Evidence map›Paper›PMID 38625583›Full record

ArticleDiabetologia2024

Trajectories of clinical characteristics, complications and treatment choices in data-driven subgroups of type 2 diabetes.

Xinyu Li, Louise A Donnelly, Roderick C Slieker, Joline W J Beulens, Leen M 't Hart, Petra J M Elders, Ewan R Pearson, Anoukh van Giessen, Jose Leal, Talitha Feenstra

Abstract 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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

10 authors.

Xinyu LiGroningen Research Institute of Pharmacy, Faculty of Science and Engineering, University of Groningen, Groningen, the Netherlands. li.xinyu@rug.nl.ORCID http://orcid.org/0000-0002-0225-6937
Louise A DonnellyDivision of Population Health and Genomics, Ninewells Hospital and School of Medicine, University of Dundee, Dundee, UK.
Roderick C SliekerDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.ORCID http://orcid.org/0000-0003-0961-9152
Joline W J BeulensDepartment of Epidemiology and Data Science, Amsterdam UMC, Location Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-4181-0937
Leen M 't HartDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.ORCID http://orcid.org/0000-0003-4401-2938
Petra J M EldersAmsterdam Public Health, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-5907-7219
Ewan R PearsonDivision of Population Health and Genomics, Ninewells Hospital and School of Medicine, University of Dundee, Dundee, UK.ORCID http://orcid.org/0000-0001-9237-8585
Anoukh van GiessenNational Institute of Public Health and the Environment, Bilthoven, the Netherlands.ORCID http://orcid.org/0000-0003-4521-9500
Jose LealHealth Economics Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-7870-6730
Talitha FeenstraGroningen Research Institute of Pharmacy, Faculty of Science and Engineering, University of Groningen, Groningen, the Netherlands.ORCID http://orcid.org/0000-0002-5788-0454

Funding

Horizon 2020 Framework Programme 115881
6 · The paper itself

Abstract

aims/hypothesisThis study aimed to explore the added value of subgroups that categorise individuals with type 2 diabetes by k-means clustering for two primary care registries (the Netherlands and Scotland), inspired by Ahlqvist's novel diabetes subgroups and previously analysed by Slieker et al.

methodsWe used two Dutch and Scottish diabetes cohorts (N=3054 and 6145; median follow-up=11.2 and 12.3 years, respectively) and defined five subgroups by k-means clustering with age at baseline, BMI, HbA

resultsSubgroups' risk factors were significantly different, and these differences remained generally consistent over follow-up. Among all subgroups, individuals with severe insulin resistance faced a significantly higher risk of myocardial infarction both before (HR 1.65; 95% CI 1.40, 1.94) and after adjusting for age effect (HR 1.72; 95% CI 1.46, 2.02) compared with mild diabetes with high HDL-cholesterol. Individuals with severe insulin-deficient diabetes were most intensively treated, with more than 25% prescribed insulin at 10 years of diagnosis. For severe insulin-deficient diabetes relative to mild diabetes, the relative risks for using insulin relative to no common treatment would be expected to increase by a factor of 3.07 (95% CI 2.73, 3.44), holding other factors constant. Clustering indicators were better predictors of progression variation relative to subgroups, but prediction accuracy may improve after combining both. Clusters were consistent over 8 years with an accuracy ranging from 59% to 72%. CONCLUSIONS/

interpretationData-driven subgroup allocations were generally consistent over follow-up and captured significant differences in risk factor trajectories, medication patterns and complication risks. Subgroups serve better as a complement rather than as a basis for compressing clustering indicators.

Indexed as

Diabetes Mellitus, Type 2AdultAgedBody Mass IndexCholesterol, HDLCluster AnalysisC-PeptideDisease ProgressionFemaleGlycated HemoglobinHumansInsulin ResistanceMaleMiddle AgedNetherlandsRegistriesCholesterol, HDLC-PeptideGlycated HemoglobinData-driven subgroupsLongitudinal analysisReal-world dataRoutine careStratification of diabetes

Identifiers

PMID38625583
PMCPMC11153261

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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.