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Plasma Homocysteine and Autonomic Nervous Dysfunction: Association and Clinical Relevance in OSAS

OBJECTIVE: Elevated plasma homocysteine (Hcy) is an independent risk factor for cardiovascular diseases, but the precise mechanism of Hcy in cardiovascular disease remains elusive. This study is aimed at evaluating the association between Hcy levels and autonomic nervous system and at investigating...

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Autores principales: Liu, Lei, Wu, Qiansheng, Yan, Hong, Zheng, Xilong, Zhou, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368224/
https://www.ncbi.nlm.nih.gov/pubmed/32695242
http://dx.doi.org/10.1155/2020/4378505
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author Liu, Lei
Wu, Qiansheng
Yan, Hong
Zheng, Xilong
Zhou, Qiang
author_facet Liu, Lei
Wu, Qiansheng
Yan, Hong
Zheng, Xilong
Zhou, Qiang
author_sort Liu, Lei
collection PubMed
description OBJECTIVE: Elevated plasma homocysteine (Hcy) is an independent risk factor for cardiovascular diseases, but the precise mechanism of Hcy in cardiovascular disease remains elusive. This study is aimed at evaluating the association between Hcy levels and autonomic nervous system and at investigating their clinical relevance in obstructive sleep apnea syndrome (OSAS). METHODS: A total of 191 subjects with OSAS were enrolled for this cross-sectional study. Heart rate variability (HRV) represents the status of the autonomic nervous system and is a well-known index that allows studying the autonomic modulation. HRV and polysomnography parameters were collected based on Holter monitors and polysomnography system. The software computed all the basic HRV parameters including SDANN, SDNN and pNN50. Correlation analyses between Hcy and HRV parameters and echocardiographic parameters were performed. RESULTS: Compared with the mild-moderate OSAS group, the prevalence of male and smoking and Hcy levels were considerably higher in the severe OSAS group (P = 0.01, P = 0.02, and P = 0.01, respectively). Also, there were significant linear relationships between Hcy quartiles with the proportion of severe OSAS (P = 0.01 for the trend). Interesting, there is a negative linear correlation between SDANN and Hcy quartiles (P = 0.02 for the trend). Spearman's correlation analysis showed a significant negative correlation between SDANN and Hcy levels (r = −0.17, P = 0.02). Interestingly, the relationship of it remains significant after adjustment for clinical covariates (r = −0.15, P = 0.04). However, echocardiographic parameters were not significantly correlated with Hcy or HRV parameters (all P > 0.05). CONCLUSIONS: Elevated plasma Hcy level is linearly correlated with cardiac autonomic nervous function disorders in patients with OSAS.
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spelling pubmed-73682242020-07-20 Plasma Homocysteine and Autonomic Nervous Dysfunction: Association and Clinical Relevance in OSAS Liu, Lei Wu, Qiansheng Yan, Hong Zheng, Xilong Zhou, Qiang Dis Markers Research Article OBJECTIVE: Elevated plasma homocysteine (Hcy) is an independent risk factor for cardiovascular diseases, but the precise mechanism of Hcy in cardiovascular disease remains elusive. This study is aimed at evaluating the association between Hcy levels and autonomic nervous system and at investigating their clinical relevance in obstructive sleep apnea syndrome (OSAS). METHODS: A total of 191 subjects with OSAS were enrolled for this cross-sectional study. Heart rate variability (HRV) represents the status of the autonomic nervous system and is a well-known index that allows studying the autonomic modulation. HRV and polysomnography parameters were collected based on Holter monitors and polysomnography system. The software computed all the basic HRV parameters including SDANN, SDNN and pNN50. Correlation analyses between Hcy and HRV parameters and echocardiographic parameters were performed. RESULTS: Compared with the mild-moderate OSAS group, the prevalence of male and smoking and Hcy levels were considerably higher in the severe OSAS group (P = 0.01, P = 0.02, and P = 0.01, respectively). Also, there were significant linear relationships between Hcy quartiles with the proportion of severe OSAS (P = 0.01 for the trend). Interesting, there is a negative linear correlation between SDANN and Hcy quartiles (P = 0.02 for the trend). Spearman's correlation analysis showed a significant negative correlation between SDANN and Hcy levels (r = −0.17, P = 0.02). Interestingly, the relationship of it remains significant after adjustment for clinical covariates (r = −0.15, P = 0.04). However, echocardiographic parameters were not significantly correlated with Hcy or HRV parameters (all P > 0.05). CONCLUSIONS: Elevated plasma Hcy level is linearly correlated with cardiac autonomic nervous function disorders in patients with OSAS. Hindawi 2020-07-08 /pmc/articles/PMC7368224/ /pubmed/32695242 http://dx.doi.org/10.1155/2020/4378505 Text en Copyright © 2020 Lei Liu et al. http://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
Liu, Lei
Wu, Qiansheng
Yan, Hong
Zheng, Xilong
Zhou, Qiang
Plasma Homocysteine and Autonomic Nervous Dysfunction: Association and Clinical Relevance in OSAS
title Plasma Homocysteine and Autonomic Nervous Dysfunction: Association and Clinical Relevance in OSAS
title_full Plasma Homocysteine and Autonomic Nervous Dysfunction: Association and Clinical Relevance in OSAS
title_fullStr Plasma Homocysteine and Autonomic Nervous Dysfunction: Association and Clinical Relevance in OSAS
title_full_unstemmed Plasma Homocysteine and Autonomic Nervous Dysfunction: Association and Clinical Relevance in OSAS
title_short Plasma Homocysteine and Autonomic Nervous Dysfunction: Association and Clinical Relevance in OSAS
title_sort plasma homocysteine and autonomic nervous dysfunction: association and clinical relevance in osas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368224/
https://www.ncbi.nlm.nih.gov/pubmed/32695242
http://dx.doi.org/10.1155/2020/4378505
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