| Literature DB >> 25482224 |
Min Jung Chang1, Jung-Woo Chae2, Hwi-Yeol Yun2, Jangik I Lee1, Hye Duck Choi3, Jihye Kim4, Jong Sun Park5, Young-Jae Cho5, Ho Il Yoon5, Choon-Taek Lee5, Wan Gyoon Shin4, Jae-Ho Lee6.
Abstract
Diabetes mellitus (DM) is a well-known risk factor to develop tuberculosis (TB). Some reports indicate the serum concentrations of anti-TB drugs are lower in patients with TB and DM than those with TB only. Therefore, we developed a nonlinear mixed-effects model (NONMEM) to determine the population PK parameters of rifampin and assessed the effects of DM status in patients with TB. One-compartment linear modeling with first-order absorption was evaluated using the 206 plasma samples of rifampin from 54 patients with DM. Based on the final model, DM affected the absorption rate constant (ka) and the volume of distribution (Vd) of rifampin. The body mass index (BMI) of the patients affected rifampin clearance (CL). The ka of rifampin in patients with TB and DM was greater than that in patients with TB only. Further, the predicted Vd in patients with DM was greater than that in patients without DM. As Vd is inversely correlated with plasma concentrations, the rifampin concentrations were predicted to be lower in the patients with DM. The authors recommend administering the greater doses of rifampin for the treatment of TB in patients with DM compared with the doses for the patients without DM to prevent treatment failure.Entities:
Keywords: Antituberculosis agents; NONMEM; Population pharmacokinetics; Rifampin; Tuberculosis
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Year: 2014 PMID: 25482224 DOI: 10.1016/j.tube.2014.10.013
Source DB: PubMed Journal: Tuberculosis (Edinb) ISSN: 1472-9792 Impact factor: 3.131