β-cell function in morbidly obese subjects during free living: Long-term effects of weight loss

Stefania Camastra, Melania Manco, Andrea Mari, Simona Baldi, Amalia Gastaldelli, Aldo V. Greco, Gertrude Mingrone, Ele Ferrannini

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Abstract

Insulin hypersecretion and insulin resistance are physiologically linked features of obesity. We tested whether extreme hypersecretion impairs β-cell function under free-living conditions and whether major weight loss modifies insulin hypersecretion, insulin sensitivity, and β-cell function. Plasma glucose, C-peptide, and free fatty acid concentrations were measured at hourly intervals during 24 h of normal life (including calorie-standardized meals) in 20 morbidly obese nondiabetic patients (BMI 48.4 ± 1.7 kg/m2) and 7 nonobese age- and sex-matched control subjects; 8 of the obese patients were restudied 6 months and 2 years following biliopancreatic diversion. Insulin secretion was reconstructed from C-peptide levels by deconvolution and related to concurrent glucose levels through a mathematical model incorporating key features of β-cell function: rate sensitivity, β-cell glucose sensitivity, and potentiation. Insulin sensitivity (by the euglycemic insulin clamp technique) was reduced by 50% in obese subjects (23.1 ± 2.5 of obese subjects vs. 52.9 ± 4.9 μmol · min -1 · kgFFM-1 of control subjects, means ± SE, P = 0.0004) as was mean 24-h insulin clearance (median 809 [interquartile range 451] vs. 1,553 [520] ml · min-1 · m-2, P <0.001) due to a 50% reduction in hepatic insulin extraction (P <0.01). Over 24 h, insulin secretion was doubled in obese subjects (468 nmol [202] in obese subjects vs. 235 [85] of control subjects, P = 0.0002). Despite the hypersecretion, β-cell glucose sensitivity, rate sensitivity, and potentiation were similar in obese and control subjects. Six months postoperatively (weight loss = 33 ± 3 kg), both insulin hypersecretion (282 nmol [213]) and insulin sensitivity (51.6 ± 3.7 μmol · min-1 · kgFFM-1) were normalized. At 2 years (weight loss = 50 ± 8 kg), insulin sensitivity was supernormal (68.7 ± 3.3 μmol · min-1 · kgFFM-1) and insulin secretion was lower than normal (167 nmol [37]) (both P <0.05 vs. control subjects). In conclusion, severe uncomplicated obesity is characterized by gross insulin hypersecretion and insulin resistance, but the dynamic aspects of β-cell function are intact. Malabsorptive bariatric surgery corrects both the insulin hypersecretion and the insulin resistance at a time when BMI is still high. With continued weight loss over a 2-year period, moderately obese subjects become supersensitive to insulin and, correspondingly, insulin hyposecretors.

Original languageEnglish
Pages (from-to)2382-2389
Number of pages8
JournalDiabetes
Volume54
Issue number8
DOIs
Publication statusPublished - Aug 2005

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ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism

Cite this

Camastra, S., Manco, M., Mari, A., Baldi, S., Gastaldelli, A., Greco, A. V., Mingrone, G., & Ferrannini, E. (2005). β-cell function in morbidly obese subjects during free living: Long-term effects of weight loss. Diabetes, 54(8), 2382-2389. https://doi.org/10.2337/diabetes.54.8.2382