The role of gluten consumption at an early age in celiac disease development: a further analysis of the prospective PreventCD cohort study

卷:105

Crespo-Escobar, Paula ; Mearin, Maria Luisa ; Hervas, David ; Auricchio, Renata ; Castillejo, Gemma ; Gyimesi, Judit ; Martinez-Ojinaga, Eva ; Werkstetter, Katharina ; Vriezinga, Sabine Lisa ; Korponay-Szabo, Ilma Rita ; Polanco, Isabel ; Troncone, Riccardo ; Stoopman, Els ; Kolacek, Sanja ; Shamir, Raanan ; Szajewska, Hania ; Koletzko, Sibylle ; Ribes-Koninckx, Carmen

Med Res Inst La Fe

关键词: celiac disease;    children;    gluten;    HLA;    European cohort;   

DOI  :  10.3945/ajcn.116.144352

学科分类：食品科学和技术

【 摘 要 】

Background: We previously found that the introduction of small quantities of gluten at 4-6 mo of age did not reduce the risk of celiac disease (CD) in a group of high-risk children. However, the consumption of high amounts of gluten early in life has been suggested to increase CD risk. Objective: The aim of this study was to evaluate this hypothesis by using data from the previous study of the PreventCD trial (www.preventcd.com). Design: Gluten intake was prospectively quantified by using specific food records between 11 and 36 mo of age in 715 children positive for the human leukocyte antigen (HLA)-DQ2 and/or HLA-DQ8 from 5 European countries. According to the PreventCD protocol, infants received 100 mg immunologically active gluten/d or placebo from 4 to 6 mo of age, with a stepwise and fixed gluten increase until age 10 mo and unrestricted intake thereafter. The primary outcome of the present study was the impact of the amount of gluten consumed from age 10 mo onward on CD development. Results: Mean daily gluten intakes from 10 mo onward were significantly different between countries for children at all ages (P < 0.001) but not between children who developed CD and those who did not within the same country (P > 0.05). The variables country, sex, intervention group, and gluten consumption pattern did not show significant associations with CD development risk (HRs not significant). In addition, the interaction between HLA risk group and gluten consumption pattern showed no significant risk on CD development, except for the DQ2.2/DQ7 haplotype (HR: 5.81; 95% CI: 1.18, 28.74; P = 0.031). Conclusions: Gluten consumption patterns as well as the amount of gluten consumed at 11-36 mo of age do not influence CD development for most related HLA genotypes in children with a genetic risk. This study reports the gluten consumption pattern in children at risk of CD from different European countries.