The role of efavirenz compared with protease inhibitors in the body fat changes associated with highly active antiretroviral therapy

被引:30
作者
Perez-Molina, Jose A. [1 ]
Domingo, Pere [2 ]
Martinez, Esteban [3 ]
Moreno, Santiago
机构
[1] Hosp Univ Ramon & Cajal, Dept Infect Dis, Trop Med & Clin Parasitol Unit, Madrid, Spain
[2] Univ Autonoma Barcelona, Hosp Santa Creu & San Pau, Infect Dis Unit, E-08193 Barcelona, Spain
[3] Univ Barcelona IDIBAPS, Hosp Clin, Infect Dis Unit, Barcelona, Spain
关键词
lipodystrophy; lopinavir; DEXA scan; antiretroviral drugs; HAART;
D O I
10.1093/jac/dkn191
中图分类号
R51 [传染病];
学科分类号
100401 [流行病与卫生统计学];
摘要
Highly active antiretroviral therapy plays a central role in the development of lipodystrophy syndrome, which may affect up to 50% of patients depending on the diagnostic criteria used. Most protease inhibitors and nucleoside reverse transcriptase inhibitors (NRTIs) are involved in body fat changes and associated metabolic disturbances. In contrast, non-NRTIs have not been directly related to the onset of this syndrome. One of the most widely used methods to evaluate body fat changes is dual-energy X-ray absorptiometry (DEXA), which can detect differences in the distribution of body fat in patients with and without lipodystrophy. New information from a randomized open-label clinical trial suggests that efavirenz could have greater potential for causing lipoatrophy than lopinavir+ritonavir. This paper examines the impact of efavirenz on adipose tissue and body fat composition in order to evaluate whether this drug plays a role in the development of lipodystrophy. We have focused on the evidence obtained from comparative randomized clinical trials that use an objective measurement of fat distribution, such as DEXA. We analysed available in vitro data and evidence from non-comparative clinical trials.
引用
收藏
页码:234 / 245
页数:12
相关论文
共 100 条
[1]
Aldeguer L, 2007, ENFERM INFEC MICR CL, V25, P32, DOI 10.1157/13096750
[2]
Efficacy and tolerability of a nucleoside reverse transcriptase inhibitor-sparing combination of lopinavir/ritonavir and efavirenz in HIV-1-infected patients [J].
Allavena, C ;
Ferré, V ;
Brunet-François, C ;
Delfraissy, JF ;
Lafeuillade, A ;
Valantin, MA ;
Bentata, M ;
Michelet, C ;
Poizot-Martin, I ;
Dailly, E ;
Launay, O ;
Raffi, F .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2005, 39 (03) :300-306
[3]
Intracellular and plasma pharmacokinetics of efavirenz in HIV-infected individuals [J].
Almond, LM ;
Hoggard, PG ;
Edirisinghe, D ;
Khoo, SH ;
Back, DJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (04) :738-744
[4]
Association between altered expression of adipogenic factor SREBP1 in lipoatrophic adipose tissue from HIV-1-infected patients and abnormal adipocyte differentiation and insulin resistance [J].
Bastard, JP ;
Caron, M ;
Vidal, H ;
Jan, V ;
Auclair, M ;
Vigouroux, C ;
Luboinski, J ;
Laville, M ;
Malachi, M ;
Girard, PM ;
Rozenbaum, W ;
Levan, P ;
Capeau, J .
LANCET, 2002, 359 (9311) :1026-1031
[5]
Cardiovascular risk in patients with HIV infection - Impact of antiretroviral therapy [J].
Bergersen, Bente Magny .
DRUGS, 2006, 66 (15) :1971-1987
[6]
Bogner JR, 2001, J ACQ IMMUN DEF SYND, V27, P237, DOI 10.1097/00126334-200107010-00004
[7]
Mitochondrial toxicity induced by nucleoside-analogue reverse-transcriptase inhibitors is a key factor in the pathogenesis of antiretroviral-therapy-related lipodystrophy [J].
Brinkman, K ;
Smeitink, JA ;
Romijn, JA ;
Reiss, P .
LANCET, 1999, 354 (9184) :1112-1115
[8]
Interpatient variability in the pharmacokinetics of the HIV non-nucleoside reverse transcriptase inhibitor efavirenz:: the effect of gender, race, and CYP2B6 polymorphism [J].
Burger, D ;
van der Heiden, I ;
la Porte, C ;
van der Ende, M ;
Groeneveld, P ;
Richter, C ;
Koopmans, P ;
Kroon, F ;
Sprenger, H ;
Lindemans, J ;
Schenk, P ;
van Schaik, R .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 61 (02) :148-154
[9]
CAMERON D, 2008, 15 C RETR OPP INF BO
[10]
Some HIV protease inhibitors alter lamin A/C maturation and stability, SREBP-1 nuclear localization and adipocyte differentiation [J].
Caron, M ;
Auclair, M ;
Sterlingot, H ;
Kornprobst, M ;
Capeau, J .
AIDS, 2003, 17 (17) :2437-2444