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呼气肌力量作为全身型重症肌无力患者功能运动能力的预测指标

Expiratory muscle strength as a predictor of functional exercise capacity in generalized myasthenia gravis.

作者信息

Calik-Kutukcu Ebru, Salci Yeliz, Karanfil Ecem, Fil-Balkan Ayla, Bekircan-Kurt Can Ebru, Armutlu Kadriye

机构信息

Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Hacettepe University, Ankara, Turkey. E-mail:

出版信息

Neurosciences (Riyadh). 2019 Apr;24(2):95-100. doi: 10.17712/nsj.2019.2.20180024.

Abstract

OBJECTIVE

To investigate the correlations between the 6-minute walk test and disease severity, pulmonary functions, and respiratory muscle performance in patients with generalized myasthenia gravis (MG) and to determine whether MG disease severity, pulmonary functions, and respiratory muscle performance contribute to 6-minute walk test distance in generalized MG.

METHODS

This cross-sectional trial was conducted at Hacettepe University in Ankara, Turkey. The study was carried out from February to August 2017. Twenty-eight class II-III MG patients participated in the study. Patients` disease severity was determined with the Myasthenia gravis composite scale. All participants underwent the 6-minute walk test, pulmonary function tests, and respiratory muscle strength and endurance assessment.

RESULTS

Approximately 40% of patients` expiratory muscle strength were under the lower limit of normal. Multiple linear regression analysis revealed that the percentage of predicted expiratory muscle strength that patients reached were significant and independent predictor of percentage of 6-minute walk test distance that patients reached according to reference values (R2=0.493, F [1-27]=25.275, p less than 0.001).

CONCLUSION

Expiratory muscle strength is a significant determinant of functional exercise performance in generalized MG with mild or moderate weakness affecting muscles other than the ocular muscles.

摘要

目的

探讨全身型重症肌无力(MG)患者6分钟步行试验与疾病严重程度、肺功能及呼吸肌功能之间的相关性,并确定MG疾病严重程度、肺功能及呼吸肌功能是否对全身型MG患者的6分钟步行试验距离有影响。

方法

本横断面试验在土耳其安卡拉的哈杰泰佩大学进行。研究于2017年2月至8月开展。28例II-III级MG患者参与了研究。采用重症肌无力综合量表确定患者的疾病严重程度。所有参与者均接受6分钟步行试验、肺功能测试以及呼吸肌力量和耐力评估。

结果

约40%患者的呼气肌力量低于正常下限。多元线性回归分析显示,患者达到的预计呼气肌力量百分比是患者根据参考值达到的6分钟步行试验距离百分比的显著且独立预测因素(R2=0.493,F [1-27]=25.275,p<0.001)。

结论

呼气肌力量是全身型MG患者功能运动表现的重要决定因素,此类患者存在轻度或中度肌无力,累及眼外肌以外的肌肉。

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本文引用的文献

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Myasthenia gravis and risks for comorbidity.重症肌无力与共病风险。
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Muscle strength in myasthenia gravis.重症肌无力的肌肉力量。
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Myasthenia gravis and the neuromuscular junction.重症肌无力与神经肌肉接头
Curr Opin Neurol. 2013 Oct;26(5):459-65. doi: 10.1097/WCO.0b013e328364c079.

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