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Early-Onset Noncommunicable Disease and Multimorbidity Among Adults With Pediatric-Onset Disabilities
Daniel G Whitney1, Rachael T Whitney2, Neil S Kamdar3
1Department of Physical Medicine and Rehabilitation, Michigan Medicine, University of Michigan, Ann Arbor.
Insights
Young adults with pediatric-onset disabilities (PoDs) face significantly higher risks of developing major noncommunicable diseases and multimorbidity. Early detection and management are crucial for this vulnerable population.
Area of Science:
- Public Health
- Epidemiology
- Disability Studies
Background:
- Pediatric-onset disabilities (PoDs) can significantly impact long-term health trajectories.
- Noncommunicable diseases (NCDs) are a leading cause of global mortality and morbidity.
- Understanding NCD prevalence in young adults with PoDs is critical for targeted interventions.
Purpose of the Study:
- To determine the prevalence of major noncommunicable diseases (NCDs) in young adults with pediatric-onset disabilities (PoDs).
- To compare NCD prevalence and multimorbidity in young adults with and without PoDs.
- To identify specific NCDs disproportionately affecting young adults with PoDs.
Main Methods:
- Utilized a de-identified nationwide claims database (Optum Clinformatics Data Mart).
- Included beneficiaries aged 18-40 years with diagnostic codes for childhood-originating PoDs.
- Identified NCDs using ICD-9-CM codes and compared prevalence between groups, adjusting for sociodemographics.
Main Results:
- Adults with PoDs exhibited significantly higher prevalences and odds of all studied NCDs (OR, 2.1-9.0; P<.05) and multimorbidity (OR, 3.8; 95% CI, 3.7-3.9).
- All PoD categories, except for genital organ PoDs regarding ischemic and cerebrovascular diseases, showed increased NCD and multimorbidity prevalence.
- This highlights a substantial burden of early-onset NCDs in young adults with PoDs.
Conclusions:
- Young adults with PoDs experience an accelerated onset of major noncommunicable diseases.
- These findings underscore the significant contribution of PoDs to the global disease and mortality burden.
- Proactive healthcare strategies are essential for managing NCDs in this population.
Objective:
To determine the prevalence of major noncommunicable diseases among young adults with pediatric-onset disabilities (PoDs) compared with young adults without PoDs.
Patients And Methods:
Data were obtained from the Optum Clinformatics Data Mart, a de-identified nationwide claims database of beneficiaries from a single private payer in the United States. Beneficiaries were included if they were 18 to 40 years old and had an International Classification of Diseases, Ninth Revision, Clinical Modification diagnostic code for a PoD known to originate in childhood. Diagnostic codes were used to identify high-burden noncommunicable diseases: ischemic heart disease, cerebrovascular disease, hypertensive and other cardiovascular disease, type 2 diabetes, malignant cancer, osteoporosis, mood affective disorders, chronic obstructive pulmonary disease, chronic kidney disease, and liver disease. The prevalence of noncommunicable diseases and multimorbidity (≥2 diseases) was compared between adults with (N=47,077) and without (N=2,180,250) PoDs, before and after adjusting for sociodemographic characteristics. This study was conducted between July 1, 2018, and February 1, 2019.
Results:
Adults with PoDs had higher prevalences and adjusted odds of all noncommunicable diseases (odds ratio, 2.1-9.0; all P<.05) and multimorbidity (odds ratio, 3.8; 95% CI, 3.7-3.9) compared with adults without PoDs. After stratifying by the type of PoD (eg, musculoskeletal, circulatory), all PoD categories had higher prevalence of all noncommunicable diseases and multimorbidity compared with young adults without PoDs, except for ischemic heart disease and cerebrovascular disease among adults with PoDs of the genital organs.
Conclusion:
Young adults with PoDs have an early onset of several noncommunicable diseases that represent major contributors to the global and national burden of disease and mortality.
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