Translational Research Center for Gastrointestinal Disorders (TARGID), Department of Chronic Diseases and Metabolism (ChroMeta), Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Translational Cell & Tissue Research, Department of Imaging & Pathology, Katholieke Universiteit Leuven, Leuven, Belgium.
Clin Transl Gastroenterol. 2024 Jul 1;15(7):e00725. doi: 10.14309/ctg.0000000000000725.
INTRODUCTION: The diagnosis of eosinophilic gastrointestinal diseases is largely based on mucosal eosinophil counts, but thresholds and normal ranges beyond the esophagus are debated, calling for much-needed methodological standardization. We aimed to develop a standardized workflow for duodenal cell quantification and estimate duodenal eosinophil and mast cell numbers in healthy controls. METHODS: Software-based histological cell quantification using free-sized or fixed-sized regions was developed and applied to digitized hematoxylin and eosin (H&E)-stained slides from 58 individuals (healthy controls [HCs] and patients with functional dyspepsia). Intraclass correlation coefficients (ICCs) compared inter-rater reliability between software-based and microscopic quantification. Reproducibility of the software-based method was validated in an independent cohort of 37 control and functional dyspepsia subjects. Eosinophil identification on H&E staining was compared to immunohistochemistry (IHC). Normal eosinophil (H&E) and mast cell (cKit) ranges were determined in 70 adult HCs. RESULTS: Eosinophil quantification on digitized slides demonstrated excellent (ICC = 0.909) and significantly improved reproducibility over microscopic evaluation (ICC = 0.796, P = 0.0014), validated in an independent cohort (ICC = 0.910). Duodenal eosinophils were more abundant around crypts than in villi ( P < 0.0001), while counts were similar on matched H&E- and IHC-stained slides ( P = 0.55). Mean ± SD (95th percentile) duodenal eosinophils and mast cells in HC were 228.8/mm 2 ± 94.7 (402.8/mm 2 ) and 419.5/mm 2 ± 132.2 (707.6/mm 2 ), respectively. DISCUSSION: We developed and validated a standardized approach to duodenal histological cell quantification, generalizable to various mucosal cell types. Implementation of software-based quantification identified 400 eosinophils/mm 2 and 700 mast cells/mm 2 as thresholds for abnormal duodenal infiltration.
简介:嗜酸性粒细胞性胃肠道疾病的诊断在很大程度上基于黏膜嗜酸性粒细胞计数,但食管以外的阈值和正常范围仍存在争议,因此需要进行急需的方法学标准化。我们旨在开发一种标准化的十二指肠细胞定量工作流程,并估计健康对照者的十二指肠嗜酸性粒细胞和肥大细胞数量。 方法:使用基于软件的组织学细胞定量方法,使用自由大小或固定大小的区域进行开发,并应用于 58 个人(健康对照者[HC]和功能性消化不良患者)的数字化苏木精和伊红(H&E)染色幻灯片。组内相关系数(ICC)比较了基于软件和显微镜定量之间的观察者间可靠性。在 37 名对照和功能性消化不良受试者的独立队列中验证了基于软件的方法的重现性。在 H&E 染色上比较嗜酸性粒细胞的鉴定与免疫组织化学(IHC)。在 70 名成人 HC 中确定了正常嗜酸性粒细胞(H&E)和肥大细胞(cKit)范围。 结果:数字化幻灯片上的嗜酸性粒细胞定量显示出极好的(ICC = 0.909)和显著优于显微镜评估的重现性(ICC = 0.796,P = 0.0014),在独立队列中得到验证(ICC = 0.910)。十二指肠嗜酸性粒细胞在隐窝周围比在绒毛中更为丰富(P <0.0001),而在匹配的 H&E 和 IHC 染色载玻片上的计数相似(P = 0.55)。HC 中十二指肠嗜酸性粒细胞和肥大细胞的平均值±SD(95%百分位数)分别为 228.8/mm 2 ±94.7(402.8/mm 2 )和 419.5/mm 2 ±132.2(707.6/mm 2 )。 讨论:我们开发并验证了一种标准化的十二指肠组织学细胞定量方法,适用于各种黏膜细胞类型。基于软件的定量识别出 400 个嗜酸性粒细胞/mm 2 和 700 个肥大细胞/mm 2 作为异常十二指肠浸润的阈值。
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