Long-term complications in youth-onset type 2 diabetes
Open accessAbstract
BACKGROUND: The prevalence of type 2 diabetes in youth is increasing, but little is known regarding the occurrence of related complications as these youths transition to adulthood. METHODS: We previously conducted a multicenter clinical trial (from 2004 to 2011) to evaluate the effects of one of three treatments (metformin, metformin plus rosiglitazone, or metformin plus an intensive lifestyle intervention) on the time to loss of glycemic control in participants who had onset of type 2 diabetes in youth. After completion of the trial, participants were transitioned to metformin with or without insulin and were enrolled in an observational follow-up study (performed from 2011 to 2020), which was conducted in two phases; the results of this follow-up study are reported here. Assessments for diabetic kidney disease, hypertension, dyslipidemia, and nerve disease were performed annually, and assessments for retinal disease were performed twice. Complications related to diabetes identified outside the study were confirmed and adjudicated. RESULTS: At the end of the second phase of the follow-up study (January 2020), the mean (±SD) age of the 500 participants who were included in the analyses was 26.4±2.8 years, and the mean time since the diagnosis of diabetes was 13.3±1.8 years. The cumulative incidence of hypertension was 67.5%, the incidence of dyslipidemia was 51.6%, the incidence of diabetic kidney disease was 54.8%, and the incidence of nerve disease was 32.4%. The prevalence of retinal disease, including more advanced stages, was 13.7% in the period from 2010 to 2011 and 51.0% in the period from 2017 to 2018. At least one complication occurred in 60.1% of the participants, and at least two complications occurred in 28.4%. Risk factors for the development of complications included minority race or ethnic group, hyperglycemia, hypertension, and dyslipidemia. No adverse events were recorded during follow-up. CONCLUSIONS: Among participants who had onset of type 2 diabetes in youth, the risk of complications, including microvascular complications, increased steadily over time and affected most participants by the time of young adulthood. Complications were more common among participants of minority race and ethnic group and among those with hyperglycemia, hypertension, and dyslipidemia. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases and others; ClinicalTrials.gov numbers, NCT01364350 and NCT02310724.).
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Most children and adolescents who develop type 2 diabetes will have microvascular complications by young adulthood.
“Most children and adolescents who develop type 2 diabetes will have microvascular complications by young adulthood (274);”
The IDx-DR autonomous AI system was US FDA De Novo authorized in 2018 for adults with diabetes.
“The autonomous AI system (IDx-DR, Digital Diagnostics, Coralville, Iowa, USA) for diagnosing diabetic eye disease (DED) was US FDA De Novo authorized (“FDA approval”) in 2018 for adults with diabetes15.”
From Autonomous artificial intelligence increases screening and follow-up for diabetic retinopathy in youth: the ACCESS randomized control trial (2024) · cites this paper as [15]
The Methods section, “Diabetic Eye Disease” (page not provided), describes fundus photography graded at a centralized reading center, not the IDx-DR system. Searches for IDx-DR, FDA De Novo authorization, and autonomous AI found no passage in our copy addressing the claimed 2018 authorization for adults with diabetes. (LLM, conf=0.77)
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- Authors
- TODAY Study Group
- Corresponding author
- TODAY Study Group
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2021-07-29
- Volume
- 385
- Issue
- 5
- Pages
- 416-426
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- PMC
- PMC8697255
- OpenAlex
- W3187052158
- Cited by
- 546
- References
- 34
- Citations by year
- 2026: 85 · 2025: 121 · 2024: 123 · 2023: 97 · 2022: 97 · 2021: 22
- FWCI
- 63.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Digital Commons@Becker (Washington University School of Medicine) (submittedVersion)
- Funders
- National Center for Research Resources (M01-RR00036, M01-RR00043-45, M01-RR00069, M01-RR00084, M01-RR00125, M01-RR01066, M01-RR14467, UL1-RR024134, UL1-RR024139, UL1-RR024153, UL1-RR024989, UL1-RR024992, UL1-RR025758, UL1-RR025780)
- National Institute of Diabetes and Digestive and Kidney Diseases (U01-DK61212, U01-DK61230, U01-DK61239, U01-DK61242, U01-DK61254)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Keywords
- youth-onset type 2 diabetes, late complications, diabetic nephropathy, hypertension, dyslipidemia, diabetic retinopathy, microvascular complications, hyperglycemia, racial and ethnic disparities, metformin, coming of age, risk factors for complications, lifestyle intervention, rosiglitazone, insulin therapy, glycemic control
- MeSH terms
- Adolescent, Child, Diabetes Mellitus, Type 2, Female, Follow-Up Studies, Humans, Hypertension, Hypoglycemic Agents, Male, Metformin, Risk Factors, Diabetes Complications, Dyslipidemias
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