Longitudinal Modeling of Cardiometabolic Dysfunction in Patients With Type 2 Diabetes Using Item Response Theory
- 1Pharmacometrics Research Group, Department of Pharmacy Uppsala University Uppsala Sweden
- 2Université Paris Cité and Université Sorbonne Paris Nord, Inserm, IAME Paris France
Abstract
Cardiometabolic dysfunction in patients with type 2 diabetes (T2D) is reflected by multiple risk factors and cannot be fully characterized by any single biomarker. Item response theory (IRT) provides a framework for integrating observed risk factors into latent measures of underlying cardiometabolic dysfunction. Routinely collected measurements of systolic and diastolic blood pressure (sBP and dBP), high‐ and low‐density lipoproteins (HDL and LDL), triglycerides (TG), HbA1c, and BMI from 33,396 adults newly diagnosed with T2D were analyzed, with biomarkers categorized into four ordered levels. A two‐dimensional model described the data better than a unidimensional, identifying a blood pressure‐related latent variable (ψ 1) primarily informed by sBP and dBP, and a metabolic latent variable (ψ 2) primarily informed by HDL, HbA1c, TG, and BMI, while LDL showed low discrimination on both dimensions. At baseline, age at T2D diagnosis was associated with both latent variables, with opposing effects of 0.02 for ψ 1 and −0.07 for ψ 2. Sex was associated with ψ 2, with women scoring 0.43 units lower than men on the latent variable scale. Longitudinally, ψ 1 and ψ
2 showed post‐baseline offsets of −0.10 and −0.22, respectively, followed by separately estimated annual slopes of approximately −0.03 year−1. HbA1c exhibited a distinct trajectory with an initial post‐baseline improvement followed by deterioration, requiring an item‐specific slope of 0.45 year−1. The ψ 2 contributed modest additional information for all‐cause mortality beyond age and sex. This framework integrated routinely collected biomarkers into continuous latent measures of multidimensional cardiometabolic dysfunction while accounting for differences in their contributions to the latent dimensions.
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BibTeX
@article{yu2026longitudinal,
title = {{Longitudinal Modeling of Cardiometabolic Dysfunction in Patients With Type 2 Diabetes Using Item Response Theory}},
author = {Chengli Yu and Hanna Kunina and Gustaf J. Wellhagen and Maria C. Kjellsson},
journal = {CPT: Pharmacometrics \& Systems Pharmacology},
year = {2026},
month = oct,
doi = {10.1002/psp4.70349},
url = {https://doi.org/10.1002/psp4.70349},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Longitudinal Modeling of Cardiometabolic Dysfunction in Patients With Type 2 Diabetes Using Item Response Theory
AU - Chengli Yu
AU - Hanna Kunina
AU - Gustaf J. Wellhagen
AU - Maria C. Kjellsson
PY - 2026
DA - 2026/10/15
JO - CPT: Pharmacometrics & Systems Pharmacology
DO - 10.1002/psp4.70349
UR - https://doi.org/10.1002/psp4.70349
AB - Cardiometabolic dysfunction in patients with type 2 diabetes (T2D) is reflected by multiple risk factors and cannot be fully characterized by any single biomarker. Item response theory (IRT) provides a framework for integrating observed risk factors into latent measures of underlying cardiometabolic dysfunction. Routinely collected measurements of systolic and diastolic blood pressure (sBP and dBP), high‐ and low‐density lipoproteins (HDL and LDL), triglycerides (TG), HbA1c, and BMI from 33,396 adults newly diagnosed with T2D were analyzed, with biomarkers categorized into four ordered levels. A two‐dimensional model described the data better than a unidimensional, identifying a blood pressure‐related latent variable (ψ 1) primarily informed by sBP and dBP, and a metabolic latent variable (ψ 2) primarily informed by HDL, HbA1c, TG, and BMI, while LDL showed low discrimination on both dimensions. At baseline, age at T2D diagnosis was associated with both latent variables, with opposing effects of 0.02 for ψ 1 and −0.07 for ψ 2. Sex was associated with ψ 2, with women scoring 0.43 units lower than men on the latent variable scale. Longitudinally, ψ 1 and ψ 2 showed post‐baseline offsets of −0.10 and −0.22, respectively, followed by separately estimated annual slopes of approximately −0.03 year−1. HbA1c exhibited a distinct trajectory with an initial post‐baseline improvement followed by deterioration, requiring an item‐specific slope of 0.45 year−1. The ψ 2 contributed modest additional information for all‐cause mortality beyond age and sex. This framework integrated routinely collected biomarkers into continuous latent measures of multidimensional cardiometabolic dysfunction while accounting for differences in their contributions to the latent dimensions.
SN - 2163-8306
ER -