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胃轻瘫综合征的再思考。

Reconsideration of the Gastroparetic Syndrome.

作者信息

Gilbert Richard J, Siamwala Jamila H, Kumar Vivek, Thompson Christopher C, Shikora Scott A

机构信息

Research Service, Providence VA Medical Center, Providence, RI, USA.

Department of Molecular Physiology, Pharmacology, and Biotechnology, Warren Alpert Medical School of Brown University, Providence, RI, USA.

出版信息

Curr Gastroenterol Rep. 2023 Apr;25(4):75-90. doi: 10.1007/s11894-023-00865-w. Epub 2023 Apr 1.

Abstract

PURPOSE OF REVIEW

Gastroparesis is a chronic disorder characterized by a constellation of foregut symptoms, including postprandial nausea, vomiting, distension, epigastric pain, and regurgitation in the absence of gastric outlet obstruction. Despite considerable research over the past decades, there remains to be only nominal understanding of disease classification, diagnostic criteria, pathogenesis, and preferred therapy.

RECENT FINDINGS

We critically reassess current approaches for disease identification and stratification, theories of causation, and treatment for gastroparesis. Gastric scintigraphy, long considered a diagnostic standard, has been re-evaluated in light of evidence showing low sensitivity, whereas newer testing modalities are incompletely validated. Present concepts of pathogenesis do not provide a unified model linking biological impairments with clinical manifestations, whereas available pharmacological and anatomical treatments lack explicit selection criteria or evidence for sustained effectiveness. We propose a disease model that embodies the re-programming of distributed neuro-immune interactions in the gastric wall by inflammatory perturbants. These interactions, combined with effects on the foregut hormonal milieu and brain-gut axis, are postulated to generate the syndromic attributes characteristically linked with gastroparesis. Research linking models of immunopathogenesis with diagnostic and therapeutic paradigms will lead to reclassifications of gastroparesis that guide future trials and technological developments.

KEY POINTS

• The term gastroparesis embodies a heterogenous array of symptoms and clinical findings based on a complex assimilation of afferent and efferent mechanisms, gastrointestinal locations, and pathologies. • There currently exists no single test or group of tests with sufficient capacity to be termed a definitional standard for gastroparesis. • Present research regarding pathogenesis suggests the importance of immune regulation of intrinsic oscillatory activity involving myenteric nerves, interstitial cells of Cajal, and smooth muscle cells. • Prokinetic pharmaceuticals remain the mainstay of management, although novel treatments are being studied that are directed to alternative muscle/nerve receptors, electromodulation of the brain-gut axis, and anatomical (endoscopic, surgical) interventions.

摘要

综述目的

胃轻瘫是一种慢性疾病,其特征为一系列前肠症状,包括餐后恶心、呕吐、腹胀、上腹部疼痛以及在无胃出口梗阻情况下的反流。尽管在过去几十年中进行了大量研究,但对于疾病分类、诊断标准、发病机制和首选治疗方法仍只有初步了解。

最新发现

我们对胃轻瘫的疾病识别和分层、病因理论及治疗的当前方法进行了批判性重新评估。长期以来被视为诊断标准的胃闪烁显像,鉴于其低敏感性的证据已被重新评估,而新的检测方式尚未得到充分验证。目前的发病机制概念并未提供一个将生物学损伤与临床表现联系起来的统一模型,而现有的药物和解剖学治疗缺乏明确的选择标准或持续有效性的证据。我们提出了一种疾病模型,该模型体现了炎症干扰物对胃壁中分布式神经免疫相互作用的重新编程。这些相互作用,再加上对前肠激素环境和脑 - 肠轴的影响,被假定会产生与胃轻瘫典型相关的综合征属性。将免疫发病机制模型与诊断和治疗范式联系起来的研究将导致胃轻瘫的重新分类,从而指导未来的试验和技术发展。

关键点

• “胃轻瘫”一词体现了基于传入和传出机制、胃肠道位置及病理的复杂综合所产生的一系列异质性症状和临床发现。

• 目前不存在单一的检测或一组检测具有足够能力被称为胃轻瘫的定义标准。

• 目前关于发病机制的研究表明,涉及肌间神经、Cajal间质细胞和平滑肌细胞的内在振荡活动的免疫调节具有重要性。

• 促动力药物仍然是治疗的主要手段,尽管正在研究针对替代肌肉/神经受体、脑 - 肠轴的电调制以及解剖学(内镜、手术)干预的新治疗方法。

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