Key result
Biologic sex influences blood-based cardiovascular biomarkers across central pathways including myocardial stretch, inflammation, adipose tissue metabolism, and fibrosis.
Why the study?
Sex-based differences in cardiovascular disease are well established, but mechanistic understanding and translation to clinical applications remain limited.
Understanding sexual dimorphism in cardiovascular biomarkers can enhance insights into disease pathogenesis and potentially translate to improved individualized care.
May support sex-adjusted biomarker thresholds clinically; extends dimorphism evidence but leaves outcome benefits open to prospective trials.
Sex-based differences in cardiovascular disease presentation, diagnosis, and response to therapies are well established, but mechanistic understanding and translation to clinical applications are limited. Blood-based biomarkers have become an important tool for interrogating biologic pathways. Understanding sexual dimorphism in the relationship between biomarkers and cardiovascular disease will enhance our insights into cardiovascular disease pathogenesis in women, with potential to translate to improved individualized care for men and women with or at risk for cardiovascular disease. In this review, we examine how biologic sex associates with differential levels of blood-based biomarkers and influences the effect of biomarkers on disease outcomes. We further summarize key differences in blood-based cardiovascular biomarkers along central biologic pathways, including myocardial stretch/injury, inflammation, adipose tissue metabolism, and fibrosis pathways in men versus women. Finally, we present recommendations for leveraging our current knowledge of sex differences in blood-based biomarkers for future research and clinical innovation.
No takes yet. Share an insight, caveat, or question.
A 2022 study conducted a review in Cardiovascular disease. Biologic sex and blood-based cardiovascular biomarkers was evaluated. Biologic sex influences blood-based cardiovascular biomarkers across central pathways including myocardial stretch, inflammation, adipose tissue metabolism, and fibrosis.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: