Age at gluten introduction and risk of celiac disease

Carin Andrén Aronsson1, Hye-Seung Lee2, Edwin Liu3

  • 1Department of Clinical Sciences, Lund University, Malmö, Sweden; carin.andren_aronsson@med.lu.se.

Pediatrics
|January 21, 2015
PubMed

Insights

Early or late gluten introduction in genetically predisposed infants was not linked to celiac disease (CD) risk. This finding from the TEDDY study suggests gluten timing isn't an independent risk factor for CD development.

Area of Science:

  • Pediatric gastroenterology
  • Immunology
  • Genetics

Background:

  • Celiac disease (CD) is an autoimmune disorder triggered by gluten in genetically susceptible individuals.
  • The optimal timing for introducing gluten to infants to prevent CD remains a subject of research.
  • The Environmental Determinants of Diabetes in the Young (TEDDY) study investigates environmental factors influencing CD development.

Purpose of the Study:

  • To investigate the association between the age of gluten introduction and the risk of developing celiac disease (CD) in genetically predisposed children.
  • To analyze differences in gluten introduction timing across participating countries within the TEDDY study.

Main Methods:

  • Prospective birth cohort study (TEDDY) involving 6,436 newborns screened for high-risk HLA-genotypes for CD.
  • Follow-up included infant feeding information collection every three months.
  • Outcomes assessed were persistent positive tissue transglutaminase autoantibodies (tTGA) and confirmed CD diagnoses.

Main Results:

  • Swedish infants were introduced to gluten significantly earlier (median 21.7 weeks) than infants in Finland, Germany, and the US (median 30.4 weeks).
  • Over a median follow-up of 5.0 years, 12% developed tTGA and 5% developed CD.
  • Gluten introduction before 17 weeks or after 26 weeks was not associated with an increased risk for tTGA or CD, after adjusting for covariates.

Conclusions:

  • The age of first gluten introduction was not found to be an independent risk factor for developing celiac disease in the TEDDY study.
  • These findings contribute to understanding the complex interplay of genetics and environmental factors in CD pathogenesis.
Abstract

Related Concept Videos

Type I Diabetes I: Introduction01:12

Type I Diabetes I: Introduction

Type 1 diabetes mellitus is a chronic metabolic disorder characterized by an absolute deficiency of insulin resulting from the autoimmune destruction of pancreatic β-cells. Although it can occur at any age, it is most commonly diagnosed in childhood, adolescence, or early adulthood. The loss of insulin production impairs cellular glucose uptake, resulting in persistent hyperglycemia and necessitating lifelong insulin therapy.Autoimmune Destruction of β-CellsThe hallmark of type 1...
1
Gastritis II: Pathophysiology01:26

Gastritis II: Pathophysiology

The pathophysiology of gastritis begins with the colonization of the stomach lining by Helicobacter pylori (H. pylori). This bacterium spreads mainly via the oral-oral route through saliva or shared utensils, and can also be transmitted in overcrowded or unhygienic environments through contaminated water, despite its brief survival outside the body.ColonizationOnce ingested, H. pylori enters the stomach and begins colonization by navigating through the mucus layer lining the stomach wall. It...
2
Glucose Transporters01:27

Glucose Transporters

Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
28.5K
Development of Human Microbiota01:30

Development of Human Microbiota

The human microbiota begins developing at birth and undergoes continual change as we age. Infancy marks a critical period of microbial sensitivity, offering a “window of opportunity” during which beneficial microbes help mature the immune system. By age three, children typically develop a more stable and diverse microbial community. Newborns acquire microbes from their immediate environment; vaginal delivery favors maternal vaginal microbes, while cesarean births favor microbes from...
50
Anatomy of the Intestines01:23

Anatomy of the Intestines

Although digestion of proteins, carbohydrates, and lipids may begin in the stomach, it is completed in the intestine. The absorption of nutrients, water, and electrolytes from food and drink also occurs in the intestine. The intestines can be divided into two structurally distinct organs—the small and large intestines.
Small Intestines
The small intestine is an ~7 meter-long tube with an inner diameter of just 2.5 cm. Since most nutrients are absorbed here, the inner lining of the...
92.7K
Inflammatory Bowel Disease III: Crohn's Disease01:25

Inflammatory Bowel Disease III: Crohn's Disease

Crohn’s disease is a chronic, relapsing form of inflammatory bowel disease characterized by segmental, transmural inflammation that can affect any part of the gastrointestinal tract. Its pathogenesis arises from a combination of genetic susceptibility, environmental exposures, epithelial barrier dysfunction, and immune dysregulation. Together, these factors lead to an exaggerated immune response against components of the gut microbiome.Genetic and Environmental InfluencesMultiple genetic...
2