Longitudinal evaluation and risk factors of lipodystrophy and associated metabolic changes in HIV-infected children

被引:89
作者
Beregszaszi, M
Dollfus, C
Levine, M
Faye, A
Deghmoun, S
Bellal, N
Houang, M
Chevenne, D
Hankard, R
Bresson, JL
Blanche, SP
Levy-Marchal, C
机构
[1] Hop Robert Debre, INSERM, Unit 690, F-75019 Paris, France
[2] Hop Trousseau, Serv Hemato Immunol, F-75571 Paris, France
[3] Hop Robert Debre, Serv Hemato Immunol, F-75019 Paris, France
[4] Hop Enfants Malad, Unit Immunol & Hematol, Paris, France
[5] Hop Robert Debre, Hormonal Lab, F-75019 Paris, France
[6] Hop Enfants Malad, Ctr Invest Clin, Paris, France
[7] Hop Robert Debre, Ctr Invest Clin, F-75019 Paris, France
[8] Hop Trousseau, Lab Endocrinol, F-75571 Paris, France
关键词
children; HIV; treatment; lipodystrophy; insulin resistance; puberty;
D O I
10.1097/01.qai.0000178930.93033.f2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To assess the rate of progression of lipodystrophy and the associated metabolic disturbances over a 2-year period in children and to assess risk factors associated with lipodystrophy and metabolic disturbances. Design: Multicenter 2-year prospective study with a standardized evaluation. Methods: One hundred thirty children (median age = 10 years, 64 boys and 66 girls) receiving antiretroviral therapy were recruited in 3 pediatric clinics. Lipodystrophy was defined based on 4 skinfold thickness measurements. Fasting lipids and glucose profile were measured in all children. Results: The proportion of children presenting with lipodystrophy was 24.6%. Nineteen percent of children had high-density lipoprotein values less than 1 mmol/L. Twenty-two percent and 15% of children had values greater than 2 standard deviations for age and gender for cholesterol and triglycerides, respectively. A total of 13.2% showed insulin resistance. A total of 42.7% showed at least I of these biologic disturbances. Prospective follow-up showed no progression at all over 2 years, except for a doubling of the number of children with insulin resistance. In multivariate analyses, ethnicity, previous severe clinical condition, duration of HIV infection, and nucleoside reverse transcriptase inhibitor treatment were significantly associated with lipodystrophy. Tanner stage V of puberty, severe clinical symptoms and protease inhibitor treatment were independently associated with the risk of metabolic disturbances. Conclusions: Puberty seems to be the time when HIV-infected children taking potent antiretroviral therapy are more likely to develop lipodystrophy and metabolic complications, especially in children with a severe underlying HIV infection. Once developed, lipodystrophy and metabolic changes seem to be extremely stable with time.
引用
收藏
页码:161 / 168
页数:8
相关论文
共 21 条
[1]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[2]  
2-S
[3]   Lipodystrophy syndrome in human immunodeficiency virus-infected children [J].
Amaya, RA ;
Kozinetz, CA ;
McMeans, A ;
Schwarzwald, H ;
Kline, MW .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2002, 21 (05) :405-410
[4]  
[Anonymous], 1994, MMWR
[5]  
Arpadi SM, 2001, J ACQ IMMUN DEF SYND, V27, P30, DOI 10.1097/00126334-200105010-00005
[6]   Evidence of human immunodeficiency virus-associated lipodystrophy syndrome in children treated with protease inhibitors [J].
Bockhorst, JL ;
Ksseiry, I ;
Toye, M ;
Chipkin, SR ;
Stechenberg, BW ;
Fisher, DJ ;
Allen, HF .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2003, 22 (05) :463-465
[7]   Highly active antiretroviral-treated HIV-infected children show fat distribution changes even in absence of lipodystrophy [J].
Brambilla, P ;
Bricalli, D ;
Sala, N ;
Renzetti, F ;
Manzoni, P ;
Vanzulli, A ;
Chiumello, G ;
di Natale, B ;
Viganò, A .
AIDS, 2001, 15 (18) :2415-2422
[8]   An objective case definition of lipodystrophy in HIV-infected adults: a case-control study [J].
Carr, A ;
Emery, S ;
Law, I ;
Puls, R ;
Lundgren, JD ;
Powderly, WG ;
Carr, B ;
Cooper, DA ;
Grinspoon, S ;
Ioannidis, J ;
Lewis, R ;
Law, M ;
Lichtenstein, K ;
Murray, J ;
Pizzuti, D ;
Rozenbaum, W ;
Schambelan, M ;
Moore, A ;
Miller, J .
LANCET, 2003, 361 (9359) :726-735
[9]   Toxicity of antiretroviral therapy and implications for drug development [J].
Carr, A .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (08) :624-634
[10]   PLASMA-CHOLESTEROL AND TRIGLYCERIDE DISTRIBUTIONS IN 13,665 CHILDREN AND ADOLESCENTS - PREVALENCE STUDY OF THE LIPID RESEARCH CLINICS PROGRAM [J].
CHRISTENSEN, B ;
GLUECK, C ;
KWITEROVICH, P ;
DEGROOT, I ;
CHASE, G ;
HEISS, G ;
MOWERY, R ;
TAMIR, I ;
RIFKIND, B .
PEDIATRIC RESEARCH, 1980, 14 (03) :194-202