NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW

Detalhes bibliográficos
Autor(a) principal: Machado, Alessandra Aparecida Vieira
Data de Publicação: 2023
Outros Autores: Souza, José Carlos Rosa Pires de, Bottino, Breno
Tipo de documento: Artigo
Idioma: por
Título da fonte: Arquivos Médicos dos Hospitais e da Faculdade de Ciências Médicas da Santa Casa de São Paulo (Online)
Texto Completo: http://arquivosmedicos.fcmsantacasasp.edu.br/index.php/AMSCSP/article/view/904
Resumo: Narcolepsy is a sleep disorder that causes physical, psychological and social damage which total or partial work or academic incapacity. Objectives: Present the main findings in the scientific literature about the neurobiological, immunological/genetic and diagnostic aspects of narclepsy. Method: Integrative literature review. The databases used in the search were: Scielo, Pubmed, LILACS and Science, basically using the descriptors “narcolepsy”, “orexin”, “cataplexy” and “neurobiology”, with the Boolean operator “and” or “or”. Results: We found 151 articles, and 23 were selected for analysis. The International Classification of Sleep Disorders (ICSD-3) differentiates narcolepsy into two pathologies, type 1 (NT1), is characterized by periods of irresistible need for sleep, cataplexy, and sometimes symptoms such as hypnagogic hallucinations, sleep paralysis and disturbed night sleep. It ischaracterized by the loss of hypocretin neurons in the hypothalamus, possibly linked to an autoimmune process. In NT2, cataplexy is absent and CSF hypocretin levels are normal. The etiopathogenesis and pathophysiology involve several genetic, immunological and hormonal aspects. Diagnosis is made with polysomnography, multiple sleep latency testing, human leukocyte antigen (HLA) typing, cerebrospinal fluid (CSF) hypocretin level, or neuroimaging in suspected narcolepsy secondary to another pathology. Conclusion: neurosciences and related ones have advanced in discoveries about the neurobiology and natural history of narcolepsy; however, new studies should relate it to other aspects, such as endocrinology
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spelling NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEWAspectos neurobiológicos, genéticos e imunológicos da narcolepsia: revisão integrativa da literatura / Neurobiological, genetic and immunological aspects of narcolepsy: integrative literature reviewNarcolepsy is a sleep disorder that causes physical, psychological and social damage which total or partial work or academic incapacity. Objectives: Present the main findings in the scientific literature about the neurobiological, immunological/genetic and diagnostic aspects of narclepsy. Method: Integrative literature review. The databases used in the search were: Scielo, Pubmed, LILACS and Science, basically using the descriptors “narcolepsy”, “orexin”, “cataplexy” and “neurobiology”, with the Boolean operator “and” or “or”. Results: We found 151 articles, and 23 were selected for analysis. The International Classification of Sleep Disorders (ICSD-3) differentiates narcolepsy into two pathologies, type 1 (NT1), is characterized by periods of irresistible need for sleep, cataplexy, and sometimes symptoms such as hypnagogic hallucinations, sleep paralysis and disturbed night sleep. It ischaracterized by the loss of hypocretin neurons in the hypothalamus, possibly linked to an autoimmune process. In NT2, cataplexy is absent and CSF hypocretin levels are normal. The etiopathogenesis and pathophysiology involve several genetic, immunological and hormonal aspects. Diagnosis is made with polysomnography, multiple sleep latency testing, human leukocyte antigen (HLA) typing, cerebrospinal fluid (CSF) hypocretin level, or neuroimaging in suspected narcolepsy secondary to another pathology. Conclusion: neurosciences and related ones have advanced in discoveries about the neurobiology and natural history of narcolepsy; however, new studies should relate it to other aspects, such as endocrinologyIntrodução: A narcolepsia é um distúrbio do sono que causa sérios prejuízos físicos, psicológicos e sociais, podendo causar incapacidade laboral ou acadêmica, total ou parcial. Objetivo: Discutir as nuances relacionadas ao paciente com narcolepsia sobre os aspectos neurobiológicos, imunológicos, genéticos e diagnósticos. Método: Revisão de literatura do tipo integrativa. As bases de dados utilizadas na busca foram: SciELO, PubMed, LILACS e Science, utilizando-se basicamente os descritores “narcolepsy”, “orexin”, “cataplexy” e “neurobiology”, com o operadorbooleano “and” ou “or”. Resultados: Dos 151 artigos localizados, 23 foram selecionados para análise. A Classificação Internacional de Distúrbios do Sono (ICSD-3) diferencia a narcolepsia em duas patologias, sendo que a do tipo 1 (NT1) é caracterizada por períodos de necessidade irresistível de dormir, cataplexia, e, por vezes, sintomas como alucinações hipnagógicas, paralisia do sono e sono noturno perturbado. Caracteriza-se pela perda de neurônios de hipocretina no hipotálamo, possivelmente ligados a um processo autoimune. Já na NT2, a cataplexia está ausente, e os níveis de hipocretina no líquor (LCR) são normais. A etiopatogenia e fisiopatologia envolvem diversos aspectos genéticos, imunológicos e hormonais. O diagnóstico é feito com polissonografia, teste de latências múltiplas do sono, tipagem de antígenos leucocitários humanos (HLA), punção lombar para medir o nível de hipocretina no LCR ou neuroimagem na suspeita de narcolepsia secundária a outra patologia. Conclusão: Asneurociências e outras correlatas avançaram nas descobertas sobre a neurobiologia e a história natural da narcolepsia, entretanto novos estudos devem relacioná-la com outros aspectos como, por exemplo, endocrinológicos.Palavras-chave: Narcolepsia, Orexinas, Neurobiologia, Cataplexia. ABSTRACT Introduction: Narcolepsy is a sleep disorder that causes physical, psychological and social damage, which total or partial, work or academic, incapacity. Objective: To present the main findings in the scientific literature about the neurobiological, immunological/genetic and diagnostic aspects of narcolepsy. Method: Integrative literature review. The databases used in the search were: Scientific Electronic Library Online (SciELO), United States National Library of Medicine (PubMed), Literatura Latino-Americana e do Caribe em Ciências da Saúde (LILACS) and Science,basically using the descriptors “narcolepsy”, “orexin”, “cataplexy” and “neurobiology”, with the Boolean operator “and” or “or”. Results: We found 151 articles, and 23 were selected for analysis. The International Classification of Sleep Disorders (ICSD-3) differentiates narcolepsy into two pathologies: type 1 (NT1) is characterized by periods of irresistible need for sleep, cataplexy, and sometimes symptoms such as hypnagogic hallucinations, sleep paralysis and disturbed night sleep. It is characterized by the loss of hypocretin neurons in the hypothalamus, possibly linkedto an autoimmune process. In type 2 (NT2), cataplexy is absent and CSF hypocretin levels are normal. The etiopathogenesis and pathophysiology involve several genetic, immunological and hormonal aspects. Diagnosis is made with polysomnography, multiple sleep latency testing, human leukocyte antigen (HLA) typing, cerebrospinal fluid (CSF) hypocretin level, or neuroimaging in suspected narcolepsy secondary to another pathology. Conclusion: Neurosciences and related fields have advanced in discoveries about the neurobiology and natural history of narcolepsy; however, new studies should relate it to other aspects, such as endocrinology.Keywords: Narcolepsy, Orexins, Neurobiology, CataplexyFaculdade de Ciências Médicas da Santa Casa de São Paulo2023-10-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://arquivosmedicos.fcmsantacasasp.edu.br/index.php/AMSCSP/article/view/90410.26432/1809-3019.2023.68.014Arquivos Médicos dos Hospitais e da Faculdade de Ciências Médicas da Santa Casa de São Paulo; V. 68 (2023): Jan/Dez; 1 of 91809-30190101-6067reponame:Arquivos Médicos dos Hospitais e da Faculdade de Ciências Médicas da Santa Casa de São Paulo (Online)instname:Faculdade de Ciências Médicas da Santa Casa de São Pauloinstacron:FCMSCSPporhttp://arquivosmedicos.fcmsantacasasp.edu.br/index.php/AMSCSP/article/view/904/1214Copyright (c) 2023 Alessandra Aparecida Vieira Machado, José Carlos, Breno Bottinohttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessMachado, Alessandra Aparecida VieiraSouza, José Carlos Rosa Pires deBottino, Breno2023-10-11T18:09:24Zoai:ojs2.arquivosmedicos.fcmsantacasasp.edu.br:article/904Revistahttp://arquivosmedicos.fcmsantacasasp.edu.br/index.php/AMSCSPONGhttp://arquivosmedicos.fcmsantacasasp.edu.br/index.php/AMSCSP/oaiarquivosmedicos@fcmsantacasasp.edu.br||1809-30190101-6067opendoar:2023-10-11T18:09:24Arquivos Médicos dos Hospitais e da Faculdade de Ciências Médicas da Santa Casa de São Paulo (Online) - Faculdade de Ciências Médicas da Santa Casa de São Paulofalse
dc.title.none.fl_str_mv NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW
Aspectos neurobiológicos, genéticos e imunológicos da narcolepsia: revisão integrativa da literatura / Neurobiological, genetic and immunological aspects of narcolepsy: integrative literature review
title NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW
spellingShingle NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW
Machado, Alessandra Aparecida Vieira
title_short NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW
title_full NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW
title_fullStr NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW
title_full_unstemmed NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW
title_sort NEUROBIOLOGICAL, GENETIC AND IMMUNOLOGICAL ASPECTS OF NARCOLEPSY: INTEGRATIVE LITERATURE REVIEW
author Machado, Alessandra Aparecida Vieira
author_facet Machado, Alessandra Aparecida Vieira
Souza, José Carlos Rosa Pires de
Bottino, Breno
author_role author
author2 Souza, José Carlos Rosa Pires de
Bottino, Breno
author2_role author
author
dc.contributor.author.fl_str_mv Machado, Alessandra Aparecida Vieira
Souza, José Carlos Rosa Pires de
Bottino, Breno
description Narcolepsy is a sleep disorder that causes physical, psychological and social damage which total or partial work or academic incapacity. Objectives: Present the main findings in the scientific literature about the neurobiological, immunological/genetic and diagnostic aspects of narclepsy. Method: Integrative literature review. The databases used in the search were: Scielo, Pubmed, LILACS and Science, basically using the descriptors “narcolepsy”, “orexin”, “cataplexy” and “neurobiology”, with the Boolean operator “and” or “or”. Results: We found 151 articles, and 23 were selected for analysis. The International Classification of Sleep Disorders (ICSD-3) differentiates narcolepsy into two pathologies, type 1 (NT1), is characterized by periods of irresistible need for sleep, cataplexy, and sometimes symptoms such as hypnagogic hallucinations, sleep paralysis and disturbed night sleep. It ischaracterized by the loss of hypocretin neurons in the hypothalamus, possibly linked to an autoimmune process. In NT2, cataplexy is absent and CSF hypocretin levels are normal. The etiopathogenesis and pathophysiology involve several genetic, immunological and hormonal aspects. Diagnosis is made with polysomnography, multiple sleep latency testing, human leukocyte antigen (HLA) typing, cerebrospinal fluid (CSF) hypocretin level, or neuroimaging in suspected narcolepsy secondary to another pathology. Conclusion: neurosciences and related ones have advanced in discoveries about the neurobiology and natural history of narcolepsy; however, new studies should relate it to other aspects, such as endocrinology
publishDate 2023
dc.date.none.fl_str_mv 2023-10-11
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dc.identifier.uri.fl_str_mv http://arquivosmedicos.fcmsantacasasp.edu.br/index.php/AMSCSP/article/view/904
10.26432/1809-3019.2023.68.014
url http://arquivosmedicos.fcmsantacasasp.edu.br/index.php/AMSCSP/article/view/904
identifier_str_mv 10.26432/1809-3019.2023.68.014
dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv http://arquivosmedicos.fcmsantacasasp.edu.br/index.php/AMSCSP/article/view/904/1214
dc.rights.driver.fl_str_mv Copyright (c) 2023 Alessandra Aparecida Vieira Machado, José Carlos, Breno Bottino
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2023 Alessandra Aparecida Vieira Machado, José Carlos, Breno Bottino
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Faculdade de Ciências Médicas da Santa Casa de São Paulo
publisher.none.fl_str_mv Faculdade de Ciências Médicas da Santa Casa de São Paulo
dc.source.none.fl_str_mv Arquivos Médicos dos Hospitais e da Faculdade de Ciências Médicas da Santa Casa de São Paulo; V. 68 (2023): Jan/Dez; 1 of 9
1809-3019
0101-6067
reponame:Arquivos Médicos dos Hospitais e da Faculdade de Ciências Médicas da Santa Casa de São Paulo (Online)
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