Amyotrophic lateral sclerosis (ALS) and the endocrine system: Are there any further ties to be explored?

Amyotrophic Lateral Sclerosis (ALS) belongs to the family of neurodegenerative disorders and is classified as fronto-temporal dementia (FTD), progressive muscular atrophy, primary lateral sclerosis, and pseudobulbar palsy. Even though endocrine dysfunction independently impacts the ALS-related survi...

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Autores principales: Alexios-Fotios A. Mentis, Anastasia M. Bougea, George P. Chrousos
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/1e15cc60d549476cb898c0639cb47e88
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spelling oai:doaj.org-article:1e15cc60d549476cb898c0639cb47e882021-11-10T04:40:21ZAmyotrophic lateral sclerosis (ALS) and the endocrine system: Are there any further ties to be explored?2589-958910.1016/j.nbas.2021.100024https://doaj.org/article/1e15cc60d549476cb898c0639cb47e882021-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2589958921000207https://doaj.org/toc/2589-9589Amyotrophic Lateral Sclerosis (ALS) belongs to the family of neurodegenerative disorders and is classified as fronto-temporal dementia (FTD), progressive muscular atrophy, primary lateral sclerosis, and pseudobulbar palsy. Even though endocrine dysfunction independently impacts the ALS-related survival rate, the complex connection between ALS and the endocrine system has not been studied in depth. Here we review earlier and recent findings on how ALS interacts with hormones a) of the hypothalamus and pituitary gland, b) the thyroid gland, c) the pancreas, d) the adipose tissue, e) the parathyroid glands, f) the bones, g) the adrenal glands, and h) the gonads (ovaries and testes). Of note, endocrine issues should always be explored in patients with ALS, especially those with low skeletal muscle and bone mass, vitamin D deficiency, and decreased insulin sensitivity (diabetes mellitus). Because ALS is a progressively deteriorating disease, addressing any potential endocrine co-morbidities in patients with this malady is quite important for decreasing the overall ALS-associated disease burden. Importantly, as this burden is estimated to increase globally in the decades to follow, in part because of an increasingly aging population, it is high time for future multi-center, multi-ethnic studies to assess the link between ALS and the endocrine system in significantly larger patient populations. Last, the psychosocial stress experienced by patients with ALS and its psycho-neuro-endocrinological sequelae, including hypothalamic–pituitaryadrenal dysregulation, should become an area of intensive study in the future.Alexios-Fotios A. MentisAnastasia M. BougeaGeorge P. ChrousosElsevierarticleAmyotrophic lateral sclerosisEndocrinologyAgingThyroidAdrenal glandsVitamin DNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571ENAging Brain, Vol 1, Iss , Pp 100024- (2021)
institution DOAJ
collection DOAJ
language EN
topic Amyotrophic lateral sclerosis
Endocrinology
Aging
Thyroid
Adrenal glands
Vitamin D
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
spellingShingle Amyotrophic lateral sclerosis
Endocrinology
Aging
Thyroid
Adrenal glands
Vitamin D
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Alexios-Fotios A. Mentis
Anastasia M. Bougea
George P. Chrousos
Amyotrophic lateral sclerosis (ALS) and the endocrine system: Are there any further ties to be explored?
description Amyotrophic Lateral Sclerosis (ALS) belongs to the family of neurodegenerative disorders and is classified as fronto-temporal dementia (FTD), progressive muscular atrophy, primary lateral sclerosis, and pseudobulbar palsy. Even though endocrine dysfunction independently impacts the ALS-related survival rate, the complex connection between ALS and the endocrine system has not been studied in depth. Here we review earlier and recent findings on how ALS interacts with hormones a) of the hypothalamus and pituitary gland, b) the thyroid gland, c) the pancreas, d) the adipose tissue, e) the parathyroid glands, f) the bones, g) the adrenal glands, and h) the gonads (ovaries and testes). Of note, endocrine issues should always be explored in patients with ALS, especially those with low skeletal muscle and bone mass, vitamin D deficiency, and decreased insulin sensitivity (diabetes mellitus). Because ALS is a progressively deteriorating disease, addressing any potential endocrine co-morbidities in patients with this malady is quite important for decreasing the overall ALS-associated disease burden. Importantly, as this burden is estimated to increase globally in the decades to follow, in part because of an increasingly aging population, it is high time for future multi-center, multi-ethnic studies to assess the link between ALS and the endocrine system in significantly larger patient populations. Last, the psychosocial stress experienced by patients with ALS and its psycho-neuro-endocrinological sequelae, including hypothalamic–pituitaryadrenal dysregulation, should become an area of intensive study in the future.
format article
author Alexios-Fotios A. Mentis
Anastasia M. Bougea
George P. Chrousos
author_facet Alexios-Fotios A. Mentis
Anastasia M. Bougea
George P. Chrousos
author_sort Alexios-Fotios A. Mentis
title Amyotrophic lateral sclerosis (ALS) and the endocrine system: Are there any further ties to be explored?
title_short Amyotrophic lateral sclerosis (ALS) and the endocrine system: Are there any further ties to be explored?
title_full Amyotrophic lateral sclerosis (ALS) and the endocrine system: Are there any further ties to be explored?
title_fullStr Amyotrophic lateral sclerosis (ALS) and the endocrine system: Are there any further ties to be explored?
title_full_unstemmed Amyotrophic lateral sclerosis (ALS) and the endocrine system: Are there any further ties to be explored?
title_sort amyotrophic lateral sclerosis (als) and the endocrine system: are there any further ties to be explored?
publisher Elsevier
publishDate 2021
url https://doaj.org/article/1e15cc60d549476cb898c0639cb47e88
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