Evidence map›Paper›PMID 42254809›Full record

ArticleThe Lancet regional health. Europe2026

Metabolic Trajectories Before Diabetes Diagnosis Across Subgroups: A Pooled Analysis of Prospective European Cohort Studies.

Liisa Hakaste, Mette K Andersen, Lars Ängquist, Haifa Maalmi, Jagadish Vangipurapu, Türküler Cakmak, Anna Möllsten, Björn Tavelin, Mikko Lehtovirta, Most Champa Begum and 14 more

Erratum issuedAbstract read
In one paragraph

Article in The Lancet regional health. Europe, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Liisa HakasteFolkhälsan Research Center, Helsinki, Finland.
Mette K AndersenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Lars ÄngquistNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Haifa MaalmiInstitute for Clinical Diabetology, German Diabetes Center (DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Jagadish VangipurapuInstitute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Finland.
Türküler CakmakBiostatistics and Data analysis core facility (BIOS), Faculty of Medicine, University of Bergen, Bergen, Norway.
Anna MöllstenDepartment of Public Health and Clinical Medicine, Family Medicine, Umeå University, Umeå, Sweden.
Björn TavelinClinical Research Unit, Cancer Centrum, Region Vasterbotten, Umea University Hospital, Umea, Sweden.
Mikko LehtovirtaInstitute for Molecular Medicine Finland and Research Program of Clinical and Molecular Medicine, University of Helsinki, Helsinki, Finland.
Most Champa BegumDepartment of Clinical Science, Mohn Center for Diabetes Research, University of Bergen, Bergen, Norway.
Rashmi B PrasadDepartment of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Annette PetersInstitute of Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Barbara ThorandInstitute of Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Allan LinnebergCenter for Clinical Research and Prevention, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Copenhagen, Denmark.
Markku LaaksoInstitute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Finland.
Olov RolandssonDepartment of Public Health and Clinical Medicine, Family Medicine, Umeå University, Umeå, Sweden.
Bjørn Olav ÅsvoldHUNT Center for Molecular and Clinical Epidemiology, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
Valeriya LyssenkoDepartment of Clinical Science, Mohn Center for Diabetes Research, University of Bergen, Bergen, Norway.
Peter M NilssonDepartment of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Christian HerderInstitute for Clinical Diabetology, German Diabetes Center (DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Michael RodenInstitute for Clinical Diabetology, German Diabetes Center (DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Torben HansenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Emma AhlqvistDepartment of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Tiinamaija TuomiFolkhälsan Research Center, Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Adult-onset diabetes comprises subgroups differing in pathophysiology, clinical presentation, and risk of comorbidities. We investigated early phenotypic differences between individuals who later developed diabetes, stratified by subgroup at diabetes diagnosis. Methods: We conducted a pooled analysis of nine prospective European cohorts with 3309 individuals developing incident diabetes and 13,963 age- and sex-matched controls without diabetes. Cases were assigned to previously defined cluster-based subgroups: severe autoimmune (SAID), insulin-deficient (SIDD), or insulin-resistant diabetes (SIRD), and moderate obesity- (MOD) or age-related diabetes (MARD). Clinical and metabolic characteristics were retroactively assessed for three time periods (>12, 6-12, 1-6 years) before diagnosis. Findings: Despite similarly high body mass index (BMI) in MOD and SIRD at diagnosis, MOD differed from controls already >12 years before diagnosis (31% higher than controls), while BMI increased progressively in SIRD (from 14% to 25% higher than controls). Compared to controls in period 1-6 years, age-, sex-, and BMI-adjusted insulin-glucose ratio was higher in SIRD, MOD and MARD at fasting (88%, 45% and 14%, respectively) and 120 min (110%, 70%, 26%) during an oral glucose tolerance test (p < 0.0001 for all), and the first-phase insulin-glucose ratio was higher in SIRD (23% [6; 43] p = 0.0072) but lower in SIDD (-30% [-37; -22], p < 0.0001) and MARD (-29% [-34; -24], p < 0.0001). The autoimmune subgroup SAID also exhibited features of metabolic syndrome. Despite differences in HOMA2-B and HbA1c at diagnosis, insulin and glucose levels did not differ significantly between the SIDD and MARD subgroups 1-6 years earlier suggesting a rapid deterioration in glycemic control in SIDD around diagnosis. Interpretation: Subgroups of diabetes display different trajectories of insulin resistance, insulin deficiency, and features of the metabolic syndrome before diagnosis. Funding: ERC, local governments, private foundations, University of Helsinki, and Research councils of Finland and Sweden.

Indexed as

ClassificationDiabetesDiabetes stratificationDiabetes subgroupDiabetes subtypePrecision medicine

Identifiers

PMID42254809
PMCPMC13233758

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.