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Maternal Diabetes in Youth-Onset Type 2 Diabetes Is Associated With Progressive Dysglycemia and Risk of Complications
Rachana D Shah1, Steven D Chernausek2, Laure El Ghormli3
1Department of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Insights
Maternal diabetes history negatively impacts glycemic control and increases risks for complications in youth with type 2 diabetes (T2D). These findings suggest potential in utero programming effects influencing long-term health outcomes.
Area of Science:
- Endocrinology and Metabolism
- Pediatric Health
- Cardiometabolic Disease Research
Background:
- Prenatal exposures like parental diabetes are known risk factors for cardiometabolic diseases.
- Limited data exist on the impact of parental diabetes on disease progression in youth-onset type 2 diabetes (T2D).
Purpose of the Study:
- To analyze the effects of parental diabetes history on glycemic outcomes, beta-cell function, and complications in a US cohort of youth-onset T2D.
- To investigate the association between maternal and paternal diabetes and disease progression in adolescents with T2D.
Main Methods:
- Analysis of data from 699 participants (aged 10-17 years) in the TODAY and TODAY2 studies, followed for up to 12 years.
- Assessment of maternal and paternal diabetes history in relation to glycemic control (HbA1c), glomerular hyperfiltration, and heart rate variability.
Main Results:
- Maternal diabetes, irrespective of timing (during or after pregnancy), was significantly associated with loss of glycemic control (HbA1c ≥ 8%).
- Paternal diabetes showed no significant association with these outcomes.
- Maternal diabetes was linked to increased risks of glomerular hyperfiltration and low heart rate variability over 12 years.
Conclusions:
- Maternal diabetes is a significant factor associated with poorer glycemic control and adverse cardiometabolic complications in youth with T2D.
- The findings suggest a potential role for in utero programming in the development of T2D complications.
- Further research is warranted to elucidate the mechanisms behind maternal diabetes's influence on T2D progression in offspring.
Context:
Prenatal exposures, including undernutrition, overnutrition, and parental diabetes, are recognized risk factors for future cardiometabolic disease. There are currently no data on effects of parental diabetes on disease progression or complications in youth-onset type 2 diabetes (T2D).
Objective:
We analyzed effects of parental diabetes history on glycemic outcomes, β-cell function, and complications in a US cohort of youth-onset T2D.
Methods:
Participants (N = 699) aged 10 to 17 years with T2D were enrolled at 15 US centers and followed for up to 12 years as part of the TODAY (Treatment Options for type 2 Diabetes in Adolescents and Youth) and TODAY2 follow-up studies. Information about diabetes diagnosis in biological mothers was available for 621 participants (never = 301; before or during pregnancy = 218; after pregnancy = 102) and in biological fathers for 519 (no diabetes = 352; paternal diabetes = 167).
Results:
Maternal, but not paternal, diabetes was associated with loss of glycemic control over time, defined as glycated hemoglobin A1c greater than or equal to 8% for more than 6 months (P = .001). Similarly, maternal, but not paternal, diabetes was associated with increased risk of glomerular hyperfiltration (P = .01) and low heart rate variability (P = .006) after 12 years of follow-up. Effects were largely independent of age, sex, race/ethnicity, and household income. Maternal diabetes during vs after pregnancy had similar effects on outcomes.
Conclusion:
Maternal diabetes, regardless of whether diagnosed during vs after pregnancy, is associated with worse glycemic control, glomerular hyperfiltration, and reduced heart rate variability in youth with T2D in TODAY. The strong associations of diabetes outcomes with maternal diabetes suggest a possible role for in utero programming.
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