Journal article
Tenofovir-based Antiretroviral Therapy in Hepatitis B Virus HIV Co-infection - Results from the TREAT Asia HIV Observational Database
David C Boettiger Stephen Kerr Rossana Ditangco Romanee Chaiwarith Patrick CK Li Ketut Tuti Parwati Merati Thuy Thi Thanh Pham Sasisopin Kiertiburanakul Nagalingeswaran Kumarasamy Saphonn Vonthanak Christopher KC Lee Nguyen Van Kinh Sanjay Pujari Wing Wai Wong Adeeba Kamarulzaman
Volume : 21 Nomor : 1 Published : 2017, January
Antiviral Therapy
Abstrak
Abstract Background—The World Health Organisation recommends Hepatitis B virus (HBV)/HIV co-infected individuals start antiretroviral therapy containing tenofovir. Here we describe first-line tenofovir use and treatment outcomes in co-infected patients in Asia. Methods—HBV surface antigen positive patients enrolled in the TREAT Asia HIV Observational Database who started first-line antiretroviral therapy were included. Logistic regression adjusted for period of treatment initiation was used to determine factors associated with tenofovir use. Generalised estimating equations were used to evaluate factors associated with alanine transaminase levels and CD4 cell count on treatment. Results—There were 548 eligible patients, of whom 149 (27.2%) started tenofovir. Patients treated in high/high-middle income countries (odds ratio 4.4 vs. low/low-middle, 95%CI 2.6-7.4, p<0.001) and those with elevated baseline alanine transaminase (odds ratio 4.2 vs. normal, 95%CI 2.4-7.2, p<0.001) were more likely to receive tenofovir. Hepatitis C antibody positive patients (odds ratio 0.4 vs. negative, 95%CI 0.2-0.8, p=0.008) were less likely. In those starting antiretroviral therapy with elevated alanine transaminase, mean reduction after tenofovir initiation was 11.2 IU/L (95%CI 0.9-21.6, p=0.034) lower compared with those using a non-tenofovir-based regimen although this did not significantly increase the chance of alanine transaminase normalization. Tenofovir use was not associated with a superior CD4 response. Conclusions—HBV/HIV co-infected patients in Asia are most likely to receive tenofovir if they are treated in a high/high-middle income country, have elevated alanine transaminase levels, and are hepatitis C antibody negative. Compared to other antiretroviral therapy, tenofovir-based regimens more effectively reduce liver inflammation in HBV/HIV co-infection but do not result in superior CD4 recovery.