Nutritional status impairments in HIV-infected patients are associated with increased TNF-α and IL-6 serum levels but not with viral load

Cytokines may alter metabolic pathways and contribute to malnutrition among human immunodefiency virus (HIV)-positive individuals. Tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), soluble IL-2 receptors (sIL-2R), beta2-microglobulin serum levels and plasma viral load of 45 HIV-positive...

Full description

Saved in:
Bibliographic Details
Published in:Infection Vol. 29; no. 5; pp. 257 - 261
Main Authors: GALHARDO, M. C. G, DE CARVALHO, M. G. C, GEORG, I, PEREZ, M, MORGADO, M. G, DE AZEVEDO, L. M. S, SAMPAIO, E. P, SARNO, E. N
Format: Journal Article
Language:English
Published: Heidelberg Springer 01-10-2001
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Cytokines may alter metabolic pathways and contribute to malnutrition among human immunodefiency virus (HIV)-positive individuals. Tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), soluble IL-2 receptors (sIL-2R), beta2-microglobulin serum levels and plasma viral load of 45 HIV-positive patients were determined and correlated to nutritional status impairment. Patients were grouped by CD4 counts into categories I (< 200/microl), II (200-499/microl), III (> or = 500/microl). There were 15 healthy controls. A nutritional grading system, based on anthropometric and laboratory data, was devised. Scores ranged from 0 to 5 (eutrophic to malnutrition). AIDS patients' cytokines and immune marker levels were significantly higher than those of the controls, but not always higher than those of other categories. AIDS patients had higher nutritional deficit grades than category III (p < 0.05) or the controls (p < 0.02) which, except for viral load, correlated with the parameters studied. Nutritional status impairments in HIV-positive individuals were associated with immune activation but not with viral load.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0300-8126
1439-0973
DOI:10.1007/s15010-001-1074-1