Nemzeti Kardiovaszkuláris Laboratórium(RRF-2.3.1-21-2022-00003) Támogató: NKFIH
(135784) Támogató: NKFIH
(101004093/EUniWell/EAC-A02- 2019/EAC-A02-2019-1)
Szakterületek:
Orvos- és egészségtudomány
Cerebral microhemorrhages (CMHs, also known as cerebral microbleeds) are a critical
but frequently underestimated aspect of cerebral small vessel disease (CSVD), bearing
substantial clinical consequences. Detectable through sensitive neuroimaging techniques,
CMHs reveal an extensive pathological landscape. They are prevalent in the aging population,
with multiple CMHs often being observed in a given individual. CMHs are closely associated
with accelerated cognitive decline and are increasingly recognized as key contributors
to the pathogenesis of vascular cognitive impairment and dementia (VCID) and Alzheimer's
disease (AD). This review paper delves into the hypothesis that atherosclerosis, a
prevalent age-related large vessel disease, extends its pathological influence into
the cerebral microcirculation, thereby contributing to the development and progression
of CSVD, with a specific focus on CMHs. We explore the concept of vascular aging as
a continuum, bridging macrovascular pathologies like atherosclerosis with microvascular
abnormalities characteristic of CSVD. We posit that the same risk factors precipitating
accelerated aging in large vessels (i.e., atherogenesis), primarily through oxidative
stress and inflammatory pathways, similarly instigate accelerated microvascular aging.
Accelerated microvascular aging leads to increased microvascular fragility, which
in turn predisposes to the formation of CMHs. The presence of hypertension and amyloid
pathology further intensifies this process. We comprehensively overview the current
body of evidence supporting this interconnected vascular hypothesis. Our review includes
an examination of epidemiological data, which provides insights into the prevalence
and impact of CMHs in the context of atherosclerosis and CSVD. Furthermore, we explore
the shared mechanisms between large vessel aging, atherogenesis, microvascular aging,
and CSVD, particularly focusing on how these intertwined processes contribute to the
genesis of CMHs. By highlighting the role of vascular aging in the pathophysiology
of CMHs, this review seeks to enhance the understanding of CSVD and its links to systemic
vascular disorders. Our aim is to provide insights that could inform future therapeutic
approaches and research directions in the realm of neurovascular health.