Etiologies underlying subtypes of long-standing type 2 diabetes

PLoS One. 2024 May 28;19(5):e0304036. doi: 10.1371/journal.pone.0304036. eCollection 2024.

Abstract

Background: Attempts to subtype, type 2 diabetes (T2D) have mostly focused on newly diagnosed European patients. In this study, our aim was to subtype T2D in a non-white Emirati ethnic population with long-standing disease, using unsupervised soft clustering, based on etiological determinants.

Methods: The Auto Cluster model in the IBM SPSS Modeler was used to cluster data from 348 Emirati patients with long-standing T2D. Five predictor variables (fasting blood glucose (FBG), fasting serum insulin (FSI), body mass index (BMI), hemoglobin A1c (HbA1c) and age at diagnosis) were used to determine the appropriate number of clusters and their clinical characteristics. Multinomial logistic regression was used to validate clustering results.

Results: Five clusters were identified; the first four matched Ahlqvist et al subgroups: severe insulin-resistant diabetes (SIRD), severe insulin-deficient diabetes (SIDD), mild age-related diabetes (MARD), mild obesity-related diabetes (MOD), and a fifth new subtype of mild early onset diabetes (MEOD). The Modeler algorithm allows for soft assignments, in which a data point can be assigned to multiple clusters with different probabilities. There were 151 patients (43%) with membership in cluster peaks with no overlap. The remaining 197 patients (57%) showed extensive overlap between clusters at the base of distributions.

Conclusions: Despite the complex picture of long-standing T2D with comorbidities and complications, our study demonstrates the feasibility of identifying subtypes and their underlying causes. While clustering provides valuable insights into the architecture of T2D subtypes, its application to individual patient management would remain limited due to overlapping characteristics. Therefore, integrating simplified, personalized metabolic profiles with clustering holds greater promise for guiding clinical decisions than subtyping alone.

MeSH terms

  • Adult
  • Aged
  • Blood Glucose / analysis
  • Body Mass Index
  • Cluster Analysis
  • Diabetes Mellitus, Type 2* / blood
  • Diabetes Mellitus, Type 2* / complications
  • Female
  • Glycated Hemoglobin / analysis
  • Humans
  • Insulin / blood
  • Insulin Resistance
  • Male
  • Middle Aged
  • United Arab Emirates / epidemiology

Substances

  • Blood Glucose
  • Glycated Hemoglobin
  • Insulin

Grants and funding

This study was supported by an internal grant [MBRU-CM-RG2019-06] awarded on May 29, 2019, by the College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, UAE. Further support was obtained from Sandooq Al Watan, Grant Number: SWARD-F22-013 awarded on August 30, 2022. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.