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タイトル: Association between Plasma Neutrophil Gelatinase Associated Lipocalin Level and Obstructive Sleep Apnea or Nocturnal Intermittent Hypoxia.
著者: Murase, Kimihiko
Mori, Kiyoshi
Yoshimura, Chikara
Aihara, Kensaku
Chihara, Yuichi
Azuma, Masanori
Harada, Yuka
Toyama, Yoshiro
Tanizawa, Kiminobu  KAKEN_id  orcid https://orcid.org/0000-0002-5719-0744 (unconfirmed)
Handa, Tomohiro  kyouindb  KAKEN_id
Hitomi, Takefumi  KAKEN_id
Oga, Toru  KAKEN_id
Mishima, Michiaki
Chin, Kazuo  KAKEN_id
著者名の別形: 村瀬, 公彦
陳, 和夫
発行日: Jan-2013
出版者: Public Library of Science
誌名: PloS one
巻: 8
号: 1
論文番号: e54184
抄録: [Background]Both obstructive sleep apnea (OSA) and a novel lipocalin, neutrophil gelatinase associated lipocalin (Ngal), have been reported to be closely linked with cardiovascular disease and loss of kidney function through chronic inflammation. However, the relationship between OSA and Ngal has never been investigated. [Objectives]To evaluate the relationship between Ngal and OSA in clinical practice. [Methods]In 102 patients, polysomnography was performed to diagnose OSA and plasma Ngal levels were measured. The correlations between Ngal levels and OSA severity and other clinical variables were evaluated. Of the 46 patients who began treatment with continuous positive airway pressure (CPAP), Ngal levels were reevaluated after three months of treatment in 25 patients. [Results]The Ngal level correlated significantly with OSA severity as determined by the apnea hypopnea index (r = 0.24, p = 0.01) and 4% oxygen desaturation index (ODI) (r = 0.26, p = 0.01). Multiple regression analysis showed that the Ngal level was associated with 4%ODI independently of other clinical variables. Compliance was good in 13 of the 25 patients who used CPAP. Although the OSA (4%ODI: 33.1±16.7 to 1.1±1.9/h, p<0.01) had significantly improved in those with good compliance, the Ngal levels were not significantly changed (60.5±18.1 before CPAP vs 64.2±13.9 ng/ml after CPAP, p = 0.27). [Conclusions]Plasma Ngal levels were positively associated with the severity of OSA. However, the contribution rate of OSA to systemic Ngal secretion was small and changes in Ngal levels appeared to be influenced largely by other confounding factors. Therefore, it does not seem reasonable to use the Ngal level as a specific biomarker of OSA in clinical practice.
著作権等: © 2013 Murase et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
URI: http://hdl.handle.net/2433/169767
DOI(出版社版): 10.1371/journal.pone.0054184
PubMed ID: 23342100
出現コレクション:学術雑誌掲載論文等

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