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Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients
Central nervous system (CNS) barrier impairment has been reported in amyotrophic lateral sclerosis (ALS), highlighting its potential significance in the disease. In this context, we aim to shed light on its involvement in the disease, by determining albumin quotient (QAlb) at the time of diagnosis o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10342931/ https://www.ncbi.nlm.nih.gov/pubmed/37446372 http://dx.doi.org/10.3390/ijms241311196 |
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author | Alarcan, Hugo Vourc’h, Patrick Berton, Lise Benz-De Bretagne, Isabelle Piver, Eric Andres, Christian R. Corcia, Philippe Veyrat-Durebex, Charlotte Blasco, Hélène |
author_facet | Alarcan, Hugo Vourc’h, Patrick Berton, Lise Benz-De Bretagne, Isabelle Piver, Eric Andres, Christian R. Corcia, Philippe Veyrat-Durebex, Charlotte Blasco, Hélène |
author_sort | Alarcan, Hugo |
collection | PubMed |
description | Central nervous system (CNS) barrier impairment has been reported in amyotrophic lateral sclerosis (ALS), highlighting its potential significance in the disease. In this context, we aim to shed light on its involvement in the disease, by determining albumin quotient (QAlb) at the time of diagnosis of ALS in a large cohort of patients. Patients from the university hospital of Tours (n = 307) were included in this monocentric, retrospective study. In total, 92 patients (30%) had elevated QAlb levels. This percentage was higher in males (43%) than in females (15%). Interestingly, QAlb was not associated with age of onset, age at sampling or diagnostic delay. However, we found an association with ALS functional rating scale-revised (ALSFRS-r) at diagnosis but this was significant only in males. The QAlb levels were not linked to the presence of a pathogenic mutation. Finally, we performed a multivariate survival analysis and found that QAlb was significantly associated with survival in male patients (HR = 2.3, 95% CI = 1.2–4.3, p = 0.009). A longitudinal evaluation of markers of barrier impairment, in combination with inflammatory biomarkers, could give insight into the involvement of CNS barrier impairment in the pathogenesis of the disease. The gender difference might guide the development of new drugs and help personalise the treatment of ALS. |
format | Online Article Text |
id | pubmed-10342931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103429312023-07-14 Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients Alarcan, Hugo Vourc’h, Patrick Berton, Lise Benz-De Bretagne, Isabelle Piver, Eric Andres, Christian R. Corcia, Philippe Veyrat-Durebex, Charlotte Blasco, Hélène Int J Mol Sci Article Central nervous system (CNS) barrier impairment has been reported in amyotrophic lateral sclerosis (ALS), highlighting its potential significance in the disease. In this context, we aim to shed light on its involvement in the disease, by determining albumin quotient (QAlb) at the time of diagnosis of ALS in a large cohort of patients. Patients from the university hospital of Tours (n = 307) were included in this monocentric, retrospective study. In total, 92 patients (30%) had elevated QAlb levels. This percentage was higher in males (43%) than in females (15%). Interestingly, QAlb was not associated with age of onset, age at sampling or diagnostic delay. However, we found an association with ALS functional rating scale-revised (ALSFRS-r) at diagnosis but this was significant only in males. The QAlb levels were not linked to the presence of a pathogenic mutation. Finally, we performed a multivariate survival analysis and found that QAlb was significantly associated with survival in male patients (HR = 2.3, 95% CI = 1.2–4.3, p = 0.009). A longitudinal evaluation of markers of barrier impairment, in combination with inflammatory biomarkers, could give insight into the involvement of CNS barrier impairment in the pathogenesis of the disease. The gender difference might guide the development of new drugs and help personalise the treatment of ALS. MDPI 2023-07-07 /pmc/articles/PMC10342931/ /pubmed/37446372 http://dx.doi.org/10.3390/ijms241311196 Text en © 2023 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 Alarcan, Hugo Vourc’h, Patrick Berton, Lise Benz-De Bretagne, Isabelle Piver, Eric Andres, Christian R. Corcia, Philippe Veyrat-Durebex, Charlotte Blasco, Hélène Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients |
title | Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients |
title_full | Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients |
title_fullStr | Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients |
title_full_unstemmed | Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients |
title_short | Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients |
title_sort | implication of central nervous system barrier impairment in amyotrophic lateral sclerosis: gender-related difference in patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10342931/ https://www.ncbi.nlm.nih.gov/pubmed/37446372 http://dx.doi.org/10.3390/ijms241311196 |
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