Cargando…

Inflammatory Blood Biomarker Kynurenine Is Linked With Elevated Neuroinflammation and Neurodegeneration in Older Adults: Evidence From Two 1H-MRS Post-Processing Analysis Methods

RATIONALE AND OBJECTIVES: Pro-inflammatory processes have been argued to play a role in conditions associated with cognitive decline and neurodegeneration, like aging and obesity. Only a limited number of studies have tried to measure both peripheral and central biomarkers of inflammation and examin...

Descripción completa

Detalles Bibliográficos
Autores principales: Vints, Wouter A. J., Kušleikiene, Simona, Sheoran, Samrat, Šarkinaite, Milda, Valatkevičiene, Kristina, Gleizniene, Rymante, Kvedaras, Mindaugas, Pukenas, Kazimieras, Himmelreich, Uwe, Cesnaitiene, Vida J., Levin, Oron, Verbunt, Jeanine, Masiulis, Nerijus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035828/
https://www.ncbi.nlm.nih.gov/pubmed/35479493
http://dx.doi.org/10.3389/fpsyt.2022.859772
_version_ 1784693384859877376
author Vints, Wouter A. J.
Kušleikiene, Simona
Sheoran, Samrat
Šarkinaite, Milda
Valatkevičiene, Kristina
Gleizniene, Rymante
Kvedaras, Mindaugas
Pukenas, Kazimieras
Himmelreich, Uwe
Cesnaitiene, Vida J.
Levin, Oron
Verbunt, Jeanine
Masiulis, Nerijus
author_facet Vints, Wouter A. J.
Kušleikiene, Simona
Sheoran, Samrat
Šarkinaite, Milda
Valatkevičiene, Kristina
Gleizniene, Rymante
Kvedaras, Mindaugas
Pukenas, Kazimieras
Himmelreich, Uwe
Cesnaitiene, Vida J.
Levin, Oron
Verbunt, Jeanine
Masiulis, Nerijus
author_sort Vints, Wouter A. J.
collection PubMed
description RATIONALE AND OBJECTIVES: Pro-inflammatory processes have been argued to play a role in conditions associated with cognitive decline and neurodegeneration, like aging and obesity. Only a limited number of studies have tried to measure both peripheral and central biomarkers of inflammation and examined their interrelationship. The primary aim of this study was to examine the hypothesis that chronic peripheral inflammation would be associated with neurometabolic changes that indicate neuroinflammation (the combined elevation of myoinositol and choline), brain gray matter volume decrease, and lower cognitive functioning in older adults. MATERIALS AND METHODS: Seventy-four older adults underwent bio-impedance body composition analysis, cognitive testing with the Montreal Cognitive Assessment (MoCA), blood serum analysis of inflammatory markers interleukin-6 (IL-6) and kynurenine, magnetic resonance imaging (MRI), and proton magnetic resonance spectroscopy ((1)H-MRS) of the brain. Neurometabolic findings from both Tarquin and LCModel (1)H-MRS post-processing software packages were compared. The regions of interest for MRI and (1)H-MRS measurements were dorsal posterior cingulate cortex (DPCC), left hippocampal cortex (HPC), left medial temporal cortex (MTC), left primary sensorimotor cortex (SM1), and right dorsolateral prefrontal cortex (DLPFC). RESULTS: Elevated serum kynurenine levels were associated with signs of neuroinflammation, specifically in the DPCC, left SM1 and right DLPFC, and signs of neurodegeneration, specifically in the left HPC, left MTC and left SM1, after adjusting for age, sex and fat percentage (fat%). Elevated serum IL-6 levels were associated with increased Glx levels in left HPC, left MTC, and right DLPFC, after processing the (1)H-MRS data with Tarquin. Overall, the agreement between Tarquin and LCModel results was moderate-to-strong for tNAA, tCho, mIns, and tCr, but weak to very weak for Glx. Peripheral inflammatory markers (IL-6 and kynurenine) were not associated with older age, higher fat%, decreased brain gray matter volume loss or decreased cognitive functioning within a cohort of older adults. CONCLUSION: Our results suggest that serum kynurenine may be used as a peripheral inflammatory marker that is associated with neuroinflammation and neurodegeneration, although not linked to cognition. Future studies should consider longitudinal analysis to assess the causal inferences between chronic peripheral and neuroinflammation, brain structural and neurometabolic changes, and cognitive decline in aging.
format Online
Article
Text
id pubmed-9035828
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90358282022-04-26 Inflammatory Blood Biomarker Kynurenine Is Linked With Elevated Neuroinflammation and Neurodegeneration in Older Adults: Evidence From Two 1H-MRS Post-Processing Analysis Methods Vints, Wouter A. J. Kušleikiene, Simona Sheoran, Samrat Šarkinaite, Milda Valatkevičiene, Kristina Gleizniene, Rymante Kvedaras, Mindaugas Pukenas, Kazimieras Himmelreich, Uwe Cesnaitiene, Vida J. Levin, Oron Verbunt, Jeanine Masiulis, Nerijus Front Psychiatry Psychiatry RATIONALE AND OBJECTIVES: Pro-inflammatory processes have been argued to play a role in conditions associated with cognitive decline and neurodegeneration, like aging and obesity. Only a limited number of studies have tried to measure both peripheral and central biomarkers of inflammation and examined their interrelationship. The primary aim of this study was to examine the hypothesis that chronic peripheral inflammation would be associated with neurometabolic changes that indicate neuroinflammation (the combined elevation of myoinositol and choline), brain gray matter volume decrease, and lower cognitive functioning in older adults. MATERIALS AND METHODS: Seventy-four older adults underwent bio-impedance body composition analysis, cognitive testing with the Montreal Cognitive Assessment (MoCA), blood serum analysis of inflammatory markers interleukin-6 (IL-6) and kynurenine, magnetic resonance imaging (MRI), and proton magnetic resonance spectroscopy ((1)H-MRS) of the brain. Neurometabolic findings from both Tarquin and LCModel (1)H-MRS post-processing software packages were compared. The regions of interest for MRI and (1)H-MRS measurements were dorsal posterior cingulate cortex (DPCC), left hippocampal cortex (HPC), left medial temporal cortex (MTC), left primary sensorimotor cortex (SM1), and right dorsolateral prefrontal cortex (DLPFC). RESULTS: Elevated serum kynurenine levels were associated with signs of neuroinflammation, specifically in the DPCC, left SM1 and right DLPFC, and signs of neurodegeneration, specifically in the left HPC, left MTC and left SM1, after adjusting for age, sex and fat percentage (fat%). Elevated serum IL-6 levels were associated with increased Glx levels in left HPC, left MTC, and right DLPFC, after processing the (1)H-MRS data with Tarquin. Overall, the agreement between Tarquin and LCModel results was moderate-to-strong for tNAA, tCho, mIns, and tCr, but weak to very weak for Glx. Peripheral inflammatory markers (IL-6 and kynurenine) were not associated with older age, higher fat%, decreased brain gray matter volume loss or decreased cognitive functioning within a cohort of older adults. CONCLUSION: Our results suggest that serum kynurenine may be used as a peripheral inflammatory marker that is associated with neuroinflammation and neurodegeneration, although not linked to cognition. Future studies should consider longitudinal analysis to assess the causal inferences between chronic peripheral and neuroinflammation, brain structural and neurometabolic changes, and cognitive decline in aging. Frontiers Media S.A. 2022-04-11 /pmc/articles/PMC9035828/ /pubmed/35479493 http://dx.doi.org/10.3389/fpsyt.2022.859772 Text en Copyright © 2022 Vints, Kušleikiene, Sheoran, Šarkinaite, Valatkevičiene, Gleizniene, Kvedaras, Pukenas, Himmelreich, Cesnaitiene, Levin, Verbunt and Masiulis. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Vints, Wouter A. J.
Kušleikiene, Simona
Sheoran, Samrat
Šarkinaite, Milda
Valatkevičiene, Kristina
Gleizniene, Rymante
Kvedaras, Mindaugas
Pukenas, Kazimieras
Himmelreich, Uwe
Cesnaitiene, Vida J.
Levin, Oron
Verbunt, Jeanine
Masiulis, Nerijus
Inflammatory Blood Biomarker Kynurenine Is Linked With Elevated Neuroinflammation and Neurodegeneration in Older Adults: Evidence From Two 1H-MRS Post-Processing Analysis Methods
title Inflammatory Blood Biomarker Kynurenine Is Linked With Elevated Neuroinflammation and Neurodegeneration in Older Adults: Evidence From Two 1H-MRS Post-Processing Analysis Methods
title_full Inflammatory Blood Biomarker Kynurenine Is Linked With Elevated Neuroinflammation and Neurodegeneration in Older Adults: Evidence From Two 1H-MRS Post-Processing Analysis Methods
title_fullStr Inflammatory Blood Biomarker Kynurenine Is Linked With Elevated Neuroinflammation and Neurodegeneration in Older Adults: Evidence From Two 1H-MRS Post-Processing Analysis Methods
title_full_unstemmed Inflammatory Blood Biomarker Kynurenine Is Linked With Elevated Neuroinflammation and Neurodegeneration in Older Adults: Evidence From Two 1H-MRS Post-Processing Analysis Methods
title_short Inflammatory Blood Biomarker Kynurenine Is Linked With Elevated Neuroinflammation and Neurodegeneration in Older Adults: Evidence From Two 1H-MRS Post-Processing Analysis Methods
title_sort inflammatory blood biomarker kynurenine is linked with elevated neuroinflammation and neurodegeneration in older adults: evidence from two 1h-mrs post-processing analysis methods
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035828/
https://www.ncbi.nlm.nih.gov/pubmed/35479493
http://dx.doi.org/10.3389/fpsyt.2022.859772
work_keys_str_mv AT vintswouteraj inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT kusleikienesimona inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT sheoransamrat inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT sarkinaitemilda inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT valatkevicienekristina inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT gleiznienerymante inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT kvedarasmindaugas inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT pukenaskazimieras inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT himmelreichuwe inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT cesnaitienevidaj inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT levinoron inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT verbuntjeanine inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods
AT masiulisnerijus inflammatorybloodbiomarkerkynurenineislinkedwithelevatedneuroinflammationandneurodegenerationinolderadultsevidencefromtwo1hmrspostprocessinganalysismethods