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Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up

Congenital Central Hypoventilation Syndrome (CCHS) is a rare genetic disorder of the autonomic nervous system and in particular of the respiratory control during sleep. No drug therapy is, to date, available; therefore, the survival of these patients depends on lifelong ventilatory support during sl...

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Autores principales: Peruzzi, Marta, Ramazzotti, Matteo, Damiano, Roberta, Vasarri, Marzia, la Marca, Giancarlo, Arzilli, Cinzia, Piumelli, Raffaele, Nassi, Niccolò, Degl'Innocenti, Donatella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138029/
https://www.ncbi.nlm.nih.gov/pubmed/35624794
http://dx.doi.org/10.3390/antiox11050929
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author Peruzzi, Marta
Ramazzotti, Matteo
Damiano, Roberta
Vasarri, Marzia
la Marca, Giancarlo
Arzilli, Cinzia
Piumelli, Raffaele
Nassi, Niccolò
Degl'Innocenti, Donatella
author_facet Peruzzi, Marta
Ramazzotti, Matteo
Damiano, Roberta
Vasarri, Marzia
la Marca, Giancarlo
Arzilli, Cinzia
Piumelli, Raffaele
Nassi, Niccolò
Degl'Innocenti, Donatella
author_sort Peruzzi, Marta
collection PubMed
description Congenital Central Hypoventilation Syndrome (CCHS) is a rare genetic disorder of the autonomic nervous system and in particular of the respiratory control during sleep. No drug therapy is, to date, available; therefore, the survival of these patients depends on lifelong ventilatory support during sleep. Reactive oxygen species (ROS)-induced oxidative stress is a recognized risk factor involved in the pathogenesis of several chronic diseases. Therefore, monitoring systemic oxidative stress could provide important insights into CCHS outcomes. Because ROS-induced oxidative products are excreted as stable metabolites in urine, we performed an HPLC-MS/MS analysis for the quantitative determination of the three main representative oxidative biomarkers (i.e., diY, MDA, and 8-OHdG) in the urine of CCHS patients. Higher levels of urinary MDA were found in CCHS patients compared with age-matched control subjects. The noteworthy finding is the identification of urinary MDA as relevant biomarker of systemic oxidative status in CCHS patients. This study is a concise and smart communication about the impact that oxidative stress has in CCHS, and suggests the monitoring of urinary MDA levels as a useful tool for the management of these patients.
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spelling pubmed-91380292022-05-28 Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up Peruzzi, Marta Ramazzotti, Matteo Damiano, Roberta Vasarri, Marzia la Marca, Giancarlo Arzilli, Cinzia Piumelli, Raffaele Nassi, Niccolò Degl'Innocenti, Donatella Antioxidants (Basel) Communication Congenital Central Hypoventilation Syndrome (CCHS) is a rare genetic disorder of the autonomic nervous system and in particular of the respiratory control during sleep. No drug therapy is, to date, available; therefore, the survival of these patients depends on lifelong ventilatory support during sleep. Reactive oxygen species (ROS)-induced oxidative stress is a recognized risk factor involved in the pathogenesis of several chronic diseases. Therefore, monitoring systemic oxidative stress could provide important insights into CCHS outcomes. Because ROS-induced oxidative products are excreted as stable metabolites in urine, we performed an HPLC-MS/MS analysis for the quantitative determination of the three main representative oxidative biomarkers (i.e., diY, MDA, and 8-OHdG) in the urine of CCHS patients. Higher levels of urinary MDA were found in CCHS patients compared with age-matched control subjects. The noteworthy finding is the identification of urinary MDA as relevant biomarker of systemic oxidative status in CCHS patients. This study is a concise and smart communication about the impact that oxidative stress has in CCHS, and suggests the monitoring of urinary MDA levels as a useful tool for the management of these patients. MDPI 2022-05-09 /pmc/articles/PMC9138029/ /pubmed/35624794 http://dx.doi.org/10.3390/antiox11050929 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 Communication
Peruzzi, Marta
Ramazzotti, Matteo
Damiano, Roberta
Vasarri, Marzia
la Marca, Giancarlo
Arzilli, Cinzia
Piumelli, Raffaele
Nassi, Niccolò
Degl'Innocenti, Donatella
Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up
title Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up
title_full Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up
title_fullStr Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up
title_full_unstemmed Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up
title_short Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up
title_sort urinary biomarkers as a proxy for congenital central hypoventilation syndrome patient follow-up
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138029/
https://www.ncbi.nlm.nih.gov/pubmed/35624794
http://dx.doi.org/10.3390/antiox11050929
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