Fedulovs Aleksejs, Tzivian Lilian, Zalizko Polina, Ivanova Santa, Bumane Renāte, Janeviča Jana, Krūzmane Lelde, Krustins Eduards, Sokolovska Jelizaveta
Faculty of Medicine, University of Latvia, Jelgavas Street 3, LV 1004 Riga, Latvia.
Pauls Stradins Clinical University Hospital, Pilsoņu Street 13, LV 1002 Riga, Latvia.
Biomedicines. 2023 Sep 29;11(10):2679. doi: 10.3390/biomedicines11102679.
(1) Background: Little research is conducted on the link between diabetic kidney disease (DKD) progression and diabetic gastroenteropathy in type 1 diabetes (T1D). (2) Methods. We performed a cross-sectional study with 100 T1D patients; 27 of them had progressive DKD, defined as an estimated glomerular filtration rate (eGFR) decline ≥3 mL/min/year or increased albuminuria stage, over a mean follow-up time of 5.89 ± 1.73 years. A newly developed score with 17 questions on gastrointestinal (GI) symptoms was used. Faecal calprotectin was measured by ELISA. Lower GI endoscopies were performed in 21 patients. (3) Results: The gastrointestinal symptom score demonstrated high reliability (Cronbach's α = 0.78). Patients with progressive DKD had higher GI symptom scores compared to those with stable DKD ( = 0.019). The former group demonstrated more frequent bowel movement disorders ( < 0.01). The scores correlated negatively with eGFR (r = -0.335; = 0.001), positively with albuminuria (r = 0.245; = 0.015), Hba1c (r = 0.305; = 0.002), and diabetes duration (r = 0.251; = 0.012). Faecal calprotectin levels did not differ between DKD groups significantly. The most commonly reported histopathological findings of enteric mucosa were infiltration with eosinophils, lymphocytes, plasmacytes, the presence of lymphoid follicles, and lymphoid aggregates. Conclusion: The progression of DKD is positively correlated with gastrointestinal symptoms; however, more research is needed to clarify the causal relationships of the gut-kidney axis in T1D.
(1) 背景:关于1型糖尿病(T1D)中糖尿病肾病(DKD)进展与糖尿病胃肠病之间的联系,相关研究较少。(2) 方法。我们对100例T1D患者进行了一项横断面研究;其中27例患有进展性DKD,定义为在平均5.89±1.73年的随访时间内,估计肾小球滤过率(eGFR)下降≥3 mL/min/年或蛋白尿分期增加。使用了一个新开发的包含17个关于胃肠道(GI)症状问题的评分系统。通过酶联免疫吸附测定(ELISA)法检测粪便钙卫蛋白。对21例患者进行了下消化道内镜检查。(3) 结果:胃肠道症状评分显示出高可靠性(Cronbach's α = 0.78)。与稳定DKD患者相比,进展性DKD患者的GI症状评分更高(P = 0.019)。前一组出现排便障碍的频率更高(P < 0.01)。这些评分与eGFR呈负相关(r = -0.335;P = 0.001),与蛋白尿呈正相关(r = 0.245;P = 0.015),与糖化血红蛋白(Hba1c)呈正相关(r = 0.305;P = 0.002),与糖尿病病程呈正相关(r = 0.251;P = 0.012)。DKD组之间粪便钙卫蛋白水平无显著差异。肠道黏膜最常报告的组织病理学发现是嗜酸性粒细胞、淋巴细胞、浆细胞浸润,存在淋巴滤泡和淋巴样聚集。结论:DKD的进展与胃肠道症状呈正相关;然而,需要更多研究来阐明T1D中肠 - 肾轴的因果关系。