Marital status and genetic liability independently predict coronary heart disease incidence

Karri Silventoinen*, Hannu Lahtinen, Kaarina Korhonen, George Davey Smith, Samuli Ripatti, Tim T Morris, Pekka Martikainen

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

1 Citation (Scopus)
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Abstract

Aims:
Married individuals have a lower coronary heart disease (CHD) risk than non-married, but the mechanisms behind this are not fully understood. We analyzed whether genetic liability to CHD may affect these associations.
Methods:

Marital status, a polygenic score of CHD (PGS-CHD), and other risk factors for CHD were measured from 35,444 participants (53% female) in Finnish population-based surveys conducted between 1992 and 2012. During the register-based follow-up until 2020, there were 2439 fatal and non-fatal incident CHD cases. The data were analyzed using linear and Cox regression models.
Results:

Divorced and cohabiting men and women had a higher genetic risk of CHD than married individuals, but the difference was very small (0.023–0.058 standard deviation of PGS-CHD, p-values 0.011–0.429). Both marital status and PGS-CHD were associated with CHD incidence, but the associations were largely independent. Adjusting for behavioral and metabolic risk factors for CHD explained part of these associations (11–20%). No interaction was found between marital status and PGS-CHD for CHD incidence.

Conclusions:
We showed minor differences between the marital status categories in PGS-CHD and demonstrated that marital status and genetic liability predicted CHD incidence largely independently. This emphasizes the need to measure multiple risk factors when predicting CHD risk.
Original languageEnglish
JournalScandinavian Journal of Public Health
Early online date7 Sept 2022
DOIs
Publication statusE-pub ahead of print - 7 Sept 2022

Bibliographical note

Funding Information:
The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: Pekka Martikainen was supported by the Academy of Finland [grant numbers 308247 and 345219], the European Research Council under the European Union’s Horizon 2020 research and innovation program [grant number 101019329]. Hannu Lahtinen was supported by the Academy of Finland [grant number 345219]. George Davey Smith and Tim Morris were supported by the UK Medical Research Council [grant number MC_UU_00011/1].

Publisher Copyright:
© Author(s) 2022.

Research Groups and Themes

  • Bristol Population Health Science Institute

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