TY - JOUR
T1 - Metabolic disorders in vertically HIV-infected children: Future adults at risk for cardiovascular disease
AU - Dapena, Marta
AU - Jiménez, Beatriz
AU - Noguera-Julian, Antoni
AU - Soler-Palacín, Pere
AU - Fortuny, Clàudia
AU - Lahoz, Rebeca
AU - Aracil, Francisco Javier
AU - Figueras, Concepción
AU - De José, María Isabel
PY - 2012/6/1
Y1 - 2012/6/1
N2 - Background: Despite metabolic disorders in HIV-infected children being widely described, there is still a lack of agreed criteria for diagnoses and management. Numerous studies are coming from other settings and results are heterogeneous when assessing several analytical and clinical parameters. Objectives: To describe the prevalence of metabolic disorders and associated risk factors in the Spanish National cohort of HIV-infected pediatric patients (CoRISpe). Methods: This was a cross-sectional study following all vertically HIV-infected children and adolescents in three referral centers included in the CoRISpe. Metabolic data (fasting lipids, glucose and insulin levels and thyroid hormone levels) were collected. Fat distribution was clinically assessed by expert clinicians. Results: We included 157 patients [median age 13 years, interquartile range (IQR) 10-16]. Median duration of antiretroviral therapy was 10.2 years (IQR 5.0-13.0). Almost 20 % of patients had insulin resistance and this was associated with hepatitis C co-infection, current use of stavudine (d4T) and hypertriglyceridemia. Hypercholesterolemia and hypertriglyceridemia were found in 23.9 % and 24.8 % of patients and were associated with current use of protease inhibitors (p = 0.042 and p = 0.022, respectively). Abnormal fat distribution was observed in 63 patients (40.5 % ): lipoatrophy in 32 (20.4 % ), lipohypertrophy in eight (5.1 % ) and a mixed pattern in 23 patients (14.6 % ), and it was significantly associated with previous exposure to stavudine (p < 0.001). Conclusions: Metabolic disorders are a significant problem in our HIV-infected pediatric population. We need to encourage the development of global strategies and the creation of consensus guidelines that can decrease the cardiovascular risk in this population. © 2012 by Walter de Gruyter Berlin Boston.
AB - Background: Despite metabolic disorders in HIV-infected children being widely described, there is still a lack of agreed criteria for diagnoses and management. Numerous studies are coming from other settings and results are heterogeneous when assessing several analytical and clinical parameters. Objectives: To describe the prevalence of metabolic disorders and associated risk factors in the Spanish National cohort of HIV-infected pediatric patients (CoRISpe). Methods: This was a cross-sectional study following all vertically HIV-infected children and adolescents in three referral centers included in the CoRISpe. Metabolic data (fasting lipids, glucose and insulin levels and thyroid hormone levels) were collected. Fat distribution was clinically assessed by expert clinicians. Results: We included 157 patients [median age 13 years, interquartile range (IQR) 10-16]. Median duration of antiretroviral therapy was 10.2 years (IQR 5.0-13.0). Almost 20 % of patients had insulin resistance and this was associated with hepatitis C co-infection, current use of stavudine (d4T) and hypertriglyceridemia. Hypercholesterolemia and hypertriglyceridemia were found in 23.9 % and 24.8 % of patients and were associated with current use of protease inhibitors (p = 0.042 and p = 0.022, respectively). Abnormal fat distribution was observed in 63 patients (40.5 % ): lipoatrophy in 32 (20.4 % ), lipohypertrophy in eight (5.1 % ) and a mixed pattern in 23 patients (14.6 % ), and it was significantly associated with previous exposure to stavudine (p < 0.001). Conclusions: Metabolic disorders are a significant problem in our HIV-infected pediatric population. We need to encourage the development of global strategies and the creation of consensus guidelines that can decrease the cardiovascular risk in this population. © 2012 by Walter de Gruyter Berlin Boston.
KW - Antiretroviral
KW - Dyslipidemia
KW - HIV
KW - HIV-associated lipodystrophy syndrome
KW - Insulin resistance
UR - https://www.scopus.com/pages/publications/84865639216
U2 - 10.1515/jpem-2012-0005
DO - 10.1515/jpem-2012-0005
M3 - Article
SN - 0334-018X
VL - 25
SP - 529
EP - 535
JO - Journal of Pediatric Endocrinology and Metabolism
JF - Journal of Pediatric Endocrinology and Metabolism
IS - 5-6
ER -