Celiac disease without villous atrophy in children: a prospective study.
Study Goal
The researchers aimed to determine whether children who are EmA positive with normal small-bowel villi are gluten-sensitive and benefit from early treatment with a gluten-free diet.
Results Summary
Children with normal villi who continued gluten consumption experienced disease exacerbation, while those on a gluten-free diet saw resolution of gastrointestinal symptoms and abnormal antibodies. The study concluded that EmA-positive children benefit from early gluten-free diet treatment despite normal mucosal structure.
Population
Children who were EmA positive with normal small-bowel mucosal villi, compared to EmA-positive children with villous atrophy and seronegative controls.
Effective Dosage
Not specified
Duration
1 year
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
gluten-free diet | decrease | celiac-type disorder | children who are EmA positive with normal small-bowel mucosal villi | - | benefit from early treatment | #1 |
gluten consumption | increase | celiac-type disorder | children who were EmA positive with normal villi | - | disease was exacerbated | #2 |
gluten-free diet | decrease | gastrointestinal symptoms | children who were EmA positive with normal villi | - | gastrointestinal symptoms disappeared | #3 |
gluten-free diet | decrease | abnormal antibodies | children who were EmA positive with normal villi | - | abnormal antibodies disappeared | #4 |
OBJECTIVE: To establish whether children who are endomysial antibody (EmA) positive and have normal small-bowel mucosal villous morphology are truly gluten-sensitive and may benefit from early treatment with a gluten-free diet. STUDY DESIGN: Children who were EmA positive with normal small-bowel mucosal villi were compared with children who were seropositive with villous atrophy by using several markers of untreated celiac disease. Thereafter, children with normal villous structure either continued on a normal diet or were placed on a gluten-free diet and re-investigated after 1 year. Seventeen children who were seronegative served as control subjects for baseline investigations. RESULTS: Normal villous morphology was noted in 17 children who were EmA positive, and villous atrophy was noted in 42 children who were EmA positive. These children were comparable in all measured variables regardless of the degree of enteropathy, but differed significantly from the seronegative control subjects. During the dietary intervention, in children who were EmA positive with normal villi, the disease was exacerbated in children who continued gluten consumption, whereas in all children who started the gluten-free diet, both the gastrointestinal symptoms and abnormal antibodies disappeared. CONCLUSIONS: The study provided evidence that children who are EmA positive have a celiac-type disorder and benefit from early treatment despite normal mucosal structure, indicating that the diagnostic criteria for celiac disease should be re-evaluated.