Evidence map›Paper›PMID 41919194›Full record

ArticleBMJ public health2026

Younger adults are not alright, but older adults are? Examining mortality disparities among the children of migrants aged 15-44 and 45-64 in Sweden, 1990-2023: a total-population cohort study.

Matthew Wallace

Abstract read
In one paragraph

Article in BMJ public health, 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

1 author.

Matthew WallaceCentre for Research on Inclusive Society, University of Salford, Salford, UK.ORCID https://orcid.org/0000-0002-8318-7952

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Younger working age children of migrants have higher mortality risks relative to younger working age non-migrants in Europe. Yet, these are unique ages of mortality where the absolute risk of death is low and driven by external causes (ie, accidents, injuries and suicides). It remains unclear whether this higher mortality risk presents among older working age children of migrants-ages at which the absolute risk of death begins to increase exponentially and becomes dictated by chronic morbidities. We aim to fill this gap. Methods: We fit survival models on Swedish total population register data using an extended, competing risks approach. We investigate all-cause and mortality from natural causes and external causes, drugs and alcohol among the children of migrants, migrants and non-migrants aged 15-44 and 45-64 from 1990 to 2023. We report both HRs and regression-standardised cumulative probabilities of death. Results: Younger working age children of migrants from an array of origins exhibit higher external, drug and alcohol mortality relative to non-migrants that drives their higher all-cause mortality risk. Older working age children of migrants from multiple origins also present with a higher risk of external, drug and alcohol mortality, but only exhibit comparable all-cause mortality to non-migrants, owing to their similar to lower mortality from natural causes. Disparities in socioeconomic background largely attenuate these risks. A diverse range of younger and older working age migrants exhibit lower all-cause, natural, and external, drug and alcohol mortality than non-migrants do. Conclusions: Interventions should be made to address the elevated avoidable and preventable external, drugs and alcohol mortality that presents among both older and younger working age children of migrants. Doing so will generate reductions in their all-cause mortality risk.

Indexed as

Community HealthDemographyEpidemiologyPublic HealthSociodemographic Factors

Identifiers

PMID41919194
PMCPMC13034282

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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.