Phenotyping Kidney Function in Young Adults With High Blood Pressure: The African-PREDICT Study.

IF 2.7 3区 医学 Q2 PERIPHERAL VASCULAR DISEASE
Anja Degenaar, Ruan Kruger, Adriaan Jacobs, Catharina M C Mels
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引用次数: 0

Abstract

Biomarkers of kidney function, including glomerular, tubular, and fibrotic markers, have been associated with blood pressure in elderly populations and individuals with kidney and cardiovascular diseases. However, limited information is available in young adults. In this study, we compared levels of several kidney function biomarkers between normotensive and hypertensive young adults and explored the associations of these biomarkers with blood pressure within these groups. In this cross-sectional assessment, twenty-four-hour (24-h) blood pressure measurements of 1055 participants (mean age = 24.6 years) were used to classify hypertension as per the 2018 ESC/ESH guidelines. Biomarkers of kidney function included estimated glomerular filtration rate, urinary albumin, alpha-1 microglobulin (uA1M), neutrophil gelatinase-associated lipocalin (uNGAL), uromodulin (uUMOD), and the CKD273 classifier. All urinary biomarkers, except for the CKD273 classifier, were standardized for urinary creatinine (Cr). In the hypertensive group (61.0% White; 73.2% men), urinary albumin-to-creatinine ratio (uACR), uNGAL/Cr and uUMOD/Cr were lower than the normotensive group. In multiple regression analyses, 24-h systolic blood pressure (SBP) (β = 0.14; p = 0.042), 24-h diastolic blood pressure (DBP) (β = 0.14; p = 0.040), and 24-h mean arterial pressure (MAP) (β = 0.16; p = 0.020) associated positively with uA1M/Cr in the hypertensive group, while 24-h MAP positively associated with uACR (β = 0.17; p = 0.017). In exploratory factor analysis, positive associations of 24-h DBP and 24-h MAP with a factor pattern including tubular biomarkers were observed in the hypertensive group (24-h DBP: β = 0.18; p = 0.026, 24-h MAP: β = 0.17; p = 0.032). In the setting of hypertension, high perfusion pressure in the kidneys may play a role in the development of proximal tubule damage and promote early deterioration in kidney function in young adults. Trial Registration: ClinicalTrials.gov identifier: NCT03292094.

年轻成人高血压患者肾功能的表型分析:非洲-PREDICT 研究。
肾功能生物标志物(包括肾小球、肾小管和纤维化标志物)与老年人群以及肾脏和心血管疾病患者的血压有关。然而,有关青壮年的信息却很有限。在这项研究中,我们比较了血压正常的年轻人和高血压年轻人的几种肾功能生物标志物的水平,并探讨了这些生物标志物与这些群体的血压之间的关系。在这项横断面评估中,1055 名参与者(平均年龄 = 24.6 岁)的二十四小时(24-h)血压测量值被用于根据 2018 ESC/ESH 指南对高血压进行分类。肾功能生物标志物包括估计肾小球滤过率、尿白蛋白、α-1微球蛋白(uA1M)、中性粒细胞明胶酶相关脂褐质(uNGAL)、尿调蛋白(uUMOD)和CKD273分类器。除 CKD273 分类器外,所有尿液生物标记物均以尿肌酐(Cr)为标准。高血压组(61.0% 白人;73.2% 男性)的尿白蛋白与肌酐比值(uACR)、uNGAL/Cr 和 uUMOD/Cr 均低于正常血压组。在多元回归分析中,高血压组的 24 小时收缩压(SBP)(β = 0.14;p = 0.042)、24 小时舒张压(DBP)(β = 0.14;p = 0.040)和 24 小时平均动脉压(MAP)(β = 0.16;p = 0.020)与 uA1M/Cr 呈正相关,而 24 小时平均动脉压与 uACR 呈正相关(β = 0.17;p = 0.017)。在探索性因子分析中,观察到高血压组 24 小时 DBP 和 24 小时 MAP 与包括肾小管生物标志物在内的因子模式呈正相关(24 小时 DBP:β = 0.18;p = 0.026,24 小时 MAP:β = 0.17;p = 0.032)。在高血压的情况下,肾脏的高灌注压可能会在近端肾小管损伤的发展过程中发挥作用,并促进青壮年肾功能的早期恶化。试验注册:临床试验注册:ClinicalTrials.gov identifier:NCT03292094。
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来源期刊
Journal of Clinical Hypertension
Journal of Clinical Hypertension PERIPHERAL VASCULAR DISEASE-
CiteScore
5.80
自引率
7.10%
发文量
191
审稿时长
4-8 weeks
期刊介绍: The Journal of Clinical Hypertension is a peer-reviewed, monthly publication that serves internists, cardiologists, nephrologists, endocrinologists, hypertension specialists, primary care practitioners, pharmacists and all professionals interested in hypertension by providing objective, up-to-date information and practical recommendations on the full range of clinical aspects of hypertension. Commentaries and columns by experts in the field provide further insights into our original research articles as well as on major articles published elsewhere. Major guidelines for the management of hypertension are also an important feature of the Journal. Through its partnership with the World Hypertension League, JCH will include a new focus on hypertension and public health, including major policy issues, that features research and reviews related to disease characteristics and management at the population level.
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