Clinical characteristics and manometric findings of esophageal achalasia-a systematic review regarding differences among three subtypes.

Q3 Medicine
Ryo Katsumata, Noriaki Manabe, Hiroyuki Sakae, Kenta Hamada, Maki Ayaki, Takahisa Murao, Minoru Fujita, Tomoari Kamada, Hirofumi Kawamoto, Ken Haruma
{"title":"Clinical characteristics and manometric findings of esophageal achalasia-a systematic review regarding differences among three subtypes.","authors":"Ryo Katsumata,&nbsp;Noriaki Manabe,&nbsp;Hiroyuki Sakae,&nbsp;Kenta Hamada,&nbsp;Maki Ayaki,&nbsp;Takahisa Murao,&nbsp;Minoru Fujita,&nbsp;Tomoari Kamada,&nbsp;Hirofumi Kawamoto,&nbsp;Ken Haruma","doi":"10.1540/jsmr.59.14","DOIUrl":null,"url":null,"abstract":"<p><p>Esophageal achalasia is classified into three subtypes according to manometric findings. Since several factors, including clinical characteristics and treatment response, have been reported to differ among the subtypes, the underlying pathogenesis may also differ. However, a comprehensive understanding regarding the differences is still lacking. We therefore performed a systematic review of the differences among the three subtypes of achalasia to clarify the current level of comprehension. In terms of clinical features, type III, which is the least frequently diagnosed of the three subtypes, showed the oldest age and most severe symptoms, such as chest pain. In contrast, type I showed a higher prevalence of lung complications, and type II showed weight loss more frequently than the other types. Histopathologically, type I showed a high loss of ganglion cells in esophagus, and on a molecular basis, type III had elevated serum pro-inflammatory cytokine levels. In addition to peristalsis and the lower esophageal sphincter (LES) function, the upper esophageal sphincter (UES) function of achalasia has attracted attention, as an impaired UES function is associated with severe aspiration pneumonia, a fatal complication of achalasia. Previous studies have indicated that type II shows a higher UES pressure than the other subtypes, while an earlier decline in the UES function has been confirmed in type I. Differences in the treatment response are also crucial for managing achalasia patients. A number of studies have reported better responses in type II cases and less favorable responses in type III cases to pneumatic dilatation. These differences help shed light on the pathogenesis of achalasia and support its clinical management according to the subtype.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"59 ","pages":"14-27"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e7/5d/jsmr-59-014.PMC10036217.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Smooth Muscle Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1540/jsmr.59.14","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1

Abstract

Esophageal achalasia is classified into three subtypes according to manometric findings. Since several factors, including clinical characteristics and treatment response, have been reported to differ among the subtypes, the underlying pathogenesis may also differ. However, a comprehensive understanding regarding the differences is still lacking. We therefore performed a systematic review of the differences among the three subtypes of achalasia to clarify the current level of comprehension. In terms of clinical features, type III, which is the least frequently diagnosed of the three subtypes, showed the oldest age and most severe symptoms, such as chest pain. In contrast, type I showed a higher prevalence of lung complications, and type II showed weight loss more frequently than the other types. Histopathologically, type I showed a high loss of ganglion cells in esophagus, and on a molecular basis, type III had elevated serum pro-inflammatory cytokine levels. In addition to peristalsis and the lower esophageal sphincter (LES) function, the upper esophageal sphincter (UES) function of achalasia has attracted attention, as an impaired UES function is associated with severe aspiration pneumonia, a fatal complication of achalasia. Previous studies have indicated that type II shows a higher UES pressure than the other subtypes, while an earlier decline in the UES function has been confirmed in type I. Differences in the treatment response are also crucial for managing achalasia patients. A number of studies have reported better responses in type II cases and less favorable responses in type III cases to pneumatic dilatation. These differences help shed light on the pathogenesis of achalasia and support its clinical management according to the subtype.

Abstract Image

Abstract Image

食管贲门失弛缓症的临床特征和压力测量结果——关于三种亚型差异的系统综述。
食道贲门失弛缓症根据测压结果可分为三种亚型。由于包括临床特征和治疗反应在内的几个因素在亚型之间存在差异,因此潜在的发病机制也可能存在差异。然而,对这些差异的全面认识仍然缺乏。因此,我们对失弛缓症的三种亚型之间的差异进行了系统的回顾,以澄清目前的理解水平。在临床特征方面,III型是三种亚型中诊断频率最低的,年龄最大,症状最严重,如胸痛。相比之下,I型患者肺部并发症的患病率更高,II型患者体重下降的频率高于其他类型。在组织病理学上,I型表现为食道神经节细胞的大量损失,而在分子基础上,III型表现为血清促炎细胞因子水平升高。贲门失弛缓症除了蠕动和下食管括约肌(LES)功能外,上食管括约肌(UES)功能也引起了人们的关注,因为UES功能受损与严重吸入性肺炎有关,这是贲门失弛缓症的致命并发症。先前的研究表明,II型比其他亚型表现出更高的UES压力,而在i型中证实了更早的UES功能下降。治疗反应的差异对于治疗失弛缓症患者也是至关重要的。许多研究报告了II型病例更好的反应,而III型病例对气动扩张的反应不太有利。这些差异有助于揭示贲门失弛缓症的发病机制,并根据亚型支持其临床管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Smooth Muscle Research
Journal of Smooth Muscle Research Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
2.30
自引率
0.00%
发文量
7
审稿时长
10 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信