TY - JOUR
T1 - Association of highly active antiretroviral treatment with incident tuberculosis in people living with HIV/AIDS
AU - Yen, Yung Feng
AU - Jen, I. An
AU - Chuang, Pei Hung
AU - Chen, Marcelo
AU - Lan, Yu Ching
AU - Lee, Chun Yuan
AU - Arthur Chen, Yi Ming
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Purpose: To determine the short-term and long-term effects of highly active antiretroviral therapy (HAART) on incident tuberculosis (TB) in people living with HIV/AIDS (PLWHA). Methods: From 2000 to 2012, we identified adult PLWHA from Taiwan Centers for Disease Control HIV Surveillance System. All PLWHA were followed up until December 31, 2012, and observed for TB occurrence. Time-dependent Cox proportional hazards models were used to determine the short-term and long-term effects of HAART on incident TB. Results: Of 20,072 PLWHA, 628 (3.13%) had incident TB, corresponding to an incident rate of 701/100,000 person-years. After adjusting for potential confounders, PLWHA receiving HAART were more likely to develop TB than those not receiving the drugs (adjusted hazard ratio [AHR] 1.56; 95% confidence interval [CI] 1.18–2.05). While the short-term and long-term effects of HAART on incident TB were considered, HAART was a risk factor for TB development within the first 90 days (AHR 6.06; 95% CI 4.58–8.01) and between 90 and 180 days of treatment (AHR 1.80; 95% CI 1.11–2.94) but was a protective factor after 180 days of HAART use (AHR 0.51; 95% CI 0.39–0.66). Conclusions: HAART is a risk factor for the development of TB in the short term but a protective factor in the long term.
AB - Purpose: To determine the short-term and long-term effects of highly active antiretroviral therapy (HAART) on incident tuberculosis (TB) in people living with HIV/AIDS (PLWHA). Methods: From 2000 to 2012, we identified adult PLWHA from Taiwan Centers for Disease Control HIV Surveillance System. All PLWHA were followed up until December 31, 2012, and observed for TB occurrence. Time-dependent Cox proportional hazards models were used to determine the short-term and long-term effects of HAART on incident TB. Results: Of 20,072 PLWHA, 628 (3.13%) had incident TB, corresponding to an incident rate of 701/100,000 person-years. After adjusting for potential confounders, PLWHA receiving HAART were more likely to develop TB than those not receiving the drugs (adjusted hazard ratio [AHR] 1.56; 95% confidence interval [CI] 1.18–2.05). While the short-term and long-term effects of HAART on incident TB were considered, HAART was a risk factor for TB development within the first 90 days (AHR 6.06; 95% CI 4.58–8.01) and between 90 and 180 days of treatment (AHR 1.80; 95% CI 1.11–2.94) but was a protective factor after 180 days of HAART use (AHR 0.51; 95% CI 0.39–0.66). Conclusions: HAART is a risk factor for the development of TB in the short term but a protective factor in the long term.
KW - Highly active antiretroviral treatment
KW - HIV
KW - Short-term and long-term risk
KW - Tuberculosis
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U2 - 10.1016/j.annepidem.2018.03.011
DO - 10.1016/j.annepidem.2018.03.011
M3 - Article
AN - SCOPUS:85045220511
SN - 1047-2797
VL - 28
SP - 886-892.e3
JO - Annals of Epidemiology
JF - Annals of Epidemiology
IS - 12
ER -