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Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study
S Hatun1, G Yesiltepe Mutlu1, P Cinaz2
1Koç University School of Medicine, Division of Pediatric Endocrinology and Diabetes, Turkey.
Insights
Opportunistic screening is vital for early detection of Type 2 diabetes in children, as over half were asymptomatic. Accurate diagnosis remains a challenge, with a significant exclusion rate indicating diagnostic difficulties even for specialists.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Public Health
Background:
- Type 2 diabetes in children and adolescents is a growing concern.
- Understanding baseline characteristics and treatment patterns is crucial for effective management.
Purpose of the Study:
- To describe the clinical and laboratory findings of children and adolescents with Type 2 diabetes in Turkey.
- To analyze initial treatment modalities used in this population.
Main Methods:
- Data from 367 children newly diagnosed with Type 2 diabetes across 37 centers were collected.
- A standardized questionnaire was used, and analysis included 227 children after exclusions.
Main Results:
- The study included 227 children (68% female, mean age 13.8 years) with a high prevalence of family history (86%) and obesity (mean BMI Z-score 2.4).
- Over half (57%) were identified via opportunistic screening, often asymptomatic.
- Initial treatments varied, with metformin (40.5%) and combined insulin/metformin (33.5%) being common; higher HbA1c levels were observed in insulin-treated groups.
Conclusions:
- Opportunistic screening is essential for asymptomatic children at high risk.
- A high exclusion rate (38%) highlights ongoing diagnostic challenges for Type 2 diabetes in youth.
Aims:
To describe the baseline clinical and laboratory findings and treatment modalities of 367 children and adolescents diagnosed with Type 2 diabetes in various paediatric endocrinology centres in Turkey.
Methods:
A standard questionnaire regarding clinical and laboratory characteristics at onset was uploaded to an online national database system. Data for 367 children (aged 6-18 years) newly diagnosed with Type 2 diabetes at 37 different paediatric endocrinology centres were analysed.
Results:
After exclusion of the children with a BMI Z-score < 1 SD, those with genetic syndromes associated with Type 2 diabetes, and those whose C-peptide and/or insulin levels were not available, 227 cases were included in the study. Mean age was 13.8 ± 2.2 (range 6.5-17.8) years, with female preponderance (68%). Family history of Type 2 diabetes was positive in 86% of the children. The mean BMI was 31.3 ± 6.5 kg/m2 (range 18.7-61) and BMI Z-score was 2.4 ± 0.8 (range 1-5). More than half (57%) of the children were identified by an opportunistic diabetes screening due to existing risk markers without typical symptoms of diabetes. Only 13% (n = 29) were treated solely by lifestyle modification, while 40.5% (n = 92) were treated with metformin, 13% (n = 30) were treated with insulin, and 33.5% (n = 76) were treated with a combination of insulin and metformin initially. Mean HbA1C levels of the insulin and combination of insulin and metformin groups were 98 (11.1%) and 102 mmol/mol (11.5%), respectively, and also were significantly higher than the lifestyle modification only and metformin groups mean HbA1C levels (70(8.6%) and 67 mmol/mol (8.3%), respectively).
Conclusions:
An opportunistic screening of children who are at high risk of Type 2 diabetes is essential, as our data showed that > 50% of the children were asymptomatic at diagnosis. The other important result of our study was the high rate of exclusion from the initial registration (38%), suggesting that accurate diagnosis of Type 2 diabetes in youth is still problematic, even for paediatric endocrinologists.
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