Evidence map›Paper›PMID 38517484›Full record

ArticleDiabetologia2024

The INNODIA Type 1 Diabetes Natural History Study: a European cohort of newly diagnosed children, adolescents and adults.

M Loredana Marcovecchio, A Emile J Hendriks, Carl Delfin, Tadej Battelino, Thomas Danne, Mark L Evans, Jesper Johannesen, Simranjeet Kaur, Mikael Knip, Lut Overbergh and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
13.2field-weighted citation impact, top 1% of its field
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

23 citing papers in PubMed, 24 citations in OpenAlex.

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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

17 authors at 9 institutions in 7 countries.

M Loredana MarcovecchioDepartment of Paediatrics, University of Cambridge, Cambridge, UK. mlm45@medschl.cam.ac.uk.ORCID http://orcid.org/0000-0002-4415-316X
A Emile J HendriksDepartment of Paediatrics, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-0795-1832
Carl DelfinDepartment of Pharmacometrics, Novo Nordisk A/S, Søborg, Denmark.ORCID http://orcid.org/0000-0003-4827-7650
Tadej BattelinoDepartment of Endocrinology, Diabetes and Metabolism, University Children's Hospital, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Thomas DanneCentre for Paediatric Endocrinology, Diabetology, and Clinical Research, Auf Der Bult Children's Hospital, Hannover, Germany.ORCID http://orcid.org/0000-0002-8424-3944
Mark L EvansWellcome MRC Institute of Metabolic Science, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-8122-8987
Jesper JohannesenTranslational Type 1 Diabetes Research, Clinical Research, Steno Diabetes Center Copenhagen, Herlev, Denmark.ORCID http://orcid.org/0000-0003-2772-2567
Simranjeet KaurTranslational Type 1 Diabetes Research, Clinical Research, Steno Diabetes Center Copenhagen, Herlev, Denmark.
Mikael KnipResearch Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0003-0474-0033
Lut OverberghClinical and Experimental Endocrinology, Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0001-7126-356X
Flemming PociotTranslational Type 1 Diabetes Research, Clinical Research, Steno Diabetes Center Copenhagen, Herlev, Denmark.
John A ToddCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-2740-8148
Bart Van der SchuerenClinical and Experimental Endocrinology, Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.
Linda S WickerCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-7771-0324
Mark PeakmanImmunology & Inflammation Research Therapeutic Area, Sanofi, MA, USA.
Chantal MathieuClinical and Experimental Endocrinology, Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-4055-5233
INNODIA consortium
KU Leuven · BESteno Diabetes Centers · DKUniversity of Cambridge · GBCentre for Human Genetics · GBKinderkrankenhaus auf der Bult · DENovo Nordisk (Denmark) · DKSanofi (United States) · USUniversity of Helsinki · FIUniversity of Ljubljana · SI

Funding

Innovative Medicines Initiative 115797
6 · The paper itself

Abstract

aims/hypothesisType 1 diabetes is an heterogenous condition. Characterising factors explaining differences in an individual's clinical course and treatment response will have important clinical and research implications. Our aim was to explore type 1 diabetes heterogeneity, as assessed by clinical characteristics, autoantibodies, beta cell function and glycaemic outcomes, during the first 12 months from diagnosis, and how it relates to age at diagnosis.

methodsData were collected from the large INNODIA cohort of individuals (aged 1.0-45.0 years) newly diagnosed with type 1 diabetes, followed 3 monthly, to assess clinical characteristics, C-peptide, HbA

resultsThe study population included 649 individuals (57.3% male; age 12.1±8.3 years), 96.9% of whom were positive for one or more diabetes-related antibodies. Baseline (IQR) fasting C-peptide was 242.0 (139.0-382.0) pmol/l (AUC 749.3 [466.2-1106.1] pmol/l × min), with levels increasing with age (p<0.001). Over time, C-peptide remained lower in participants aged <10 years but it declined in all age groups. In parallel, glucose levels progressively increased. Lower baseline fasting C-peptide, BMI SD score and presence of diabetic ketoacidosis at diagnosis were associated with lower stimulated C-peptide over time. HbA CONCLUSIONS/

interpretationIn this large cohort with newly diagnosed type 1 diabetes, we identified age-related differences in clinical and biochemical variables. Of note, C-peptide was lower in younger children but there were no main age differences in its rate of decline.

Indexed as

AutoantibodiesC-PeptideDiabetes Mellitus, Type 1Glycated HemoglobinAdolescentAdultBlood GlucoseChildChild, PreschoolCohort StudiesEuropeFemaleHumansInfantInsulin-Secreting CellsMaleAutoantibodiesBlood GlucoseC-PeptideGlycated HemoglobinAgeBeta cell functionC-peptidePreventionSubgroupsTreatmentType 1 diabetes

Identifiers

PMID38517484
PMCPMC11058619
OpenAlexW4393085378

What OpenQuestion holds

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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.