1. Metabolic abnormalities in human immunodeficiency virus-infected children: two-year follow-up.
- Author
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Krause JC, Toye MP, Fisher DJ, Stechenberg BW, Reiter EO, and Allen HF
- Subjects
- Adiponectin blood, Antiretroviral Therapy, Highly Active adverse effects, Child, Cholesterol blood, Cholesterol, LDL blood, Dyslipidemias etiology, Fatty Acids, Nonesterified, Female, HIV Infections complications, Humans, Insulin-Like Growth Factor Binding Protein 3, Insulin-Like Growth Factor Binding Proteins blood, Insulin-Like Growth Factor I metabolism, Male, Prospective Studies, Triglycerides blood, HIV Infections blood, HIV-Associated Lipodystrophy Syndrome etiology
- Abstract
Background: HIV-associated lipodystrophy (LD) manifests with fat maldistribution, dyslipidemia, and insulin resistance in some HIV-infected children on antiretroviral therapy., Aim: To assess whether lipid abnormalities in patients with HIV are stable over time., Patients: The perinatally HIV-infected cohort at a medium-sized urban US teaching hospital., Methods: This prospective, observational study consisted of five visits (at entry and 3, 6, 24, and 30 months after entry) during which fasting venous blood samples were drawn for HIV-1 RNA, CD4 lymphocytes, lipid profile, free fatty acids (FFA), glucose, insulin, and adiponectin. IGF-I/IGFBP-3 levels were measured at the first and fifth visits., Results: Of 36 study participants, seven were lipodystrophic, and 30 patients completed all five study visits. LDL-cholesterol, total cholesterol (TC), triglycerides (TG), and FFA levels were significantly higher in patients taking protease inhibitors (PIs). Patients with LD had higher TC and TG levels (both p < 0.05), and higher FFA (p = 0.0532). Adiponectin levels did not differ between PI/non-PI and LD/non-LD groups. HDL-cholesterol seemed to decrease, and FFA to increase over time. All IGF-I and all but one IGFBP-3 level were within normal range for age and Tanner stage., Conclusion: Dyslipidemia remained relatively constant over our study period. Adiponectin was not useful as a marker of LD in our population.
- Published
- 2009
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