher American Society for Microbiology
dc.relation.ispartofseries Antimicrobial Agents and Chemotherapy
dc.rights info:eu-repo/semantics/restrictedAccess
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.subject Humans en_US
dc.subject Controlled Study en_US
dc.subject Major Clinical Study en_US
dc.subject Sex Difference en_US
dc.subject Comorbidity en_US
dc.subject Rifampicin en_US
dc.subject HIV Infections en_US
dc.subject Human Immunodeficiency Virus Infection en_US
dc.subject Sex Factors en_US
dc.subject Treatment Outcome en_US
dc.subject Mycobacterium Tuberculosis en_US
dc.subject Tuberculosis en_US
dc.subject Tuberculosis Pulmonary en_US
dc.subject Antitubercular Agents en_US
dc.subject Treatment Response en_US
dc.subject Blood Sampling en_US
dc.subject Diabetes Mellitus en_US
dc.subject Rifampin en_US
dc.subject Maximum Plasma Concentration en_US
dc.subject Drug Absorption en_US
dc.subject Time To Maximum Plasma Concentration en_US
dc.subject Diabetes Complications en_US
dc.subject Directly Observed Therapy en_US
dc.subject Regression Analysis en_US
dc.title Pharmacokinetics of rifampin in peruvian tuberculosis patients with and without comorbid diabetes or HIV en_US
dc.type info:eu-repo/semantics/article
dc.identifier.doi https://doi.org/10.1128/AAC.06059-11
dc.subject.ocde https://purl.org/pe-repo/ocde/ford#3.02.21
dc.relation.issn 1098-6596


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