Dziedzic-Jankowska Katarzyna, Szyszka Michał, Bujanowicz Adam, Stelmaszczyk-Emmel Anna, Skrzypczyk Piotr
Department of Pediatrics and Nephrology, Medical University of Warsaw, 02-091 Warsaw, Poland.
Department of Pediatrics and Nephrology, Doctoral School, Medical University of Warsaw, 02-091 Warsaw, Poland.
J Clin Med. 2025 Aug 13;14(16):5737. doi: 10.3390/jcm14165737.
: Increased blood pressure variability (BPV) was found in adults with primary (essential) hypertension (PH) and is associated with increased cardiovascular risk. Our study aimed to analyze the relation between BPV and low-grade inflammation in children with primary hypertension. : In 56 treatment-naive pediatric patients with PH (15.1 ± 2.1 years) and 30 healthy children (14.9 ± 1.4 years), we evaluated BPV: BP dipping, standard deviation (SD) of ambulatory blood pressure measurements (ABPMs), pulse pressure (PP)/systolic blood pressure ratio (24 h PP/SBP), rate-pressure index (24 h RPI), 24-h weighted BPV (24 h WSBPV, 24 h WDBV, 24 h WMAPV), coefficient of variation (24 h CoVSBP, 24 h CoVDBP, 24 h CoVMAP), ambulatory arterial stiffness index (AASI), and morning BP surge. We also analyzed indices of subclinical inflammation (markers derived from complete blood count, high-sensitivity C-reactive protein (CRP), interleukin 18), and office and ambulatory BP. : Patients with PH had significantly higher hsCRP, neutrophils, monocytes, and platelets, neutrophil-to-lymphocyte (NLR), platelet-to-mean platelet volume (PMPVR), and lower monocyte-to-neutrophil (MNR) ratios, and higher BPV: 24 h ABPM SBP SD, 24 h ABPM MAP SD, 24 h RPI, 24 h WSBPV, 24 h WDBV, 24 h WMAPV, and 24 h CoVSBP. Low-grade inflammation markers correlated with BPV indices in both groups. In multivariate analysis, MNR predicted 24 h ABPM MAP SD (beta = 0.290, 95CI: 0.029-0.551), 24 h RPI (beta = -0.348, 95CI: -0.587--0.108), and 24 h WDBPV (beta = 0.286, 95CI: 0.032-0.540); monocyte count-24 h RPI (beta = 0.281, 95CI: 0.041-0.521), and hsCRP-24 h WDBV (beta = 0.310, 95CI: 0.055-0.564). ROC analysis revealed a good diagnostic profile for lymphocyte count as a positive determinant of non-dipping status in PH children (cut-off point 2.59 [×10/µL]). : BPV is higher in children with PH compared to healthy peers and is associated with low-grade inflammation. MNR may be the most helpful indicator of BPV, whereas high lymphocyte count predicts the best non-dipping status in these patients.
在原发性(特发性)高血压(PH)成人患者中发现血压变异性(BPV)增加,且其与心血管风险增加相关。我们的研究旨在分析原发性高血压儿童中BPV与低度炎症之间的关系。:在56例未经治疗的PH儿科患者(15.1±2.1岁)和30例健康儿童(14.9±1.4岁)中,我们评估了BPV:血压波动、动态血压测量(ABPM)的标准差(SD)、脉压(PP)/收缩压比值(24小时PP/SBP)、速率压力指数(24小时RPI)、24小时加权BPV(24小时WSBPV、24小时WDBV、24小时WMAPV)、变异系数(24小时CoVSBP、24小时CoVDBP、24小时CoVMAP)、动态动脉僵硬度指数(AASI)和晨起血压激增。我们还分析了亚临床炎症指标(源自全血细胞计数的标志物、高敏C反应蛋白(CRP)、白细胞介素18)以及诊室血压和动态血压。:PH患者的hsCRP、中性粒细胞、单核细胞和血小板水平显著更高,中性粒细胞与淋巴细胞比值(NLR)、血小板与平均血小板体积比值(PMPVR)更高,单核细胞与中性粒细胞比值(MNR)更低,且BPV更高:24小时ABPM收缩压SD、24小时ABPM平均动脉压SD、24小时RPI、24小时WSBPV、24小时WDBV、24小时WMAPV和24小时CoVSBP。两组中低度炎症标志物均与BPV指标相关。在多变量分析中,MNR可预测24小时ABPM平均动脉压SD(β = 0.290,95%CI:0.029 - 0.551)、24小时RPI(β = -0.348,95%CI:-0.587 - -0.108)和24小时WDBPV(β = 0.286,95%CI:0.032 - 0.540);单核细胞计数 - 24小时RPI(β = 0.281,95%CI:0.041 - 0.521),以及hsCRP - 24小时WDBV(β = 0.310,95%CI:0.055 - 0.564)。ROC分析显示淋巴细胞计数作为PH儿童非勺型状态的阳性决定因素具有良好的诊断特征(截断点为2.59[×10/µL])。:与健康同龄人相比,PH儿童的BPV更高,且与低度炎症相关。MNR可能是BPV最有用的指标,而高淋巴细胞计数预示着这些患者最佳的非勺型状态。