Evidence map›Paper›PMID 39379808›Full record

ArticleBMC geriatrics2024

Heterogeneity in the association between social support and mental distress in old-age retirees - a computational approach using longitudinal cohort data.

Jere Lahelma, Eero Lahelma, Mikko Laaksonen, Susan Kuivalainen, Mikko Koivisto, Tea Lallukka

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Article in BMC geriatrics, 2024. 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jere LahelmaDepartment of Computer Science, University of Helsinki, Helsinki, Finland. jere.lahelma@iki.fi.ORCID http://orcid.org/0009-0006-8881-1562
Eero LahelmaDepartment of Public Health, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0002-1064-1333
Mikko LaaksonenFinnish Centre for Pensions, Helsinki, Finland.ORCID http://orcid.org/0000-0002-6979-9872
Susan KuivalainenFinnish Centre for Pensions, Helsinki, Finland.ORCID http://orcid.org/0000-0001-9621-3710
Mikko KoivistoDepartment of Computer Science, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0001-9662-3605
Tea LallukkaDepartment of Public Health, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0003-3841-3129

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMental distress among retirees and older people is a severe public health challenge, and information on new risk groups is needed. This study aims to identify subgroups of old-age retirees with varying associations between low social support and mental distress by applying model-based recursive partitioning (MOB).

methodsWe used the Helsinki Health Study follow-up survey data of old-age retired former municipal sector employees of the City of Helsinki, Finland. Phase 1 data were collected in 2000-2002, when all participants were employed, Phase 2 in 2007, Phase 3 in 2012, Phase 4 in 2017, and Phase 5 in 2022 (n = 4,466, 81% women). Social support and covariates were measured at each Phase 1-5 and the outcome, mental distress (Depression Anxiety Stress Scales [DASS-21]) was measured at a single occasion, during Phase 5. The three subscales and the common factor of general distress were analysed separately. An approach rooted in computational statistics was used to investigate risk factor heterogeneity in the association of low social support and mental distress. MOB combines decision trees with regression analysis to identify subgroups with the most significant heterogeneity among risk factors.

resultsMedian (IQR) general distress score from DASS-21 was 5.7 (3.0, 9.0), while Social Support Questionnaire number-score (SSQN) was 1.5 (1.15, 2.05). The primary effect modifier for the association between social support and general distress was education (p < 0.001). Those with high education had a different association of low social support and general distress than those with low or medium education. Additionally, the subgroup with low and medium education had a significant effect modification for age (p = 0.01). For the association between low social support and depressive symptoms, the moderating effect of education was dependent on gender, as men with medium-high education had the weakest association, while for women with medium-high education the association was strongest.

conclusionsOur results suggest that stratification by sociodemographic variables is justifiable when investigating risk factors of mental distress in old-age retirees. The incongruent association of low social support and depressive symptoms in men with medium-high education compared to women with medium-high education is a promising target for confirmatory research.

Indexed as

Psychological DistressRetirementSocial SupportAgedAged, 80 and overCohort StudiesFemaleFinlandFollow-Up StudiesHumansLongitudinal StudiesMaleMiddle AgedRisk FactorsStress, PsychologicalDASS-21Decision treeLongitudinal studyMental distressModel-based recursive partitioningOld-age retireeSocial supportSubgroup analysis

Identifiers

PMID39379808
PMCPMC11460196

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