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Exploring Sex Differences in Pain Manifestation of Coronary Artery Disease through Mendelian Randomization
Ruben Methorst1, Monique R M Jongbloed1,2, Raymond Noordam3
1Department of Anatomy and Embryology, Leiden University Medical Centre, 2300 RC Leiden, The Netherlands.
Insights
Coronary artery disease (CAD) pain differs in men and women. Genetic predisposition for CAD increases chest pain risk in both sexes, but women also show higher risks for back and neck/shoulder pain.
Area of Science:
- Cardiovascular Genetics
- Pain Medicine
- Epidemiology
Background:
- Coronary artery disease (CAD) pain presentation varies between sexes.
- Understanding these differences is crucial for accurate diagnosis and treatment.
Purpose of the Study:
- To investigate sex-specific pain manifestations associated with CAD using Mendelian randomization.
- To explore genetic links between CAD and various pain types in men and women.
Main Methods:
- Utilized sex-stratified genome-wide association study data from UK Biobank (>450,000 participants).
- Employed two-sample Mendelian randomization and sensitivity analyses.
- Examined associations between genetically influenced CAD and self-reported/clinically diagnosed pain (chest, neck/shoulder, back, facial).
Main Results:
- Genetically influenced CAD associated with increased chest pain risk in both men and women.
- Women with genetically influenced CAD showed a higher risk for back pain (OR: 1.35) and neck/shoulder pain (OR: 1.22).
- Sensitivity analyses ruled out significant directional pleiotropy.
Conclusions:
- Genetic predisposition to CAD reveals distinct pain patterns in men and women.
- While chest pain is common in both, women exhibit increased risk for back and neck/shoulder pain, aligning with atypical angina symptoms.
- Findings support sex-specific considerations in CAD pain assessment.
Abstract:
Pain manifestation following coronary artery disease (CAD) disease differs between men and women. Here, we aimed to provide evidence favoring possible differences in pain manifestation between men and women following CAD using Mendelian randomization (MR). We used summary-level data from sex-stratified genome-wide association studies on CAD and self-reported and clinically diagnosed chest, neck and shoulder, back, and facial pain using data from the UK Biobank cohort (N > 450,000) followed by two-sample MR (sensitivity) analyses. We identified 32 and 19 independent genetic variants associated with CAD for men and women, respectively, as instrumental variables. Genetically influenced CAD was associated with a higher risk of self-reported chest pain in both men (OR: 1.27, CI: 1.2-1.33) and women (OR: 1.44, CI: 1.20-1.73), with similar results for clinically diagnosed chest pain (men OR: 1.22, CI: 1.17-1.26; women OR: 1.31, CI: 1.18-1.46). In addition, in women only, genetically influenced CAD was associated with a higher risk of back pain (OR: 1.35, CI: 1.03-1.66) and neck and shoulder pain (OR: 1.22, CI: 0.91-1.63) (p-values for interaction with men: 0.030 and 0.041, respectively). Sensitivity analysis did not indicate the results were biased by directional pleiotropy. We found evidence, based on genetic predisposition for CAD, for different pain manifestations of CAD in men and women. While CAD was associated with chest pain in both sexes, we only found evidence for a higher risk of back pain and neck and shoulder pain in women, supporting common notions that women may present more often with uncharacteristic anginal symptoms.
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