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

CCHS oxidative stress rare disease urinary biomarkers

Journal

Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981

Informations de publication

Date de publication:
09 May 2022
Historique:
received: 25 02 2022
revised: 25 04 2022
accepted: 06 05 2022
entrez: 28 5 2022
pubmed: 29 5 2022
medline: 29 5 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 35624794
pii: antiox11050929
doi: 10.3390/antiox11050929
pmc: PMC9138029
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : University of Florence
ID : Fondi di Ateneo 2020 to D.D. and M.R.
Organisme : A.I.S.I.C.C. (Associazione Italiana per la Sindrome da Ipoventilazione Centrale Congenita)
ID : 2021
Organisme : CCHS Foundation
ID : Grant Application 2018 (to R.P.)

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Auteurs

Marta Peruzzi (M)

Sleep Breathing Disorders and SIDS Centre, A. Meyer Children's Hospital, 50134 Florence, Italy.

Matteo Ramazzotti (M)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.

Roberta Damiano (R)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.
Newborn Screening, Biochemistry and Pharmacology Laboratory, A. Meyer Children's Hospital, 50134 Florence, Italy.

Marzia Vasarri (M)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.

Giancarlo la Marca (G)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.
Newborn Screening, Biochemistry and Pharmacology Laboratory, A. Meyer Children's Hospital, 50134 Florence, Italy.

Cinzia Arzilli (C)

Sleep Breathing Disorders and SIDS Centre, A. Meyer Children's Hospital, 50134 Florence, Italy.

Raffaele Piumelli (R)

Sleep Breathing Disorders and SIDS Centre, A. Meyer Children's Hospital, 50134 Florence, Italy.

Niccolò Nassi (N)

Sleep Breathing Disorders and SIDS Centre, A. Meyer Children's Hospital, 50134 Florence, Italy.

Donatella Degl'Innocenti (D)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.

Classifications MeSH