Evidence map›Paper›PMID 39809916›Full record

ArticleGeroScience2025

Analysis of sex-specific disease patterns associated with human lifespan.

Sara Cruces-Salguero, Joaquim Sol, Igor Larrañaga, Reinald Pamplona, Javier Mar, Mariona Jove, Ander Matheu

Abstract read
In one paragraph

Article in GeroScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Sara Cruces-SalgueroCellular Oncology Group, Biogipuzkoa (Biodonostia) Health Research Institute, San Sebastian, Spain.
Joaquim SolCatalan Health Institute, Lleida Research Support Unit, Fundació Institut Universitari Per a La Recerca en Atenció Primària de Salut Jordi Gol I Gurina, Lleida, Spain.
Igor LarrañagaOsakidetza Basque Health Service, Debagoiena Integrated Healthcare Organisation, Research Unit, Mondragon, Spain.
Reinald PamplonaDepartment of Experimental Medicine, University of Lleida-Lleida Biomedical Research Institute, Lleida, Spain.
Javier MarOsakidetza Basque Health Service, Debagoiena Integrated Healthcare Organisation, Research Unit, Mondragon, Spain.
Mariona JoveDepartment of Experimental Medicine, University of Lleida-Lleida Biomedical Research Institute, Lleida, Spain.
Ander MatheuCellular Oncology Group, Biogipuzkoa (Biodonostia) Health Research Institute, San Sebastian, Spain. ander.matheu@biodonostia.org.ORCID 0000-0002-1848-0781

Funding

Departament de Salut, Generalitat de Catalunya 2021SGR00990Diputación Foral de Gipuzkoa FA547/2022Instituto de Salud Carlos III PI22/01905
6 · The paper itself

Abstract

Disability and multimorbidity increase with aging and constitute a challenge for the health system. However, different individuals display different aging trajectories, and understanding the underlying relationships between lifespan and disease is fundamental for identifying the different patterns in human lifespan. A previous study explored associations between lifespan and age of onset of diseases of different organ systems, prevalence of escapers, and percentage of life free of disease (health span), comparing them between genders in Catalonian population. In this retrospective study, we analyzed a cohort of 41,063 old individuals (20,722 men, with a mean lifespan of 79 years [50-109], and 20,341 women, with a mean lifespan of 84 years [50-109]) deceased between 2014 and 2019 in Gipuzkoa (Basque Country, Spain) taken from the Basque Health Service electronic health records data lake and analyzed and contrasted the above cited characteristics. Longevity, defined by age above the mean lifespan of the population, showed a protective effect against developing diseases, with higher lifespans delaying the onset of all diseases both at single and multisystemic levels. Furthermore, individuals with the lowest and highest lifespans were the ones presenting the healthier profiles, with fewer systems altered. There were specific differences according to sex, with women exhibiting decreased mortality risk despite having greater multimorbidity and men having less multimorbidity. In addition, men reached the highest lifespans with a smaller number of comorbidities. These results define the aging trajectories of the Basque population, extend the characterization of the human aging, and provide insight into sex-specific differences in multimorbidity and survival risk.

Indexed as

LongevityAgedAged, 80 and overAgingFemaleHumansMaleMiddle AgedMultimorbidityRetrospective StudiesSex FactorsSpainHealth spanLifespansSex-specific disease patterns

Identifiers

PMID39809916
PMCPMC12181580

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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.