Role of Plasma Proteins in the Association Between Socioeconomic Status and Cardiovascular Disease Events: Results From Trans-Omics for Precision Medicine Cohorts.

J Am Heart AssocOct 23, 2026 (epub)

LáShauntá M Glover, Madeline G Gillman, Michael D Green et al.

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In 30 seconds

This meta-analysis examined socioeconomic status (SES), plasma proteins, and incident coronary heart disease (CHD) and stroke in participants from three cohorts. SES was scored using education, income, and employment; associations with events and 1,270 proteins were assessed, followed by mediation analyses. Higher SES scores were associated with lower CHD risk (hazard ratio [HR], 0.74 [95% CI, 0.63-0.87]) and lower stroke risk (HR, 0.81 [95% CI, 0.66-1.00]). Of 233 proteins associated with SES after multiple-testing correction, 21 showed a significant indirect effect on the SES–CHD association.

Key findings

  • Higher SES scores were associated with lower CHD risk (HR, 0.74 [95% CI, 0.63-0.87]).
  • Higher SES scores were associated with lower stroke risk (HR, 0.81 [95% CI, 0.66-1.00]).
  • After multiple-testing correction, 233 proteins were associated with SES; 21 had a significant indirect effect on the SES–CHD association.
  • Proteins were not tested as mediators of stroke because the SES–stroke association was not statistically significant.

Why it matters

The findings connect a social determinant of health with measurable plasma-protein patterns and CHD events across multiple cohorts. The mediation results offer candidate biological pathways for further study, while underscoring that proteomic associations do not establish a causal mechanism. Considering social conditions alongside biological risk factors may help frame research into cardiovascular health disparities.

What to keep in mind

The cohort-based analyses and regression mediation approach identify associations and statistical indirect effects, not causal pathways. The SES–stroke association was not statistically significant, so mediation was not assessed for stroke.

Source

Published in J Am Heart Assoc. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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