Association of endometriosis with cardiovascular disease: Genetic aspects (Review)

Cardiovascular disease (CVD) comprises a broad spectrum of pathological conditions that affect the heart or blood vessels, including sequelae that arise from damaged vasculature in other organs of the body, such as the brain, kidneys or eyes. Atherosclerosis is a chronic inflammatory disease of the arterial intima and is the primary cause of coronary artery disease, peripheral vascular disease, heart attack, stroke and renal pathology. It represents a leading cause of mortality worldwide and the loss of human productivity that is marked by an altered immune response. Endometriosis is a heritable, heterogeneous, common gynecological condition influenced by multiple genetic, epigenetic and environmental factors, affecting up to 10% of the female population of childbearing age, causing pain and infertility; it is characterized by the ectopic growth of endometrial tissue outside the uterine cavity. Of note, epidemiological data obtained thus far have suggested a link between endometriosis and the risk of developing CVD. The similarities observed in specific molecular and cellular pathways of endometriosis and CVD may be partially explained by a shared genetic background. The present review presents and discusses the shared genetic factors which have been reported to be associated with the development of both disorders.

Automated summary

Cardiovascular disease refers to a range of pathological conditions impacting the heart or blood vessels, including sequelae arising from damaged blood vessels in other organs. Atherosclerosis, a chronic inflammatory disease, is the main cause of coronary artery disease, peripheral vascular disease, heart attack, stroke, and renal pathology. Endometriosis, a common gynecological condition, is characterized by ectopic growth of endometrial tissue outside the uterus, affecting up to 10% of women of childbearing age. Recent epidemiological data suggests a link between endometriosis and the risk of developing cardiovascular disease. Shared genetic factors may explain the observed similarities in molecular and cellular pathways of both disorders.