Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity

Detalhes bibliográficos
Ano de defesa: 2025
Autor(a) principal: Spilari, Sarah
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: eng
Instituição de defesa: Biblioteca Digitais de Teses e Dissertações da USP
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://www.teses.usp.br/teses/disponiveis/61/61132/tde-20052025-170225/
Resumo: Introduction: 22q11.2 Deletion Syndrome (22q11.2DS), also known as DiGeorge Syndrome or Velocardiofacial Syndrome, presents multisystemic manifestations, including cardiac, gastrointestinal, craniofacial malformations, and sleep-disordered breathing, which can impact quality of life. Objective: To determine the occurrence of obstructive sleep-disordered breathing in individuals with 22q11.2DS and assess its relationship with nasal patency and cardiorespiratory capacity. Methods: Eleven patients (mean age 10.6±3.64 years) with molecular (n=6) or clinical (n=5) diagnoses of 22q11.2DS were evaluated. Questionnaires on sleep disorders, as Pediatric Sleep Questionnaire (PSQ) and Sleep Disturbance Scale for Children (SDSC) in subscales Sleep Disturbance Breathing (SDB) and Excessive Daytime Sleepiness (EDS), oral breathing, and nasal patency (CQ-5 and VAS) were administered. The 6-Minute Walk Test (6MWT) was conducted to assess cardiorespiratory capacity. A significance level of 5% (p<0.05) was adopted. Results: Positive scores for obstructive sleep apnea (OSA) were found in 54% of patients on the PSQ and 18% on the SDSC, with a positive correlation between PSQ and SDB (p=<0,05 r=0,84), and PSQ with EDS (p=<0,03 r=0,63). Daytime oral breathing was observed in 65% and nighttime oral breathing in 81%, while nasal obstruction was present in 54% of the individuals (CQ-5). The mean distance covered in the 6MWT was 401.67m (±94.02), with physiological increases in BORG escale, heart rate, respiratory frequency, and systolic blood pressure post-exercise. Diastolic blood pressure rose from 71.25 mmHg (±13.30) to 88.33 mmHg (±9.83) and showed a significant positive correlation with PSQ (p<0,05 r=0,76). Conclusion: Children and adolescents with 22q11.2DS have a high prevalence of OSA symptoms and are predominantly oral breathers with impaired nasal patency. Increased diastolic pressure during exercise may indicate future cardiovascular risk, highlighting the need for cardiovascular monitoring.
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spelling Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacityOcorrência de distúrbios respiratórios do sono em indivíduos com síndrome de deleção do cromossomo 22q11.2 e relação com a obstrução nasal e capacidade cardiorrespiratóriaApneia obstrutiva do sonoCriançasPediatricsSíndrome da deleção 22q11Sleep disordersVelocardiofacial syndromeIntroduction: 22q11.2 Deletion Syndrome (22q11.2DS), also known as DiGeorge Syndrome or Velocardiofacial Syndrome, presents multisystemic manifestations, including cardiac, gastrointestinal, craniofacial malformations, and sleep-disordered breathing, which can impact quality of life. Objective: To determine the occurrence of obstructive sleep-disordered breathing in individuals with 22q11.2DS and assess its relationship with nasal patency and cardiorespiratory capacity. Methods: Eleven patients (mean age 10.6±3.64 years) with molecular (n=6) or clinical (n=5) diagnoses of 22q11.2DS were evaluated. Questionnaires on sleep disorders, as Pediatric Sleep Questionnaire (PSQ) and Sleep Disturbance Scale for Children (SDSC) in subscales Sleep Disturbance Breathing (SDB) and Excessive Daytime Sleepiness (EDS), oral breathing, and nasal patency (CQ-5 and VAS) were administered. The 6-Minute Walk Test (6MWT) was conducted to assess cardiorespiratory capacity. A significance level of 5% (p<0.05) was adopted. Results: Positive scores for obstructive sleep apnea (OSA) were found in 54% of patients on the PSQ and 18% on the SDSC, with a positive correlation between PSQ and SDB (p=<0,05 r=0,84), and PSQ with EDS (p=<0,03 r=0,63). Daytime oral breathing was observed in 65% and nighttime oral breathing in 81%, while nasal obstruction was present in 54% of the individuals (CQ-5). The mean distance covered in the 6MWT was 401.67m (±94.02), with physiological increases in BORG escale, heart rate, respiratory frequency, and systolic blood pressure post-exercise. Diastolic blood pressure rose from 71.25 mmHg (±13.30) to 88.33 mmHg (±9.83) and showed a significant positive correlation with PSQ (p<0,05 r=0,76). Conclusion: Children and adolescents with 22q11.2DS have a high prevalence of OSA symptoms and are predominantly oral breathers with impaired nasal patency. Increased diastolic pressure during exercise may indicate future cardiovascular risk, highlighting the need for cardiovascular monitoring.Introdução: A síndrome de deleção do 22q11.2 (SD22q11.2), Síndrome de DiGeorge ou Síndrome Velocardiofacial apresenta manifestações multissistêmicas, como malformações cardíacas, gastrointestinais, craniofaciais e distúrbios respiratórios do sono (DRS), que podem afetar a qualidade de vida. Objetivo: Determinar a ocorrência de DRS em indivíduos com SD22q11.2 e correlacionar a permeabilidade nasal e capacidade cardiorrespiratória. Métodos: Foram avaliados 11 pacientes (idade média 10,6±3,64 anos), com diagnóstico molecular (n=6) ou clínico (n=5) de SD22q11.2. Questionários sobre distúrbios do sono, como o Questionário Pediátrico do Sono (PSQ) e a Escala de Distúrbios do Sono em Crianças (EDSC) nas subescalas Desordens Respiratórias do Sono (DRS) e Sonolência Excessiva Diurna (SED), respiração oral e permeabilidade nasal (CQ-5 e EVA) foram aplicados, e o TC6 (Teste de Caminhada de 6 minutos), para avaliação da capacidade cardiorrespiratória. Adotou-se nível de significância 5% (p<0,05). Resultados: Escores positivos para AOS foram encontrados em 54% dos pacientes pelo PSQ e 18% pela EDSC, havendo correlação positiva entre as escalas PSQ e DRS (p=<0,05 r=0,84748) e PSQ com SED (p=<0,03 r=0,63). A respiração oral diurna está presente em 65% e noturna em 81% da amostra, enquanto a obstrução nasal foi relatada por 54% dos indivíduos (CQ-5). A distância média percorrida no TC6 foi de 401.67m²(±94,02), com aumento fisiológico da escala BORG, frequência cardíaca, frequência respiratória e pressão arterial sistólica. Após exercício, observou-se que a pressão arterial diastólica aumentou em média de 71,25mmHg (±13,30) para 88,33mmHg(±9,83), sendo observada uma correlação positiva com a escala PSQ (p<0,05 r=0,76). Conclusão: Crianças e adolescentes com SD2q11.2 apresentam sintomas frequentes de AOS, além de serem, em sua maioria, respiradores orais com alteração de permeabilidade nasal. O aumento da pressão diastólica durante o exercício pode sugerir risco cardiovascular futuro, indicando necessidade monitoramento cardiovascular.Biblioteca Digitais de Teses e Dissertações da USPTrindade, Sergio Henrique KiemleSpilari, Sarah2025-02-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttps://www.teses.usp.br/teses/disponiveis/61/61132/tde-20052025-170225/reponame:Biblioteca Digital de Teses e Dissertações da USPinstname:Universidade de São Paulo (USP)instacron:USPLiberar o conteúdo para acesso público.info:eu-repo/semantics/openAccesseng2025-06-30T18:48:02Zoai:teses.usp.br:tde-20052025-170225Biblioteca Digital de Teses e Dissertaçõeshttp://www.teses.usp.br/PUBhttp://www.teses.usp.br/cgi-bin/mtd2br.plvirginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.bropendoar:27212025-06-30T18:48:02Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity
Ocorrência de distúrbios respiratórios do sono em indivíduos com síndrome de deleção do cromossomo 22q11.2 e relação com a obstrução nasal e capacidade cardiorrespiratória
title Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity
spellingShingle Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity
Spilari, Sarah
Apneia obstrutiva do sono
Crianças
Pediatrics
Síndrome da deleção 22q11
Sleep disorders
Velocardiofacial syndrome
title_short Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity
title_full Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity
title_fullStr Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity
title_full_unstemmed Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity
title_sort Occurrence of sleep-disordered breathing in individuals with 22q11.2 deletion syndrome and its relationship with nasal obstruction and cardiorespiratory capacity
author Spilari, Sarah
author_facet Spilari, Sarah
author_role author
dc.contributor.none.fl_str_mv Trindade, Sergio Henrique Kiemle
dc.contributor.author.fl_str_mv Spilari, Sarah
dc.subject.por.fl_str_mv Apneia obstrutiva do sono
Crianças
Pediatrics
Síndrome da deleção 22q11
Sleep disorders
Velocardiofacial syndrome
topic Apneia obstrutiva do sono
Crianças
Pediatrics
Síndrome da deleção 22q11
Sleep disorders
Velocardiofacial syndrome
description Introduction: 22q11.2 Deletion Syndrome (22q11.2DS), also known as DiGeorge Syndrome or Velocardiofacial Syndrome, presents multisystemic manifestations, including cardiac, gastrointestinal, craniofacial malformations, and sleep-disordered breathing, which can impact quality of life. Objective: To determine the occurrence of obstructive sleep-disordered breathing in individuals with 22q11.2DS and assess its relationship with nasal patency and cardiorespiratory capacity. Methods: Eleven patients (mean age 10.6±3.64 years) with molecular (n=6) or clinical (n=5) diagnoses of 22q11.2DS were evaluated. Questionnaires on sleep disorders, as Pediatric Sleep Questionnaire (PSQ) and Sleep Disturbance Scale for Children (SDSC) in subscales Sleep Disturbance Breathing (SDB) and Excessive Daytime Sleepiness (EDS), oral breathing, and nasal patency (CQ-5 and VAS) were administered. The 6-Minute Walk Test (6MWT) was conducted to assess cardiorespiratory capacity. A significance level of 5% (p<0.05) was adopted. Results: Positive scores for obstructive sleep apnea (OSA) were found in 54% of patients on the PSQ and 18% on the SDSC, with a positive correlation between PSQ and SDB (p=<0,05 r=0,84), and PSQ with EDS (p=<0,03 r=0,63). Daytime oral breathing was observed in 65% and nighttime oral breathing in 81%, while nasal obstruction was present in 54% of the individuals (CQ-5). The mean distance covered in the 6MWT was 401.67m (±94.02), with physiological increases in BORG escale, heart rate, respiratory frequency, and systolic blood pressure post-exercise. Diastolic blood pressure rose from 71.25 mmHg (±13.30) to 88.33 mmHg (±9.83) and showed a significant positive correlation with PSQ (p<0,05 r=0,76). Conclusion: Children and adolescents with 22q11.2DS have a high prevalence of OSA symptoms and are predominantly oral breathers with impaired nasal patency. Increased diastolic pressure during exercise may indicate future cardiovascular risk, highlighting the need for cardiovascular monitoring.
publishDate 2025
dc.date.none.fl_str_mv 2025-02-17
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.identifier.uri.fl_str_mv https://www.teses.usp.br/teses/disponiveis/61/61132/tde-20052025-170225/
url https://www.teses.usp.br/teses/disponiveis/61/61132/tde-20052025-170225/
dc.language.iso.fl_str_mv eng
language eng
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dc.rights.driver.fl_str_mv Liberar o conteúdo para acesso público.
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Liberar o conteúdo para acesso público.
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
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dc.publisher.none.fl_str_mv Biblioteca Digitais de Teses e Dissertações da USP
publisher.none.fl_str_mv Biblioteca Digitais de Teses e Dissertações da USP
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reponame:Biblioteca Digital de Teses e Dissertações da USP
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Biblioteca Digital de Teses e Dissertações da USP
collection Biblioteca Digital de Teses e Dissertações da USP
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)
repository.mail.fl_str_mv virginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.br
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