Insulin Resistance and Diabetes Mellitus in HIV-Infected Patients Receiving Antiretroviral Therapy

被引:23
作者
Calza, Leonardo [1 ]
Manfredi, Roberto [1 ]
Chiodo, Francesco [1 ]
机构
[1] Univ Bologna, Dept Clin & Expt Med, Infect Dis Sect, S Orsola Hosp, I-40138 Bologna, Italy
关键词
D O I
10.1089/met.2004.2.241
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The introduction of highly active antiretroviral therapy (HAART) has dramatically improved the long-term prognosis of human immunodeficiency virus (HIV)-infected patients, but several abnormalities of lipid and glucose metabolism have recently been reported with increasing frequency in patients receiving potent new antiretroviral combinations. Although a rare occurrence before the HAART era, insulin resistance has now been described as an important component of the lipodystrophy syndrome, including body fat redistribution, hypertriglyceridemia, hypercholesterolemia, hyperinsulinemia, and hyperglycemia. The etiology of such abnormalities remains unclear; but protease inhibitors and, to a lesser extent, nucleoside reverse transcriptase inhibitors are believed to contribute to the pathogenetic mechanism. The potential clinico-pathological consequences of glucose metabolism dysregulation, such as atherosclerosis and coronary heart disease, all make the management of insulin resistance and diabetes mellitus a challenge in the management of HIV-infected patients. Because of similarities to pathogenesis and clinical presentation of type 2 diabetes mellitus, treatment of HAART-associated hyperinsulinemia and hyperglycemia could follow the recommendations of the American Diabetes Association, but the most effective and safe management of these metabolic alterations is still unknown. The present review evaluated the most recently published data about incidence, risk factors, pathogenesis, clinical complications, and management of glucose disorders associated with antiretroviral therapy.
引用
收藏
页码:241 / 250
页数:10
相关论文
共 59 条
[1]  
Amer Diabet Assoc, 2000, DIABETES CARE, V23, pS43
[2]   Lipodystrophy in human immunodeficiency virus patients impairs insulin action and induces defects in β-cell function [J].
Andersen, O ;
Haugaard, SB ;
Andersen, LB ;
Friis-Moller, N ;
Storgaard, H ;
Volund, A ;
Nielsen, JO ;
Iversen, J ;
Madsbad, S .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2003, 52 (10) :1343-1353
[3]   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
[4]   Impaired glucose tolerance, beta cell function and lipid metabolism in HIV patients under treatment with protease inhibitors [J].
Behrens, G ;
Dejam, A ;
Schmidt, H ;
Balks, HJ ;
Brabant, G ;
Körner, T ;
Stoll, M ;
Schmidt, RE .
AIDS, 1999, 13 (10) :F63-F70
[5]   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
[6]   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
[7]   Dyslipidaemia associated with antiretroviral therapy in HIV-infected patients [J].
Calza, L ;
Manfredi, R ;
Chiodo, F .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 53 (01) :10-14
[8]   Hyperlipidaemia in patients with HIV-1 infection receiving highly active antiretroviral therapy: epidemiology, pathogenesis, clinical course and management [J].
Calza, L ;
Manfredi, R ;
Chiodo, F .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2003, 22 (02) :89-99
[9]   HIV lipodystrophy: risk factors, pathogenesis, diagnosis and management [J].
Carr, A .
AIDS, 2003, 17 :S141-S148
[10]   Diagnosis, prediction, and natural course of HIV-1 protease-inhibitor-associated lipodystrophy, hyperlipidaemia, and diabetes mellitus: a cohort study [J].
Carr, A ;
Samaras, K ;
Thorisdottir, A ;
Kaufmann, GR ;
Chisholm, DJ ;
Cooper, DA .
LANCET, 1999, 353 (9170) :2093-2099