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Isolated ventricular septal defect is not a risk factor for celiac disease: evidence from a large real-world data
Ramon Cohen1,2, Haitham Abu Khadija3, Shay Nemet2
1Department of Internal Medicine B, Kaplan Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Clalit Health Services, Rehovot, Israel.
Insights
Ventricular septal defect (VSD) in children is not independently linked to celiac disease (CD). However, other conditions like type 1 diabetes and autoimmune diseases are associated with CD, warranting targeted screening.
Area of Science:
- Pediatrics
- Gastroenterology
- Cardiology
Background:
- Ventricular septal defect (VSD) is a common congenital heart defect.
- Celiac disease (CD) is linked to autoimmune and chromosomal conditions.
- The association between isolated VSD and CD is not well-established.
Purpose of the Study:
- To investigate if isolated VSD is an independent risk factor for developing celiac disease in children.
- To compare the association of VSD with CD to other known risk factors.
Main Methods:
- Population-based retrospective cohort study using electronic health records.
- Followed 493,382 children aged 0-10 years for up to 10 years.
- Used multivariable Cox proportional hazards models adjusted for comorbidities.
Main Results:
- Isolated VSD was not independently associated with an increased risk of CD (HR 1.25).
- Type 1 diabetes mellitus (HR 10.26), chromosomal anomalies (HR 5.20), and autoimmune diseases (HR 2.07) showed strong associations with CD.
- Established comorbidities demonstrated significant links to CD development.
Conclusions:
- Isolated VSD is not an independent risk factor for celiac disease in children.
- Findings do not support routine CD screening based solely on VSD presence.
- Targeted screening for CD is recommended for children with type 1 diabetes, chromosomal anomalies, and autoimmune diseases.
Background:
Ventricular septal defect (VSD) is one of the most common congenital heart defects in children. Celiac disease (CD) is known to cluster with autoimmune conditions and chromosomal syndromes, but it remains unclear whether isolated VSD is independently associated with CD.
Methods:
We performed a population-based retrospective cohort study using electronic records from Clalit Health Services. Children aged 0-10 years were followed for up to 10 years to identify incident cases of CD. Multivariable Cox proportional hazards models were used to estimate adjusted hazard ratios (HRs) with 97.5% confidence intervals (CIs) for the association between VSD and CD. The models were adjusted for age, sex, type 1 diabetes mellitus, autoimmune diseases, immunodeficiency, and chromosomal anomalies.
Results:
The Cox model included 493,382 children. VSD was not independently associated with an increased risk of CD (HR 1.25, 97.5% CI 0.85-1.82). In contrast, established comorbidities showed strong associations with CD: type 1 diabetes mellitus (HR 10.26, 97.5% CI 8.15-12.91), chromosomal anomalies (HR 5.20, 97.5% CI 3.67-7.37), and autoimmune diseases (HR 2.07, 97.5% CI 1.39-3.10).
Conclusion:
In this large real-world data, isolated VSD was not an independent risk factor for CD, whereas type 1 diabetes mellitus, chromosomal anomalies, and other autoimmune diseases were strongly associated with CD. These findings do not support routine CD screening based solely on the presence of VSD in children.
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