Kanika Sehgal, June Tome, Amrit K Kamboj, Ross A Dierkhising, Darrell S Pardi, Sahil Khanna
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Histological change from one subtype to the other and resolution were tracked with univariate and multivariable Cox proportional hazards models.</p><p><strong>Results: </strong>Overall, 416 patients with a median age at diagnosis of 63.9 years with >1 histopathological assessment were identified. Histology at initial diagnosis was CC in 218 (52.4%) patients and LC in 198 (47.6%). No medications were associated with a histological change. However, histological resolution was more likely with the use of aspirin [hazard ratio (HR): 2.10, 95% confidence interval (CI): 1.34-3.31, <i>p</i> = 0.001) and proton-pump inhibitors (PPIs; HR: 2.01, 95% CI: 1.34-3.02, <i>p</i> = 0.001). Histological resolution was more likely with budesonide treatment (HR: 1.86, 95% CI: 1.16-3.00, <i>p</i> = 0.010) and less likely with mesalamine (HR: 0.40, 95% CI: 0.19-0.83, <i>p</i> = 0.014), compared to medications such as prednisone, loperamide, and bismuth. Patients with CC were less likely to change their histology compared to patients with LC (HR: 0.24, 95% CI: 0.14-0.42, <i>p</i> < 0.001). There was no difference in histological resolution between the two subtypes (HR: 0.70, 95% CI: 0.47-1.05, <i>p</i> = 0.084).</p><p><strong>Conclusion: </strong>Patients with LC have a higher chance of changing their histology as compared to CC. 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Little is known about the natural progression of disease with time and with treatment.</p><p><strong>Objectives: </strong>We aimed to assess histological changes over time.</p><p><strong>Design: </strong>We designed a retrospective study including adults diagnosed with MC from January 1992 to January 2020 at Mayo Clinic.</p><p><strong>Methods: </strong>Pathology reports were reviewed until 31 October 2020. Histological assessments at least 8 weeks apart were considered as adequate follow-up. Histological change from one subtype to the other and resolution were tracked with univariate and multivariable Cox proportional hazards models.</p><p><strong>Results: </strong>Overall, 416 patients with a median age at diagnosis of 63.9 years with >1 histopathological assessment were identified. Histology at initial diagnosis was CC in 218 (52.4%) patients and LC in 198 (47.6%). No medications were associated with a histological change. However, histological resolution was more likely with the use of aspirin [hazard ratio (HR): 2.10, 95% confidence interval (CI): 1.34-3.31, <i>p</i> = 0.001) and proton-pump inhibitors (PPIs; HR: 2.01, 95% CI: 1.34-3.02, <i>p</i> = 0.001). Histological resolution was more likely with budesonide treatment (HR: 1.86, 95% CI: 1.16-3.00, <i>p</i> = 0.010) and less likely with mesalamine (HR: 0.40, 95% CI: 0.19-0.83, <i>p</i> = 0.014), compared to medications such as prednisone, loperamide, and bismuth. Patients with CC were less likely to change their histology compared to patients with LC (HR: 0.24, 95% CI: 0.14-0.42, <i>p</i> < 0.001). There was no difference in histological resolution between the two subtypes (HR: 0.70, 95% CI: 0.47-1.05, <i>p</i> = 0.084).</p><p><strong>Conclusion: </strong>Patients with LC have a higher chance of changing their histology as compared to CC. 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引用次数: 0
摘要
背景:显微镜下结肠炎(MC)引起慢性腹泻。它有两种组织学亚型:淋巴细胞性结肠炎(LC)和胶原性结肠炎(CC)。人们对疾病随时间和治疗的自然进展知之甚少。目的:我们旨在评估组织学随时间的变化。设计:我们设计了一项回顾性研究,纳入了1992年1月至2020年1月在梅奥诊所诊断为MC的成年人。方法:回顾病理报告,直到2020年10月31日。至少间隔8周的组织学评估被认为是充分的随访。用单变量和多变量Cox比例风险模型跟踪从一种亚型到另一种亚型的组织学变化和解决方案。结果:总共有416例患者,诊断时的中位年龄为63.9岁,组织病理学评估>1。初诊组织学为CC 218例(52.4%),LC 198例(47.6%)。没有药物与组织学改变相关。然而,使用阿司匹林(风险比:2.10,95%可信区间:1.34-3.31,p = 0.001)和质子泵抑制剂(ppi;HR: 2.01, 95% CI: 1.34-3.02, p = 0.001)。与强尼松、洛哌丁胺和铋等药物相比,布地奈德治疗更可能出现组织学缓解(HR: 1.86, 95% CI: 1.16-3.00, p = 0.010),美沙拉胺治疗更不可能出现组织学缓解(HR: 0.40, 95% CI: 0.19-0.83, p = 0.014)。与LC患者相比,CC患者组织学改变的可能性较小(HR: 0.24, 95% CI: 0.14-0.42, p p = 0.084)。结论:与CC相比,LC患者组织学改变的机会更高,然而,组织学改变与使用PPIs和阿司匹林以及布地奈德治疗有关。
The natural history of histological changes in microscopic colitis.
Background: Microscopic colitis (MC) causes chronic diarrhea. It has two histologic subtypes: lymphocytic colitis (LC) and collagenous colitis (CC). Little is known about the natural progression of disease with time and with treatment.
Objectives: We aimed to assess histological changes over time.
Design: We designed a retrospective study including adults diagnosed with MC from January 1992 to January 2020 at Mayo Clinic.
Methods: Pathology reports were reviewed until 31 October 2020. Histological assessments at least 8 weeks apart were considered as adequate follow-up. Histological change from one subtype to the other and resolution were tracked with univariate and multivariable Cox proportional hazards models.
Results: Overall, 416 patients with a median age at diagnosis of 63.9 years with >1 histopathological assessment were identified. Histology at initial diagnosis was CC in 218 (52.4%) patients and LC in 198 (47.6%). No medications were associated with a histological change. However, histological resolution was more likely with the use of aspirin [hazard ratio (HR): 2.10, 95% confidence interval (CI): 1.34-3.31, p = 0.001) and proton-pump inhibitors (PPIs; HR: 2.01, 95% CI: 1.34-3.02, p = 0.001). Histological resolution was more likely with budesonide treatment (HR: 1.86, 95% CI: 1.16-3.00, p = 0.010) and less likely with mesalamine (HR: 0.40, 95% CI: 0.19-0.83, p = 0.014), compared to medications such as prednisone, loperamide, and bismuth. Patients with CC were less likely to change their histology compared to patients with LC (HR: 0.24, 95% CI: 0.14-0.42, p < 0.001). There was no difference in histological resolution between the two subtypes (HR: 0.70, 95% CI: 0.47-1.05, p = 0.084).
Conclusion: Patients with LC have a higher chance of changing their histology as compared to CC. However, histological resolution was associated with the use of PPIs and aspirin, and treatment with budesonide.
期刊介绍:
Therapeutic Advances in Gastroenterology is an open access journal which delivers the highest quality peer-reviewed original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of gastrointestinal and hepatic disorders. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in gastroenterology and related disciplines, providing an online forum for rapid dissemination of recent research and perspectives in this area.
The editors welcome original research articles across all areas of gastroenterology and hepatology.
The journal publishes original research articles and review articles primarily. Original research manuscripts may include laboratory, animal or human/clinical studies – all phases. Letters to the Editor and Case Reports will also be considered.