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  1. Artikel ; Online: Cohort profile: Celiac disease genomic, environmental, microbiome and metabolome study; a prospective longitudinal birth cohort study of children at-risk for celiac disease.

    Leonard, Maureen M / Kenyon, Victoria / Valitutti, Francesco / Pennacchio-Harrington, Rita / Piemontese, Pasqua / Francavilla, Ruggiero / Norsa, Lorenzo / Passaro, Tiziana / Crocco, Marco / Baldassarre, Mariella / Trovato, Chiara Maria / Fasano, Alessio

    PloS one

    2023  Band 18, Heft 3, Seite(n) e0282739

    Abstract: The Celiac Disease Genomic, Environmental, Microbiome and Metabolomic (CDGEMM) study is an international prospective birth cohort in children at-risk of developing celiac disease (CD). The CDGEMM study has been designed to take a multi-omic approach to ... ...

    Abstract The Celiac Disease Genomic, Environmental, Microbiome and Metabolomic (CDGEMM) study is an international prospective birth cohort in children at-risk of developing celiac disease (CD). The CDGEMM study has been designed to take a multi-omic approach to predicting CD onset in at-risk individuals. Participants are required to have a first-degree family member with biopsy diagnosed CD and must be enrolled prior to the introduction of solid food. Participation involves providing blood and stool samples longitudinally over a period of five years as well as answering questionnaires related to the participant, their family, and environment. Recruitment and data collection have been ongoing since 2014. As of 2022 we have a total of 554 participants and the average age of the cohort is 56.4 months. A total of 54 participants have developed positive antibodies for CD and 31 have confirmed CD. Approximately 80% of the 54 participants with CD have developed it by 3 years of age. To date we have identified several microbial strains, pathways, and metabolites occurring in increased abundance and detected before CD onset, which have previously been linked to autoimmune and inflammatory conditions while others occurred in decreased abundance before CD onset and are known to have anti-inflammatory effects. Our ongoing analysis includes expanding our metagenomic and metabolomic analyses, evaluating environmental risk factors linked to CD onset, and mechanistic studies investigating how alterations in the microbiome and metabolites may protect against or contribute to CD development.
    Mesh-Begriff(e) Humans ; Child ; Child, Preschool ; Celiac Disease ; Prospective Studies ; Cohort Studies ; Birth Cohort ; Metabolome ; Genomics ; Microbiota/genetics
    Sprache Englisch
    Erscheinungsdatum 2023-03-08
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0282739
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Zonulin as a Biomarker for the Development of Celiac Disease.

    DaFonte, Tracey M / Valitutti, Francesco / Kenyon, Victoria / Locascio, Joseph J / Montuori, Monica / Francavilla, Ruggiero / Passaro, Tiziana / Crocco, Marco / Norsa, Lorenzo / Piemontese, Pasqua / Baldassarre, Mariella / Fasano, Alessio / Leonard, Maureen M

    Pediatrics

    2023  Band 153, Heft 1

    Mesh-Begriff(e) Biomarkers ; Celiac Disease/blood ; Celiac Disease/diagnosis ; Humans ; Infant ; Child, Preschool ; Child ; Haptoglobins/analysis ; Male ; Female ; Anti-Bacterial Agents/administration & dosage ; Protein Precursors/blood
    Chemische Substanzen zonulin ; Biomarkers ; Haptoglobins ; Anti-Bacterial Agents ; Protein Precursors
    Sprache Englisch
    Erscheinungsdatum 2023-12-07
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 207677-9
    ISSN 1098-4275 ; 0031-4005
    ISSN (online) 1098-4275
    ISSN 0031-4005
    DOI 10.1542/peds.2023-063050
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Novel Bacteroides Vulgatus strain protects against gluten-induced break of human celiac gut epithelial homeostasis: a pre-clinical proof-of-concept study.

    Tran, Tina / Senger, Stefania / Baldassarre, Mariella / Brosnan, Rachel A / Cristofori, Fernanda / Crocco, Marco / De Santis, Stefania / Elli, Luca / Faherty, Christina S / Francavilla, Ruggero / Goodchild-Michelman, Isabella / Kenyon, Victoria A / Leonard, Maureen M / Lima, Rosiane S / Malerba, Federica / Montuori, Monica / Morelli, Annalisa / Norsa, Lorenzo / Passaro, Tiziana /
    Piemontese, Pasqua / Reed, James C / Sansotta, Naire / Valitutti, Francesco / Zomorrodi, Ali R / Fasano, Alessio

    Pediatric research

    2024  Band 95, Heft 5, Seite(n) 1254–1264

    Abstract: Background and aims: We have identified a decreased abundance of microbial species known to have a potential anti-inflammatory, protective effect in subjects that developed Celiac Disease (CeD) compared to those who did not. We aim to confirm the ... ...

    Abstract Background and aims: We have identified a decreased abundance of microbial species known to have a potential anti-inflammatory, protective effect in subjects that developed Celiac Disease (CeD) compared to those who did not. We aim to confirm the potential protective role of one of these species, namely Bacteroides vulgatus, and to mechanistically establish the effect of bacterial bioproducts on gluten-dependent changes on human gut epithelial functions.
    Methods: We identified, isolated, cultivated, and sequenced a unique novel strain (20220303-A2) of B. vulgatus found only in control subjects. Using a human gut organoid system developed from pre-celiac patients, we monitored epithelial phenotype and innate immune cytokines at baseline, after exposure to gliadin, or gliadin plus B. vulgatus cell free supernatant (CFS).
    Results: Following gliadin exposure, we observed increases in epithelial cell death, epithelial monolayer permeability, and secretion of pro-inflammatory cytokines. These effects were mitigated upon exposure to B. vulgatus 20220303-A2 CFS, which had matched phenotype gene product mutations. These protective effects were mediated by epigenetic reprogramming of the organoids treated with B. vulgatus CFS.
    Conclusions: We identified a unique strain of B. vulgatus that may exert a beneficial role by protecting CeD epithelium against a gluten-induced break of epithelial tolerance through miRNA reprogramming.
    Impact: Gut dysbiosis precedes the onset of celiac disease in genetically at-risk infants. This dysbiosis is characterized by the loss of protective bacterial strains in those children who will go on to develop celiac disease. The paper reports the mechanism by which one of these protective strains, B. vulgatus, ameliorates the gluten-induced break of gut epithelial homeostasis by epigenetically re-programming the target intestinal epithelium involving pathways controlling permeability, immune response, and cell turnover.
    Sprache Englisch
    Erscheinungsdatum 2024-01-04
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 4411-8
    ISSN 1530-0447 ; 0031-3998
    ISSN (online) 1530-0447
    ISSN 0031-3998
    DOI 10.1038/s41390-023-02960-0
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Prevalence and detection rate of celiac disease in Italy: Results of a SIGENP multicenter screening in school-age children.

    Lionetti, Elena / Pjetraj, Dorina / Gatti, Simona / Catassi, Giulia / Bellantoni, Antonella / Boffardi, Massimo / Cananzi, Mara / Cinquetti, Mauro / Francavilla, Ruggiero / Malamisura, Basilio / Montuori, Monica / Zuccotti, Gianvincenzo / Cristofori, Fernanda / Gaio, Paola / Passaro, Tiziana / Penagini, Francesca / Testa, Alessandra / Trovato, Chiara Maria / Catassi, Carlo

    Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver

    2023  Band 55, Heft 5, Seite(n) 608–613

    Abstract: Background: Celiac disease is a common lifelong disorder. Recent studies indicate that the number of clinically detected cases has increased over the last decades, however little is known about changes in the prevalence and the detection rate of celiac ... ...

    Abstract Background: Celiac disease is a common lifelong disorder. Recent studies indicate that the number of clinically detected cases has increased over the last decades, however little is known about changes in the prevalence and the detection rate of celiac disease.
    Aim: To evaluate the current prevalence and detection rate of celiac disease in Italy by a multicenter, mass screening study on a large sample of school-age children.
    Methods: children aged 5-11 years were screened at school by HLA-DQ2 and -DQ8 determination on a drop of blood in six Italian cities; total serum IgA and IgA anti-transglutaminase were determined in children showing HLA-DQ2 and/or -DQ8 positivity. Diagnosis of celiac disease was confirmed according to the European guidelines.
    Results: 5994 children were eligible, 4438 participated and 1873 showed predisposing haplotypes (42.2%, 95% CI=40.7-43.7). The overall prevalence of celiac disease was 1.65% (95% CI, 1.34%-2.01%). Only 40% of celiac children had been diagnosed prior to the school screening. Symptoms evoking celiac disease were as common in celiac children as in controls.
    Conclusion: In this multicenter study the prevalence of celiac disease in school-age Italian children was one of the highest in the world. Determination of HLA predisposing genotypes is an easy and fast first-level screening test for celiac disease. Without a mass screening strategy, 60% of celiac patients remain currently undiagnosed in Italy.
    Mesh-Begriff(e) Humans ; Child ; Celiac Disease/diagnosis ; Celiac Disease/epidemiology ; Celiac Disease/genetics ; Prevalence ; Genotype ; Italy/epidemiology ; Transglutaminases/genetics ; Immunoglobulin A
    Chemische Substanzen Transglutaminases (EC 2.3.2.13) ; Immunoglobulin A
    Sprache Englisch
    Erscheinungsdatum 2023-01-21
    Erscheinungsland Netherlands
    Dokumenttyp Multicenter Study ; Journal Article
    ZDB-ID 1459373-7
    ISSN 1878-3562 ; 1125-8055
    ISSN (online) 1878-3562
    ISSN 1125-8055
    DOI 10.1016/j.dld.2022.12.023
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Early Antibody Dynamics in a Prospective Cohort of Children At Risk of Celiac Disease.

    Valitutti, Francesco / Leonard, Maureen M / Kenyon, Victoria / Montuori, Monica / Piemontese, Pasqua / Francavilla, Ruggiero / Malamisura, Basilio / Norsa, Lorenzo / Calvi, Angela / Lionetti, Maria Elena / Baldassarre, Mariella / Trovato, Chiara Maria / Perrone, Michela / Passaro, Tiziana / Sansotta, Naire / Crocco, Marco / Morelli, Annalisa / Raguseo, Lidia Celeste / Malerba, Federica /
    Elli, Luca / Cristofori, Fernanda / Catassi, Carlo / Fasano, Alessio

    The American journal of gastroenterology

    2023  Band 118, Heft 3, Seite(n) 574–577

    Abstract: Introduction: The purpose of this study was to identify possible serum biomarkers predicting celiac disease (CD) onset in children at risk.: Methods: A subgroup from an ongoing, international prospective study of children at risk of CD was classified ...

    Abstract Introduction: The purpose of this study was to identify possible serum biomarkers predicting celiac disease (CD) onset in children at risk.
    Methods: A subgroup from an ongoing, international prospective study of children at risk of CD was classified according to an early trajectory of deamidated gliadin peptides (DGPs) immunoglobulin (Ig) G and clinical outcomes (CD, potential CD, and CD autoimmunity).
    Results: Thirty-eight of 325 children developed anti-tissue transglutaminase IgA antibody (anti-tTG IgA) seroconversion. Twenty-eight of 38 children (73.6%) showed an increase in anti-DGPs IgG before their first anti-tTG IgA seroconversion.
    Discussion: Anti-DGPs IgG can represent an early preclinical biomarker predicting CD onset in children at risk.
    Mesh-Begriff(e) Child ; Humans ; Celiac Disease ; Prospective Studies ; Gliadin ; Immunoglobulin A ; Autoantibodies ; Immunoglobulin G ; Biomarkers ; Transglutaminases
    Chemische Substanzen Gliadin (9007-90-3) ; Immunoglobulin A ; Autoantibodies ; Immunoglobulin G ; Biomarkers ; Transglutaminases (EC 2.3.2.13)
    Sprache Englisch
    Erscheinungsdatum 2023-01-20
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 390122-1
    ISSN 1572-0241 ; 0002-9270
    ISSN (online) 1572-0241
    ISSN 0002-9270
    DOI 10.14309/ajg.0000000000002192
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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