Breathing Abnormalities During Sleep and Wakefulness in Rett Syndrome: Clinical Relevance and Paradoxical Relationship With Circulating Pro-oxidant Markers
Breathing abnormalities are common in Rett syndrome (RTT), a pervasive neurodevelopmental disorder almost exclusively affecting females. RTT is linked to mutations in the methyl-CpG-binding protein 2 ( ) gene. Our aim was to assess the clinical relevance of apneas during sleep-wakefulness cycle in a...
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Published in | Frontiers in neurology Vol. 13; p. 833239 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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29.03.2022
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Abstract | Breathing abnormalities are common in Rett syndrome (RTT), a pervasive neurodevelopmental disorder almost exclusively affecting females. RTT is linked to mutations in the methyl-CpG-binding protein 2 (
) gene. Our aim was to assess the clinical relevance of apneas during sleep-wakefulness cycle in a population with RTT and the possible impact of apneas on circulating oxidative stress markers.
Female patients with a clinical diagnosis of typical RTT (
= 66),
gene mutation, and apneas were enrolled (mean age: 12.5 years). Baseline clinical severity, arterial blood gas analysis, and red blood cell count were assessed. Breathing was monitored during the wakefulness and sleep states (average recording time: 13 ± 0.5 h) with a portable polygraphic screening device. According to prevalence of breath holdings, the population was categorized into the wakefulness apnea (WA) and sleep apnea (SA) groups, and apnea-hypopnea index (AHI) was calculated. The impact of respiratory events on oxidative stress was assessed by plasma and intra-erythrocyte non-protein-bound iron (P-NPBI and IE-NPBI, respectively), and plasma F
-isoprostane (F
-IsoP) assays.
Significant prevalence of obstructive apneas with values of AHI > 15 was present in 69.7% of the population with RTT. The group with SA showed significantly increased AHI values > 15 (
= 0.0032), total breath holding episodes (
= 0.007), and average SpO
(
= 0.0001) as well as lower nadir SpO
(
= 0.0004) compared with the patients with WAs. The subgroups of patients with WA and SA showed no significant differences in arterial blood gas analysis variables (
> 0.089). Decreased mean cell hemoglobin (MCH) (
= 0.038) was observed in the group with WAs. P-NPBI levels were significantly higher in the group with WA than in that with SAs (
= 0.0001). Stepwise multiple linear regression models showed WA being related to nadir SpO
, average SpO
, and P-NPBI (adjusted
= 0.613, multiple correlation coefficient = 0.795
< 0.0001), and P-NPBI being related to average SpO
, blood PaCO
, red blood cell mean corpuscular volume (MCV), age, and topiramate treatment (adjusted
= 0.551, multiple correlation coefficient = 0.765,
< 0.0001).
Our findings indicate that the impact of apneas in RTT is uneven according to the sleep-wakefulness cycle, and that plasma redox active iron represents a potential novel therapeutic target. |
---|---|
AbstractList | Breathing abnormalities are common in Rett syndrome (RTT), a pervasive neurodevelopmental disorder almost exclusively affecting females. RTT is linked to mutations in the methyl-CpG-binding protein 2 (MeCP2) gene. Our aim was to assess the clinical relevance of apneas during sleep-wakefulness cycle in a population with RTT and the possible impact of apneas on circulating oxidative stress markers.BackgroundBreathing abnormalities are common in Rett syndrome (RTT), a pervasive neurodevelopmental disorder almost exclusively affecting females. RTT is linked to mutations in the methyl-CpG-binding protein 2 (MeCP2) gene. Our aim was to assess the clinical relevance of apneas during sleep-wakefulness cycle in a population with RTT and the possible impact of apneas on circulating oxidative stress markers.Female patients with a clinical diagnosis of typical RTT (n = 66), MECP2 gene mutation, and apneas were enrolled (mean age: 12.5 years). Baseline clinical severity, arterial blood gas analysis, and red blood cell count were assessed. Breathing was monitored during the wakefulness and sleep states (average recording time: 13 ± 0.5 h) with a portable polygraphic screening device. According to prevalence of breath holdings, the population was categorized into the wakefulness apnea (WA) and sleep apnea (SA) groups, and apnea-hypopnea index (AHI) was calculated. The impact of respiratory events on oxidative stress was assessed by plasma and intra-erythrocyte non-protein-bound iron (P-NPBI and IE-NPBI, respectively), and plasma F2-isoprostane (F2-IsoP) assays.MethodsFemale patients with a clinical diagnosis of typical RTT (n = 66), MECP2 gene mutation, and apneas were enrolled (mean age: 12.5 years). Baseline clinical severity, arterial blood gas analysis, and red blood cell count were assessed. Breathing was monitored during the wakefulness and sleep states (average recording time: 13 ± 0.5 h) with a portable polygraphic screening device. According to prevalence of breath holdings, the population was categorized into the wakefulness apnea (WA) and sleep apnea (SA) groups, and apnea-hypopnea index (AHI) was calculated. The impact of respiratory events on oxidative stress was assessed by plasma and intra-erythrocyte non-protein-bound iron (P-NPBI and IE-NPBI, respectively), and plasma F2-isoprostane (F2-IsoP) assays.Significant prevalence of obstructive apneas with values of AHI > 15 was present in 69.7% of the population with RTT. The group with SA showed significantly increased AHI values > 15 (p = 0.0032), total breath holding episodes (p = 0.007), and average SpO2 (p = 0.0001) as well as lower nadir SpO2 (p = 0.0004) compared with the patients with WAs. The subgroups of patients with WA and SA showed no significant differences in arterial blood gas analysis variables (p > 0.089). Decreased mean cell hemoglobin (MCH) (p = 0.038) was observed in the group with WAs. P-NPBI levels were significantly higher in the group with WA than in that with SAs (p = 0.0001). Stepwise multiple linear regression models showed WA being related to nadir SpO2, average SpO2, and P-NPBI (adjusted R 2 = 0.613, multiple correlation coefficient = 0.795 p < 0.0001), and P-NPBI being related to average SpO2, blood PaCO2, red blood cell mean corpuscular volume (MCV), age, and topiramate treatment (adjusted R 2 = 0.551, multiple correlation coefficient = 0.765, p < 0.0001).ResultsSignificant prevalence of obstructive apneas with values of AHI > 15 was present in 69.7% of the population with RTT. The group with SA showed significantly increased AHI values > 15 (p = 0.0032), total breath holding episodes (p = 0.007), and average SpO2 (p = 0.0001) as well as lower nadir SpO2 (p = 0.0004) compared with the patients with WAs. The subgroups of patients with WA and SA showed no significant differences in arterial blood gas analysis variables (p > 0.089). Decreased mean cell hemoglobin (MCH) (p = 0.038) was observed in the group with WAs. P-NPBI levels were significantly higher in the group with WA than in that with SAs (p = 0.0001). Stepwise multiple linear regression models showed WA being related to nadir SpO2, average SpO2, and P-NPBI (adjusted R 2 = 0.613, multiple correlation coefficient = 0.795 p < 0.0001), and P-NPBI being related to average SpO2, blood PaCO2, red blood cell mean corpuscular volume (MCV), age, and topiramate treatment (adjusted R 2 = 0.551, multiple correlation coefficient = 0.765, p < 0.0001).Our findings indicate that the impact of apneas in RTT is uneven according to the sleep-wakefulness cycle, and that plasma redox active iron represents a potential novel therapeutic target.ConclusionOur findings indicate that the impact of apneas in RTT is uneven according to the sleep-wakefulness cycle, and that plasma redox active iron represents a potential novel therapeutic target. Breathing abnormalities are common in Rett syndrome (RTT), a pervasive neurodevelopmental disorder almost exclusively affecting females. RTT is linked to mutations in the methyl-CpG-binding protein 2 ( ) gene. Our aim was to assess the clinical relevance of apneas during sleep-wakefulness cycle in a population with RTT and the possible impact of apneas on circulating oxidative stress markers. Female patients with a clinical diagnosis of typical RTT ( = 66), gene mutation, and apneas were enrolled (mean age: 12.5 years). Baseline clinical severity, arterial blood gas analysis, and red blood cell count were assessed. Breathing was monitored during the wakefulness and sleep states (average recording time: 13 ± 0.5 h) with a portable polygraphic screening device. According to prevalence of breath holdings, the population was categorized into the wakefulness apnea (WA) and sleep apnea (SA) groups, and apnea-hypopnea index (AHI) was calculated. The impact of respiratory events on oxidative stress was assessed by plasma and intra-erythrocyte non-protein-bound iron (P-NPBI and IE-NPBI, respectively), and plasma F -isoprostane (F -IsoP) assays. Significant prevalence of obstructive apneas with values of AHI > 15 was present in 69.7% of the population with RTT. The group with SA showed significantly increased AHI values > 15 ( = 0.0032), total breath holding episodes ( = 0.007), and average SpO ( = 0.0001) as well as lower nadir SpO ( = 0.0004) compared with the patients with WAs. The subgroups of patients with WA and SA showed no significant differences in arterial blood gas analysis variables ( > 0.089). Decreased mean cell hemoglobin (MCH) ( = 0.038) was observed in the group with WAs. P-NPBI levels were significantly higher in the group with WA than in that with SAs ( = 0.0001). Stepwise multiple linear regression models showed WA being related to nadir SpO , average SpO , and P-NPBI (adjusted = 0.613, multiple correlation coefficient = 0.795 < 0.0001), and P-NPBI being related to average SpO , blood PaCO , red blood cell mean corpuscular volume (MCV), age, and topiramate treatment (adjusted = 0.551, multiple correlation coefficient = 0.765, < 0.0001). Our findings indicate that the impact of apneas in RTT is uneven according to the sleep-wakefulness cycle, and that plasma redox active iron represents a potential novel therapeutic target. BackgroundBreathing abnormalities are common in Rett syndrome (RTT), a pervasive neurodevelopmental disorder almost exclusively affecting females. RTT is linked to mutations in the methyl-CpG-binding protein 2 (MeCP2) gene. Our aim was to assess the clinical relevance of apneas during sleep-wakefulness cycle in a population with RTT and the possible impact of apneas on circulating oxidative stress markers.MethodsFemale patients with a clinical diagnosis of typical RTT (n = 66), MECP2 gene mutation, and apneas were enrolled (mean age: 12.5 years). Baseline clinical severity, arterial blood gas analysis, and red blood cell count were assessed. Breathing was monitored during the wakefulness and sleep states (average recording time: 13 ± 0.5 h) with a portable polygraphic screening device. According to prevalence of breath holdings, the population was categorized into the wakefulness apnea (WA) and sleep apnea (SA) groups, and apnea-hypopnea index (AHI) was calculated. The impact of respiratory events on oxidative stress was assessed by plasma and intra-erythrocyte non-protein-bound iron (P-NPBI and IE-NPBI, respectively), and plasma F2-isoprostane (F2-IsoP) assays.ResultsSignificant prevalence of obstructive apneas with values of AHI > 15 was present in 69.7% of the population with RTT. The group with SA showed significantly increased AHI values > 15 (p = 0.0032), total breath holding episodes (p = 0.007), and average SpO2 (p = 0.0001) as well as lower nadir SpO2 (p = 0.0004) compared with the patients with WAs. The subgroups of patients with WA and SA showed no significant differences in arterial blood gas analysis variables (p > 0.089). Decreased mean cell hemoglobin (MCH) (p = 0.038) was observed in the group with WAs. P-NPBI levels were significantly higher in the group with WA than in that with SAs (p = 0.0001). Stepwise multiple linear regression models showed WA being related to nadir SpO2, average SpO2, and P-NPBI (adjusted R2 = 0.613, multiple correlation coefficient = 0.795 p < 0.0001), and P-NPBI being related to average SpO2, blood PaCO2, red blood cell mean corpuscular volume (MCV), age, and topiramate treatment (adjusted R2 = 0.551, multiple correlation coefficient = 0.765, p < 0.0001).ConclusionOur findings indicate that the impact of apneas in RTT is uneven according to the sleep-wakefulness cycle, and that plasma redox active iron represents a potential novel therapeutic target. |
Author | Scandurra, Valeria Hayek, Joussef Rossi, Marcello Canitano, Roberto Boasiako, Lidia Ciccoli, Lucia Leoncini, Silvia Signorini, Cinzia De Felice, Claudio |
AuthorAffiliation | 4 Child Neuropsychiatry Unit, University Hospital, Azienda Ospedaliera Universitaria Senese , Siena , Italy 1 Rett Syndrome Trial Center, Child Neuropsychiatry Unit, University Hospital Azienda Ospedaliera Universitaria Senese , Siena , Italy 5 Respiratory Pathophysiology and Rehabilitation Unit, University Hospital, Azienda Ospedaliera Universitaria Senese , Siena , Italy 2 Neonatal Intensive Care Unit, University Hospital Azienda Ospedaliera Universitaria Senese , Siena , Italy 3 Department of Molecular and Developmental Medicine, University of Siena , Siena , Italy |
AuthorAffiliation_xml | – name: 1 Rett Syndrome Trial Center, Child Neuropsychiatry Unit, University Hospital Azienda Ospedaliera Universitaria Senese , Siena , Italy – name: 2 Neonatal Intensive Care Unit, University Hospital Azienda Ospedaliera Universitaria Senese , Siena , Italy – name: 3 Department of Molecular and Developmental Medicine, University of Siena , Siena , Italy – name: 4 Child Neuropsychiatry Unit, University Hospital, Azienda Ospedaliera Universitaria Senese , Siena , Italy – name: 5 Respiratory Pathophysiology and Rehabilitation Unit, University Hospital, Azienda Ospedaliera Universitaria Senese , Siena , Italy |
Author_xml | – sequence: 1 givenname: Silvia surname: Leoncini fullname: Leoncini, Silvia – sequence: 2 givenname: Cinzia surname: Signorini fullname: Signorini, Cinzia – sequence: 3 givenname: Lidia surname: Boasiako fullname: Boasiako, Lidia – sequence: 4 givenname: Valeria surname: Scandurra fullname: Scandurra, Valeria – sequence: 5 givenname: Joussef surname: Hayek fullname: Hayek, Joussef – sequence: 6 givenname: Lucia surname: Ciccoli fullname: Ciccoli, Lucia – sequence: 7 givenname: Marcello surname: Rossi fullname: Rossi, Marcello – sequence: 8 givenname: Roberto surname: Canitano fullname: Canitano, Roberto – sequence: 9 givenname: Claudio surname: De Felice fullname: De Felice, Claudio |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35422749$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_3390_ijms24086962 crossref_primary_10_1016_j_atherosclerosis_2024_118600 crossref_primary_10_3389_fneur_2024_1388506 crossref_primary_10_1007_s10286_023_00958_6 crossref_primary_10_1016_j_ncl_2023_01_004 crossref_primary_10_1002_ppul_26796 crossref_primary_10_3390_children10091442 |
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ContentType | Journal Article |
Copyright | Copyright © 2022 Leoncini, Signorini, Boasiako, Scandurra, Hayek, Ciccoli, Rossi, Canitano and De Felice. Copyright © 2022 Leoncini, Signorini, Boasiako, Scandurra, Hayek, Ciccoli, Rossi, Canitano and De Felice. 2022 Leoncini, Signorini, Boasiako, Scandurra, Hayek, Ciccoli, Rossi, Canitano and De Felice |
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Keywords | non-protein-bound iron oxidative stress respiratory dysfunction Rett syndrome sleep-wakefulness cycle |
Language | English |
License | Copyright © 2022 Leoncini, Signorini, Boasiako, Scandurra, Hayek, Ciccoli, Rossi, Canitano and De Felice. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Maurizio Elia, IRCCS Oasi Maria SS, Italy; Rosa Peraita- Adrados, Complutense University of Madrid, Spain Edited by: Karen Spruyt, Institut National de la Santé et de la Recherche Médicale (INSERM), France This article was submitted to Pediatric Neurology, a section of the journal Frontiers in Neurology |
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Snippet | Breathing abnormalities are common in Rett syndrome (RTT), a pervasive neurodevelopmental disorder almost exclusively affecting females. RTT is linked to... BackgroundBreathing abnormalities are common in Rett syndrome (RTT), a pervasive neurodevelopmental disorder almost exclusively affecting females. RTT is... |
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SubjectTerms | Neurology non-protein-bound iron oxidative stress respiratory dysfunction Rett syndrome sleep-wakefulness cycle |
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Title | Breathing Abnormalities During Sleep and Wakefulness in Rett Syndrome: Clinical Relevance and Paradoxical Relationship With Circulating Pro-oxidant Markers |
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