Reduced Levels of Serum FGF19 and Impaired Expression of Receptors for Endocrine FGFs in Adipose Tissue From HIV-Infected Patients


Por: Gallego-Escuredo, JM, Domingo, P, Gutierrez, MD, Mateo, MG, Cabeza, MC, Fontanet, A, Vidal, F, Domingo, JC, Giralt, M, Villarroya, F

Publicada: 15 dic 2012
Resumen:
Background: To determine the role of fibroblast growth factor (FGF)-19 and FGF21 and the endocrine FGFs receptor system in the metabolic alterations that manifest in HIV-1-infected patients undergoing highly active antiretroviral treatment (HAART). Methods: Serum FGF19 and FGF21 levels were determined in 4 groups of individuals as follows: (1) HIV-1-infected HAART patients with lipodystrophy (n = 38); or (2) without lipodystrophy (n = 34); (3) untreated (naive) HIV-1-infected patients (n = 34); and (4) healthy controls (n = 31). Serum FGF19 levels were correlated with anthropometric, metabolic, HIV-1 infection-related, and HAART-related parameters and with FGF21 levels. The gene expression of FGF receptor 1 and the coreceptor beta-Klotho was analyzed in adipose tissue from 10 individuals from each group. Results: Serum FGF19 levels were significantly reduced in all groups of HIV-1-infected patients, whereas FGF21 levels were increased. FGF19 levels were negatively correlated with insulin resistance and insulin levels and positively correlated with high-density lipoprotein cholesterol. FGF19 was inversely correlated with cumulative exposure to nucleoside reverse transcriptase inhibitor and non-nucleoside reverse transcriptase inhibitor drugs. The expression of FGF receptor 1 and coreceptor beta-Klotho was reduced in adipose tissue from all groups of HIV-infected patients. Conclusions: FGF19 levels are reduced in HIV-1-infected patients, in contrast with FGF21 levels. Impaired expression of the corresponding receptor and coreceptor, which mediate the actions of endocrine FGFs in adipose tissue, suggests a resistance to the metabolic effects of FGF19 and FGF21 in HIV-1-infected patients. Considering the beneficial effects of endocrine FGFs on metabolism, the observed reduction in FGF19 levels and decreased sensitivity to endocrine FGFs in adipose tissue may contribute to metabolic alterations in HIV-1-infected patients.

Filiaciones:
Gallego-Escuredo, JM:
 Univ Barcelona, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain

 Univ Barcelona, Inst Biomed, E-08028 Barcelona, Spain

 Minist Sanidad & Consumo, Inst Salud Carlos III, CIBER Fisiopatol Obesidad & Nutr, Madrid, Spain

Domingo, P:
 Autonomous Univ Barcelona, Hosp Santa Creu & St Pau, Infect Dis Unit, Barcelona, Spain

Gutierrez, MD:
 Autonomous Univ Barcelona, Hosp Santa Creu & St Pau, Infect Dis Unit, Barcelona, Spain

Mateo, MG:
 Autonomous Univ Barcelona, Hosp Santa Creu & St Pau, Infect Dis Unit, Barcelona, Spain

Cabeza, MC:
 Autonomous Univ Barcelona, Hosp Santa Creu & St Pau, Infect Dis Unit, Barcelona, Spain

 Red Invest SIDA RIS, Barcelona, Spain

Fontanet, A:
 Autonomous Univ Barcelona, Hosp Santa Creu & St Pau, Infect Dis Unit, Barcelona, Spain

 Red Invest SIDA RIS, Barcelona, Spain

Vidal, F:
 Univ Rovira & Virgili, Hosp Univ Tarragona Joan 23, IISPV, Dept Internal Med, Tarragona, Catalonia, Spain

Domingo, JC:
 Univ Barcelona, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain

 Univ Barcelona, Inst Biomed, E-08028 Barcelona, Spain

 Minist Sanidad & Consumo, Inst Salud Carlos III, CIBER Fisiopatol Obesidad & Nutr, Madrid, Spain

Giralt, M:
 Univ Barcelona, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain

 Univ Barcelona, Inst Biomed, E-08028 Barcelona, Spain

 Minist Sanidad & Consumo, Inst Salud Carlos III, CIBER Fisiopatol Obesidad & Nutr, Madrid, Spain

Villarroya, F:
 Univ Barcelona, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain

 Univ Barcelona, Inst Biomed, E-08028 Barcelona, Spain

 Minist Sanidad & Consumo, Inst Salud Carlos III, CIBER Fisiopatol Obesidad & Nutr, Madrid, Spain
ISSN: 15254135





JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
Editorial
LIPPINCOTT WILLIAMS & WILKINS, TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 61 Número: 5
Páginas: 527-534
WOS Id: 000311790300006
ID de PubMed: 23187887

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