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Autonomic Abnormalities in Patients With Primary Sjogren’s Syndrome – Preliminary Results

机译:原发性干燥综合征患者的自主神经异常–初步结果

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摘要

Primary Sjögren’s syndrome (pSS) is an autoimmune disease affecting exocrine glands and extra-glandular organs. There are conflicting reports on the presence of autonomic dysfunction in pSS and no data are available on the functional status of sympathetic outflow to the vessels and baroreceptor [baroreflex sensitivity (BRS)] control mechanisms. We investigated the cardiac (cBRS) and sympathetic (sBRS) baroreceptor modulation in both time and frequency domains and the cardiovascular autonomic profile in pSS patients compared to healthy controls. Autonomic symptoms were quantified by the Composite Autonomic Symptom Scale (COMPASS31) three-item questionnaire. The EULAR Sjogren’s syndrome patient reported index (ESSPRI) questionnaire evaluated the magnitude of pSS clinical symptoms, i.e., fatigue, pain, and sicca symptoms. Electrocardiogram, beat-by-beat arterial pressure (AP) and respiratory activity were continuously recorded in 17 pSS patients and 16 healthy controls, while supine and during 75° head-up tilt. In seven patients and seven controls, muscle sympathetic nerve activity (MSNA) was measured. Spectrum analysis of RR variability provided markers of cardiac vagal modulation (HFRR nu) and sympatho-vagal balance [low frequency (LF)/high frequency (HF)]. The power of LF (0.1 Hz) oscillations of systolic arterial pressure (SAP) variability (LFSAP) evaluated the vasomotor response to sympathetic stimulation. Compared to controls, pSS patients scored higher in total COMPASS31 (p < 0.0001) and all ESSPRI subdomains (fatigue, p = 0.005; pain, p = 0.0057; dryness, p < 0.0001). Abnormal scialometry (<1.5 ml/15 min) and Schirmer tests (<5 mm/5 min) were found in pSS patients and salivary flow rate was negatively associated with ESSPRI dryness (p = 0.0014). While supine, pSS patients had lower SEQcBRS index of cardiac baroreceptor sensitivity, higher HFRRnu (p = 0.021), lower LF/HF (p = 0.007), and greater MSNA (p = 0.038) than controls. No differences were observed in LFSAP between groups. During orthostatic challenge, although LFSAP increased similarly in both groups, MSNA was greater in pSS patients (p = 0.003). At rest pSS patients showed lower cBR control and greater parasympathetic modulation. Furthermore, greater sympathetic nerve activity was observed in pSS patients while supine and in response to gravitational challenge. We hypothesized that such enhanced sympathetic vasoconstrictor activity might reflect an attempt to maintain blood pressure in a setting of likely reduced vascular responsiveness.
机译:原发性干燥综合征(pSS)是一种自身免疫性疾病,会影响外分泌腺和腺外器官。关于pSS中存在自主神经功能障碍的报道相互矛盾,尚无有关交感性血管功能状态和压力感受器[压力反射敏感性(BRS)]控制机制的数据。与健康对照组相比,我们研究了pSS患者在时域和频域中的心脏(cBRS)和交感(sBRS)压力感受器调节以及心血管自主神经系统。通过复合自主神经症状量表(COMPASS31)三项问卷对自主神经症状进行量化。 EULAR干燥综合征患者报告指数(ESSPRI)调查表评估了pSS临床症状(即疲劳,疼痛和干燥症状)的严重程度。在17名pSS患者和16名健康对照者中,在仰卧时和75°抬头俯仰期间,连续记录心电图,逐次搏动的动脉压(AP)和呼吸活动。在7位患者和7位对照中,测量了肌肉交感神经活动(MSNA)。 RR变异性的频谱分析提供了心脏迷走神经调制(HFRR nu)和交感迷走神经平衡[低频(LF)/高频(HF)]的标志。收缩压(SAP)变异性(LFSAP)的LF(0.1 Hz)振荡的功率评估了对交感刺激的血管舒缩反应。与对照组相比,pSS患者在COMPASS31总评分(p <0.0001)和所有ESSPRI子域(疲劳,p = 0.005;疼痛,p = 0.0057;干燥,p <0.0001)上得分更高。在pSS患者中发现异常的社会计量学(<1.5 ml / 15 min)和Schirmer测试(<5 mm / 5 min),唾液流速与ESSPRI干燥度呈负相关(p = 0.0014)。仰卧时,pSS患者的心脏压力感受器敏感性的SEQcBRS指数较低,HFRRnu较高(p = 0.021),LF / HF较低(p = 0.007),MSNA较高(p = 0.038)。两组之间在LFSAP中未观察到差异。在体位挑战期间,尽管两组的LFSAP均增加,但pSS患者的MSNA更高(p = 0.003)。静息pSS患者表现出较低的cBR控制和更大的副交感调节。此外,仰卧和对重力挑战的反应,在pSS患者中观察到更大的交感神经活动。我们假设这种增强的交感性血管收缩药活性可能反映了在可能降低的血管反应性的情况下维持血压的尝试。

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