# β-Cell Function and Glucose Tolerance in Persons With Multiple Islet Autoantibodies Randomized to a Gluten-free Diet

**Authors:** Marlena Maziarz, Jaakko J Koskenniemi, Maria Månsson Martinez, Lampros Spiliopoulos, Falastin Salami, Jorma Toppari, Jukka Kero, Riitta Veijola, Päivi Tossavainen, Sauli Palmu, Carin Andrén Aronsson, Markus Lundgren, Henrik Borg, Anastasia Katsarou, Helena Elding Larsson, Mikael Knip, Olivia Lou, Jessica L Dunne, Carina Törn, Åke Lernmark

PMC · DOI: 10.1210/jendso/bvaf073 · Journal of the Endocrine Society · 2025-05-07

## TL;DR

A study found that a gluten-free diet did not improve β-cell function or glucose tolerance in people with multiple islet autoantibodies over 18 months.

## Contribution

This is the first randomized clinical trial to evaluate the effect of a gluten-free diet on β-cell function in individuals with multiple islet autoantibodies.

## Key findings

- No differences were observed between the gluten-free diet and normal diet groups in glucose tolerance outcomes.
- The gluten-free diet did not preserve β-cell function better than a normal diet.
- No adverse events related to the gluten-free diet were reported.

## Abstract

A randomized clinical trial was conducted to evaluate the impact of a gluten-free diet (GFD) on β-cell function and glucose tolerance in persons with multiple islet autoantibodies.

Individuals (n = 59; median age 11 years) with multiple islet autoantibodies were recruited to a randomized clinical trial between April 2016 and April 2021. The participants were randomized to a GFD (n = 30; female n = 14) or a normal diet (ND) (n = 29; female n = 16). The study was conducted at 6 clinical research centers in Finland and Sweden, with a dietary intervention for 17 months followed by a 6-month washout on a ND. The primary outcomes were (1) the proportion of participants going from normal glucose tolerance at the time of the randomization to abnormal glucose tolerance by 18 months, (2) a change in first-phase insulin response in IV glucose tolerance tests between randomization and 18 months, and (3) a change in C-peptide area under the curve in oral glucose tolerance test between randomization and 18 months.

We did not find differences between participants randomized to GFD and ND in any of the glucose tolerance outcomes. No serious adverse events or adverse events related to a GFD were noted.

Being on a GFD was not found to differ from being on a ND in preserving β-cell function or maintaining normal glucose tolerance in persons with multiple islet autoantibodies.

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** abnormal glucose tolerance (MESH:D018149)
- **Chemicals:** Glucose (MESH:D005947)

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12146266/full.md

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Source: https://tomesphere.com/paper/PMC12146266