Evidence map›Paper›PMID 40214701›Full record

ArticleDiabetes care2025

Subphenotype-Dependent Benefits of Bariatric Surgery for Individuals at Risk for Type 2 Diabetes.

Leontine Sandforth, Violeta Raverdy, Arvid Sandforth, Pierre Bauvin, Estelle Chatelain, Helene Verkindt, Geltrude Mingrone, Caterina Guidone, Ornella Verrastro, Karin Zhou and 22 more

Abstract read
In one paragraph

Article in Diabetes care, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors.

Leontine SandforthInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.
Violeta RaverdyINSERM, CHU Lille, Institut Pasteur de Lille, UMR 1190 Translational Research for Diabetes, European Genomic Institute for Diabetes, University Lille, Lille, France.ORCID 0000-0001-5754-2028
Arvid SandforthInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.
Pierre BauvinINSERM, CHU Lille, Institut Pasteur de Lille, U1190-EGID, University Lille, Lille, France.
Estelle ChatelainCNRS, INSERM, CHU Lille, Institut Pasteur de Lille, US 41-UAR 2014-PLBS, University Lille, Lille, France.
Helene VerkindtINSERM, CHU Lille, Institut Pasteur de Lille, UMR 1190 Translational Research for Diabetes, European Genomic Institute for Diabetes, University Lille, Lille, France.
Geltrude MingroneDepartment of Internal Medicine, Catholic University of the Sacred Heart, Rome, Italy.ORCID 0000-0003-2021-528X
Caterina GuidoneFondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Ornella VerrastroDepartment of Internal Medicine, Catholic University of the Sacred Heart, Rome, Italy.
Karin ZhouInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.
Rami ArchidDepartment of General, Visceral, and Transplant Surgery, University Hospital of Tübingen, Tübingen, Germany.
André MihaljevicDepartment of General, Visceral, and Transplant Surgery, University Hospital of Tübingen, Tübingen, Germany.
Robert CaiazzoINSERM, CHU Lille, Institut Pasteur de Lille, UMR 1190 Translational Research for Diabetes, European Genomic Institute for Diabetes, University Lille, Lille, France.
Gregory BaudINSERM, CHU Lille, Institut Pasteur de Lille, UMR 1190 Translational Research for Diabetes, European Genomic Institute for Diabetes, University Lille, Lille, France.
Camille MarciniakINSERM, CHU Lille, Institut Pasteur de Lille, UMR 1190 Translational Research for Diabetes, European Genomic Institute for Diabetes, University Lille, Lille, France.
Mikael ChetbounINSERM, CHU Lille, Institut Pasteur de Lille, UMR 1190 Translational Research for Diabetes, European Genomic Institute for Diabetes, University Lille, Lille, France.
Marlene GanslmeierInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.
Vitória Minelli FaiaoInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.
Martin HeniInstitute for Clinical Chemistry and Pathobiochemistry, Department for Diagnostic Laboratory Medicine, University Hospital of Tübingen, Tübingen, Germany.ORCID 0000-0002-8462-3832
Louise FritscheInstitute for Diabetes Research and Metabolic Diseases (IDM), Helmholtz Center Munich, University of Tübingen, Tübingen, Germany.
Anja MollerInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.
Konstantinos KantartzisInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.
Andreas PeterInstitute for Diabetes Research and Metabolic Diseases (IDM), Helmholtz Center Munich, University of Tübingen, Tübingen, Germany.
Rainer LehmannInstitute for Diabetes Research and Metabolic Diseases (IDM), Helmholtz Center Munich, University of Tübingen, Tübingen, Germany.
Robert WagnerGerman Center for Diabetes Research (DZD), Neuherberg, Germany.
Katsiaryna PrystupaGerman Center for Diabetes Research (DZD), Neuherberg, Germany.
Andreas FritscheInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.ORCID 0000-0002-4987-1961
Norbert StefanInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.ORCID 0000-0002-2186-9595
Hubert PreisslInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.ORCID 0000-0002-8859-4661
Andreas L BirkenfeldInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.
Reiner Jumpertz von SchwartzenbergInternal Medicine IV, Endocrinology, Diabetology and Nephrology, University Hospital of Tübingen, Tübingen, Germany.ORCID 0000-0002-5544-099X
François PattouINSERM, CHU Lille, Institut Pasteur de Lille, UMR 1190 Translational Research for Diabetes, European Genomic Institute for Diabetes, University Lille, Lille, France.

Funding

Agence National de la Recherche ANR-10-LABX-46Agence National de la Recherche Precinash-16-RHUS-0006Cluster of Excellence Controlling Microbes to Fight Infections 03.007EFPIAEU Horizon 2020 research and innovation programEuropean Commission FEDER 12003944Federal Ministry of Education and ResearchFondation Coeur et Arteres FCA R15112EEFondation Francophone pour la Recherche sur le Diabète FFRD-2015German Center for Diabetes Research (DZD) 01GI0925German Research AssociationHelmholtz MunichHelmholtz SocietyHelmholtz Young Investigator Group VH-NG-1619Innovative Medicines Initiative 2 Joint Undertaking 875534Innovative Medicines Initiative Joint Undertaking 115317Innovative Medicines Initiative Joint Undertaking 115881Juvenile Diabetes Research FoundationObesity Action CoalitionSeventh Framework Programme FP7/2007-2013The European Federation of Pharmaceutical Industries and Associations (EFPIA)Type 1 Diabetes Exchange
6 · The paper itself

Abstract

objectiveBariatric surgery is an effective treatment option for individuals with obesity and type 2 diabetes (T2D). However, whether outcomes in subtypes of individuals at risk for T2D and/or comorbidities (Tübingen Clusters) differ, is unknown. Of these, cluster 5 (C5) and cluster 6 (C6) are high-risk clusters for developing T2D and/or comorbidities, while cluster 4 (C4) is a low-risk cluster. We investigated bariatric surgery outcomes, hypothesizing that high-risk clusters benefit most due to great potential for metabolic improvement. RESEARCH DESIGN AND

methodsWe allocated participants without T2D but at risk for T2D, defined by elevated BMI, to the Tübingen Clusters. Participants had normal glucose regulation or prediabetes according to American Diabetes Association criteria. Two cohorts underwent bariatric surgery: a discovery (Lille, France) and a replication cohort (Rome, Italy). A control cohort (Tübingen, Germany) received behavioral modification counseling. Main outcomes included alteration of glucose regulation parameters and prediabetes remission.

resultsIn the discovery cohort, 15.0% of participants (n = 121) were allocated to C4, 22.3% (n = 180) to C5, and 62.4% (n = 503) to C6. Relative body weight loss was similar among all clusters; however, reduction of insulin resistance and improvement of β-cell function were strongest in C5. Prediabetes remission rate was lowest in low-risk C4 and highest in high-risk C5. Individuals from high-risk clusters changed to low-risk clusters in both bariatric surgery cohorts but not in the control cohort.

conclusionsParticipants in C5 had the highest benefit from bariatric surgery in terms of improvement in insulin resistance, β-cell function, and prediabetes remission. This novel classification might help identify individuals who will benefit specifically from bariatric surgery.

Indexed as

Bariatric SurgeryDiabetes Mellitus, Type 2AdultBody Mass IndexFemaleHumansMaleMiddle AgedObesityPrediabetic StateWeight Loss

Identifiers

PMID40214701
PMCPMC12094208

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