Evidence map›Paper›PMID 41188051›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2026

Survival and mortality rates in early onset dementia.

Kasper Katisko, Mikko Aaltonen, Kalle Aho, Sami Heikkinen, Ave Kivisild, Adolfina Lehtonen, Laura Leppänen, Iina Rinnankoski, Helmi Soppela, Laura Tervonen and 5 more

Abstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2026. 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

15 authors.

Kasper KatiskoInstitute of Clinical Medicine - Neurology, University of Eastern Finland, Kuopio, Finland.ORCID http://orcid.org/0000-0001-7463-1989
Mikko AaltonenLaw School, University of Eastern Finland, Joensuu, Finland.
Kalle AhoInstitute of Clinical Medicine - Neurology, University of Eastern Finland, Kuopio, Finland.
Sami HeikkinenInstitute of Clinical Medicine - Neurology, University of Eastern Finland, Kuopio, Finland.
Ave KivisildInstitute of Clinical Medicine - Neurology, University of Eastern Finland, Kuopio, Finland.
Adolfina LehtonenResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland.
Laura LeppänenResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland.
Iina RinnankoskiResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland.
Helmi SoppelaInstitute of Clinical Medicine - Neurology, University of Eastern Finland, Kuopio, Finland.
Laura TervonenResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland.
Noora Maria SuhonenNeurocenter, Neurology, Oulu University Hospital, Oulu, Finland.
Annakaisa HaapasaloA.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.
Päivi HartikainenNeuro Center - Neurology, Kuopio University Hospital, Kuopio, Finland.
Johanna KrügerResearch Unit of Clinical Medicine, Neurology, University of Oulu, Oulu, Finland.ORCID http://orcid.org/0000-0003-4346-1133
Eino SoljeInstitute of Clinical Medicine - Neurology, University of Eastern Finland, Kuopio, Finland eino.solje@uef.fi.ORCID http://orcid.org/0000-0001-9940-9524

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe socioeconomic burden of early onset dementia (EOD) defined as disease onset before the age of 65 years, is substantial due to its widespread disabling effects in relatively young individuals. While dementia is widely recognised as a major contributor to mortality among the elderly, only a limited number of studies have assessed survival and factors associated with prognosis specifically in EOD.

methodsA population-based cohort study, encompassing all incident EOD cases from two defined regions in Finland. The survival and all-cause mortality rates in EOD and its subtypes were evaluated from January 2010 to December 2021. All visits at the dementia outpatient clinics were reviewed and manually re-assessed (n=12 490), resulting in 794 validated EOD cases of Alzheimer's disease (AD), frontotemporal dementia (FTD), alpha-synucleinopathy (α-SYNU) and other EOD spectra. Region-, age- and sex-matched control groups without neurodegenerative diseases were created from nonselective general population data registers (1:10 case to control ratio, 7930 controls in total).

resultsThe median survival for EOD was 8.7 years, with the shortest survival in the FTD (6.9 years) and α-SYNU groups (7.0 years), followed by the AD group (9.9 years). Compared with controls, mortality was significantly higher in the total EOD group (HR=6.56, 95% CI=5.56-7.74, p<0.001). Among the dementia subtypes, FTD spectrum patients had the highest all-cause mortality risk compared with controls (HR=13.75, 95% CI=10.25-18.43, p<0.001). Male sex, older age, several comorbidities and lower level of education were associated with increased mortality, but these were not EOD-specific.

conclusionEOD diagnosis significantly deteriorates patients' survival, with significant variation between different diagnostic groups and in relation to patients' demographic factors.

Indexed as

DementiaAgedAge of OnsetAlzheimer DiseaseCohort StudiesFemaleFinlandFrontotemporal DementiaHumansMaleMiddle AgedSurvival RateALZHEIMER'S DISEASEEPIDEMIOLOGYFRONTOTEMPORAL DEMENTIAPrognosisVASCULAR DEMENTIA

Identifiers

PMID41188051
PMCPMC13018774

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Registered trials

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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.