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Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis

Estrogens have neuroprotective actions depending on estrogen type, dose, and timing in both preclinical models and in women during health and disease. Serum neurofilament light chain is a putative biomarker of neurodegeneration in multiple sclerosis, aging, and other neurodegenerative diseases. Here...

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Autores principales: Voskuhl, Rhonda, Kuhle, Jens, Siddarth, Prabha, Itoh, Noriko, Patel, Kevin, MacKenzie‐Graham, Allan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380170/
https://www.ncbi.nlm.nih.gov/pubmed/35770318
http://dx.doi.org/10.1002/acn3.51622
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author Voskuhl, Rhonda
Kuhle, Jens
Siddarth, Prabha
Itoh, Noriko
Patel, Kevin
MacKenzie‐Graham, Allan
author_facet Voskuhl, Rhonda
Kuhle, Jens
Siddarth, Prabha
Itoh, Noriko
Patel, Kevin
MacKenzie‐Graham, Allan
author_sort Voskuhl, Rhonda
collection PubMed
description Estrogens have neuroprotective actions depending on estrogen type, dose, and timing in both preclinical models and in women during health and disease. Serum neurofilament light chain is a putative biomarker of neurodegeneration in multiple sclerosis, aging, and other neurodegenerative diseases. Here, oral treatment with an estrogen unique to pregnancy (estriol) using an 8 mg dose to induce a mid‐pregnancy blood estriol level reduced serum neurofilament light chain in nonpregnant MS women at mean age of 37 years. This is consistent with estriol‐mediated protection from neuro‐axonal injury and supports the use of serum neurofilament light chain as a biomarker in MS.
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spelling pubmed-93801702022-08-19 Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis Voskuhl, Rhonda Kuhle, Jens Siddarth, Prabha Itoh, Noriko Patel, Kevin MacKenzie‐Graham, Allan Ann Clin Transl Neurol Brief Communications Estrogens have neuroprotective actions depending on estrogen type, dose, and timing in both preclinical models and in women during health and disease. Serum neurofilament light chain is a putative biomarker of neurodegeneration in multiple sclerosis, aging, and other neurodegenerative diseases. Here, oral treatment with an estrogen unique to pregnancy (estriol) using an 8 mg dose to induce a mid‐pregnancy blood estriol level reduced serum neurofilament light chain in nonpregnant MS women at mean age of 37 years. This is consistent with estriol‐mediated protection from neuro‐axonal injury and supports the use of serum neurofilament light chain as a biomarker in MS. John Wiley and Sons Inc. 2022-06-29 /pmc/articles/PMC9380170/ /pubmed/35770318 http://dx.doi.org/10.1002/acn3.51622 Text en © 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communications
Voskuhl, Rhonda
Kuhle, Jens
Siddarth, Prabha
Itoh, Noriko
Patel, Kevin
MacKenzie‐Graham, Allan
Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis
title Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis
title_full Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis
title_fullStr Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis
title_full_unstemmed Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis
title_short Decreased neurofilament light chain levels in estriol‐treated multiple sclerosis
title_sort decreased neurofilament light chain levels in estriol‐treated multiple sclerosis
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380170/
https://www.ncbi.nlm.nih.gov/pubmed/35770318
http://dx.doi.org/10.1002/acn3.51622
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