# Polygenic Risks for Mood Disorders and Economic Well‐being: Study of Finnish Cohorts

**Authors:** Aaro Hazak, Johanna Liuhanen, Katri Kantojärvi, Merike Kukk, Sonja Sulkava, Tuija Jääskeläinen, Veikko Salomaa, Seppo Koskinen, Markus Perola, Tiina Paunio

PMC · DOI: 10.1155/da/1008569 · Depression and Anxiety · 2026-02-23

## TL;DR

This study explores how genetic risks for mood disorders like depression and bipolar disorder relate to economic outcomes such as employment and income in the general population.

## Contribution

The study reveals distinct and sometimes opposing genetic associations between mood disorders and economic outcomes, mediated by education.

## Key findings

- Polygenic scores for bipolar disorder are linked to higher education and knowledge work, especially in females.
- Depression polygenic scores are associated with lower education and worse economic outcomes.
- Overall mood disorder scores show no link to education but are tied to lower income and satisfaction.

## Abstract

Polygenic scores (PGS) for mood disorders provide population‐level measures of genetic liability, allowing examination of how common mental health‐related traits associate with socio‐economic outcomes. This study investigated how PGS for depression (DPGS), bipolar disorder (BDPGS) and overall mood disorders (MDPGS) predict economic outcomes in the general population.

We studied genetic and socio‐economic registry data alongside repeated cross‐sectional surveys from six Finnish cohorts (1992–2017; N = 20,121; ages 25–64), representative of various regions. Using multiple regression models, we examined associations between PGS and educational attainment, employment status, occupational type, equivalent income and economic satisfaction.

All PGS were negatively associated with employment probability, although their associations with other economic outcomes varied depending on educational attainment as a mediating factor. BDPGS was positively associated with higher educational attainment and engagement in knowledge work, particularly among females. However, BDPGS showed no significant associations with equivalent income or economic satisfaction. In contrast, DPGS was negatively associated with educational attainment and demonstrated negative associations with knowledge work, equivalent income and economic satisfaction. MDPGS, consolidating depression and bipolar disorder (BD) risks, showed no significant association with educational attainment but was negatively associated with equivalent income and economic satisfaction. Additionally, DPGS and MDPGS were linked to a lower likelihood of self‐employment among males.

The genetic predispositions for depression and BD exhibit distinct and sometimes opposing relationships with economic outcomes, mediated by education. Although effect sizes were substantial, genetic risks could still be mitigated by environmental factors, such as education and institutional frameworks, that foster economic resilience. The lack of association between MDPGS and educational level highlights the offsetting effects of its components, suggesting that focusing on specific mental disorders rather than generalisations offers clearer insights into the genetic underpinnings of brain health‐related economic disparities in the general population.

## Linked entities

- **Diseases:** depression (MONDO:0002050), bipolar disorder (MONDO:0004985)

## Full-text entities

- **Genes:** PCSK1 (proprotein convertase subtilisin/kexin type 1) [NCBI Gene 5122] {aka BMIQ12, NEC1, PC1, PC1/3, PC3, SPC3}
- **Diseases:** BD (MESH:D001714), Depression (MESH:D003866), FH (OMIM:143890), functioning (MESH:D003291), Mood Disorders (MESH:D019964), MDD (MESH:D003865), inability to work (MESH:D000073397), mental disorder (MESH:D001523), impaired (MESH:D060825)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12927894/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927894/full.md

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Source: https://tomesphere.com/paper/PMC12927894