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Systems Biology Genetic Approach Identifies Serotonin Pathway as a Possible Target for Obstructive Sleep Apnea: Results from a Literature Search Review

RATIONALE: Overall validity of existing genetic biomarkers in the diagnosis of obstructive sleep apnea (OSA) remains unclear. The objective of this systematic genetic study is to identify “novel” biomarkers for OSA using systems biology approach. METHODS: Candidate genes for OSA were extracted from...

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Autores principales: Jagannathan, Ram, Seixas, Azizi, St-Jules, David, Jagannathan, Lakshmanan, Rogers, April, Hu, Lu, Jean-Louis, Girardin, Sevick, Mary Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625807/
https://www.ncbi.nlm.nih.gov/pubmed/29057124
http://dx.doi.org/10.1155/2017/6768323
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author Jagannathan, Ram
Seixas, Azizi
St-Jules, David
Jagannathan, Lakshmanan
Rogers, April
Hu, Lu
Jean-Louis, Girardin
Sevick, Mary Ann
author_facet Jagannathan, Ram
Seixas, Azizi
St-Jules, David
Jagannathan, Lakshmanan
Rogers, April
Hu, Lu
Jean-Louis, Girardin
Sevick, Mary Ann
author_sort Jagannathan, Ram
collection PubMed
description RATIONALE: Overall validity of existing genetic biomarkers in the diagnosis of obstructive sleep apnea (OSA) remains unclear. The objective of this systematic genetic study is to identify “novel” biomarkers for OSA using systems biology approach. METHODS: Candidate genes for OSA were extracted from PubMed, MEDLINE, and Embase search engines and DisGeNET database. The gene ontology (GO) analyses and candidate genes prioritization were performed using Enrichr tool. Genes pertaining to the top 10 pathways were extracted and used for Ingenuity Pathway Analysis. RESULTS: In total, we have identified 153 genes. The top 10 pathways associated with OSA include (i) serotonin receptor interaction, (ii) pathways in cancer, (iii) AGE-RAGE signaling in diabetes, (iv) infectious diseases, (v) serotonergic synapse, (vi) inflammatory bowel disease, (vii) HIF-1 signaling pathway, (viii) PI3-AKT signaling pathway, (ix) regulation lipolysis in adipocytes, and (x) rheumatoid arthritis. After removing the overlapping genes, we have identified 23 candidate genes, out of which >30% of the genes were related to the genes involved in the serotonin pathway. Among these 4 serotonin receptors SLC6A4, HTR2C, HTR2A, and HTR1B were strongly associated with OSA. CONCLUSIONS: This preliminary report identifies several potential candidate genes associated with OSA and also describes the possible regulatory mechanisms.
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spelling pubmed-56258072017-10-22 Systems Biology Genetic Approach Identifies Serotonin Pathway as a Possible Target for Obstructive Sleep Apnea: Results from a Literature Search Review Jagannathan, Ram Seixas, Azizi St-Jules, David Jagannathan, Lakshmanan Rogers, April Hu, Lu Jean-Louis, Girardin Sevick, Mary Ann Sleep Disord Research Article RATIONALE: Overall validity of existing genetic biomarkers in the diagnosis of obstructive sleep apnea (OSA) remains unclear. The objective of this systematic genetic study is to identify “novel” biomarkers for OSA using systems biology approach. METHODS: Candidate genes for OSA were extracted from PubMed, MEDLINE, and Embase search engines and DisGeNET database. The gene ontology (GO) analyses and candidate genes prioritization were performed using Enrichr tool. Genes pertaining to the top 10 pathways were extracted and used for Ingenuity Pathway Analysis. RESULTS: In total, we have identified 153 genes. The top 10 pathways associated with OSA include (i) serotonin receptor interaction, (ii) pathways in cancer, (iii) AGE-RAGE signaling in diabetes, (iv) infectious diseases, (v) serotonergic synapse, (vi) inflammatory bowel disease, (vii) HIF-1 signaling pathway, (viii) PI3-AKT signaling pathway, (ix) regulation lipolysis in adipocytes, and (x) rheumatoid arthritis. After removing the overlapping genes, we have identified 23 candidate genes, out of which >30% of the genes were related to the genes involved in the serotonin pathway. Among these 4 serotonin receptors SLC6A4, HTR2C, HTR2A, and HTR1B were strongly associated with OSA. CONCLUSIONS: This preliminary report identifies several potential candidate genes associated with OSA and also describes the possible regulatory mechanisms. Hindawi 2017 2017-09-19 /pmc/articles/PMC5625807/ /pubmed/29057124 http://dx.doi.org/10.1155/2017/6768323 Text en Copyright © 2017 Ram Jagannathan et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jagannathan, Ram
Seixas, Azizi
St-Jules, David
Jagannathan, Lakshmanan
Rogers, April
Hu, Lu
Jean-Louis, Girardin
Sevick, Mary Ann
Systems Biology Genetic Approach Identifies Serotonin Pathway as a Possible Target for Obstructive Sleep Apnea: Results from a Literature Search Review
title Systems Biology Genetic Approach Identifies Serotonin Pathway as a Possible Target for Obstructive Sleep Apnea: Results from a Literature Search Review
title_full Systems Biology Genetic Approach Identifies Serotonin Pathway as a Possible Target for Obstructive Sleep Apnea: Results from a Literature Search Review
title_fullStr Systems Biology Genetic Approach Identifies Serotonin Pathway as a Possible Target for Obstructive Sleep Apnea: Results from a Literature Search Review
title_full_unstemmed Systems Biology Genetic Approach Identifies Serotonin Pathway as a Possible Target for Obstructive Sleep Apnea: Results from a Literature Search Review
title_short Systems Biology Genetic Approach Identifies Serotonin Pathway as a Possible Target for Obstructive Sleep Apnea: Results from a Literature Search Review
title_sort systems biology genetic approach identifies serotonin pathway as a possible target for obstructive sleep apnea: results from a literature search review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625807/
https://www.ncbi.nlm.nih.gov/pubmed/29057124
http://dx.doi.org/10.1155/2017/6768323
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