Department of Cardiology, Erciyes University Medical Faculty, Kayseri, Turkey.
J Investig Med. 2013 Mar;61(3):597-603. doi: 10.2310/JIM.0b013e31828218e7.
Autosomal-dominant polycystic kidney disease (ADPKD) demonstrates cardiovascular manifestations, such as hypertension, myocardial infarction, and increased carotid intimae-media thickness. These complications are the main cause of morbidity and mortality in patients with ADPKD. Platelet activation and arterial stiffness are important manifestations that independently predict cardiovascular events. In the present study, we aimed to investigate the relation between arterial stiffness, mean platelet volume (MPV), and highly sensitive C-reactive protein (hs-CRP) in patients with normotensive polycystic kidney disease.
We included 30 normotensive subjects with ADPKD with an estimated glomerular filtration rate (eGFR) of 60 mL or more per minute per 1.73 m, 30 normotensive subjects with ADPKD with eGFR from 30 to 60 mL/min per 1.73 m, and 30 healthy controls in our study. Pulse wave velocity (PWV), eGFR, spot urine protein-creatinine ratio, MPV, and hs-CRP levels were measured in all participants. In addition, transthoracic echocardiography and ambulatory blood pressure monitoring were performed.
Age, sex, biochemical markers, eGFR, hemoglobin level, and platelet count were similar in the ADPKD subjects and the controls. There were significant differences in MPV (9.8 ± 0.7, 8.7 ± 0.8, and 8.0 ± 0.5 femtolitre; P < 0.001) and hs-CRP (6.8 ± 3.0, 5.3 ± 2.7, and 2.6 ± 0.52 mg/L; P < 0.001) in the groups. Additionally, PWV values were increased from healthy subjects to ADPKD patients who have decreased eGFR (5.5 ± 1.1, 8.8 ± 1.6, and 10.8 ± 1.2 m/s; P for trend <0.001). There were significant positive correlations between PWV and MPV (r = 0.401; P = 0.002) and hs-CRP (r = 0.343; P = 0.007) in the patients with ADPKD. Additionally, PWV was independently predicted by MPV (β = 0.286; P = 0.007), proteinuria (β = 0.255; P = 0.001), eGFR (β = -0.479; P < 0.001), and hs-CRP (β = 0.379; P < 0.001) in the patients with ADPKD. In addition, eGFR, as a sign of severity of disease, was independently predicted by MPV (β = -0.325; P = 0.003), PWV (β = -0.471; P < 0.001), and hs-CRP (β = -0.269; P = 0.008).
Our findings suggest that MPV and hs-CRP levels are associated with increased arterial stiffness in patients with early-stage ADPKD and those with late-stage ADPKD. Also, MPV and hs-CRP were independently associated with the severity of ADPKD.
常染色体显性遗传多囊肾病(ADPKD)表现出心血管表现,如高血压、心肌梗死和颈动脉内膜中层厚度增加。这些并发症是 ADPKD 患者发病和死亡的主要原因。血小板激活和动脉僵硬是独立预测心血管事件的重要表现。在本研究中,我们旨在研究在血压正常的多囊肾病患者中动脉僵硬、平均血小板体积(MPV)和高敏 C 反应蛋白(hs-CRP)之间的关系。
我们纳入了 30 名血压正常的 ADPKD 患者,他们的估计肾小球滤过率(eGFR)为每分钟每 1.73 m 肾小球滤过率 60 mL 或以上,30 名 eGFR 在每分钟每 1.73 m 肾小球滤过率 30 至 60 mL 的血压正常的 ADPKD 患者,以及 30 名健康对照组。所有参与者均测量脉搏波速度(PWV)、eGFR、尿蛋白肌酐比、MPV 和 hs-CRP 水平。此外,还进行了经胸超声心动图和动态血压监测。
ADPKD 患者和对照组的年龄、性别、生化标志物、eGFR、血红蛋白水平和血小板计数相似。MPV(9.8 ± 0.7、8.7 ± 0.8 和 8.0 ± 0.5 飞升;P < 0.001)和 hs-CRP(6.8 ± 3.0、5.3 ± 2.7 和 2.6 ± 0.52 mg/L;P < 0.001)在各组之间存在显著差异。此外,从健康受试者到 eGFR 降低的 ADPKD 患者,PWV 值增加(5.5 ± 1.1、8.8 ± 1.6 和 10.8 ± 1.2 m/s;P < 0.001)。ADPKD 患者的 PWV 与 MPV(r = 0.401;P = 0.002)和 hs-CRP(r = 0.343;P = 0.007)呈显著正相关。此外,MPV(β = 0.286;P = 0.007)、蛋白尿(β = 0.255;P = 0.001)、eGFR(β = -0.479;P < 0.001)和 hs-CRP(β = 0.379;P < 0.001)可独立预测 ADPKD 患者的 PWV。此外,eGFR 作为疾病严重程度的标志,可独立预测 MPV(β = -0.325;P = 0.003)、PWV(β = -0.471;P < 0.001)和 hs-CRP(β = -0.269;P = 0.008)。
我们的研究结果表明,MPV 和 hs-CRP 水平与早期和晚期 ADPKD 患者的动脉僵硬增加有关。此外,MPV 和 hs-CRP 与 ADPKD 的严重程度独立相关。