Infectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.
Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
J Antimicrob Chemother. 2019 Jan 1;74(1):135-138. doi: 10.1093/jac/dky379.
To report the efavirenz serum concentrations in TB/HIV-coinfected Ugandan adults on concomitant anti-TB treatment and analyse factors associated with elevated concentrations in this specific population.
Serum efavirenz concentrations in TB/HIV-coinfected Ugandan adults on efavirenz-based ART (600 mg daily) were measured onsite at 2, 8, 12 and 24 weeks of concomitant anti-TB treatment, including rifampicin. Genetic analysis was done retrospectively through real-time PCR by allelic discrimination (CYP2B6 516G>T, rs3745274). Univariable and multivariable logistic regression analyses were done to assess factors potentially associated with elevated efavirenz serum concentrations.
A total of 166 patients were included in the analysis. The median age was 34 (IQR = 30-40) years, 99 (59.6%) were male, the median CD4 cell count was 195 (IQR = 71-334) cells/mm3 and the median BMI was 19 (IQR = 17.6-21.5) kg/m2. Almost half of all patients (82, 49.4%) had at least one efavirenz serum concentration above the reference range of 4 mg/L. The serum efavirenz concentrations of patients with genotype CYP2B6 516 TT were consistently above 4 mg/L and significantly higher than those of patients with GG/GT genotypes: CYP2B6 516 TT 9.6 mg/L (IQR = 7.3-13.3) versus CYP2B6 516 GT 3.4 mg/L (IQR = 2.1-5.1) and CYP2B6 516 GG 2.6 mg/L (IQR = 1.3-4.0) (Wilcoxon rank-sum test: P < 0.0001).
A large proportion of our study participants had at least one efavirenz serum concentration >4 mg/L. The CYP2B6 516 TT genotype was the strongest predictor of high concentration. Physicians should be vigilant that efavirenz serum concentrations may be elevated in patients on concomitant anti-TB treatment and that individualized care is warranted whenever possible.
报告同时接受抗结核治疗的乌干达合并结核和 HIV 感染的成年患者中依非韦伦的血清浓度,并分析该特定人群中浓度升高的相关因素。
在同时接受抗结核治疗(包括利福平)的乌干达合并结核和 HIV 感染的成年患者中,通过实时 PCR 等位基因鉴别(CYP2B6 516G>T,rs3745274)进行依非韦伦的血清浓度现场检测。采用单变量和多变量逻辑回归分析评估可能与依非韦伦血清浓度升高相关的因素。
共纳入 166 例患者进行分析。中位年龄为 34(IQR=30-40)岁,99 例(59.6%)为男性,中位 CD4 细胞计数为 195(IQR=71-334)/mm3,中位 BMI 为 19(IQR=17.6-21.5)kg/m2。几乎一半的患者(82 例,49.4%)至少有一次依非韦伦血清浓度超过 4mg/L 的参考范围。CYP2B6 516 TT 基因型患者的血清依非韦伦浓度始终高于 4mg/L,明显高于 CYP2B6 516 GT 基因型患者:CYP2B6 516 TT 9.6mg/L(IQR=7.3-13.3)比 CYP2B6 516 GT 3.4mg/L(IQR=2.1-5.1)和 CYP2B6 516 GG 2.6mg/L(IQR=1.3-4.0)(Wilcoxon 秩和检验:P<0.0001)。
我们研究的大部分参与者至少有一次依非韦伦血清浓度>4mg/L。CYP2B6 516 TT 基因型是浓度升高的最强预测因素。医生应警惕在同时接受抗结核治疗的患者中依非韦伦血清浓度可能升高,在可能的情况下应进行个体化治疗。