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  3. Chronic kidney disease and neurological disorders: are uraemic toxins the missing piece of the puzzle?
 

Chronic kidney disease and neurological disorders: are uraemic toxins the missing piece of the puzzle?

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BORIS DOI
10.48350/161519
Date of Publication
December 28, 2021
Publication Type
Article
Contributor
Liabeuf, Sophie
Pepin, Marion
Franssen, Casper F M
Viggiano, Davide
Carriazo, Sol
Gansevoort, Ron T
Gesualdo, Loreto
Hafez, Gaye
Malyszko, Jolanta
Mayer, Christopher
Nitsch, Dorothea
Ortiz, Alberto
Pešić, Vesna
Wiecek, Andrzej
Massy, Ziad A
Series
Nephrology, dialysis, transplantation
ISSN or ISBN (if monograph)
0931-0509
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/ndt/gfab223
PubMed ID
34718753
Uncontrolled Keywords

CKD cardiovascular in...

Description
Chronic kidney disease (CKD) perturbs the crosstalk with others organs, with the interaction between the kidneys and the heart having been studied most intensively. However, a growing body of data indicates that there is an association between kidney dysfunction and disorders of the central nervous system. In epidemiological studies, CKD is associated with a high prevalence of neurological complications, such as cerebrovascular disorders, movement disorders, cognitive impairment and depression. Along with traditional cardiovascular risk factors (such as diabetes, inflammation, hypertension and dyslipidaemia), non-traditional risk factors related to kidney damage (such as uraemic toxins) may predispose patients with CKD to neurological disorders. There is increasing evidence to show that uraemic toxins, for example indoxyl sulphate, have a neurotoxic effect. A better understanding of factors responsible for the elevated prevalence of neurological disorders among patients with CKD might facilitate the development of novel treatments. Here, we review (i) the potential clinical impact of CKD on cerebrovascular and neurological complications, (ii) the mechanisms underlying the uraemic toxins' putative action (based on pre-clinical and clinical research) and (iii) the potential impact of these findings on patient care.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/57742
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gfab223.pdftextAdobe PDF2.88 MBAttribution-NonCommercial (CC BY-NC 4.0)publishedOpen
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