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A systematic review of guidelines on screening for celiac disease in children with thyroid disease and vice versa
Talia D'Ambrosio1,2, Silvia Bianchin2, Roberto Gastaldi3
1Pediatric Clinic, University of Ferrara, Ferrara, Italy.
Insights
Screening for celiac disease (CD) and autoimmune thyroid disease (ATD) in children lacks consistent guidelines. This review highlights the need for standardized protocols for early detection and management of these associated autoimmune conditions.
Area of Science:
- Immunology
- Endocrinology
- Gastroenterology
Background:
- Autoimmune thyroid diseases (ATD) are common in patients with celiac disease (CD), another autoimmune disorder.
- Both conditions can be screened for in asymptomatic individuals, but guidelines for screening children vary.
- Early detection and treatment can benefit children with co-occurring CD and ATD.
Purpose of the Study:
- To systematically review and compare recent international guidelines for screening co-occurring celiac disease and autoimmune thyroid disease in children.
- To identify discrepancies in screening protocols and suggest a practical clinical approach.
Main Methods:
- Systematic review of 20 guidelines published between January 2013 and January 2024.
- Analysis of recommendations for screening timing, methods, and follow-up for co-occurring CD and ATD.
- Comparison of European and North American gastroenterological organization guidelines.
Main Results:
- Significant variation exists in recommended screening protocols for CD and ATD in children, with limited consensus.
- Some guidelines suggest clinical follow-up only, omitting routine serological screening.
- Disagreement persists on screening asymptomatic children for TD (using TSH) with CD, and for CD (using tTG IgA and total IgA) with TD. HLA genotyping is rarely a first-line method.
Conclusions:
- International guidelines lack consensus on optimal screening strategies for co-occurring CD and ATD in children.
- Notable differences in HLA testing use and follow-up protocols complicate clinical management.
- Standardized procedures are needed for managing patients with these associated autoimmune conditions, particularly those with isolated low tTG.
Introduction:
Autoimmune thyroid diseases (ATD) are the most prevalent autoimmune disorders associated with celiac disease (CD). Both conditions can often be detected through serological screening in asymptomatic patients over several years. Various guidelines for screening thyroid disease (TD) are available in children with CD and vice versa.
Methods:
We conducted a systematic review to identify the most recent and relevant guidelines, comparing their recommendations to analyze key differences and suggesting a practical clinical approach.
Results:
Out of 1,294 articles reviewed, we identified 20 guidelines published between January 2013 and January 2024. These guidelines, primarily from gastroenterological organizations in Europe and North America, recommend different timings and methods for screening the co-occurrence of these diseases, both at diagnosis and during follow up. Some guidelines recommend only clinical follow-up without routine serological screening. There is limited consensus on screening for TD [using thyroid-stimulating hormone test (TSH)] in asymptomatic children newly diagnosed with CD, and even less agreement on screening for CD [using anti-transglutaminase antibodies (tTG) immunoglobulin A (IgA) test and total IgA] in children newly diagnosed with TD. No standardized procedures exist for managing patients with isolated low tTG and human leukocyte antigen (HLA) genotyping is rarely recommended as a first- line screening method.
Discussion:
Over the past decade, there has been a growing recognition of the importance of identifying children with co-occurrence of CD and TD who could benefit from early treatment, even in the absence of symptoms. However, international guidelines still show a lack of consensus regarding screening for these frequently associated autoimmune diseases, with notable differences in the use of HLA testing and follow-up protocols.
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