rdf:type |
|
lifeskim:mentions |
umls-concept:C0021051,
umls-concept:C0025266,
umls-concept:C0031928,
umls-concept:C0071097,
umls-concept:C0086418,
umls-concept:C0299583,
umls-concept:C0332161,
umls-concept:C0332293,
umls-concept:C0376674,
umls-concept:C0559956,
umls-concept:C0920563
|
pubmed:issue |
7
|
pubmed:dateCreated |
2011-6-20
|
pubmed:databankReference |
|
pubmed:abstractText |
Highly active antiretroviral therapy (HAART)-induced lipoatrophy is characterized by hypoleptinemia and insulin resistance. Evidence suggests that pioglitazone and recombinant methionyl human leptin (metreleptin) administration has beneficial effects in human immunodeficiency virus (HIV)-infected lipoatrophic patients. This proof-of-concept study aimed at evaluating whether the combination of metreleptin and pioglitazone has favorable effects, above and beyond pioglitazone alone, on both metabolic outcomes and peripheral lipoatrophy in HIV-infected patients on HAART. Nine HIV-positive men with at least 6 months of HAART exposure, clinical evidence of lipoatrophy, and low leptin concentrations (?4 ng/mL) were placed on pioglitazone treatment (30 mg/d per os) and were randomized to receive either metreleptin (0.04 mg/kg subcutaneously once daily; n = 5) or placebo (n = 4) for 3 months in a double-blinded fashion. Compared with placebo, metreleptin reduced fasting serum insulin concentration, increased adiponectin concentration, reduced the homeostasis model assessment index of insulin resistance, and attenuated postprandial glycemia in response to a mixed meal (all P ? .02), but did not affect trunk and peripheral fat mass. HIV control was not affected, and no major adverse effects were observed. Metreleptin administration in HIV-positive, leptin-deficient patients with lipoatrophy treated with pioglitazone improves postprandial glycemia and insulin sensitivity. Results from this pilot study should be confirmed in larger clinical trials.
|
pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/AG032030,
http://linkedlifedata.com/resource/pubmed/grant/DK 58785,
http://linkedlifedata.com/resource/pubmed/grant/DK 79929,
http://linkedlifedata.com/resource/pubmed/grant/DK 81913,
http://linkedlifedata.com/resource/pubmed/grant/K24 DK081913-01A1,
http://linkedlifedata.com/resource/pubmed/grant/K24 DK081913-04,
http://linkedlifedata.com/resource/pubmed/grant/M01-RR-01032,
http://linkedlifedata.com/resource/pubmed/grant/R01 AG032030-01A1,
http://linkedlifedata.com/resource/pubmed/grant/R01 AG032030-03,
http://linkedlifedata.com/resource/pubmed/grant/R01 DK058785-01A1,
http://linkedlifedata.com/resource/pubmed/grant/R01 DK079929-01A1,
http://linkedlifedata.com/resource/pubmed/grant/R01 DK079929-04
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
1532-8600
|
pubmed:author |
|
pubmed:copyrightInfo |
Copyright © 2011 Elsevier Inc. All rights reserved.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
60
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1045-9
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:21081243-Adiponectin,
pubmed-meshheading:21081243-Adult,
pubmed-meshheading:21081243-Antiretroviral Therapy, Highly Active,
pubmed-meshheading:21081243-Blood Glucose,
pubmed-meshheading:21081243-Body Mass Index,
pubmed-meshheading:21081243-Drug Therapy, Combination,
pubmed-meshheading:21081243-HIV-1,
pubmed-meshheading:21081243-HIV-Associated Lipodystrophy Syndrome,
pubmed-meshheading:21081243-Humans,
pubmed-meshheading:21081243-Hypoglycemic Agents,
pubmed-meshheading:21081243-Insulin,
pubmed-meshheading:21081243-Insulin Resistance,
pubmed-meshheading:21081243-Leptin,
pubmed-meshheading:21081243-Male,
pubmed-meshheading:21081243-Middle Aged,
pubmed-meshheading:21081243-Pilot Projects,
pubmed-meshheading:21081243-Postprandial Period,
pubmed-meshheading:21081243-Thiazolidinediones
|
pubmed:year |
2011
|
pubmed:articleTitle |
Leptin replacement improves postprandial glycemia and insulin sensitivity in human immunodeficiency virus-infected lipoatrophic men treated with pioglitazone: a pilot study.
|
pubmed:affiliation |
Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA. fmagkos@bidmc.harvard.edu
|
pubmed:publicationType |
Journal Article,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|