Abstract

The kidney and the brain, as high-flow end organs relying on autoregulatory mechanisms, have unique anatomic and physiological hemodynamic properties. Similarly, the two organs share a common pattern of microvascular dysfunction as a result of aging and exposure to vascular risk factors (e.g., hypertension, diabetes and smoking) and therefore progress in parallel into a systemic condition known as small vessel disease (SVD). Many epidemiological studies have shown that even mild renal dysfunction is robustly associated with acute and chronic forms of cerebrovascular disease. Beyond ischemic SVD, kidney impairment increases the risk of acute cerebrovascular events related to different underlying pathologies, notably large artery stroke and intracerebral hemorrhage. Other chronic cerebral manifestations of SVD are variably associated with kidney disease. Observational data have suggested the hypothesis that kidney function influences cerebrovascular disease independently and adjunctively to the effect of known vascular risk factors, which affect both renal and cerebral microvasculature. In addition to confirming this independent association, recent large-scale human genetic studies have contributed to disentangling potentially causal associations from shared genetic predisposition and resolving the uncertainty around the direction of causality between kidney and cerebrovascular disease. Accelerated atherosclerosis, impaired cerebral autoregulation, remodeling of the cerebral vasculature, chronic inflammation and endothelial dysfunction can be proposed to explain the additive mechanisms through which renal dysfunction leads to cerebral SVD and other cerebrovascular events. Genetic epidemiology also can help identify new pathological pathways which wire kidney dysfunction and cerebral vascular pathology together. The need for identifying additional pathological mechanisms underlying kidney and cerebrovascular disease is attested to by the limited effect of current therapeutic options in preventing cerebrovascular disease in patients with kidney impairment.

Highlights

  • Chronic kidney disease (CKD) affects around 10% of the general population globally and has an increasing prevalence, posing a major burden on public health systems [1]

  • We provide an overview of recent genetic findings that support these associations, suggest possible new pathological pathways combining kidney and brain disease, and summarize data that may help to disentangle correlations from causal associations between the two organs

  • This evidence suggests that CKD increases the risk for developing atrial fibrillation (AF) as well as the risk of thromboembolic events in the context of AF, both of which increase the risk for cardioembolic stroke

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Summary

INTRODUCTION

Chronic kidney disease (CKD) affects around 10% of the general population globally and has an increasing prevalence, posing a major burden on public health systems [1]. The mechanisms underlying associations between CKD and cerebrovascular disease have been underinvestigated [3]. In this narrative review, we highlight work exploring the intersection of chronic kidney disease and cerebrovascular disease. We discuss pathophysiological features connecting vascular damage in the two organs and summarize epidemiological data supporting the effect of CKD on acute and chronic manifestations of cerebrovascular disease. We provide an overview of recent genetic findings that support these associations, suggest possible new pathological pathways combining kidney and brain disease, and summarize data that may help to disentangle correlations from causal associations between the two organs. We discuss therapeutic options for patients suffering from chronic kidney disease, among whom cerebrovascular disease treatment is under recognized and insufficiently treated

HEMODYNAMIC PROPERTIES OF THE KIDNEY AND BRAIN VASCULATURE
Cardioembolic Stroke
Large Artery Stroke
Small Vessel Stroke
Intracerebral Hemorrhage
THERAPEUTIC OPTIONS
Findings
FUTURE DIRECTIONS
Full Text
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