The study will identify a cohort of infants at risk for celiac disease that can be followed on a long term basis for investigating the natural history the celiac disease based on the pattern of early nutrition. The study will investigate possible early feeding patterns including the timing of introduction to gluten that may protect at least in part from CD development in at risk infants.

From weaning to age 12 months the clinical data, the adherence to the dietary protocol and the amount of intervention baby-food ingested will be checked every two months Following investigations will be performed at the time of recruitment, 12 months, 18 months, 24 months, 30 months, and 36 months by taking a sample of blood (maximum 4 ml) in infants fasting form at least 4 hours: (a) quick test for IgA anti-tTG abs determination (few drops); (b) conventional ELISA for serum IgA and IgG anti-tTG determination (0.4 ml); (c) sugar permeability test with lactulose/mannitol on serum (0.25 ml); (d) serum zonulin determination (0.1 ml); (e) serum sample for T1D-related autoantibodies (0.25 ml); (f) serum sample to be stocked in the sera bank (0.25 ml); (g) whole blood sample in EDTA for validation of the quick tests (0.5 ml). All the sera samples will be frozen, stored at -20 °C and sent (boxed in dry ice) in blocks to the centre responsible for the determinations every 2 months. Cases positive for the quick-test for anti-tTG the serum sample will be frozen and immediately shipped for confirmatory determination.

If infants develop symptoms during the intervention period (6 to 12 months) the group to which infant belongs will be decoded. Infants belonging to group A (on a gluten-containing diet) presenting symptoms suggestive of CD will undergo a complete diagnostic work-up for CD. These events will be reported in a form. After age 1 year, infants developing symptoms suggestive of active CD (chronic diarrhea, failure to thrive, etc) in-between the scheduled visits will undergo a supplementary serological investigation. A small intestinal biopsy will be recommended in cases showing either serum anti-tTG abs higher than the cut-off or IgG-AGA higher than cut-off in infants with selective IgA deficiency. (Standard medical care and not part of research). The evolution of the composition of the intestinal microbiota will be evaluated in both groups at 7d, 30d, 4-6 months (prior to weaning), 12 and 18 months. The bacterial composition of stool will also be analyzed in a sub-sample of children developing active CD and in non-CD controls. All patients who develop CD will continue in the study.

Definitions:

Active CD: Children showing positive serology and signs of immune-mediated damage of the small intestinal mucosa on biopsy (ranging from isolated increase of intraepithelial lymphocytes to villous atrophy with crypt hypertrophy.)

CD serological autoimmunity positive: Children positive for IgA anti-tTG abs on two consecutive occasions.

Disruption of the small intestinal barrier: Children with an increased ratio of serum lactulose/mannitol with or without increased levels of serum zonulin.

• Celiac Disease
• Infant Nutrition

• Dietary Supplement: Gluten
• Dietary Supplement: Gluten free diet

• Active Comparator: Gluten added to diet at 6 months per American Academy of Pediatrics recommendations
• Active Comparator: Purified corn starch added to diet from 6-12 months

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Inclusion Criteria:

• Newborns and infants less than 6 months of age
• First-degree relatives of patients affected with biopsy-proven CD
• Showing positivity of HLA-DQ2 and/or DQ8 genotypes.
• On exclusive milk diet (breast milk or formula)

Exclusion Criteria:

• Infants who are negative for HLA DQ2 and/or DQ8 genotype
• Infants that have gluten introduced in their diet before 5-6 months of age
• Infants older than 6 months of age