Adamidis Petros Spyridonas, Florentin Matilda, Liberopoulos Evangelos, Koutsogianni Amalia Despoina, Anastasiou Georgia, Liamis George, Milionis Haralampos, Barkas Fotios
Department of Internal Medicine, Faculty of Medicine, School of Health Sciences, University of Ioannina, 45110 Ioannina, Greece.
1st Propedeutic Department of Medicine, School of Medicine, Laiko General Hospital, National and Kapodistrian University of Athens, 15772 Athens, Greece.
J Cardiovasc Dev Dis. 2024 Feb 15;11(2):60. doi: 10.3390/jcdd11020060.
Serum alkaline phosphatase (ALP) activity has been associated with atherosclerotic cardiovascular disease (ASCVD). We aimed to investigate the association of ALP with ASCVD in patients with dyslipidemia.
We conducted a retrospective cohort study including consecutive adults with dyslipidemia followed-up for ≥3 years (from 1999 to 2022) in the outpatient Lipid Clinic of Ioannina University General Hospital, Greece. The primary endpoint was the association between baseline ALP and incident ASCVD after adjusting for traditional risk factors (i.e., sex, age, hypertension, diabetes, smoking, and dyslipidemia), baseline ASCVD, and lipid-lowering treatment. ALP levels were stratified by tertiles as follows: low: <67 U/L, middle: 67-79 U/L, high: ≥79 U/L.
Overall, 1178 subjects were included; 44% were males, and their median age was 57 years (range: 49-65). During a 6-year median follow-up (interquartile range: IQR: 4-9), 78 new ASCVD events (6.6%) occurred. A statistically significant association between baseline ALP levels and incident ASCVD was demonstrated (Odds Ratio, OR: 6.99; 95% Confidence Interval, CI: 2.29-21.03, = 0.001). Subjects in the highest ALP tertile had the highest odds for ASCVD when compared with those in the lowest tertile (OR: 2.35; 95% CI: 1.24-4.41, = 0.008).
The present study indicates an association between ALP and the development of ASCVD in patients with dyslipidemia, which underscores the potential of ALP as a predictive tool or a therapeutic target in the realm of ASCVD prevention within this population.
血清碱性磷酸酶(ALP)活性与动脉粥样硬化性心血管疾病(ASCVD)有关。我们旨在研究血脂异常患者中ALP与ASCVD的关联。
我们进行了一项回顾性队列研究,纳入了希腊约阿尼纳大学总医院门诊脂质诊所连续就诊的血脂异常成年人,随访时间≥3年(从1999年至2022年)。主要终点是在调整传统危险因素(即性别、年龄、高血压、糖尿病、吸烟和血脂异常)、基线ASCVD和降脂治疗后,基线ALP与新发ASCVD之间的关联。ALP水平按三分位数分层如下:低:<67 U/L,中:67 - 79 U/L,高:≥79 U/L。
总体而言,共纳入1178名受试者;44%为男性,中位年龄为57岁(范围:49 - 65岁)。在中位6年的随访期间(四分位间距:IQR:4 - 9),发生了78例新发ASCVD事件(6.6%)。基线ALP水平与新发ASCVD之间存在统计学显著关联(比值比,OR:6.99;95%置信区间,CI:2.29 - 21.03,P = 0.001)。与最低三分位数的受试者相比,最高ALP三分位数的受试者发生ASCVD的几率最高(OR:2.35;95% CI:1.24 - 4.41,P = 0.008)。
本研究表明血脂异常患者中ALP与ASCVD的发生有关,这突出了ALP作为该人群ASCVD预防领域预测工具或治疗靶点的潜力。