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May 24, 2023Research ArticleOpen Access

Association of Chronic Kidney Disease With Plasma NfL and Other Biomarkers of Neurodegeneration: The H70 Birth Cohort Study in Gothenburg

Anna Dittrich, View ORCID ProfileNicholas J Ashton, View ORCID ProfileHenrik Zetterberg, View ORCID ProfileKaj Blennow, Anna Zettergren, View ORCID ProfileJoel Simrén, Tobias Skillbäck, Sara Shams, Alejandra Machado, View ORCID ProfileEric Westman, View ORCID ProfileMichael Schöll, Ingmar Skoog, Silke Kern
First published May 24, 2023, DOI: https://doi.org/10.1212/WNL.0000000000207419
Anna Dittrich
1Neuropsychiatric Epidemiology Unit, Sahlgrenska Academy, University of Gothenburg, Gothenburg Sweden
2Department of Psychiatry Cognition and Old Age Psychiatry, Sahlgrenska University Hospital, Mölndal Sweden
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  • For correspondence: anna.dittrich@vgregion.se
Nicholas J Ashton
3Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal Campus, Sweden
4King's College London, Institute of Psychiatry, Psychology and Neuroscience, Maurice Wohl Institute Clinical Neuroscience Institute, London UK
5NIHR Biomedical Research Centre for Mental Health and Biomedical Research Unit for Dementia at South London and Maudsley NHS Foundation, London UK
6Centre for Age-Related Medicine, Stavanger University Hospital, Stavanger, Norway
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  • ORCID record for Nicholas J Ashton
Henrik Zetterberg
3Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal Campus, Sweden
7Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal Sweden
8UK Dementia Research Institute at UCL, UCL Institute of Neurology, London UK
9Department of Neurodegenerative Disease, UCL Institute of Neurology, London UK
10Hong Kong Center for Neurodegenerative Diseases, Hong Kong, China
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  • ORCID record for Henrik Zetterberg
Kaj Blennow
3Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal Campus, Sweden
7Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal Sweden
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  • ORCID record for Kaj Blennow
Anna Zettergren
1Neuropsychiatric Epidemiology Unit, Sahlgrenska Academy, University of Gothenburg, Gothenburg Sweden
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Joel Simrén
3Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal Campus, Sweden
7Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal Sweden
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  • ORCID record for Joel Simrén
Tobias Skillbäck
1Neuropsychiatric Epidemiology Unit, Sahlgrenska Academy, University of Gothenburg, Gothenburg Sweden
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Sara Shams
11Care Sciences and Society, Karolinska Institutet, and Department of Radiology, Karolinska University Hospital, Stockholm Sweden
12Department of Clinical Neuroscience, Karolinska University Hospital, Stockholm Sweden
13Department of Radiology, Stanford University, Stanford California, USA
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Alejandra Machado
14Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society (NVS), Karolinska University Hospital, Stockholm Sweden
15Division of Insurance Medicine, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
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Eric Westman
14Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society (NVS), Karolinska University Hospital, Stockholm Sweden
16Department of Neuroimaging, Centre for Neuroimaging Sciences, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, UK
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Michael Schöll
3Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal Campus, Sweden
9Department of Neurodegenerative Disease, UCL Institute of Neurology, London UK
17Wallenberg Center of Molecular and Translational Medicine, University of Gothenburg, Gothenburg Sweden
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Ingmar Skoog
1Neuropsychiatric Epidemiology Unit, Sahlgrenska Academy, University of Gothenburg, Gothenburg Sweden
2Department of Psychiatry Cognition and Old Age Psychiatry, Sahlgrenska University Hospital, Mölndal Sweden
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Silke Kern
1Neuropsychiatric Epidemiology Unit, Sahlgrenska Academy, University of Gothenburg, Gothenburg Sweden
2Department of Psychiatry Cognition and Old Age Psychiatry, Sahlgrenska University Hospital, Mölndal Sweden
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Citation
Association of Chronic Kidney Disease With Plasma NfL and Other Biomarkers of Neurodegeneration: The H70 Birth Cohort Study in Gothenburg
Anna Dittrich, Nicholas J Ashton, Henrik Zetterberg, Kaj Blennow, Anna Zettergren, Joel Simrén, Tobias Skillbäck, Sara Shams, Alejandra Machado, Eric Westman, Michael Schöll, Ingmar Skoog, Silke Kern
Neurology May 2023, 10.1212/WNL.0000000000207419; DOI: 10.1212/WNL.0000000000207419

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Abstract

Background and objectives: Studies associate chronic kidney disease (CKD) with neurodegeneration. This study investigated the relation between kidney function, blood, cerebrospinal fluid (CSF), and structural brain MRI markers of neurodegeneration, in a sample including individuals with and without CKD.

Methods: Participants from the Gothenburg H70 Birth Cohort Study, with data on plasma-neurofilament light (P-NfL), estimated glomerular filtration rate (eGFR) and structural brain MRI were included. Participants were invited to also have CSF collected. The primary endpoint of the present study was to determine any association between CKD and P-NfL. Secondary endpoints included cross-sectional associations between CKD, eGFR and cerebrospinal fluid (CSF)- and MRI-derived markers of neurodegeneration and Alzheimer’s disease (AD) pathology (MRI: cortical thickness, hippocampal volume, lateral ventricle volume, white matter lesion volume; CSF: β-amyloid (Aβ) 42, Aβ42/40, Aβ42/p-tau, t-tau, p-tau, NfL). Participants with P-NfL and eGFR at baseline were re-examined on eGFR, 5.5 (5.3; 6.1) years (median; IQR) after the first visit, and the predictive value of P-NfL levels on incident CKD was estimated longitudinally, using a Cox proportional hazards model.

Results: We included 744 participants, 668 without CKD (Age 71 (70; 71) years, 50% males) and 76 with CKD (age 71 (70;71) years, 39% males). Biomarkers from cerebrospinal fluid (CSF) were analysed in 313 participants. 558 individuals returned for a re-examination of eGFR (75% response rate, age 76 (76; 77), 48% males, 76 new cases of CKD). Participants with CKD had higher P-NfL levels than those with normal kidney function (median; 18.8 versus 14.0 pg/mL, p<0.001), while MRI and CSF markers were similar between the groups. P-NfL was independently associated with CKD after adjustment for confounding variables, including hypertension and diabetes (OR; 3.231, p<0.001), in a logistic regression model. eGFR, and CSF Aβ 42/40: R=0.23, p=0.004 correlated in participants with Aβ42 pathology. P-NfL levels in the highest quartile were associated with incident CKD at follow-up (HR; 2.08 (1.14: 4.50)).

Discussion: In a community-based cohort of 70-year olds, P-NfL was associated with both prevalent and incident CKD, while CSF and/or imaging measures did not differ by CKD status. Participants with CKD and dementia presented similar levels of P-NfL.

  • Received December 30, 2022.
  • Accepted in final form March 31, 2023.
  • Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.

This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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