Progressive deterioration of β-cell function in obese youth with type 2 diabetes: β-Cell function in youth T2DM
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OBJECTIVE: In adults, type 2 diabetes (T2DM) is characterized with progressive deterioration in insulin secretion. Data are scanty in youth. We investigated prospectively the change in β-cell function and in insulin sensitivity in youth with T2DM. RESEARCH DESIGN AND METHODS: Six adolescents with T2DM [hemoglobin A1c (HbA1c) 6.6 ± 1.0%] underwent evaluation of hepatic glucose production (HGP; [6,6-²H₂] glucose), insulin-stimulated glucose disposal (Rd; hyperinsulinemic-euglycemic clamp), first- and second-phase insulin/C-peptide secretion (hyperglycemic clamp), body composition dual energy X-ray absorptiometry (DEXA), and abdominal adiposity (computed tomography) within 3 yr of the diagnosis of diabetes and after 12-16 months of follow-up. RESULTS: Weight, body mass index (37.1 ± 6.9), HbA1c (6.3 ± 0.7%), HGP (2.8 ± 1.2 mg/kg/min), and Rd (4.9 ± 3.4 mg/kg/min) did not change significantly from baseline. However, first-phase insulin and C-peptide declined (152.6 ± 261.2 vs. 75.9 ± 108.5 μU/mL, p = 0.028; 8.0 ± 6.3 vs. 5.9 ± 4.4 ng/mL, p = 0.048, respectively) with no significant change in second-phase insulin/C-peptide. The rate of decline in β-cell function was ∼20% per year. CONCLUSIONS: After a median duration of 20 months of diabetes, youth with T2DM manifest a rapid decline in β-cell function with no significant changes in peripheral or hepatic insulin sensitivity. Interventions to retard this deterioration in β-cell function should be investigated.
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Younger people with type 2 diabetes can have up to three times more liver fat than BMI-matched non-diabetic controls and than middle-aged or older type 2 diabetes presentations.
“and younger people with T2DM can have much higher (up to 3 times) amounts of liver fat compared with BMI-matched non-diabetic controls and compared with presentations of T2DM in middle and later life 24,”
From Type 2 diabetes in adolescents and young adults (2018) · cites this paper as [24]
The Results section (‘Study subjects and fasting metabolic profile’; page unavailable) reports abdominal fat and hepatic insulin sensitivity, but not liver-fat amounts. Searches for liver fat, intrahepatic fat, and a threefold difference found no comparison with BMI-matched non-diabetic controls or older people with type 2 diabetes in our copy. (LLM, conf=0.76)
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- Authors
- Bacha, F., Gungor, N., Lee, S., & Arslanian, S. A.
- Affiliations
- University of Pittsburgh (US)
- Louisiana State University Health Sciences Center Shreveport (US)
- Corresponding author
- Bacha, Fida
- Venue
- Pediatric Diabetes
- Publisher
- Hindawi Limited
- Published
- 2012-08-23
- Volume
- 14
- Issue
- 2
- Pages
- 106-111
- ISSN
- 1399-543X (ISSN-L)
- PMC
- PMC3648791
- OpenAlex
- W1598677707
- Cited by
- 106
- References
- 23
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 12 · 2023: 8 · 2022: 12 · 2021: 11 · 2020: 9 · 2019: 7 · 2018: 6 · 2017: 9 · 2016: 6 · 2015: 5 · 2014: 4 · 2013: 2 · 2012: 1
- FWCI
- 3.89
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Pediatric Diabetes (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- U.S. Department of Defense (UL1 RR024153, K24 HD01357, MO1 RR00084, UL1TR000005)
- Deutsches Krebsforschungszentrum
- National Institutes of Health (UL1TR000005)
- U.S. Public Health Service (UL1TR000005, K24 HD01357, UL1 RR024153)
- National Center for Research Resources (MO-1-RR-00084, UL1RR024153, M01RR000084)
- National Center for Advancing Translational Sciences
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (K24HD001357)
- Children's Hospital of Pittsburgh
- Topics
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Keywords
- type 2 diabetes, adolescents, beta-cell function, insulin secretion, first-phase insulin secretion, C-peptide, insulin sensitivity, hepatic glucose production, insulin-stimulated glucose disposal, obesity, disease progression, abdominal fat
- MeSH terms
- Adolescent, Blood Glucose, Body Composition, Diabetes Mellitus, Type 2, Female, Glycated Hemoglobin, Humans, Insulin Resistance, Male, Glucose Clamp Technique, Absorptiometry, Photon, Body Mass Index, Insulin-Secreting Cells, Obesity, Abdominal
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