AIDS-related lipodystrophy/insulin resistance syndrome

被引:34
作者
Kino, T [1 ]
Mirani, M [1 ]
Alesci, S [1 ]
Chrousos, GP [1 ]
机构
[1] NICHHD, Pediat & Reprod Endrocrinol Branch, NIH, Bethesda, MD 20892 USA
关键词
adipose calls; AIDS; fat distribution; pseudo-cushing;
D O I
10.1055/s-2003-39072
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The recent development and clinical use of three different types of highly effective anti-HIV-1 drugs, including nucleotide and non-nucleotide reverse transcriptase inhibitors (NRTIs) and non-peptidic viral protease inhibitors (Pis) and their combinations, termed highly active antiretroviral therapy (HAART), have dramatically reduced the infection-related mortality of AIDS patients in developed countries. However, the prolongation of the life expectancy of HIV-1-infected patients and/or long-term use of the above antiviral agents have generated a score of new problems and complications. Among them is the relatively common AIDS-related lipodystrophy/insulin resistance syndrome, which is associated with severe metabolic disturbances such as carbo-hydrate intolerance/diabetes mellitus and severe dyslipidemia, which influence the quality of life and threaten the life expectancies of HIV-1-infected patients by increasing the risk of atherosclerotic cardiovascular disease. The etiology of this syndrome appears to be multi-factorial; the classes of anti-viral drugs listed above, hypercytokinemia in AIDS patients, and the HIV-1 infection itself could induce the pathologic changes of this syndrome or increase the vulnerability of patients to the adverse effect of the therapeutic compounds. In this article, we review our current understanding of the pathogenesis of this severe AIDS-associated metabolic disorder.
引用
收藏
页码:129 / 136
页数:8
相关论文
共 110 条
[1]   Fat cell function and fibrinolysis [J].
Alessi, MC ;
Morange, P ;
Juhan-Vague, I .
HORMONE AND METABOLIC RESEARCH, 2000, 32 (11-12) :504-508
[2]   HIV-1 viral protein R (Vpr) regulates viral replication and cellular proliferation in T cells and monocytoid cells in vitro [J].
Ayyavoo, V ;
Mahalingam, S ;
Rafaeli, Y ;
Kudchodkar, S ;
Chang, D ;
Nagashunmugam, T ;
Williams, WV ;
Weiner, DB .
JOURNAL OF LEUKOCYTE BIOLOGY, 1997, 62 (01) :93-99
[3]   Efficacy and tolerability of pravastatin for the treatment of HIV-1 protease inhibitor-associated hyperlipidaemia: a pilot study [J].
Baldini, F ;
Di Giambenedetto, S ;
Cingolani, A ;
Murri, R ;
Ammassari, A ;
De Luca, A .
AIDS, 2000, 14 (11) :1660-1662
[4]   THE ADIPSIN ACYLATION STIMULATING PROTEIN SYSTEM AND REGULATION OF INTRACELLULAR TRIGLYCERIDE SYNTHESIS [J].
BALDO, A ;
SNIDERMAN, AD ;
STLUCE, S ;
AVRAMOGLU, RK ;
MASLOWSKA, M ;
HOANG, B ;
MONGE, JC ;
BELL, A ;
MULAY, S ;
CIANFLONE, K .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) :1543-1547
[5]   Risks and benefits of replacing protease inhibitors by nevirapine in HIV-infected subjects under long-term successful triple combination therapy [J].
Barreiro, P ;
Soriano, V ;
Blanco, F ;
Casimiro, C ;
de la Cruz, JJ ;
González-Lahoz, J .
AIDS, 2000, 14 (07) :807-812
[6]   ApoE genotype and protease-inhibitor-associated hyperlipidaemia [J].
Behrens, G ;
Schmidt, HHJ ;
Stoll, M ;
Schmidt, RE .
LANCET, 1999, 354 (9172) :76-76
[7]   Lipodystrophy syndrome in HIV infection - What is it, what causes it and how can it be managed? [J].
Behrens, GMN ;
Stoll, M ;
Schmidt, RE .
DRUG SAFETY, 2000, 23 (01) :57-76
[8]   THE LDL RECEPTOR RELATED PROTEIN, LRP, IS AN APOLIPOPROTEIN-E-BINDING PROTEIN [J].
BEISIEGEL, U ;
WEBER, W ;
IHRKE, G ;
HERZ, J ;
STANLEY, KK .
NATURE, 1989, 341 (6238) :162-164
[9]   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
[10]   Adverse effects of reverse transcriptase inhibitors: mitochondrial toxicity as common pathway [J].
Brinkman, K ;
ter Hofstede, HJM ;
Burger, DM ;
Smeitinkt, JAM ;
Koopmans, PP .
AIDS, 1998, 12 (14) :1735-1744