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原发性干燥综合征中的轻度自主神经功能障碍:一项对照研究。

Mild autonomic dysfunction in primary Sjögren's syndrome: a controlled study.

作者信息

Cai Fin Z J, Lester Sue, Lu Tim, Keen Helen, Boundy Karyn, Proudman Susanna M, Tonkin Anne, Rischmueller Maureen

机构信息

Rheumatology Department, The Queen Elizabeth Hospital, Woodville Road, Woodville South, 5011, Australia.

出版信息

Arthritis Res Ther. 2008;10(2):R31. doi: 10.1186/ar2385. Epub 2008 Mar 7.

Abstract

INTRODUCTION

The aim of this study was to compare cardiovascular autonomic nervous system function in patients with primary Sjögren's syndrome (pSS) with that in control individuals, and to correlate the findings with autonomic symptoms and the presence of exocrine secretory dysfunction.

METHODS

Twenty-seven female patients with pSS and 25 control individuals completed the COMPASS (Composite Autonomic Symptom Scale) self-reported autonomic symptom questionnaire. Beat-to-beat heart rate and blood pressure data in response to five standard cardiovascular reflex tests were digitally recorded using a noninvasive finger pressure cuff and heart rate variability was analyzed by Fourier spectral analysis. Analysis was performed by analysis of variance (ANOVA), multivariate ANOVA and repeated measures ANOVA, as indicated. Factor analysis was utilized to detect relationships between positive autonomic symptoms in pSS patients.

RESULTS

Multiple, mild autonomic disturbances were observed in pSS patients relating to decreased heart rate variability, decreased blood pressure variability and increased heart rate, which were most evident in response to postural change. There was a strong trend toward an association between decreased heart rate variability and increased severity of the secretomotor, orthostatic, bladder, gastroparesis and constipation self-reported autonomic symptom cluster identified in pSS patients. This symptom cluster was also associated with fatigue and reduced unstimulated salivary flow, and therefore may be an important component of the clinical spectrum of this disease.

CONCLUSION

There was evidence of mild autonomic dysfunction in pSS as measured with both cardiovascular reflex testing and self-reported symptoms. Pathogenic autoantibodies targeting M3 muscarinic receptors remain a strong candidate for the underlying pathophysiology, but practical assays for the detection of this autoantibody remain elusive.

摘要

引言

本研究旨在比较原发性干燥综合征(pSS)患者与对照个体的心血管自主神经系统功能,并将研究结果与自主神经症状及外分泌分泌功能障碍的存在情况相关联。

方法

27例pSS女性患者和25名对照个体完成了COMPASS(综合自主神经症状量表)自我报告的自主神经症状问卷。使用无创手指压力袖带数字记录对五项标准心血管反射测试的逐搏心率和血压数据,并通过傅里叶频谱分析对心率变异性进行分析。根据需要,采用方差分析(ANOVA)、多变量ANOVA和重复测量ANOVA进行分析。利用因子分析检测pSS患者阳性自主神经症状之间的关系。

结果

在pSS患者中观察到多种轻度自主神经紊乱,表现为心率变异性降低、血压变异性降低和心率增加,在体位改变时最为明显。在pSS患者中,心率变异性降低与分泌运动、直立性、膀胱、胃轻瘫和便秘自我报告的自主神经症状群严重程度增加之间存在强烈的关联趋势。该症状群还与疲劳和未刺激唾液流量减少相关,因此可能是该疾病临床谱的重要组成部分。

结论

通过心血管反射测试和自我报告症状测量均有证据表明pSS存在轻度自主神经功能障碍。靶向M3毒蕈碱受体的致病性自身抗体仍是潜在病理生理学的有力候选因素,但检测这种自身抗体的实用检测方法仍然难以捉摸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34a7/2453776/8da34202f47e/ar2385-1.jpg

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