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在内镜下黏膜静止的溃疡性结肠炎中,缺乏帕内特细胞化生可预测临床复发。

Absence of Paneth Cell Metaplasia to Predict Clinical Relapse in Ulcerative Colitis with Endoscopically Quiescent Mucosa.

机构信息

Department of Internal Medicine, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan.

出版信息

Dig Dis Sci. 2024 Oct;69(10):3932-3941. doi: 10.1007/s10620-024-08581-9. Epub 2024 Aug 7.

DOI:10.1007/s10620-024-08581-9
PMID:39110367
Abstract

BACKGROUND

Paneth cells play multiple roles in maintaining intestinal homeostasis. However, the clinical role of Paneth cell metaplasia (PCM) in ulcerative colitis (UC) remains unclear. We aimed to investigate the relationship between PCM and relapse in patients with UC and compare the usefulness of PCM with other histological indexes, including mucin depletion (MD) and basal plasmacytosis (BP).

METHODS

Patients with UC in clinical remission (CR) who underwent colonoscopy to confirm a Mayo endoscopic subscore (MES) ≦1 with biopsies from the distal colon were enrolled into this retrospective cohort study. Biopsy samples were evaluated for histological findings of PCM, MD, and BP. Clinical relapse was defined as partial Mayo score ≧3 or medication escalation. Multivariate analysis was performed to determine independent predictors of relapse among the three histological findings, MES, and patient background, and relapse prediction models were generated.

RESULTS

Eighty-three patients were enrolled in this study (MES 0, n = 47; MES 1, n = 36). The number of PCM cases was significantly higher in patients with prolonged CR than that in those with relapse (p = 0.01). Multivariate analysis showed that the absence of PCM and MD were related to relapse in all the patients. In patients with MES 1, the absence of PCM was the only risk factor significantly and independently associated with relapse (hazard ratio, 4.51 [1.15-17.7]; p = 0.03).

CONCLUSION

The absence of PCM was a histological risk factor for relapse in patients with MES 1, implying a protective role for PCM in remission and a new index for mucosal healing.

摘要

背景

潘氏细胞在维持肠道内稳态方面发挥多种作用。然而,潘氏细胞化生(PCM)在溃疡性结肠炎(UC)中的临床作用尚不清楚。我们旨在研究 PCM 与 UC 患者复发之间的关系,并比较 PCM 与其他组织学指标(包括粘蛋白耗竭(MD)和基底浆细胞增多(BP))的有用性。

方法

本回顾性队列研究纳入了临床缓解(CR)期并接受结肠镜检查以确认 Mayo 内镜评分(MES)≦1 且远端结肠有活检的 UC 患者。对活检样本进行 PCM、MD 和 BP 的组织学检查。临床复发定义为部分 Mayo 评分≧3 或药物升级。对三种组织学发现、MES 和患者背景中的复发独立预测因子进行多变量分析,并生成复发预测模型。

结果

本研究共纳入 83 例患者(MES 0,n=47;MES 1,n=36)。与复发患者相比,持续 CR 患者的 PCM 病例数明显更多(p=0.01)。多变量分析显示,在所有患者中,无 PCM 和 MD 与复发有关。在 MES 1 的患者中,无 PCM 是唯一与复发显著且独立相关的危险因素(危险比,4.51[1.15-17.7];p=0.03)。

结论

在 MES 1 的患者中,无 PCM 是复发的组织学危险因素,这表明 PCM 在缓解期具有保护作用,是黏膜愈合的新指标。

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Intestinal commensal microbiota and cytokines regulate Fut2 Paneth cells for gut defense.肠道共生微生物群和细胞因子调节 Fut2 潘氏细胞进行肠道防御。
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Histologic Diagnosis of Inflammatory Bowel Diseases.炎症性肠病的组织学诊断。
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Histologic remission does not offer additional benefit for ulcerative colitis patients in endoscopic remission.组织学缓解对内镜缓解的溃疡性结肠炎患者没有额外获益。
Aliment Pharmacol Ther. 2020 Dec;52(11-12):1676-1682. doi: 10.1111/apt.16147. Epub 2020 Nov 1.
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Histopathological Features of Inflammatory Bowel Disease are Associated With Different CD4+ T Cell Subsets in Colonic Mucosal Lamina Propria.炎症性肠病的组织病理学特征与结肠黏膜固有层中不同的 CD4+T 细胞亚群有关。
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Histological Risk Factors to Predict Clinical Relapse in Ulcerative Colitis With Endoscopically Normal Mucosa.内镜下黏膜正常的溃疡性结肠炎的组织学危险因素预测临床复发。
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Histologic Normalization Occurs in Ulcerative Colitis and Is Associated With Improved Clinical Outcomes.组织学正常化发生在溃疡性结肠炎中,并与改善的临床结局相关。
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Histological Disease Activity as a Predictor of Clinical Relapse Among Patients With Ulcerative Colitis: Systematic Review and Meta-Analysis.组织学疾病活动作为溃疡性结肠炎患者临床复发的预测指标:系统评价和荟萃分析
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