Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry.
Rebeca LorcaAndrea AparicioMaría SalgadoRut Alvarez-VelascoIsaac PascualJuan Gómez de OñaDaniel Vazquez-CotoClaudia Garcia-LagoLucinda Velázquez-CuervoElías Cuesta-LlavonaPablo AvanzasEliecer CotoPublished in: Journal of clinical medicine (2023)
Cardiovascular disease (CVD) is the leading cause of death worldwide, with coronary artery disease (CAD) being one of its main manifestations. Both environmental and genetic factors are widely known to be related to CAD, such as smoking, diabetes mellitus, dyslipidemia, and a family history of CAD. However, there is still a lack of information about other risk factors, especially those related to genetic mutations. Sex represents a classic CAD risk factor, as men are more likely to suffer CAD, but there is lack of evidence with regard to sex-specific genetic factors. We evaluated the Y chromosome haplogroups in a cohort of young Spanish male patients who suffered from STEMI. In this cohort, haplogroup R was significantly more frequent in STEMI patients.
Keyphrases
- coronary artery disease
- percutaneous coronary intervention
- copy number
- mitochondrial dna
- risk factors
- cardiovascular events
- cardiovascular disease
- coronary artery bypass grafting
- st segment elevation myocardial infarction
- genome wide
- st elevation myocardial infarction
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- middle aged
- prognostic factors
- type diabetes
- heart failure
- adipose tissue
- dna methylation
- risk assessment
- gene expression
- acute coronary syndrome
- metabolic syndrome
- insulin resistance
- patient reported
- human health
- climate change
- weight loss