Reference intervals reimagined with IRIS for earlier detection and better disease monitoring

Reference intervals (RIs) are the universal established methodology for interpreting numerical clinical data by comparing individual test results to population-based benchmarks. The quality of these RIs significantly influences individual-level decision-making. This study aims to answer the question on how we can effectively leverage an individual's personal data in conjunction with that of their peers to compute individual reference intervals (IRIs) for key clinical parameters relevant to disease detection and progression. We describe the IRIS workflow that includes prior data processing and data quality check procedures. The computation of IRI involves the test results of multiple "healthy" data points from the same subject(s) and also from the peers. The model adjusts for covariates like sex and age, enhancing accuracy. The workflow demonstrated the potential utility of IRI in clinical and omics data from two longitudinal studies. For healthy populations, IRIs showed diagnostic value in chronic diseases, while in diseased cohorts, they enabled effective disease monitoring. An integrated application IRIS has been developed, incorporating all described steps in an easy-to-use tool in research and/or clinical practice. The IRI may assist in (1) early detection of disease transition in chronic diseases and (2) monitoring personal disease progression. It facilitates the detection of small deviations in clinical measurements, either using standard clinical biochemistry test results or omics data. With adequate data infrastructure, the IRIS workflow can be integrated into clinical practice by embedding personalised biomarker baselines into AI-enabled decision support systems Such integration provides a complementary layer that enhances the sensitivity and specificity of clinical alerts and risk stratification. Ultimately, this approach has the potential to transform personalised disease diagnosis, management, and patient outcomes.

Authors

Institutions

Publication Details

Journal
Scientific Reports
Published
2026-05-22
DOI
https://doi.org/10.1038/s41598-026-52500-z
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
0.00

Funders

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

Reference intervals reimagined with IRIS for earlier detection and better disease monitoring

Murih Pusparum, Wendy P. J. den Elzen, Gökhan Ertaylan, Olivier Thas
Scientific Reports
Genetic Associations and Epidemiology
article

Reference intervals reimagined with IRIS for earlier detection and better disease monitoring

Murih Pusparum, Wendy P. J. den Elzen, Gökhan Ertaylan, Olivier Thas
article en

Abstract

Reference intervals (RIs) are the universal established methodology for interpreting numerical clinical data by comparing individual test results to population-based benchmarks. The quality of these RIs significantly influences individual-level decision-making. This study aims to answer the question on how we can effectively leverage an individual's personal data in conjunction with that of their peers to compute individual reference intervals (IRIs) for key clinical parameters relevant to disease detection and progression. We describe the IRIS workflow that includes prior data processing and data quality check procedures. The computation of IRI involves the test results of multiple "healthy" data points from the same subject(s) and also from the peers. The model adjusts for covariates like sex and age, enhancing accuracy. The workflow demonstrated the potential utility of IRI in clinical and omics data from two longitudinal studies. For healthy populations, IRIs showed diagnostic value in chronic diseases, while in diseased cohorts, they enabled effective disease monitoring. An integrated application IRIS has been developed, incorporating all described steps in an easy-to-use tool in research and/or clinical practice. The IRI may assist in (1) early detection of disease transition in chronic diseases and (2) monitoring personal disease progression. It facilitates the detection of small deviations in clinical measurements, either using standard clinical biochemistry test results or omics data. With adequate data infrastructure, the IRIS workflow can be integrated into clinical practice by embedding personalised biomarker baselines into AI-enabled decision support systems Such integration provides a complementary layer that enhances the sensitivity and specificity of clinical alerts and risk stratification. Ultimately, this approach has the potential to transform personalised disease diagnosis, management, and patient outcomes.

Scientific Reports
HOGENT University of Applied Sciences and Arts (BE), University of Wollongong (AU), Wollongong Hospital (AU), Ghent University (BE), Amsterdam Neuroscience (NL), Public Health Service of Amsterdam (NL), Flemish Institute for Technological Research (BE), Hasselt University (BE), University of Amsterdam (NL)
Fonds Wetenschappelijk Onderzoek
Industry, innovation and infrastructure
Openalex Percentile: Top 5%
Genetic Associations and Epidemiology
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.