Screening för celiaki kan vara motiverad i högriskgrupper
Screening for celiac disease can be justified in high-risk groups
Author
Summary, in English
Coeliac disease is widespread and occurs in 0.5-1 per cent of the population. Most sufferers show atypical symptoms and might well remain undiagnosed. Endomysial or human transglutaminase autoantibody levels of type IgA can be recommended as screening instruments combined with s-IgA for exclusion of such deficiency. In contrast, there is a high frequency of false-positive IgA gliadin antibody test results, especially where coeliac disease is common, as in chronic liver disease, diabetes, thyroid disease and conditions with chromosomal aberrations (Down syndrome and Turner syndrome). Despite this, gliadin antibodies of type IgA are still the best marker for coeliac disease in children under two years of age. While mass screening is not to be recommended, case finding is worthwhile in well defined risk groups, i.e. in cohorts with autoimmune disease or chromosomal aberrations or in relatives to anyone with coeliac disease. A positive biopsy is still the gold standard for diagnosis.
Department/s
- Gastroenterology
- Chronic Inflammatory and Degenerative Diseases Research Unit
Publishing year
2004
Language
Swedish
Pages
6-3918
Publication/Series
Läkartidningen
Volume
101
Issue
48
Links
Document type
Journal article
Publisher
Swedish Medical Association
Topic
- Gastroenterology and Hepatology
Keywords
- Humans
- Gliadin: immunology
- English Abstract
- Child
- Celiac Disease: immunology
- Celiac Disease: genetics
- Celiac Disease: diagnosis
- Celiac Disease: complications
- Biological Markers: blood
- Autoimmune Diseases: diagnosis
- Adult
- Autoimmune Diseases: complications
- Transglutaminases: immunology
- Risk Factors
- Myosins: immunology
- Immunoglobulin A: blood
- Mass Screening
Status
Published
Research group
- Gastroenterology
- Chronic Inflammatory and Degenerative Diseases Research Unit
ISBN/ISSN/Other
- ISSN: 0023-7205