Zhang Li, Meng Ran, Shang Shuling, Wu Chuanjie, Wu Di, Shang Shuyi, Chen Lifeng, Zhang Yunshu, Ji Xunming
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China; Department of Neurology, The Third Hospital of Shijiazhuang, Shijiazhuang, China.
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
J Stroke Cerebrovasc Dis. 2019 Aug;28(8):2132-2139. doi: 10.1016/j.jstrokecerebrovasdis.2019.04.008. Epub 2019 May 22.
Obstructive sleep apnea (OSA) is a probable risk factor with speculative roles in the induction or aggravation of acute ischemic stroke (AIS).
The association between OSA and AIS severity was retrospectively analyzed using clinical data of first-onset AIS patients, admitted to our hospital between January 2013 and September 2016. Eligible patients were categorized based on the presence of OSA prior to stroke. Stroke severity and functional outcomes were evaluated using the National Institute of Health Stroke Severity Scale (NIHSS) and the modified Rankin scale (mRS), respectively.
No significant differences were observed among OSA and non-OSA groups for infarction volume, NIHSS at admission and discharge, or mRS at discharge and at the 3-month follow-up (all P > .05). OSA prior to stroke negatively correlated with infarction volume (P = .008), NIHSS at discharge (P = .006), and the 3-month mRS (P = .015). In addition to OSA, it was also found that infarction volume significantly correlated with large artery occlusion (LAO), anterior circulation involvement, neutrophil count, and fibrinogen level; NIHSS at discharge significantly correlated with LAO, transient ischemia attack (TIA), neutrophil count, and thrombolysis; and the 3-month mRS significantly correlated with LAO, TIA, age, neutrophil count, and thrombolysis.
OSA before AIS does not increase the severity of stroke. The negative association between OSA and infarction volume, stroke severity, and clinical outcomes suggests an endogenous neuroprotective effect.
阻塞性睡眠呼吸暂停(OSA)可能是急性缺血性卒中(AIS)诱发或加重的一个风险因素,其作用尚存在推测性。
回顾性分析2013年1月至2016年9月我院收治的首发AIS患者的临床资料,以分析OSA与AIS严重程度之间的关联。符合条件的患者根据卒中前是否存在OSA进行分类。分别使用美国国立卫生研究院卒中严重程度量表(NIHSS)和改良Rankin量表(mRS)评估卒中严重程度和功能转归。
OSA组和非OSA组在梗死体积、入院及出院时的NIHSS评分、出院时及3个月随访时的mRS评分方面均未观察到显著差异(所有P>.05)。卒中前的OSA与梗死体积(P = .008)、出院时的NIHSS评分(P = .006)及3个月时的mRS评分(P = .015)呈负相关。除OSA外,还发现梗死体积与大动脉闭塞(LAO)、前循环受累、中性粒细胞计数及纤维蛋白原水平显著相关;出院时的NIHSS评分与LAO、短暂性脑缺血发作(TIA)、中性粒细胞计数及溶栓治疗显著相关;3个月时的mRS评分与LAO、TIA、年龄、中性粒细胞计数及溶栓治疗显著相关。
AIS前的OSA不会增加卒中严重程度。OSA与梗死体积、卒中严重程度及临床转归之间的负相关表明其具有内源性神经保护作用。