Evidence map›Paper›PMID 41847870›Full record

ArticleEuropean journal of public health2026

Paths to multimorbidity: a longitudinal perspective on disease accumulation in Catalonia, Spain.

Sahar M A Ahmed, Iñaki Permanyer, Aïda Solé-Auró

Abstract read
In one paragraph

Article in European journal of public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Sahar M A AhmedCentre for Demographic Studies (CED), Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID 0000-0002-3406-1720
Iñaki PermanyerCentre for Demographic Studies (CED), Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID 0000-0002-7051-5144
Aïda Solé-AuróDemoSoc Research Group, Department of Political and Social Sciences, Universitat Pompeu Fabra, Barcelona, Spain.ORCID 0000-0003-3726-2509

Funding

Generación de Conocimiento" Project LONGHEALTH PID2021-128892OB-I00
6 · The paper itself

Abstract

With increasing life expectancy, multimorbidity represents a growing global challenge, affecting quality of life. We analyzed electronic health records of individuals aged 45-74 from Catalonia, Spain (2007-2021), who were healthy at the end of 2007. We use sequence and cluster analysis to describe and categorize monthly disease accumulation patterns, from healthy to one or multiple conditions or death, involving four disease groups with the highest global morbidity and mortality burdens. We further investigate the association between identified clusters and sociodemographic factors and the association of cluster membership with healthcare utilization. Approximately 36% of individuals remained healthy throughout the study, while the remainder transitioned to single or multiple morbidity and/or died. A higher number of conditions in a given month increased transition probability, with metabolic and hypertensive conditions being the most common entry points. We identified nine disease accumulation trajectories linked to sociodemographic characteristics: Women were more likely to be in clusters involving neurodegenerative conditions and men in those involving cardiovascular and cancer conditions. Higher-income individuals were more likely to be in lower morbidity clusters, except the cancer multimorbidity cluster. Healthcare utilization was elevated in all clusters relative to the healthy group, with notably higher emergency use in cardiovascular clusters and more hospital admissions in cancer-related clusters. The study shows that disease accumulation follows identifiable patterns linked to sociodemographic factors and underscores the propagative nature of multimorbidity. Further, healthcare utilization is shaped more by condition type than by the number, highlighting the need for targeted health services.

Indexed as

MultimorbidityAgedChronic DiseaseCluster AnalysisElectronic Health RecordsFemaleHumansLongitudinal StudiesMaleMiddle AgedPatient Acceptance of Health CareSociodemographic FactorsSocioeconomic FactorsSpain

Identifiers

PMID41847870
PMCPMC13017133

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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.