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Clinical Question
In newborns with a hereditary risk, does avoiding cow's milk formula decrease their risk of developing celiac disease?
Bottom line
In this study of newborns at higher-than-average risk, avoiding cow's milk–based formula did not decrease their likelihood of developing celiac disease. However, the study was small and could have missed a real difference if one truly exists. 1b-
Reference
Study design: Randomized controlled trial (double-blinded)
Funding: Government
Setting: Outpatient (any)
Synopsis
The researchers of this study conducted in Finland enrolled 230 infants with a first-degree relative with type 1 diabetes and a laboratory-verified predisposition to develop diabetes; both factors are associated with the development of celiac disease. The infants were randomly assigned, using concealed allocation, to receive either a cow's milk–based formula or a hydrolyzed casein–based formula (Nutramigen) to be used as desired to supplement breastfeeding for the first 6 months to 8 months of life. Breastfeeding rates were similar in both groups. Children were followed up until they were 10 years old with periodic testing for antibody development signaling celiac disease, with approximately 18% of the kids lost to drop-out. There was no difference in the development of either antibodies or symptomatic disease among the 2 groups. Using intention-to-treat analysis, 25 of the 189 participants (13.2%) developed antibodies. Ten of the children (4.3%; median age 16.7 years) were given a diagnosis of celiac disease: 6 in the control group and 4 in the cow's milk group. This was a small study with a small number of cases of celiac disease, so the study may not have had the power to identify a difference in the development of celiac disease among the 2 groups if one truly exists.
Reviewer
Allen F. Shaughnessy, PharmD, MMedEd
Professor of Family Medicine
Tufts University
Boston, MA
Comments
None
good poem
concur with conclusion : does not warrant clinical guideline other than extra attention for mothers with coeliac disease