Healthy and pro-inflammatory gut ecology plays a crucial role in the digestion and tolerance of a novel Gluten Friendly™ bread in celiac subjects : Randomized, double blind, placebo control in vivo study
Andriulli, Angelo; Bevilacqua, Antonio; Palmieri, Orazio; Latiano, Anna; Fontana, Rosanna; Gioffreda, Domenica; Castellana, Stefano; Mazza, Tommaso; Panza, Anna; Menzaghi, Claudia; Grandone, Elvira; di Mauro, Lazzaro; Decina, Ivana; Tricarico, Michele; Musaico, Daniela; Mäki, Markku; Isola, Jorma; Popp, Alina; Taavela, Juha; Petruzzi, Leonardo; Sinigaglia, Milena; Corbo, Maria Rosaria; Lamacchia, Carmela (2022-02-07)
Andriulli, Angelo
Bevilacqua, Antonio
Palmieri, Orazio
Latiano, Anna
Fontana, Rosanna
Gioffreda, Domenica
Castellana, Stefano
Mazza, Tommaso
Panza, Anna
Menzaghi, Claudia
Grandone, Elvira
di Mauro, Lazzaro
Decina, Ivana
Tricarico, Michele
Musaico, Daniela
Mäki, Markku
Isola, Jorma
Popp, Alina
Taavela, Juha
Petruzzi, Leonardo
Sinigaglia, Milena
Corbo, Maria Rosaria
Lamacchia, Carmela
07.02.2022
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202205104659
https://urn.fi/URN:NBN:fi:tuni-202205104659
Kuvaus
Peer reviewed
Tiivistelmä
Gluten Friendly™ (GF) is a new gluten achieved through a physicochemical process applied to wheat kernels. The goal of this research was to assess the in vivo effects of Gluten Friendly™ bread on celiac gut mucosa and microbiota. In a double-blind placebo-controlled intervention study, 48 celiac disease (CD) patients were randomized into 3 groups to eat 100 g of bread daily, containing different doses (0; 3 g; 6 g) of GF for 12 weeks. The small-bowel morphology (VH/CrD), intraepithelial densities of CD3+, celiac serology, MUC2, CB1, gut permeability, proinflammatory cytokines, gluten in stools, symptoms, and gut microbial composition were assessed. All 48 CD subjects experienced no symptoms. K-means analysis evidenced celiac subjects clustering around unknown parameters independent of GF dosage: K1 35%; K2 30%; K3 35%. VH/CrD significantly decreased in K1 and K2. VH/CrD did not correlate with IEL increase in K2. 33-mer was not detected in 47% and 73% of patients in both K1 and K2, respectively. VH/CrD and IEL did not change significantly and strongly correlated with the absence of 33-mer in K3. Inflammation and VH/CrD decrease are strongly related with the presence of proinflammatory species at the baseline. A boost in probiotic, butyrate-producing genera, is strongly related with GF tolerance at the end of the trial. Our research suggests that a healthy and proinflammatory ecology could play a crucial role in the digestion and tolerance of the new gluten molecule in celiac subjects. However, GF can be completely digested by gut microbiota of CD subjects and shapes it toward gut homeostasis by boosting healthy butyrate-producing populations. The clinical trial registry number is NCT03137862 (https://clinicaltrials.gov).
Kokoelmat
- TUNICRIS-julkaisut [19225]