Longitudinal Modeling of Cardiometabolic Dysfunction in Patients With Type 2 Diabetes Using Item Response Theory

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 ( 1 ) primarily informed by sBP and dBP, and a metabolic latent variable ( 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 1 and −0.07 for 2 . Sex was associated with 2 , with women scoring 0.43 units lower than men on the latent variable scale. Longitudinally, 1 and 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 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.

Authors

Institutions

Publication Details

Journal
CPT Pharmacometrics & Systems Pharmacology
Published
2026-10-15
DOI
https://doi.org/10.1002/psp4.70349
Primary Topic
Diabetes, Cardiovascular Risks, and Lipoproteins
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Longitudinal Modeling of Cardiometabolic Dysfunction in Patients With Type 2 Diabetes Using Item Response Theory

Gustaf J. Wellhagen, Hanna Kunina, Maria C. Kjellsson, Chengli Yu
CPT Pharmacometrics & Systems Pharmacology
Diabetes, Cardiovascular Risks, and Lipoproteins
article

Longitudinal Modeling of Cardiometabolic Dysfunction in Patients With Type 2 Diabetes Using Item Response Theory

Gustaf J. Wellhagen, Hanna Kunina, Maria C. Kjellsson, Chengli Yu
article en

Abstract

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 ( 1 ) primarily informed by sBP and dBP, and a metabolic latent variable ( 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 1 and −0.07 for 2 . Sex was associated with 2 , with women scoring 0.43 units lower than men on the latent variable scale. Longitudinally, 1 and 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 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.

CPT Pharmacometrics & Systems PharmacologyVol. 15(11)
Uppsala University (SE), Inserm (FR), Université Paris Cité (FR), Université Sorbonne Paris Nord (FR), Infection, Anti-microbiens, Modélisation, Evolution (FR)
Vetenskapsrådet, Uppsala Universitet
Good health and well-being
Openalex Percentile: Top 12%
Diabetes, Cardiovascular Risks, and Lipoproteins
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.