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Cerebrospinal Fluid α-Calcitonin Gene-Related Peptide: A Comparison between Alzheimer’s Disease and Multiple Sclerosis

Alzheimer’s disease (AD) and Multiple Sclerosis (MS) represent an emerging health problem on a global scale, as they are responsible for a significant contribution to the burden of disability in Western countries. Limited numbers of cerebrospinal fluid (CSF) diagnostic markers are available for each...

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Autores principales: Papiri, Giulio, Vignini, Arianna, Capriotti, Luigi, Verdenelli, Paola, Alia, Sonila, Di Paolo, Alice, Fiori, Chiara, Baldinelli, Sara, Silvestrini, Mauro, Luzzi, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961604/
https://www.ncbi.nlm.nih.gov/pubmed/35204700
http://dx.doi.org/10.3390/biom12020199
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author Papiri, Giulio
Vignini, Arianna
Capriotti, Luigi
Verdenelli, Paola
Alia, Sonila
Di Paolo, Alice
Fiori, Chiara
Baldinelli, Sara
Silvestrini, Mauro
Luzzi, Simona
author_facet Papiri, Giulio
Vignini, Arianna
Capriotti, Luigi
Verdenelli, Paola
Alia, Sonila
Di Paolo, Alice
Fiori, Chiara
Baldinelli, Sara
Silvestrini, Mauro
Luzzi, Simona
author_sort Papiri, Giulio
collection PubMed
description Alzheimer’s disease (AD) and Multiple Sclerosis (MS) represent an emerging health problem on a global scale, as they are responsible for a significant contribution to the burden of disability in Western countries. Limited numbers of cerebrospinal fluid (CSF) diagnostic markers are available for each disease (amyloid and tau deposition markers for AD and oligoclonal bands for MS) representing mostly state markers that provide few, if any, clues about the severity of the clinical phenotype. α-CGRP is a neuropeptide implied in nociception, vasodilation, synaptic plasticity and immune functions. This neuropeptide is expressed in encephalic regions connected to memory, attention, autonomic and behavioral functions and is also expressed by spinal motor neurons. The present work confronted α-CGRP levels between 19 AD, 27 MS and 17 control subjects using an ELISA/EIA assay. We measured higher CSF α-CGRP contents in control subjects with respect to AD, as shown in previous studies, as well as in MS patients in comparison to AD. The control subjects and MS patients did not significantly differ between each other. We did not observe a relationship between CSF protein content, albumin quotient and α-CGRP. We also describe, retrospectively, an association between higher CSF CGRP content and higher MRI overall lesion count in MS and between lower α-CGRP and worse attention and visuo-perceptual skills in AD. We speculate that α-CGRP could be differentially involved in both disabling diseases.
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spelling pubmed-89616042022-03-30 Cerebrospinal Fluid α-Calcitonin Gene-Related Peptide: A Comparison between Alzheimer’s Disease and Multiple Sclerosis Papiri, Giulio Vignini, Arianna Capriotti, Luigi Verdenelli, Paola Alia, Sonila Di Paolo, Alice Fiori, Chiara Baldinelli, Sara Silvestrini, Mauro Luzzi, Simona Biomolecules Article Alzheimer’s disease (AD) and Multiple Sclerosis (MS) represent an emerging health problem on a global scale, as they are responsible for a significant contribution to the burden of disability in Western countries. Limited numbers of cerebrospinal fluid (CSF) diagnostic markers are available for each disease (amyloid and tau deposition markers for AD and oligoclonal bands for MS) representing mostly state markers that provide few, if any, clues about the severity of the clinical phenotype. α-CGRP is a neuropeptide implied in nociception, vasodilation, synaptic plasticity and immune functions. This neuropeptide is expressed in encephalic regions connected to memory, attention, autonomic and behavioral functions and is also expressed by spinal motor neurons. The present work confronted α-CGRP levels between 19 AD, 27 MS and 17 control subjects using an ELISA/EIA assay. We measured higher CSF α-CGRP contents in control subjects with respect to AD, as shown in previous studies, as well as in MS patients in comparison to AD. The control subjects and MS patients did not significantly differ between each other. We did not observe a relationship between CSF protein content, albumin quotient and α-CGRP. We also describe, retrospectively, an association between higher CSF CGRP content and higher MRI overall lesion count in MS and between lower α-CGRP and worse attention and visuo-perceptual skills in AD. We speculate that α-CGRP could be differentially involved in both disabling diseases. MDPI 2022-01-24 /pmc/articles/PMC8961604/ /pubmed/35204700 http://dx.doi.org/10.3390/biom12020199 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Papiri, Giulio
Vignini, Arianna
Capriotti, Luigi
Verdenelli, Paola
Alia, Sonila
Di Paolo, Alice
Fiori, Chiara
Baldinelli, Sara
Silvestrini, Mauro
Luzzi, Simona
Cerebrospinal Fluid α-Calcitonin Gene-Related Peptide: A Comparison between Alzheimer’s Disease and Multiple Sclerosis
title Cerebrospinal Fluid α-Calcitonin Gene-Related Peptide: A Comparison between Alzheimer’s Disease and Multiple Sclerosis
title_full Cerebrospinal Fluid α-Calcitonin Gene-Related Peptide: A Comparison between Alzheimer’s Disease and Multiple Sclerosis
title_fullStr Cerebrospinal Fluid α-Calcitonin Gene-Related Peptide: A Comparison between Alzheimer’s Disease and Multiple Sclerosis
title_full_unstemmed Cerebrospinal Fluid α-Calcitonin Gene-Related Peptide: A Comparison between Alzheimer’s Disease and Multiple Sclerosis
title_short Cerebrospinal Fluid α-Calcitonin Gene-Related Peptide: A Comparison between Alzheimer’s Disease and Multiple Sclerosis
title_sort cerebrospinal fluid α-calcitonin gene-related peptide: a comparison between alzheimer’s disease and multiple sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961604/
https://www.ncbi.nlm.nih.gov/pubmed/35204700
http://dx.doi.org/10.3390/biom12020199
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