Manosuthi Weerawat, Sukasem Chonlaphat, Thongyen Supeda, Nilkamhang Samruay, Manosuthi Sukanya, Sungkanuparph Somnuek
Bamrasnaradura Infectious Diseases Institute, Ministry of Public Health, Nonthaburi, Thailand.
Antimicrob Agents Chemother. 2014;58(4):2268-73. doi: 10.1128/AAC.02384-13. Epub 2014 Feb 3.
Data regarding the effect of the CYP2B6 18492T→C polymorphism on plasma efavirenz concentrations and 96-week virologic responses in patients coinfected with HIV and tuberculosis (TB) are still unavailable. A total of 139 antiretroviral-naive HIV-infected adults with active TB were prospectively enrolled to receive efavirenz 600 mg-tenofovir 300 mg-lamivudine 300 mg. Eight single nucleotide polymorphisms (SNPs) within CYP2B6 were genotyped. Seven SNPs, including 64C→T, 499C→G, 516G→T, 785A→G, 1375A→G, 1459C→T, and 21563C→T, were included for CYP2B6 haplotype determination. The CYP2B6 18492T→C polymorphism was studied in 48 patients who carried haplotype *1/*1. At 12 and 24 weeks after antiretroviral therapy, plasma efavirenz concentrations at 12 h after dosing were measured. Plasma HIV RNA was monitored every 12 weeks for 96 weeks. Of 48 patients {body weight [mean±standard deviation (SD)], 56±10 kg}, 77% received a rifampin-containing anti-TB regimen. No drug resistance-associated mutation was detected at baseline. The frequencies of the wild type (18492TT) and the heterozygous (18492TC) and homozygous (18492CC) mutants of the CYP2B6 18492T→C polymorphism were 39%, 42%, and 19%, respectively. At 12 weeks, mean (±SD) efavirenz concentrations of patients who carried the 18492TT, 18492TC, and 18492CC mutants were 2.8±1.6, 1.7±0.9, and 1.4±0.5 mg/liter, respectively (P=0.005). At 24 weeks, the efavirenz concentrations of the corresponding groups were 2.4±0.8, 1.7±0.8, and 1.2±0.4 mg/liter, respectively (P=0.003). A low efavirenz concentration was independently associated with 18492T→C (β=-0.937, P=0.004) and high body weight (β=-0.032, P=0.046). At 96 weeks, 19%, 17%, and 28% of patients carrying the 18492TT, 18492TC, and 18492CC mutants, respectively, had plasma HIV RNA levels of >40 copies/ml and developed efavirenz-associated mutations (P=0.254). In summary, the CYP2B6 18492T→C polymorphism compromises efavirenz concentrations in patients who carry CYP2B6 haplotype *1/*1 and are coinfected with HIV and tuberculosis.
关于CYP2B6 18492T→C基因多态性对合并感染人类免疫缺陷病毒(HIV)和结核病(TB)患者血浆依非韦伦浓度及96周病毒学应答影响的数据仍然缺乏。共有139例初治的活动性TB合并HIV感染的成人前瞻性入组,接受600 mg依非韦伦+300 mg替诺福韦+300 mg拉米夫定治疗。对CYP2B6基因内的8个单核苷酸多态性(SNP)进行基因分型。包括64C→T、499C→G、516G→T、785A→G、1375A→G、1459C→T和21563C→T在内的7个SNP用于CYP2B6单倍型的确定。在48例携带单倍型*1/1的患者中研究了CYP2B6 18492T→C基因多态性。在抗逆转录病毒治疗后12周和24周,测定给药后12小时的血浆依非韦伦浓度。每12周监测血浆HIV RNA,共监测96周。48例患者(体重[均值±标准差(SD)],56±10 kg)中,77%接受含利福平的抗结核治疗方案。基线时未检测到耐药相关突变。CYP2B6 18492T→C基因多态性的野生型(18492TT)、杂合子(18492TC)和纯合子(18492CC)突变体的频率分别为39%、42%和19%。在12周时,携带18492TT、18492TC和18492CC突变体的患者依非韦伦平均(±SD)浓度分别为2.8±1.6、1.7±0.9和1.4±0.5 mg/升(P=0.005)。在24周时,相应组的依非韦伦浓度分别为2.4±0.8、1.7±0.8和1.2±0.4 mg/升(P=0.003)。依非韦伦低浓度与18492T→C(β=-0.937,P=0.004)和高体重(β=-0.032,P=0.046)独立相关。在96周时,携带18492TT、18492TC和18492CC突变体的患者中,分别有19%、17%和28%的患者血浆HIV RNA水平>40拷贝/ml并出现依非韦伦相关突变(P=0.254)。总之,CYP2B6 18492T→C基因多态性会降低携带CYP2B6单倍型1/*1且合并感染HIV和TB患者的依非韦伦浓度。