Cardiovascular-kidney-metabolic syndrome - An integrative review.

Katiana Simões Kittelson, Arquimedes Gasparotto Junior, Natasha Fillmore, Roberto da Silva Gomes
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引用次数: 0

Abstract

The American Heart Association recently defined the complex interactions among the cardiovascular, renal, and metabolic systems as CKM syndrome. To promote better patient outcomes, having a more profound understanding of CKM pathophysiology and pursuing holistic preventative and therapy strategies is critical. Despite many gaps in understanding CKM syndrome, this study attempts to elucidate two of these gaps: the new emerging biomarkers for screening and the role of inflammation in its pathophysiology. For this review, an extensive search for specific terms was conducted in the following databases: PubMed, Scopus, Web of Science, and Google Scholar. Studies were first assessed by title, abstract, keywords, and selected for portfolio according to eligibility criteria, which led to 38 studies. They provided background information about CKM syndrome; data suggested that serum uric acid, leptin, aldosterone, bilirubin, soluble neprilysin, lipocalin-type-prostaglandin-D-synthase, and endocan could be valuable biomarkers for CKM screening; and finally, the inflammation role in CKM.

心血管-肾脏-代谢综合征--综述。
美国心脏协会最近将心血管、肾脏和代谢系统之间复杂的相互作用定义为 CKM 综合征。为了改善患者的预后,更深入地了解 CKM 病理生理学并采取全面的预防和治疗策略至关重要。尽管对 CKM 综合征的认识还存在许多空白,但本研究试图阐明其中的两个空白:用于筛查的新兴生物标志物以及炎症在其病理生理学中的作用。为了撰写这篇综述,我们在以下数据库中对特定术语进行了广泛搜索:PubMed、Scopus、Web of Science 和 Google Scholar。首先根据标题、摘要和关键词对研究进行评估,然后根据资格标准筛选出 38 篇研究。这些研究提供了有关 CKM 综合征的背景信息;数据表明,血清尿酸、瘦素、醛固酮、胆红素、可溶性肾酶、脂钙素型-前列腺素-D-合成酶和内切酶可能是筛查 CKM 的有价值的生物标志物;最后,研究了炎症在 CKM 中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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