2014-2020年Ahwaz教学医院就诊的2型糖尿病合并CKD患者蛋白尿正常至轻度增高频率的评估

S. Ghaderian, Torkan Rezaie, S. Mousavi, H. Rashidi, F. Hayati
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引用次数: 0

摘要

研究-数据收集,统计-数据解释,-背景。糖尿病肾病是糖尿病患者肾功能受损和慢性肾病(CKD)的主要原因。目标。本研究的目的是评估2型糖尿病(T2DM)合并慢性肾脏疾病患者正常至轻度蛋白尿增高的患病率和特征。材料和方法。本回顾性研究对2014-2020年间在Ahvaz医院就诊的310例诊断为T2DM并肾功能不全(eGFR < 60 mL/min/1.73 m2)的患者进行了研究。从患者的医疗记录中提取了人口统计和临床数据以及实验室参数。在考虑了纳入标准(成人糖尿病患者合并肾功能衰竭(eGFR < 60 mL/min/1.73 m2)和排除标准(高血压、心血管疾病(缺血性心脏病、慢性心力衰竭、外周血管疾病、脑血管疾病)、尿路感染、尿路解剖紊乱、肾结石、良性前列腺增生、利尿剂使用史、肾毒性药物如ACEI、ARB、NSAIDs、生理原因引起蛋白尿,如长时间站立和运动、系统性疾病(如系统性红斑狼疮)和透析患者,根据年龄、性别、糖尿病病程、血脂、视网膜病变和神经病变、HbA 1C,根据蛋白尿严重程度(白蛋白与肌酐比值)将患者分为正常至轻度蛋白尿升高(ACR < 30 mg/g)、中度升高(ACR:ACR > 300 mg/g,急性加重。结果。T2DM患者平均年龄±9.5岁,女性164例(52.9%),男性146例(47.1%),其中正常蛋白尿4例(1.3%),轻度增高蛋白尿76例(24.5%),中度增高蛋白尿142例(45.8%),重度增高蛋白尿88例(28.4%)。与中度至重度蛋白尿相比,正常至轻度蛋白尿升高的个体糖尿病病程、年龄、creati9、视网膜病变、神经病变、HbA 1c、LDL、Tchol (p < 0.001)、GFR升高(p < 0.001)和TG降低(p = 0.003)较短,而HDL-c (p = 0.07)和患者性别(p = 0.2)差异无统计学意义。优势比(OR)检查显示,视网膜病变、高年龄和高hba1c水平对中度至重度蛋白尿的发展影响最大,而GFR升高和低密度脂蛋白的少量升高对中度至重度蛋白尿有预防作用。伴有糖尿病和肾功能不全者尿白蛋白正常至轻度增高。这限制了微量白蛋白尿作为检测糖尿病肾病发病的筛查工具的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the frequency of normal to mildly increased albuminuria, in patients with type 2 diabetes with CKD referred to clinics of Ahwaz teaching Hospitals in the years 2014–2020
Study – Data Collection, Statistical – Data Interpretation, – Background. Diabetic nephropathy is the main cause of impaired renal function and chronic kidney disease (CKD) in dia betic patients. Objectives. The aim of this study was to estimate the prevalence and characteristics of normal to mildly increased albuminuria in type 2 diabetes mellitus (T2DM) patients with chronic kidney disease. Material and methods. This retrospective study was performed on 310 patients diagnosed with T2DM and renal insufficiency (eGFR < 60 mL/min/1.73 m 2 ) referred to Ahvaz hospitals between 2014–2020. Demographic and clinical data, as well as laboratory param -eters, were extracted from patients’ medical records. After considering the inclusion criteria (adult diabetic patients with renal failure (eGFR < 60 mL/min/1.73 m 2 ) and exclusion criteria (patients with hypertension, cardiovascular disease (ischemic heart disease, chronic heart failure, peripheral vascular disease, cerebrovascular disease), urinary tract infection, anatomical disorders of the urinary tract, kidney stones, benign prostatic hyperplasia, history of diuretic use, nephrotoxic drugs such as ACEI, ARB, NSAIDs, physiological causes of albuminuria such as prolonged standing and exercise, systematic disease (e.g. systemic lupus erythematosus) and dialysis patients), in terms of age, gender and duration of diabetes and lipid profile and retinopathy and neuropathy and HbA 1C , patients were divided into three groups based on the severity of albuminuria (albumin-to-creatinine ratio): normal to mildly increased albuminuria (ACR < 30 mg/g), moderately increased (ACR: 30–300 mg/g) and severely increased (ACR > 300 mg/g). Results. T2DM patients with a mean age of ± 9.5 years, including 164 women (52.9%) and 146 men (47.1%), par ticipated in the study, of which 4 patients (1.3%) had normal albuminuria, 76 patients (24.5%) had mildly increased albuminuria, 142 patients (45.8%) had moderately increased albuminuria, and 88 patients (28.4%) had severely increased albuminuria. Individuals with normal to mildly increased albuminuria compared with moderate to severe albuminuria had lower duration of diabetes, age, creati -nine, retinopathy, neuropathy, HbA 1c , LDL, Tchol ( p < 0.001), higher GFR ( p < 0.001) and lower TG ( p = 0.003), while HDL-c ( p = 0.07) and patients’ gender ( p = 0.2) were not significantly different. Examination of the odds ratio (OR) showed that retinopathy, high age and high HbA 1c levels had the greatest effect on the development of moderate to severe albuminuria, whereas increased GFR and a small increase in LDL had a preventive effect on moderate to severe albuminuria. with diabetes and renal insufficiency had normal to mildly increased albuminuria. This can limit the role of microalbuminuria as a screening tool to detect the onset of diabetic nephropathy.
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