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Contribution of Glucose Tolerance and Gender to Cardiac Adiposity.

Articolo
Data di Pubblicazione:
2009
Abstract:
Context and Objective: To examine whether pericardial and myocardial fat depots may contribute
to the association between diabetes and cardiovascular risk, including sex-related differences, and
the role of adiponectin, we evaluated data in patients with obesity and without diabetes [nondiabetic
(ND)] or with impaired glucose tolerance or type 2 diabetes and in lean ND controls.
Methods: Magnetic resonance imaging and spectroscopy were used to measure left ventricular
(LV) function and abdominal sc and visceral fat areas to estimate respective masses, pericardial fat
depots, and myocardial triglyceride content in 53 subjects (10 lean ND, 25 obese ND, six impairedglucose-
tolerance, and 12 type 2 diabetic patients with macrovascular disease); gender effects and
adiponectin levels were evaluated in the available subset of subjects.
Results: Myocardial and pericardial fat increased progressively across study groups. They were lower
in obesewomenthanmen(P0.002), but cardiac steatosis caughtupin hyperglycemicwomen(81%
vs. ND, P 0.01). Adiponectin was inversely related with both fat depots (P 0.01) and LV mass (P
0.003) and positively with LV function (P 0.03). In multiple regression analysis, myocardial and pericardial
fat were independently related with plasma glucose levels, only pericardial fat mass was associated
with visceral adiposity and myocardial fat with cardiac output and work.
Conclusions:Weconclude that glycemia, gender, adiponectin,andcardiac workload are associated
with, and hyperglycemia and male gender are independent positive predictors of, heart adiposity.
Once glucose tolerance becomes impaired, the evolution of cardiac steatosis is more pronounced
in women. (J Clin Endocrinol Metab 94: 4472-4482, 2009)
Tipologia CRIS:
01.01 Articolo in rivista
Elenco autori:
Iozzo, Patricia
Autori di Ateneo:
IOZZO PATRICIA
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/46985
Pubblicato in:
THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Journal
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URL

http://jcem.endojournals.org/content/94/11/4472.long
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