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American Journal of Clinical Nutrition, Vol. 78, No. 1, 182-189, July 2003
© 2003 American Society for Clinical Nutrition


ORIGINAL RESEARCH COMMUNICATION

The protein metabolic response to HIV infection in young children1,2,3

Farook Jahoor, Stuart Abramson and William C Heird

1 From the US Department of Agriculture, Agricultural Research Service, Children’s Nutrition Research Center (FJ and WCH), and the Section of Allergy and Immunology, Department of Pediatrics, Baylor College of Medicine, Houston (SA).

Background: Growth failure often precedes secondary infections in HIV-infected infants and children, suggesting that inadequate protein deposition may be an early manifestation of infection by the virus. However, the protein metabolic response elicited by the virus in young children is unknown.

Objective: We compared children with HIV infection and age-matched children without HIV infection with regard to whole-body and splanchnic protein kinetics and synthesis of acute phase proteins (APPs).

Design: Whole-body and splanchnic leucine kinetics and fractional and absolute synthesis rates of 2 positive and 4 negative APPs were measured in 6 asymptomatic, HIV-infected children (4 males and 2 females) aged 6–17 mo and 4 uninfected children (3 females and 1 male) aged 7–9 mo who were in the fed state.

Results: Compared with the control children, the HIV-infected children had significantly lower dietary energy and protein intakes and leucine balance and significantly faster leucine flux and fractional splanchnic leucine extraction; there was no significant difference between the groups in leucine oxidation rates. The HIV-infected children also had significantly higher plasma concentrations and absolute synthesis rates of the positive APPs and a significantly higher fractional synthesis rate of fibrinogen. The concentrations of 2 of the 4 negative APPs, albumin and HDL apolipoprotein A-I, were significantly lower in the HIV-infected children but were not associated with slower synthesis rates.

Conclusions: Children with HIV infection but without secondary infection have reduced protein balance because of an inability to down-regulate protein catabolism. Furthermore, the acute phase protein response elicited by HIV infection is characterized by higher concentrations and synthesis rates of positive APPs without lower concentrations of some negative APPs.

Key Words: Leucine kinetics • acute phase proteins • HIV infection • children • stable isotope




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