慢性肾脏病(慢性肾盂肾炎)在非酒精性脂肪性肝病和肥胖患者中的病程

A. Antoniv, Z. Y. Kotsyubiychuk, Volodymyr V. Vivsyanyk, V. Smandych, L. V. Kanyovska, O. Mandryk, O. Liakhovych
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摘要

研究目的:探讨慢性肾盂肾炎(CKD)、非酒精性脂肪性肝病和肥胖随CKD分期的共病病程特点。为了实现这一目标,250年慢性肾脏疾病(CKD)患者(慢性双边肾盂肾炎)舞台》检查,其中160例患者伴随的纳什和类1肥胖(1组)和90人CKD舞台》没有纳什和肥胖(组2)。根据CKD的阶段,患者组1被分成3组:与CKD阶段I - 63病人,CKD阶段II - 52例,慢性肾病阶段III - 45的病人。组2患者也分为3个亚组:CKD I期- 32例,CKD II期- 31例,CKD III期- 27例。对照组为表面健康个体(AHIs) 30例。患者平均年龄49.8±5.8岁。该研究不包括CKD I-III期肾病综合征患者和慢性无并发症肾盂肾炎加重期患者。根据我们的研究结果,我们注意到非酒精性脂肪变性和脂肪性肝炎对I-III期CKD患者肾脏功能状态的可能影响:与无合并症的CKD患者相比,肾小球滤过率、氮排泄功能、低白蛋白血症增加、尿蛋白、红细胞、白细胞增加、细菌存在显著变化。肾小球滤过率(GFR)的降低、氧化应激强度的增加、血谷胱甘肽、硫化氢、同型半胱氨酸、细胞角蛋白-18、结缔组织成分(胶原蛋白、唾液酸)的过量产生之间存在显著相关性。在没有合并NASH和肥胖的CKD I-II期患者中,我们发现对水电解质刺激的肾功能储备明显更高,这在两组患者中都是足够的(GFR增加28-37%,而合并NASH的患者增加19-31%)。在CKD III期合并非酒精性脂肪性肝炎的患者中,我们发现肾脏功能储备显著降低(GFR增加8.9%,而非NASH患者增加17.5%),在4.9%的合并症患者中,肾脏没有功能储备(p > 0.05),表明肾脏功能状态发生了不可逆的变化。
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THE COURSE OF CHRONIC KIDNEY DISEASE (CHRONIC PYELONEPHRITIS) IN PATIENTS WITH NON-ALCOHOLIC FATTY LIVER DISEASE AND OBESITY
The aim of the research: to investigate the features of the comorbid course of chronic kidney disease (CKD) (chronic pyelonephritis), non-alcoholic fatty liver disease and obesity, depending on the stage of CKD. To achieve this goal, 250 patients with chronic kidney disease (CKD) (chronic bilateral pyelonephritis) stage I–III were examined, of which 160 patients had concomitant NASH and class 1 obesity (1 group) and 90 people had CKD stage I–III without NASH and obesity (group 2). Depending on the stage of CKD, patients of group 1 were divided into 3 subgroups: with CKD stage I – 63 patients, with CKD stage II – 52 patients, with CKD stage III – 45 patients. Patients of group 2 were also divided into 3 subgroups: with CKD stage I – 32 patients, with CKD stage II – 31 patients, with CKD stage III – 27 patients. The control group included 30 apparently healthy individuals (AHIs). The average age of patients was 49.8 ± 5.8 years. The study did not include patients with CKD stage I–III with nephrotic syndrome and patients with chronic uncomplicated pyelonephritis in the phase of exacerbation. According to the results of our study, we noted a probable effect of nonalcoholic steatosis and steatohepatitis on the functional state of the kidneys in patients with stage I–III CKD: significant changes in glomerular filtration rate, nitrogen excretory function, increased hypoalbuminemia, increased protein in the urine, erythrocytes, leukocytes, the presence of bacteria, compared with patients with CKD without comorbidity. There was a significant correlation between a decrease in glomerular filtration rate (GFR), an increase in the intensity of oxidative stress, a decrease in blood glutathione, hydrogen sulfide, hyperproduction of homocysteine, cytokeratin-18, connective tissue components (collagen, sialic acids). In patients with CKD stage I–II without comorbid NASH and obesity, we found a significantly higher renal functional reserve in response to water-electrolyte stimulation, which is sufficient in both groups of patients (increase in GFR by 28–37% vs. 19–31% for comorbidity with NASH). In patients with CKD stage III with nonalcoholic steatohepatitis we found a significantly reduced functional reserve of the kidneys (increase in GFR by 8.9% vs. 17.5% in patients without NASH), and in 4.9% of patients with comorbidity ­– no functional reserve of the kidneys (p > 0.05), indicating irreversible changes in the functional state of the kidneys.
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