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系统性硬化症和混合性结缔组织病患者的心血管自主神经功能、自身抗体及食管运动活动

Cardiovascular autonomic function, autoantibodies, and esophageal motor activity in patients with systemic sclerosis and mixed connective tissue disease.

作者信息

Stacher G, Merio R, Budka C, Schneider C, Smolen J, Tappeiner G

机构信息

Department of Surgery, University of Vienna, Austria.

出版信息

J Rheumatol. 2000 Mar;27(3):692-7.

Abstract

OBJECTIVE

To study cardiovascular autonomic nerve function and presence of autoantibodies in relation to esophageal motor activity in patients with systemic sclerosis (SSc) and mixed connective tissue disease (MCTD).

METHODS

Twenty-five patients with SSc (13 limited, 12 diffuse cutaneous disease; disease duration 1-19 yrs) and 6 patients with MCTD (disease duration 1-10 yrs) were studied. Cardiovascular autonomic function was assessed using 5 standard tests and autoantibody status determined. Esophageal motor activity and lower and upper esophageal sphincter pressures were recorded manometrically.

RESULTS

Five patients with SSc had definite, 7 borderline, and 13 no autonomic dysfunction; 23 had antinuclear. 9 anti-Sc170, 4 anticentromere, and 1 U1snRNP antibodies. Contraction amplitudes in the smooth muscle as well as the striated muscle esophagus and lower esophageal sphincter pressures were significantly lower and autonomic dysfunction more frequent in patients with than in those without anti-Sc170 (6 of 9 vs 6 of 16 patients); upper esophageal sphincter pressures did not differ. All patients with MCTD had antinuclear antibodies, 5 had definite autonomic dysfunction; their lower esophageal sphincter pressures were significantly lower than in SSc patients without anti-Sc170 and anti-U1snRNP.

CONCLUSION

Esophageal motor dysfunction may be associated with the presence of anti-Sc170 and anti-U1snRNP autoantibodies and prevail in patients with cardiovascular autonomic neuropathy.

摘要

目的

研究系统性硬化症(SSc)和混合性结缔组织病(MCTD)患者心血管自主神经功能及自身抗体与食管运动活动的关系。

方法

对25例SSc患者(13例局限性、12例弥漫性皮肤疾病;病程1 - 19年)和6例MCTD患者(病程1 - 10年)进行研究。使用5项标准测试评估心血管自主功能并确定自身抗体状态。通过测压记录食管运动活动以及食管下括约肌和上括约肌压力。

结果

5例SSc患者有明确的自主神经功能障碍,7例临界,13例无自主神经功能障碍;23例有抗核抗体,9例有抗Sc170抗体,4例有抗着丝点抗体,1例有U1snRNP抗体。抗Sc170抗体阳性患者的平滑肌及横纹肌食管收缩幅度和食管下括约肌压力显著低于抗体阴性患者,且自主神经功能障碍更常见(9例中的6例 vs 16例中的6例);食管上括约肌压力无差异。所有MCTD患者均有抗核抗体,5例有明确的自主神经功能障碍;他们的食管下括约肌压力显著低于无抗Sc170和抗U1snRNP抗体的SSc患者。

结论

食管运动功能障碍可能与抗Sc170和抗U1snRNP自身抗体的存在有关,并在心血管自主神经病变患者中更为普遍。

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