Meiring S, Aydin Ö, van Baar A C G, van der Vossen E W J, Rampanelli E, van Grieken N C T, Holleman F, Nieuwdorp M, Bergman J J G H M
Department of Gastroenterology and Hepatology, Amsterdam University Medical Centres, Location AMC, Meibergdreef 9, 1105AZ, Amsterdam, The Netherlands.
Department of Internal and Vascular Medicine, Amsterdam University Medical Centres, Location AMC, Amsterdam, The Netherlands.
Dig Dis Sci. 2025 Mar;70(3):1052-1063. doi: 10.1007/s10620-024-08710-4. Epub 2025 Jan 8.
Duodenal Mucosal Resurfacing (DMR) is an endoscopic ablation technique aimed at improving glycemia in patients with type 2 diabetes mellitus (T2DM). Although the exact underlying mechanism is still unclear, it is postulated that the DMR-induced improvements are the result of changes in the duodenal mucosa. For this reason, we assessed macroscopic and microscopic changes in the duodenal mucosa induced by DMR + GLP-1RA.
We included 16 patients with T2DM using basal insulin that received a combination treatment of a single DMR and GLP-1RA. Endoscopic evaluation was performed before the DMR procedure and 3 month after, and duodenal biopsies were obtained. Histological evaluation was performed and L and K cell density was calculated. In addition, gene-expression analysis and Western blotting was performed.
Endoscopic evaluation at 3 month showed duodenal mucosa with a normal appearance. In line, microscopic histological evaluation showed no signs of villous atrophy or inflammation and unchanged L and K cell density. Unbiased transcriptome profiling and western blotting revealed that PDZK1 expression was higher in responders at baseline and after DMR. GATA6 expression was significantly increased in responders after DMR compared to non-responders.
The absence of macroscopic and microscopic changes after 3 month suggest that improvements in glycemic parameters after DMR do not result from significant histological changes in duodenal mucosa. It is more likely that these improvements result from more subtle changes in enteroendocrine signaling. PDZK1 and GATA6 expression might play a role in DMR; this needs to be confirmed in pre-clinical studies.
十二指肠黏膜重塑(DMR)是一种内镜下消融技术,旨在改善2型糖尿病(T2DM)患者的血糖水平。尽管确切的潜在机制仍不清楚,但据推测,DMR诱导的改善是十二指肠黏膜变化的结果。因此,我们评估了DMR + GLP-1RA诱导的十二指肠黏膜的宏观和微观变化。
我们纳入了16例使用基础胰岛素的T2DM患者,他们接受了单次DMR和GLP-1RA的联合治疗。在DMR手术前和术后3个月进行内镜评估,并获取十二指肠活检组织。进行组织学评估并计算L细胞和K细胞密度。此外,还进行了基因表达分析和蛋白质印迹分析。
3个月时的内镜评估显示十二指肠黏膜外观正常。同样,微观组织学评估未显示绒毛萎缩或炎症迹象,L细胞和K细胞密度也未改变。无偏转录组分析和蛋白质印迹显示,应答者在基线和DMR后PDZK1表达较高。与无应答者相比,应答者在DMR后GATA6表达显著增加。
3个月后无宏观和微观变化表明,DMR后血糖参数的改善并非由十二指肠黏膜的显著组织学变化所致。这些改善更可能是由肠内分泌信号的更细微变化引起的。PDZK1和GATA6表达可能在DMR中起作用;这需要在临床前研究中得到证实。