Evidence map›Paper›PMID 36636731›Full record

ArticleClinical epidemiology2023

Data-Driven Identification of Long-Term Glycemia Clusters and Their Individualized Predictors in Finnish Patients with Type 2 Diabetes.

Piia Lavikainen, Gunjan Chandra, Pekka Siirtola, Satu Tamminen, Anusha T Ihalapathirana, Juha Röning, Tiina Laatikainen, Janne Martikainen

Open access · goldAbstract read
In one paragraph

Article in Clinical epidemiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Time Trends of Body Mass Index and its Impact on Glycemic Control Among Finnish Patients with Type 2 Diabetes.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2025
    Article
  5. 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

8 authors at 2 institutions in 1 country.

Piia Lavikainen *School of Pharmacy, University of Eastern Finland, Kuopio, Finland.ORCID 0000-0003-3560-8860
Gunjan Chandra *Biomimetics and Intelligent Systems Group, Faculty of ITEE, University of Oulu, Oulu, Finland.ORCID 0000-0002-0051-0268
Pekka SiirtolaBiomimetics and Intelligent Systems Group, Faculty of ITEE, University of Oulu, Oulu, Finland.ORCID 0000-0002-5995-5421
Satu TamminenBiomimetics and Intelligent Systems Group, Faculty of ITEE, University of Oulu, Oulu, Finland.ORCID 0000-0002-5215-6889
Anusha T IhalapathiranaBiomimetics and Intelligent Systems Group, Faculty of ITEE, University of Oulu, Oulu, Finland.ORCID 0000-0002-3276-2056
Juha RöningBiomimetics and Intelligent Systems Group, Faculty of ITEE, University of Oulu, Oulu, Finland.ORCID 0000-0001-9993-8602
Tiina LaatikainenJoint Municipal Authority for North Karelia Social and Health Services (Siun Sote), Joensuu, Finland.ORCID 0000-0002-6614-4782
Janne MartikainenSchool of Pharmacy, University of Eastern Finland, Kuopio, Finland.ORCID 0000-0003-0855-3921
University of Oulu · FIUniversity of Eastern Finland · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To gain an understanding of the heterogeneous group of type 2 diabetes (T2D) patients, we aimed to identify patients with the homogenous long-term HbA1c trajectories and to predict the trajectory membership for each patient using explainable machine learning methods and different clinical-, treatment-, and socio-economic-related predictors. Patients and Methods: Electronic health records data covering primary and specialized healthcare on 9631 patients having T2D diagnosis were extracted from the North Karelia region, Finland. Six-year HbA1c trajectories were examined with growth mixture models. Linear discriminant analysis and neural networks were applied to predict the trajectory membership individually. Results: Three HbA1c trajectories were distinguished over six years: "stable, adequate" (86.5%), "improving, but inadequate" (7.3%), and "fluctuating, inadequate" (6.2%) glycemic control. Prior glucose levels, duration of T2D, use of insulin only, use of insulin together with some oral antidiabetic medications, and use of only metformin were the most important predictors for the long-term treatment balance. The prediction model had a balanced accuracy of 85% and a receiving operating characteristic area under the curve of 91%, indicating high performance. Moreover, the results based on SHAP (Shapley additive explanations) values show that it is possible to explain the outcomes of machine learning methods at the population and individual levels. Conclusion: Heterogeneity in long-term glycemic control can be predicted with confidence by utilizing information from previous HbA1c levels, fasting plasma glucose, duration of T2D, and use of antidiabetic medications. In future, the expected development of HbA1c could be predicted based on the patient's unique risk factors offering a practical tool for clinicians to support treatment planning.

Indexed as

clusterHbA1cmachine learningSHAPtype 2 diabetes

Identifiers

PMID36636731
PMCPMC9829833
OpenAlexW4313588675

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.