糖尿病微量白蛋白尿病例排出的白蛋白具有假酯酶活性:探索微量白蛋白尿的新途径,或许能获得更多信息。

IF 3.2 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinica Chimica Acta Pub Date : 2024-08-30 DOI:10.1016/j.cca.2024.119947
Deepak Kumar , Pinaki Dutta , Raja Ramachandran , Rajasri Bhattacharyya , Dibyajyoti Banerjee
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引用次数: 0

摘要

背景:微量白蛋白尿与几种公众健康关注的临床症状有关。特别是在糖尿病患者中,常规微量白蛋白尿筛查可了解肾脏并发症是否已发展到微量白蛋白尿阶段。因此,微量白蛋白尿的检测备受关注。临床实验室依靠免疫化学方法进行检测。然而,人们认为免疫化学方法的灵敏度较低。因此,有必要在这一领域继续开展研究。我们认为,微量白蛋白尿病例中排泄的白蛋白的假酯酶活性是一个潜在的目标。本文对这方面进行了研究,结果表明,与明显的白蛋白尿病例不同,糖尿病微量白蛋白尿病例中排出的白蛋白仍具有假酯酶活性:研究对象包括糖尿病肾病病例和健康对照组。根据 ACR 比率将患者分为糖尿病对照组微量白蛋白尿和明显白蛋白尿组。病例的尿蛋白经离心分离。然后用电泳法和荧光法检测得到的蛋白质颗粒是否具有假酯酶活性。CD 光谱和 LC-MS 研究显示了底物对检测白蛋白伪酯酶活性的适用性。为了进一步了解结构与功能的关系,还进行了分子对接研究:结果:CD 和 LC-MS 研究证实了所用底物的适用性。电泳和荧光研究表明,微量白蛋白尿组的蛋白质保留了伪酯酶活性,而明显白蛋白尿组的蛋白质则失去了这种活性。分子对接研究表明,白蛋白结构的改变可能导致其假酯酶活性的改变:结论:糖尿病微量白蛋白尿病例的尿蛋白具有假酯酶活性。结论:糖尿病微量白蛋白尿病例的尿蛋白表现出假酯酶活性,它区分了糖尿病白蛋白尿组和明显白蛋白尿组的排泄蛋白。这是第一项显示排泄白蛋白中保留假酯酶特性的研究。此外,本研究还开发了一种简单的检测方法,可区分微量白蛋白尿组和明显白蛋白尿组的排泄白蛋白。
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Excreted albumin of diabetic microalbuminuria cases exhibits pseudo esterase activity: A new way to explore microalbuminuria, perhaps with more information

Background

Microalbuminuria is associated with several clinical conditions of public health concern. Particularly in diabetic patients, there is routine microalbuminuria screening to understand whether the renal complication has progressed to the microalbuminuria stage or not. Therefore, microalbuminuria detection is a matter of considerable interest. For such detection, the clinical labs rely on immunochemical methods. Nevertheless, the immunochemical methods are believed to be less sensitive for the purpose. So, the need arises for continuous research in the field. We believe that pseudoesterase activity of the excreted albumin in microalbuminuria cases is a potential target. This aspect is investigated here and it is shown that the excreted albumin in diabetic microalbuminuria cases retains its pseudoesterase activity, unlike the overt albuminuria cases.

Methods

The cases of diabetic nephropathy and healthy controls were included in the study. The patients were divided into diabetic controls microalbuminuria, and overt albuminuria group considering the albumin to creatinine ratio (ACR). The urinary proteins of the cases were isolated by centrifugation. The obtained protein pellet was then checked for pseudoesterase activity by electrophoretic and fluorescence-based methods. The CD spectroscopy and LC-MS study was carried out to show the suitability of the substrate for the detection of albumin pseudoesterase activity. To further, understand the structure–function relation, molecular docking studies were carried out.

Results

From the CD and LC-MS study the suitability of the used substrate was confirmed. The electrophoretic and fluorescence study showed that the protein of the microalbuminuria group retained the pseudoesterase activity whereas the same is lost in the overt albuminuria group. The molecular docking studies indicated that a change in albumin structure may result in a change in its pseudoesterase activity.

Conclusion

The urinary protein of diabetic microalbuminuria cases exhibits pseudoesterase activity. It distinguishes the excreted protein in the diabetic albuminuria group and the overt albuminuria group. This is the first study that showed the retention of pseudoesterase property in excreted albumin. Further, in this study a simple test is developed that distinguishes the excreted albumin in the microalbuminuria group and overt albuminuria group.

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来源期刊
Clinica Chimica Acta
Clinica Chimica Acta 医学-医学实验技术
CiteScore
10.10
自引率
2.00%
发文量
1268
审稿时长
23 days
期刊介绍: The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells. The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.
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