Relative contributions of diabetes and chronic kidney disease to neuropathy development in diabetic nephropathy patients.


Journal

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
ISSN: 1872-8952
Titre abrégé: Clin Neurophysiol
Pays: Netherlands
ID NLM: 100883319

Informations de publication

Date de publication:
11 2019
Historique:
received: 12 04 2019
revised: 04 07 2019
accepted: 12 08 2019
pubmed: 22 9 2019
medline: 9 6 2020
entrez: 22 9 2019
Statut: ppublish

Résumé

Chronic kidney disease (CKD) caused by diabetes is known as diabetic kidney disease (DKD). The present study aimed to examine the underlying mechanisms of axonal dysfunction and features of neuropathy in DKD compared to CKD and type 2 diabetes (T2DM) alone. Patients with DKD (n = 30), CKD (n = 28) or T2DM (n = 40) and healthy controls (n = 41) underwent nerve excitability assessments to examine axonal function. Neuropathy was assessed using the Total Neuropathy Score. A validated mathematical model of human axons was utilised to provide an indication of the underlying causes of nerve pathophysiology. Total neuropathy score was significantly higher in patients with DKD compared to those with either CKD or T2DM (p < 0.05). In DKD, nerve excitability measures (S2 accommodation and superexcitability, p < 0.05) were more severely affected compared to both CKD and T2DM and worsened with increasing serum K Patients with DKD manifested a more severe neuropathy phenotype and shared features of nerve dysfunction to that of CKD. The CKD, and not diabetes component, appears to underlie axonal pathophysiology in DKD.

Identifiants

pubmed: 31541986
pii: S1388-2457(19)31191-5
doi: 10.1016/j.clinph.2019.08.005
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2088-2095

Informations de copyright

Copyright © 2019 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.

Auteurs

Tushar Issar (T)

Prince of Wales Clinical School, UNSW Sydney, NSW 2031, Australia.

Ria Arnold (R)

School of Medical Sciences, UNSW Sydney, NSW 2052, Australia.

Natalie C G Kwai (NCG)

Prince of Wales Clinical School, UNSW Sydney, NSW 2031, Australia; Department of Exercise Physiology, UNSW Sydney, NSW 2052, Australia.

Susan Walker (S)

Prince of Wales Clinical School, UNSW Sydney, NSW 2031, Australia.

Aimy Yan (A)

Prince of Wales Clinical School, UNSW Sydney, NSW 2031, Australia.

Adeniyi A Borire (AA)

Prince of Wales Clinical School, UNSW Sydney, NSW 2031, Australia.

Ann M Poynten (AM)

Department of Endocrinology, Prince of Wales Hospital, Sydney, NSW 2031, Australia.

Bruce A Pussell (BA)

Department of Nephrology, Prince of Wales Hospital, Sydney, NSW 2031, Australia.

Zoltan H Endre (ZH)

Department of Nephrology, Prince of Wales Hospital, Sydney, NSW 2031, Australia.

Matthew C Kiernan (MC)

Brain and Mind Centre, University of Sydney and Royal Prince Alfred Hospital, Sydney, NSW 2050, Australia.

Arun V Krishnan (AV)

Prince of Wales Clinical School, UNSW Sydney, NSW 2031, Australia. Electronic address: arun.krishnan@unsw.edu.au.

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Classifications MeSH