系统性硬化症的食管运动障碍:与胃肠道外表现的关系和胸部影像学的补充作用。

IF 1.2 Q3 RHEUMATOLOGY
Inês Santos, Carlos Marques-Gomes, Mariana Diz-Lopes, Georgina Terroso, Lúcia Costa, Raquel Miriam Ferreira
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引用次数: 0

摘要

在系统性硬化症中,胸部高分辨率计算机断层扫描显示的压力测量变化与食管扩张之间的关系已经确立,但其与食管外表现的关系并不一致。本研究旨在描述系统性硬化症患者的血压测量结果,并确定与食管体运动障碍的潜在关联。方法:回顾性单中心研究,包括接受常规或高分辨率食管测压的成年系统性硬化症患者。收集了人口统计学和临床数据。评估食管运动与疾病持续时间、免疫特征、皮肤和肺部受累以及内镜或断层扫描食管改变之间的关系。结果:共纳入76例患者。60例(78.9%)进行常规测压,23例(38.3%)观察到胃蠕动,45例(75.0%)观察到食管下括约肌正常张力。16例(21.1%)患者行高分辨率食管测压,其中9例(56.3%)运动正常,9例(56.3%)食管下括约肌正常,7例(43.8%)食管下括约肌低张力。总体而言,食管体运动障碍46例(60.5%),食管下括约肌正常54例(71.1%)。大多数患者(84.2%)有局限性皮肤病。中位病程为5年(四分位数间距= 11),平均年龄为54.1±12.4岁。女性71例(93.4%)。比较运动正常和运动障碍患者与压力测量食管受累的潜在关联。胸部高分辨率计算机断层扫描显示,食管扩张在运动障碍患者中更为常见(p = 0.005)。在疾病持续时间、免疫特征、改良罗德曼皮肤评分、食管炎、巴雷特食管、肺间质性疾病、强迫肺活量或单呼吸一氧化碳弥散能力方面没有发现显著差异。讨论:食道受累在我们的样本中很常见,尽管食管下括约肌更常见。在胸部高分辨率计算机断层扫描上发现食管运动障碍与其扩张之间的关联,强调了胸部高分辨率计算机断层扫描在识别系统性硬化症中上消化道受累的实用性。血压变化与食管外表现无关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Esophageal dysmotility in systemic sclerosis: Relationship with extra-gastrointestinal manifestations and complementary utility of thoracic imaging.

Introduction: The relationship between manometric changes and esophageal dilation on chest high-resolution computed tomography is well established in systemic sclerosis, but its association with extra-esophageal manifestations is inconsistent. This study aims to characterize manometric findings in systemic sclerosis patients and to determine potential associations with esophageal body dysmotility.

Methods: Retrospective single-center study including adult systemic sclerosis patients who underwent conventional or high-resolution esophageal manometry. Demographic and clinical data were collected. Associations between esophageal motility and disease duration, immunologic profile, cutaneous and pulmonary involvement, as well as endoscopic or tomographic esophageal alterations were evaluated.

Results: A total of 76 patients were included. Conventional manometry was performed in 60 (78.9%), with aperistalsis observed in 23 (38.3%) and a normotonic lower esophageal sphincter in 45 (75.0%). Sixteen patients (21.1%) underwent high-resolution esophageal manometry, showing normal motility in 9 (56.3%), normotonic lower esophageal sphincter in 9 (56.3%), and hypotonic lower esophageal sphincter in 7 (43.8%). Overall, 46 patients (60.5%) had esophageal body dysmotility and 54 (71.1%) had normotonic lower esophageal sphincter. Most patients (84.2%) had limited cutaneous disease. Median disease duration was 5 years (interquartile range = 11) with mean age 54.1 ± 12.4 years. Seventy-one patients (93.4%) were females. Potential associations with manometric esophageal involvement were compared between patients with normal motility and dysmotility. Esophageal dilation on chest high-resolution computed tomography was more frequent among those with dysmotility (p = 0.005). No significant differences were found regarding disease duration, immunologic profile, modified Rodnan skin score, esophagitis, Barrett's esophagus, interstitial lung disease, forced vital capacity, or single-breath carbon monoxide diffusing capacity.

Discussion: Esophageal involvement was frequent in our sample, although the lower esophageal sphincter was more commonly spared. An association between esophageal dysmotility and its dilation on chest high-resolution computed tomography was found, highlighting the utility of chest high-resolution computed tomography for identification of upper gastrointestinal involvement in systemic sclerosis. No association was found between manometric changes and extra-esophageal manifestations.

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