含7的F-box WD重复结构域在1型糖尿病中的作用

Sarah W. Mohammed, Zainab M. Qassam, E. M. Taha, Nameer M. Salih
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引用次数: 0

摘要

1型糖尿病(T1DM)是一种慢性免疫系统疾病,其特征是朗格汉斯岛ß-细胞被破坏或损伤,导致胰岛素缺乏和高血糖。本研究确定了含有7的新标记物F-box和WD重复结构域(FBXW7)。在(2021年12月20日至2022年3月25日)期间,来自伊拉克三个不同地方(中央儿童医院、Alkindi糖尿病和内分泌中心、儿童教育医院)的120名1型糖尿病患者,年龄在(4-17)岁之间。患者组分为三组:第一组为健康患者(33例),第二组为新诊断的T1DM患者(20例)和经胰岛素治疗的1型糖尿病患者(67例)。采用定量酶联免疫吸附法(ELISA)生化参数定量FBXW-7蛋白水平。分光光度法测定FBG、胆固醇、甘油三酯、HDL、LDL、VLDL、HbA1c、GOT、GPT、总氧化状态、总抗氧化状态。血清FBXW-7蛋白水平明显升高(p值= 0.00)。在FBXW7蛋白方面,新组和治疗组之间存在显著差异。与健康组相比,新组之间的蛋白质水平没有显著变化。患者组血清FBXW-7蛋白与FBG、TG、胆固醇、GOT、GPT、LDL、VLDL呈正相关,与HDL呈负相关。经ROC分析,新组FBXW-7蛋白的临界值为(1.9),治疗组FBXW-7蛋白的临界值为(2.1)。糖尿病患者FBXW-7蛋白水平升高。FBXW-7蛋白在治疗组与健康组比较差异有统计学意义,而新组与健康组比较差异无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of F-box WD Repeat Domain Containing 7 in Type 1 Diabetes
Type I diabetes (T1DM) is a chronic immune system disease characterized by the devastation or injury of ß-cells in the Langerhans Island, resulting in insulin deficiency and hyperglycemia. This study determines the new marker F-box and WD repeat domain containing 7 (FBXW7). One hundred twenty type 1 diabetic patients from three different places (central child hospital, Alkindi center for diabetes and endocrinology, Children’s Education Hospital) in Iraq during the period from (20 December 2021 to 25 March 2022) an age ranges of (4-17) years. The patient group consisted of being derived to three groups: group one healthy patient group (33) was included as healthy patient, group two (20) newly diagnosed T1DM and (67) type 1 diabetic with insulin treatment. The quantitative enzyme-linked immunosorbent assay (ELISA) biochemical parameters were used to quantify the protein FBXW-7 levels. FBG, Cholesterol, Triglyceride, HDL, LDL, VLDL, HbA1c, GOT, GPT, Total Oxidant status, and Total Antioxidant status were measured through spectrophotometry. Serum FBXW-7 protein levels were considerably elevated noticeably (p-value = 0.00). In terms of FBXW7 protein, there was a significant variation between the new and therapy groups. There was no significant variation in protein levels between the new compared to healthy groups. Serum FBXW-7 protein was positively correlated with FBG, TG, cholesterol, GOT, GPT, LDL, and VLDL, and was negatively correlated with HDL in the patient group. According to ROC analysis, the cutoff value for FBXW-7 protein was (1.9) in the newly group and (2.1) in the treatment group. Levels of FBXW-7 protein are elevated in DM patients. FBXW-7 protein was significantly different in the treatment group but not different in the newly group when compared with the healthy group.
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