Nocturnal oxygen therapy prevents progress of congestive heart failure with central sleep apnea

被引:31
作者
Shigemitsu, Meiei
Nishio, Kazuaki
Kusuyama, Taro
Itoh, Seiji
Konno, Noboru
Katagiri, Takashi
机构
[1] Yamanashi Red Cross Hosp, Dept Internal Med, Yamanashi 4010301, Japan
[2] Showa Univ, Sch Med, Dept Internal Med 3, Tokyo 142, Japan
关键词
central sleep apnea; congestive heart failure; nocturnal oxygen therapy; sympathetic nerve activity;
D O I
10.1016/j.ijcard.2006.03.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Sleep disordered breathing has been reported to be associated with congestive heart failure (CHF). Nocturnal oxygen has been shown to abolish apnea. The aim of this study is to examine whether nocturnal oxygen reduces sympathetic nerve activity, and prevents progress of CHF. Methods: 93 patients with left ventricular ejection fractions < 60%, were examined with overnight saturation monitoring for an oxygen desaturation index. Subjects with oxygen desaturation of 4% >= 4/h were examined with polysomnography. Apnea-hypopnea index (AHI) was calculated as the total number of episodes of apnea and hypopnea per hour of sleep. We started nocturnal oxygen for the patients with AHI >= 20. Urinary and plasma catecholamines concentrations, serum brain natriuretic peptide, human atrial natriuretic peptide, and endothelial nitric oxide synthase levels were measured before and after starting oxygen. Results: Compared among the three groups, CHF with central sleep apnea (CHF-CSA) group had significantly higher 24-h urinary adrenaline (CHF-CSA: 4.411 +/- 2.940 mu mol/day, CHF with obstructive sleep apnea (CHF-OSA): 2.686 +/- 1.084 mu mol/day, CHF without apnea (CHF-N): 3.178 +/- 1.778 mu mol/day, P < 0.05). Oxygen therapy significantly decreased AHI and 4 serum BNP levels (from 91.75 +/- 80.35 pg/ml to 52.75 +/- 45.70 pg/ml, mean change = 33.85 pg/ml, P = 0.0208). Serum eNOS levels were lower in CHF-CSA group and CHF-OSA group than in CHF-N group (CHF-CSA: 15.89 +/- 10.75 pg/ml, CHF-OSA: 7.46 +/- 3.91 pg/ml, CHF-N: 27.33 +/- 14.83 pg/ml, P < 0.05). Conclusions: Nocturnal oxygen may prevent progress of CHF with central sleep apnea. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:354 / 360
页数:7
相关论文
共 44 条
  • [21] ADRENERGIC EFFECTS ON THE BIOLOGY OF THE ADULT MAMMALIAN CARDIOCYTE
    MANN, DL
    KENT, RL
    PARSONS, B
    COOPER, G
    [J]. CIRCULATION, 1992, 85 (02) : 790 - 804
  • [22] Raised sympathetic nerve activity in heart failure and central sleep apnea is due to heart failure severity
    Mansfield, D
    Kaye, DM
    La Rocca, HB
    Solin, P
    Esler, MD
    Naughton, MT
    [J]. CIRCULATION, 2003, 107 (10) : 1396 - 1400
  • [23] MARY SMI, 2000, AM J RESP CRIT CARE, V162, P2166
  • [24] EVIDENCE OF A SELECTIVE INCREASE IN CARDIAC SYMPATHETIC ACTIVITY IN PATIENTS WITH SUSTAINED VENTRICULAR ARRHYTHMIAS
    MEREDITH, IT
    BROUGHTON, A
    JENNINGS, GL
    ESLER, MD
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (09) : 618 - 624
  • [25] MOLECULAR MECHANISMS AND THERAPEUTIC STRATEGIES RELATED TO NITRIC-OXIDE
    MONCADA, S
    HIGGS, EA
    [J]. FASEB JOURNAL, 1995, 9 (13) : 1319 - 1330
  • [26] Early preconditioning prevents the loss of endothelial nitric oxide synthase and enhances its activity in the ischemic/reperfused rat heart
    Muscari, C
    Bonafe', F
    Gamberini, C
    Giordano, E
    Tantini, B
    Fattori, M
    Guarnieri, C
    Caldarera, CM
    [J]. LIFE SCIENCES, 2004, 74 (09) : 1127 - 1137
  • [27] EFFECTS OF NASAL CPAP ON SYMPATHETIC ACTIVITY IN PATIENTS WITH HEART-FAILURE AND CENTRAL SLEEP-APNEA
    NAUGHTON, MT
    BENARD, DC
    LIU, PP
    RUTHERFORD, R
    RANKIN, F
    BRADLEY, TD
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 152 (02) : 473 - 479
  • [28] Role of endothelin and nitric oxide imbalance in the pathogenesis of hypoxia-induced arterial hypertension
    Ni, ZM
    Bemanian, S
    Kivlighn, SD
    Vaziri, ND
    [J]. KIDNEY INTERNATIONAL, 1998, 54 (01) : 188 - 192
  • [29] Phelan MW, 1996, J CELL PHYSIOL, V167, P469, DOI 10.1002/(SICI)1097-4652(199606)167:3<469::AID-JCP11>3.3.CO
  • [30] 2-C