Piek Arnold, Smit Leonie, Suthahar Navin, Bakker Stephan J L, de Boer Rudolf A, Silljé Herman H W
Department of Cardiology, University Medical Center Groningen, University of Groningen, Hanzeplein 1, Groningen, 9713 GZ, The Netherlands.
Department of Internal Medicine, University Medical Center Groningen, University of Groningen, Hanzeplein 1, Groningen, 9713 GZ, The Netherlands.
Sci Rep. 2021 Apr 21;11(1):8642. doi: 10.1038/s41598-021-88107-9.
Dickkopf-3 (DKK3) is an emerging biomarker for cardiovascular disease (CVD) and chronic kidney disease (CKD). Herein, baseline DKK3 plasma levels were measured in 8420 subjects from the Prevention of Renal and Vascular ENd-stage Disease (PREVEND) cohort, a large general population cohort, using enzyme-linked immunosorbent assays. Associations with clinical variables and outcomes were analysed. Median DKK3 level was 32.8 ng/ml (28.0-39.0). In multivariable linear regression analysis, the strongest correlates for plasma DKK3 were age, body mass index and estimated glomerular filtration rate (eGFR). At baseline, 564 (6.7%) subjects had CVD (defined as a myocardial infarction and/or cerebrovascular accident) and 1361 (16.2%) subjects had CKD (defined as eGFR < 60 ml/min/1.73m and/or urinary albumin excretion (UAE) > 30 mg/24 h). Of subjects with known CVD and CKD follow-up status (respectively 7828 and 5548), 669 (8.5%) developed CVD and 951 (17.1%) developed CKD (median follow-up respectively 12.5 and 10.2 years). Crude logistic regression analysis revealed that DKK3 levels were associated with prevalent CVD (Odds ratio: 2.14 [1.76-2.61] per DKK3 doubling, P < 0.001) and CKD (Odds ratio: 1.84 [1.59-2.13] per DKK3 doubling, P < 0.001). In crude Cox proportional hazard regression analysis, higher DKK3 levels were associated with higher risk for new-onset CVD (Hazard ratio: 1.47 [1.13-1.91] per DKK3 doubling, P = 0.004) and CKD (Hazard ratio: 1.45, [1.25-1.69] per DKK3 doubling, P < 0.001). However, these associations remained no longer significant after correction for common clinical variables and risk factors, though independently predicted for new-onset CKD in a subgroup of subjects with the lowest UAE values. Together, DKK3 plasma levels are associated with cardiovascular risk factors, but are generally not independently associated with prevalent and new-onset CVD and CKD and only predicted for new-onset CKD in those subjects with the lowest UAE values.
Dickkopf-3(DKK3)是一种新兴的心血管疾病(CVD)和慢性肾脏病(CKD)生物标志物。在此,我们使用酶联免疫吸附测定法,对来自一般人群队列“预防肾脏和血管终末期疾病(PREVEND)队列”的8420名受试者的基线DKK3血浆水平进行了测量。分析了其与临床变量和结局的关联。DKK3水平中位数为32.8 ng/ml(28.0 - 39.0)。在多变量线性回归分析中,血浆DKK3的最强相关因素为年龄、体重指数和估计肾小球滤过率(eGFR)。基线时,564名(6.7%)受试者患有CVD(定义为心肌梗死和/或脑血管意外),1361名(16.2%)受试者患有CKD(定义为eGFR < 60 ml/min/1.73m²和/或尿白蛋白排泄量(UAE)> 30 mg/24小时)。在已知CVD和CKD随访状态的受试者中(分别为7828名和5548名),669名(8.5%)发生了CVD,951名(17.1%)发生了CKD(中位随访时间分别为12.5年和10.2年)。粗逻辑回归分析显示,DKK3水平与CVD患病率相关(比值比:每DKK3翻倍为2.14 [1.76 - 2.61],P < 0.001)和CKD患病率相关(比值比:每DKK3翻倍为1.84 [1.59 - 2.13],P < 0.001)。在粗Cox比例风险回归分析中,较高的DKK3水平与新发CVD风险较高相关(风险比:每DKK3翻倍为1.47 [1.13 - 1.91],P = 0.004)和CKD风险较高相关(风险比:每DKK3翻倍为1.45,[1.25 - 1.69],P < 0.001)。然而,在校正常见临床变量和风险因素后,这些关联不再显著,不过在UAE值最低的受试者亚组中,DKK3可独立预测新发CKD。总体而言,DKK3血浆水平与心血管危险因素相关,但通常与CVD和CKD的患病率及新发情况无独立关联,仅在UAE值最低的受试者中可预测新发CKD。