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Serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients

BACKGROUND: Chronic heart failure (HF) is known to increase the risk of developing Alzheimer’s dementia significantly. Thus, detecting and preventing mild cognitive impairment, which is common in patients with HF, is of great importance. Serum biomarkers are increasingly used in neurological disorde...

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Autores principales: Traub, Jan, Otto, Markus, Sell, Roxane, Göpfert, Dennis, Homola, György, Steinacker, Petra, Oeckl, Patrick, Morbach, Caroline, Frantz, Stefan, Pham, Mirko, Störk, Stefan, Stoll, Guido, Frey, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549648/
https://www.ncbi.nlm.nih.gov/pubmed/36217177
http://dx.doi.org/10.1186/s13195-022-01087-4
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author Traub, Jan
Otto, Markus
Sell, Roxane
Göpfert, Dennis
Homola, György
Steinacker, Petra
Oeckl, Patrick
Morbach, Caroline
Frantz, Stefan
Pham, Mirko
Störk, Stefan
Stoll, Guido
Frey, Anna
author_facet Traub, Jan
Otto, Markus
Sell, Roxane
Göpfert, Dennis
Homola, György
Steinacker, Petra
Oeckl, Patrick
Morbach, Caroline
Frantz, Stefan
Pham, Mirko
Störk, Stefan
Stoll, Guido
Frey, Anna
author_sort Traub, Jan
collection PubMed
description BACKGROUND: Chronic heart failure (HF) is known to increase the risk of developing Alzheimer’s dementia significantly. Thus, detecting and preventing mild cognitive impairment, which is common in patients with HF, is of great importance. Serum biomarkers are increasingly used in neurological disorders for diagnostics, monitoring, and prognostication of disease course. It remains unclear if neuronal biomarkers may help detect cognitive impairment in this high-risk population. Also, the influence of chronic HF and concomitant renal dysfunction on these biomarkers is not well understood. METHODS: Within the monocentric Cognition.Matters-HF study, we quantified the serum levels of phosphorylated tau protein 181 (pTau) and neurofilament light chain (NfL) of 146 extensively phenotyped chronic heart failure patients (aged 32 to 85 years; 15.1% women) using ultrasensitive bead-based single-molecule immunoassays. The clinical work-up included advanced cognitive testing and cerebral magnetic resonance imaging (MRI). RESULTS: Serum concentrations of NfL ranged from 5.4 to 215.0 pg/ml (median 26.4 pg/ml) and of pTau from 0.51 to 9.22 pg/ml (median 1.57 pg/ml). We detected mild cognitive impairment (i.e., T-score < 40 in at least one cognitive domain) in 60% of heart failure patients. pTau (p = 0.014), but not NfL, was elevated in this group. Both NfL (ρ = − 0.21; p = 0.013) and pTau (ρ = − 0.25; p = 0.002) related to the cognitive domain visual/verbal memory, as well as white matter hyperintensity volume and cerebral and hippocampal atrophy. In multivariable analysis, both biomarkers were independently influenced by age (T = 4.6 for pTau; T = 5.9 for NfL) and glomerular filtration rate (T = − 2.4 for pTau; T = − 3.4 for NfL). Markers of chronic heart failure, left atrial volume index (T = 4.6) and NT-proBNP (T = 2.8), were further cardiological determinants of pTau and NfL, respectively. In addition, pTau was also strongly affected by serum creatine kinase levels (T = 6.5) and ferritin (T = − 3.1). CONCLUSIONS: pTau and NfL serum levels are strongly influenced by age-dependent renal and cardiac dysfunction. These findings point towards the need for longitudinal examinations and consideration of frequent comorbidities when using neuronal serum biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-022-01087-4.
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spelling pubmed-95496482022-10-11 Serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients Traub, Jan Otto, Markus Sell, Roxane Göpfert, Dennis Homola, György Steinacker, Petra Oeckl, Patrick Morbach, Caroline Frantz, Stefan Pham, Mirko Störk, Stefan Stoll, Guido Frey, Anna Alzheimers Res Ther Research BACKGROUND: Chronic heart failure (HF) is known to increase the risk of developing Alzheimer’s dementia significantly. Thus, detecting and preventing mild cognitive impairment, which is common in patients with HF, is of great importance. Serum biomarkers are increasingly used in neurological disorders for diagnostics, monitoring, and prognostication of disease course. It remains unclear if neuronal biomarkers may help detect cognitive impairment in this high-risk population. Also, the influence of chronic HF and concomitant renal dysfunction on these biomarkers is not well understood. METHODS: Within the monocentric Cognition.Matters-HF study, we quantified the serum levels of phosphorylated tau protein 181 (pTau) and neurofilament light chain (NfL) of 146 extensively phenotyped chronic heart failure patients (aged 32 to 85 years; 15.1% women) using ultrasensitive bead-based single-molecule immunoassays. The clinical work-up included advanced cognitive testing and cerebral magnetic resonance imaging (MRI). RESULTS: Serum concentrations of NfL ranged from 5.4 to 215.0 pg/ml (median 26.4 pg/ml) and of pTau from 0.51 to 9.22 pg/ml (median 1.57 pg/ml). We detected mild cognitive impairment (i.e., T-score < 40 in at least one cognitive domain) in 60% of heart failure patients. pTau (p = 0.014), but not NfL, was elevated in this group. Both NfL (ρ = − 0.21; p = 0.013) and pTau (ρ = − 0.25; p = 0.002) related to the cognitive domain visual/verbal memory, as well as white matter hyperintensity volume and cerebral and hippocampal atrophy. In multivariable analysis, both biomarkers were independently influenced by age (T = 4.6 for pTau; T = 5.9 for NfL) and glomerular filtration rate (T = − 2.4 for pTau; T = − 3.4 for NfL). Markers of chronic heart failure, left atrial volume index (T = 4.6) and NT-proBNP (T = 2.8), were further cardiological determinants of pTau and NfL, respectively. In addition, pTau was also strongly affected by serum creatine kinase levels (T = 6.5) and ferritin (T = − 3.1). CONCLUSIONS: pTau and NfL serum levels are strongly influenced by age-dependent renal and cardiac dysfunction. These findings point towards the need for longitudinal examinations and consideration of frequent comorbidities when using neuronal serum biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-022-01087-4. BioMed Central 2022-10-10 /pmc/articles/PMC9549648/ /pubmed/36217177 http://dx.doi.org/10.1186/s13195-022-01087-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Traub, Jan
Otto, Markus
Sell, Roxane
Göpfert, Dennis
Homola, György
Steinacker, Petra
Oeckl, Patrick
Morbach, Caroline
Frantz, Stefan
Pham, Mirko
Störk, Stefan
Stoll, Guido
Frey, Anna
Serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients
title Serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients
title_full Serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients
title_fullStr Serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients
title_full_unstemmed Serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients
title_short Serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients
title_sort serum phosphorylated tau protein 181 and neurofilament light chain in cognitively impaired heart failure patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549648/
https://www.ncbi.nlm.nih.gov/pubmed/36217177
http://dx.doi.org/10.1186/s13195-022-01087-4
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