Ferroptosis is a new non-apoptotic form of regulatory cell death, which
is characterized by intracellular iron overload and excessive
accumulation of lipid peroxides and reactive oxygen species (ROS).
Ferroptosis is closely related to intracellular iron, amino acid, and
lipid metabolism disorders. Ferroptosis is increasingly recognized as an
important process mediating the pathogenesis and progression of acute
ischemic stroke, and it can be involved in influencing acute ischemic
stroke and acute ischemic stroke risk factors atherosclerosis, atrial
fibrillation, hypertension, diabetes mellitus, and obstructive sleep
apnea. Therefore, understanding the mechanisms of ferroptosis regulation
in different diseases may have significant implications for the
preventive treatment and improvement of prognosis in patients with acute
ischemic stroke and patients with risk factors for acute ischemic
stroke. This article reviews not only the specific important mechanisms
of ferroptosis in the development of acute ischemic stroke, but also the
relevant associations between risk factors for acute ischemic stroke and
ferroptosis, and describes the current limitations and future directions
of ferroptosis in the pathogenesis of acute ischemic stroke and its risk
factors.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.