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Altered fat differentiation and adipocytokine expression are inter-related and linked to morphological changes and insulin resistance in HIV-1-infected lipodystrophic patients.
- Source :
-
Antiviral therapy [Antivir Ther] 2004 Aug; Vol. 9 (4), pp. 555-64. - Publication Year :
- 2004
-
Abstract
- Objective: To achieve a better understand of the pathophysiology of HIV-related lipoatrophy, we compared the mRNA expression of adipocytokines in fat samples from patients and healthy HIV-seronegative controls together with fat morphology and we studied the relationship between changes in fat morphology, adipocytokine expression, markers of adipose tissue differentiation and whole body insulin sensitivity.<br />Design: Cross-sectional analytical study.<br />Subjects and Methods: The mRNA expression of adipocytokines and transcriptional factors in fat samples from 26 patients with peripheral lipoatrophy (all under anti-retroviral therapy associating protease inhibitor and nucleoside-analogue reverse transcriptase inhibitors) and from 16 non-HIV-infected controls was measured by real time quantitative RT-PCR. Fat morphology was assessed histologically on a subgroup of 10 patients and six controls: collagen fibres by Sirius Red staining, apoptosis by the TUNEL technique, vessels by smooth muscle alpha-actin staining and macrophages by CD68 staining. Insulin resistance was assessed by using the homeostasis model assessment.<br />Results: The patients' fat showed higher values of apoptosis (P=0.005), fibrosis (P<0.05), vessel density (P=0.001) and macrophage infiltration (P<0.05) than the controls' fat, together with lower adiponectin and leptin mRNA levels and higher interleukin (IL)-6 and tumour necrosis factor (TNF)alpha mRNA levels. TNFa and IL-6 expression correlated positively with the level of apoptosis (P=0.05 and P<0.05, respectively) and negatively with CCAAT-enhancer binding protein (C/EBP)alpha (P<0.001 and P<0.05, respectively). Apoptosis correlated negatively with the expression level of sterol-regulatory-element-binding-protein-1c (SREBP1c) (P=0.01) and C/EBPalpha (P=0.01) whilst the vessel density correlated negatively with SREBP1c (P<0.005), C/EBPalpha (P=0.001) and beta (P=0.001). Adiponectin and leptin expression correlated positively with each other, and also with adipogenic marker expression and overall insulin sensitivity. These relationships were also present when the patient group was studied separately. Finally, fat morphological abnormalities correlated positively with whole body insulin resistance.<br />Conclusions: Adipose tissue from patients with HIV-1-related lipoatrophy shows increased apoptosis, together with decreased adipocyte differentiation. Increased TNFalpha and IL-6 expression could be a major phenomenon linking these alterations. Decreased adiponectin and leptin expression, which may result from decreased adipocyte differentiation, could be involved in the observed whole body insulin resistance.
- Subjects :
- Adipocytes metabolism
Adiponectin
Adult
Apoptosis
Blood Vessels pathology
CCAAT-Enhancer-Binding Protein-alpha genetics
CCAAT-Enhancer-Binding Protein-alpha metabolism
CCAAT-Enhancer-Binding Protein-beta genetics
CCAAT-Enhancer-Binding Protein-beta metabolism
CCAAT-Enhancer-Binding Proteins genetics
CCAAT-Enhancer-Binding Proteins metabolism
Cross-Sectional Studies
DNA-Binding Proteins genetics
DNA-Binding Proteins metabolism
Female
Fibrosis pathology
Humans
Intercellular Signaling Peptides and Proteins genetics
Interleukin-6 genetics
Interleukin-6 metabolism
Leptin genetics
Leptin metabolism
Macrophages pathology
Male
Middle Aged
RNA, Messenger analysis
Sterol Regulatory Element Binding Protein 1
Transcription Factors genetics
Transcription Factors metabolism
Tumor Necrosis Factor-alpha genetics
Tumor Necrosis Factor-alpha metabolism
Adipose Tissue metabolism
Adipose Tissue pathology
HIV-1
HIV-Associated Lipodystrophy Syndrome metabolism
HIV-Associated Lipodystrophy Syndrome pathology
Insulin Resistance
Intercellular Signaling Peptides and Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1359-6535
- Volume :
- 9
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Antiviral therapy
- Publication Type :
- Academic Journal
- Accession number :
- 15456087