Chronic kidney disease and peripheral nerve function in the Health, Aging and Body Composition Study.


Journal

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
ISSN: 1460-2385
Titre abrégé: Nephrol Dial Transplant
Pays: England
ID NLM: 8706402

Informations de publication

Date de publication:
01 04 2019
Historique:
received: 01 01 2018
pubmed: 15 5 2018
medline: 7 1 2020
entrez: 15 5 2018
Statut: ppublish

Résumé

Chronic kidney disease (CKD) is associated with poor mobility. Peripheral nerve function alterations play a significant role in low mobility. We tested the hypothesis that early CKD is associated with altered sensory, motor and autonomic nerve function. Participants in the Health, Aging and Body Composition cohort who had kidney function measures in Year 3 (1999-2000) and nerve function measurements at Year 4 (2000-01) were analyzed (n = 2290). Sensory (vibration threshold, monofilament insensitivity to light and standard touch), motor [compound motor action potentials (CMAPs), nerve conduction velocities (NCVs)] and autonomic (heart rate response and recovery after a 400-m walk test) nerve function as well as participant characteristics were compared across cystatin C- and creatinine-based estimated glomerular filtration rate categorized as ≤60 (CKD) or >60 mL/min/1.73 m2 (non-CKD). The association between CKD and nerve function was examined with logistic regression adjusted for covariates. Participants with CKD (n = 476) were older (77 ± 3 versus 75 ± 3 years; P < 0.05) and had a higher prevalence of diabetes (20.6% versus 13.1%; P < 0.001). CKD was associated with higher odds for vibration detection threshold {odds ratio [OR] 1.7 [95% confidence interval (CI) 1.1-2.7]} and light touch insensitivity [OR 1.4 (95% CI 1.1-1.7)]. CMAPs and NCVs were not significantly different between CKD and non-CKD patients. In adjusted analyses, participants with CKD had higher odds of an abnormal heart rate response [OR 1.6 (95% CI 1.1-2.2)] and poor heart rate recovery [OR 1.5 (95% CI 1.1-2.0)]. CKD is associated with changes in sensory and autonomic nerve function, even after adjustment for demographics and comorbidities, including diabetes. Longitudinal studies in CKD are needed to determine the contribution of nerve impairments to clinically important outcomes.

Sections du résumé

BACKGROUND
Chronic kidney disease (CKD) is associated with poor mobility. Peripheral nerve function alterations play a significant role in low mobility. We tested the hypothesis that early CKD is associated with altered sensory, motor and autonomic nerve function.
METHODS
Participants in the Health, Aging and Body Composition cohort who had kidney function measures in Year 3 (1999-2000) and nerve function measurements at Year 4 (2000-01) were analyzed (n = 2290). Sensory (vibration threshold, monofilament insensitivity to light and standard touch), motor [compound motor action potentials (CMAPs), nerve conduction velocities (NCVs)] and autonomic (heart rate response and recovery after a 400-m walk test) nerve function as well as participant characteristics were compared across cystatin C- and creatinine-based estimated glomerular filtration rate categorized as ≤60 (CKD) or >60 mL/min/1.73 m2 (non-CKD). The association between CKD and nerve function was examined with logistic regression adjusted for covariates.
RESULTS
Participants with CKD (n = 476) were older (77 ± 3 versus 75 ± 3 years; P < 0.05) and had a higher prevalence of diabetes (20.6% versus 13.1%; P < 0.001). CKD was associated with higher odds for vibration detection threshold {odds ratio [OR] 1.7 [95% confidence interval (CI) 1.1-2.7]} and light touch insensitivity [OR 1.4 (95% CI 1.1-1.7)]. CMAPs and NCVs were not significantly different between CKD and non-CKD patients. In adjusted analyses, participants with CKD had higher odds of an abnormal heart rate response [OR 1.6 (95% CI 1.1-2.2)] and poor heart rate recovery [OR 1.5 (95% CI 1.1-2.0)].
CONCLUSIONS
CKD is associated with changes in sensory and autonomic nerve function, even after adjustment for demographics and comorbidities, including diabetes. Longitudinal studies in CKD are needed to determine the contribution of nerve impairments to clinically important outcomes.

Identifiants

pubmed: 29757410
pii: 4995012
doi: 10.1093/ndt/gfy102
pmc: PMC6452189
doi:

Substances chimiques

CST3 protein, human 0
Cystatin C 0
Creatinine AYI8EX34EU

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

625-632

Subventions

Organisme : NIDDK NIH HHS
ID : K23 DK102824
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG024827
Pays : United States

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

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Auteurs

Ranjani N Moorthi (RN)

Department of Medicine, Division of Nephrology, Indiana University School of Medicine, Indianapolis, IN, USA.

Simit Doshi (S)

Department of Medicine, Division of Nephrology, Indiana University School of Medicine, Indianapolis, IN, USA.

Linda F Fried (LF)

Renal Section, VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA.
Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Department of Epidemiology, University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA.

Sharon M Moe (SM)

Department of Medicine, Division of Nephrology, Indiana University School of Medicine, Indianapolis, IN, USA.
Roudebush VA Medical Center, Indianapolis, IN, USA.

Mark J Sarnak (MJ)

Department of Medicine, Division of Nephrology, Tufts Medical Center, Boston, MA, USA.

Suzanne Satterfield (S)

Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.

Ann V Schwartz (AV)

Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, USA.

Michael Shlipak (M)

Division of Nephrology, Department of Medicine, San Francisco VA Medical Center, San Francisco, CA; Kidney Health Research Collaborative, San Francisco VA Medical Center and University of California, San Francisco, CA, USA.

Brittney S Lange-Maia (BS)

Department of Preventive Medicine and Center for Community Health Equity, Rush University Medical Center, Chicago, IL, USA.

Tamara B Harris (TB)

Intramural Research Program, Laboratory of Epidemiology, and Population Sciences, National Institute on Aging, National Institutes of Health, Laboratory of Epidemiology, Demography, and Biometry, Bethesda, MD, USA.

Anne B Newman (AB)

Department of Epidemiology, University of Pittsburgh, Pittsburgh, PA, USA.

Elsa S Strotmeyer (ES)

Department of Epidemiology, University of Pittsburgh, Pittsburgh, PA, USA.

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