Abstract | OBJECTIVE: DESIGN: We studied 40 morbidly obese subjects (mean age, 40·6 ± 1·3 years; mean BMI, 53·1 ± 1·2 kg/m(2) ) divided into groups according to their glycemic status: normal fasting glucose (NFG) group, impaired fasting glucose (IFG) group and type 2 diabetes mellitus (T2D) group. NFG patients were additionally subclassified, according to the homoeostasis model assessment of insulin resistance (HOMAIR ), into a low insulin-resistance (LIR) group (HOMAIR <3·9) or a high insulin-resistance (HIR) group (HOMAIR ≥3·9). MEASUREMENTS: RESULTS: At the 180-minute postprandial reading, GLP-1 and PYY had increased in LIR-NFG subjects (41·84%, P = 0·01; 35·7%, P = 0·05; respectively), whereas no changes were observed in HIR-NFG, IFG or T2D subjects. CONCLUSIONS: These results suggest that in morbidly obese subjects, both insulin resistance and abnormal glucose metabolism (IFG or T2D) impair the GLP-1 and PYY response to fat load. The implications of this attenuated enteroendocrine response should be elucidated by further studies.
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Authors | José C Fernández-García, Mora Murri, Leticia Coin-Aragüez, Juan Alcaide, Rajaa El Bekay, Francisco J Tinahones |
Journal | Clinical endocrinology
(Clin Endocrinol (Oxf))
Vol. 80
Issue 5
Pg. 671-6
(May 2014)
ISSN: 1365-2265 [Electronic] England |
PMID | 23573808
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2013 John Wiley & Sons Ltd. |
Chemical References |
- Blood Glucose
- Lipids
- Peptide YY
- Glucagon-Like Peptide 1
|
Topics |
- Adult
- Blood Glucose
(analysis)
- Body Mass Index
- Diabetes Mellitus, Type 2
(blood)
- Fasting
- Female
- Glucagon-Like Peptide 1
(blood)
- Homeostasis
- Humans
- Insulin Resistance
- Lipids
(administration & dosage)
- Male
- Middle Aged
- Obesity, Morbid
(blood)
- Peptide YY
(blood)
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