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The DOI matches its Crossref record; 55 of the 55 references it cites were found in a registry or an index.

Faecal microbiota transplantation halts progression of human new-onset type 1 diabetes in a randomised controlled trial

Open access
de Groot, Pieter, Nikolic, Tanja, Pellegrini, Silvia, Sordi, Valeria, Imangaliyev, Sultan, Rampanelli, Elena, Hanssen, Nordin, Attaye, Ilias, Bakker, Guido, Duinkerken, Gaby, Joosten, Antoinette, Prodan, Andrei, Levin, Evgeni, Levels, Han, Potter van Loon, Bartjan, van Bon, Arianne, Brouwer, Catherina, van Dam, Sytze, Simsek, Suat, van Raalte, Daniel, Stam, Frank, Gerdes, Victor, Hoogma, Roel, Diekman, Martin, Gerding, Martin, Rustemeijer, Cees, de Bakker, Bernadette, Hoekstra, Joost, Zwinderman, Aeilko, Bergman, Jacques, Holleman, Frits, Piemonti, Lorenzo, De Vos, Willem, Roep, Bart, Nieuwdorp, Max·2021·Gut

Abstract

Objective: Type 1 diabetes (T1D) is characterised by islet autoimmunity and beta cell destruction. A gut microbiota–immunological interplay is involved in the pathophysiology of T1D. We studied microbiota-mediated effects on disease progression in patients with type 1 diabetes using faecal microbiota transplantation (FMT). Design: Patients with recent-onset (<6 weeks) T1D (18–30 years of age) were randomised into two groups to receive three autologous or allogenic (healthy donor) FMTs over a period of 4 months. Our primary endpoint was preservation of stimulated C peptide release assessed by mixed-meal tests during 12 months. Secondary outcome parameters were changes in glycaemic control, fasting plasma metabolites, T cell autoimmunity, small intestinal gene expression profile and intestinal microbiota composition. Results: Stimulated C peptide levels were significantly preserved in the autologous FMT group (n=10 subjects) compared with healthy donor FMT group (n=10 subjects) at 12 months. Small intestinal Prevotella was inversely related to residual beta cell function (r=−0.55, p=0.02), whereas plasma metabolites 1-arachidonoyl-GPC and 1-myristoyl-2-arachidonoyl-GPC levels linearly correlated with residual beta cell preservation (rho=0.56, p=0.01 and rho=0.46, p=0.042, respectively). Finally, baseline CD4 +CXCR3+T cell counts, levels of small intestinal Desulfovibrio piger and CCL22 and CCL5 gene expression in duodenal biopsies predicted preserved beta cell function following FMT irrespective of donor characteristics. Conclusion: FMT halts decline in endogenous insulin production in recently diagnosed patients with T1D in 12 months after disease onset. Several microbiota-derived plasma metabolites and bacterial strains were linked to preserved residual beta cell function. This study provides insight into the role of the intestinal gut microbiome in T1D. Trial registration number: NTR3697.

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Metadata

Authors
de Groot, P., Nikolic, T., Pellegrini, S., Sordi, V., Imangaliyev, S., Rampanelli, E., Hanssen, N., Attaye, I., Bakker, G., Duinkerken, G., Joosten, A., Prodan, A., Levin, E., Levels, H., Potter van Loon, B., van Bon, A., Brouwer, C., van Dam, S., Simsek, S., van Raalte, D., Stam, F., Gerdes, V., Hoogma, R., Diekman, M., Gerding, M., Rustemeijer, C., de Bakker, B., Hoekstra, J., Zwinderman, A., Bergman, J., Holleman, F., Piemonti, L., De Vos, W., Roep, B., & Nieuwdorp, M.
Venue
Gut
Publisher
BMJ
Published
2020-10-26
Volume
70
Issue
1
Pages
92-105
ISSN
  • 0017-5749 (ISSN-L)
  • 1468-3288
OpenAlex
W3094273450
Cited by
316
References
55
FWCI
11.41
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Faecal microbiota transplantation halts progression of human new-onset type 1 diabetes in a randomised controlled trial. https://app.cochat.ai/papers/10.1136/gutjnl-2020-322630
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de Groot, P., Nikolic, T., Pellegrini, S., Sordi, V., Imangaliyev, S., Rampanelli, E., Hanssen, N., Attaye, I., Bakker, G., Duinkerken, G., Joosten, A., Prodan, A., Levin, E., Levels, H., Potter van Loon, B., van Bon, A., Brouwer, C., van Dam, S., Simsek, S., . . . Nieuwdorp, M. (2021). Faecal microbiota transplantation halts progression of human new-onset type 1 diabetes in a randomised controlled trial. Gut. https://doi.org/10.1136/gutjnl-2020-322630

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