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Published on: July 5, 2022
Autoimmune comorbidity in type 1 diabetes and its association with metabolic control and mortality risk in young
John Samuelsson1,2, Rebecka Bertilsson3, Erik Bülow3,4
1Department of Paediatrics, Ryhov County Hospital, Jönköping, Sweden. john.samuelsson@rjl.se.
Insights
Children and young adults with type 1 diabetes have a high prevalence of autoimmune diseases, particularly celiac and thyroid conditions. However, these comorbidities do not significantly impact glycemic control (HbA1c) or increase mortality risk.
Area of Science:
- Endocrinology and Metabolism
- Immunology
- Pediatrics
Background:
- Type 1 diabetes (T1D) is an autoimmune condition often associated with other autoimmune comorbidities.
- Understanding the spectrum and impact of these comorbidities in young T1D patients is crucial for comprehensive care.
- Previous studies have not comprehensively evaluated the long-term development of various autoimmune diseases following T1D onset in pediatric populations.
Purpose of the Study:
- To describe the incidence and types of autoimmune comorbidities in children and young adults diagnosed with type 1 diabetes.
- To investigate the association between autoimmune comorbidity and glycemic control (HbA1c) in individuals with T1D.
- To examine the relationship between autoimmune comorbidity and mortality risk in a young T1D cohort.
Main Methods:
- A nationwide, register-based cohort study utilizing the Swedish National Diabetes Register.
- Included 15,188 individuals diagnosed with T1D before age 18 (2000-2019), matched with population controls.
- Autoimmune diseases identified via ICD-10 codes from the National Patient Register; mortality data from the Cause of Death Register.
Main Results:
- 19.2% of individuals with T1D were diagnosed with at least one autoimmune disease, compared to 4.0% in the control group.
- High hazard ratios (HRs) observed for celiac disease (11.6), thyroid disease (10.6), Addison's disease (18.3), and atrophic gastritis (19.6).
- Autoimmune comorbidity in T1D patients did not show a statistically significant effect on HbA1c levels or mortality risk.
Conclusions:
- This study confirms a high prevalence of autoimmune diseases in young individuals with T1D, especially celiac and thyroid disease.
- The presence of autoimmune comorbidities does not appear to negatively influence metabolic control or long-term survival in this cohort.
- Findings highlight the importance of screening for autoimmune conditions in pediatric T1D patients and suggest that management of T1D itself is key for outcomes.
Aims/Hypothesis:
This register-based study aimed to describe autoimmune comorbidity in children and young adults from type 1 diabetes onset, and to investigate whether such comorbidity was associated with a difference in HbA1c or mortality risk compared with children/young adults with type 1 diabetes without autoimmune comorbidity.
Methods:
A total of 15,188 individuals from the Swedish National Diabetes Register, registered with type 1 diabetes before 18 years of age between 2000 and 2019, were included. Five randomly selected control individuals from the Swedish population (Statistics Sweden) were matched to each individual with type 1 diabetes (n=74,210 [346 individuals with type 1 diabetes were not found in the Statistics Sweden register at the date of type 1 diabetes diagnosis, so could not be matched to control individuals]). The National Patient Register was used to attain ICD-10 codes on autoimmune diseases and the Cause of Death Register was used to identify deceased individuals.
Results:
In the total type 1 diabetes cohort, mean±SD age at onset of type 1 diabetes was 9.5±4.4 years and mean disease duration at end of follow-up was 8.8±5.7 years. Of the individuals with type 1 diabetes, 19.2% were diagnosed with at least one autoimmune disease vs 4.0% of the control group. The HRs for comorbidities within 19 years from onset of type 1 diabetes were 11.6 (95% CI 10.6, 12.6) for coeliac disease, 10.6 (95% CI 9.6, 11.8) for thyroid disease, 1.3 (95% CI 1.1, 1.6) for psoriasis, 4.1 (95% CI 3.2, 5.3) for vitiligo, 1.7 (95% CI 1.4, 2.2) for rheumatic joint disease, 1.0 (95% CI 0.8, 1.3) for inflammatory bowel disease, 1.0 (95% CI 0.7, 1.2) for systemic connective tissue disorder, 1.4 (95% CI 1.1, 1.9) for uveitis, 18.3 (95% CI 8.4, 40.0) for Addison's disease, 1.8 (95% CI 0.9, 3.6) for multiple sclerosis, 3.7 (95% CI 1.6, 8.7) for inflammatory liver disease and 19.6 (95% CI 4.2, 92.3) for atrophic gastritis. Autoimmune disease in addition to type 1 diabetes had no statistically significant effect on HbA1c or mortality risk.
Conclusions/Interpretation:
To our knowledge, this is the first comprehensive study where young individuals with type 1 diabetes were followed regarding development of a wide spectrum of autoimmune diseases, from onset of type 1 diabetes. In this nationwide and population-based study, there was already a high prevalence of autoimmune diseases in childhood, especially coeliac and thyroid disease. The presence of autoimmune comorbidity did not have a statistically significant effect on metabolic control or mortality risk.
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