Dyrbuś Krzysztof, Mędrala Zofia, Konsek Karolina, Nowowiejska-Wiewióra Alicja, Trzeciak Przemysław, Skrzypek Michał, Cieśla Daniel, Banach Maciej, Gąsior Mariusz
Silesian Center for Heart Diseases (SCHD), 3 Department of Cardiology, SMDZ in Zabrze, Medical University of Silesia in Katowice, Poland.
Department of Environmental Health, School of Public Health in Bytom, Medical University of Silesia, Katowice, Poland.
Arch Med Sci. 2024 Aug 29;20(4):1069-1076. doi: 10.5114/aoms/188294. eCollection 2024.
Lipoprotein(a) [Lp(a)] is an independent risk factor for atherosclerotic cardiovascular disease (ASCVD). Increased Lp(a) concentration > 30 mg/dl (75 nmol/l) and especially >50 mg/dl (125 nmol/l) may cause faster atherosclerosis, being an important and underdiagnosed residual cardiovascular risk factor. Thus, there is a need to characterize further the clinical phenotypes in patients at risk for ASCVD with high Lp(a) levels now and during follow-up, while also looking for the possible impact of geographical differences.
The Zabrze Lipoprotein(a) Registry (Zabrze-Lip(a)R) was founded on the basis of data from 2,001 consecutive patients with very high cardiovascular risk treated in a tertiary hospital. The registry patients will be followed for at least 5 years with the possibility of extending this period as an open label study. All-cause and cause-specific mortality, hospitalizations, and cardiovascular events, such as myocardial infarction (MI) and stroke, will be assessed.
The mean age of patients was 66.4 years (females 37.1%). The median Lp(a) concentration in the entire population was 6.6 mg/dl (16.5 nmol/l) (mean: 14.3 ±19.4 mg/dl). 540 (27%) patients had elevated Lp(a) levels above 30 mg/dl (75 nmol/l); they were significantly older (68.8 vs. 66.3 years; = 0.04), had significantly lower hemoglobin and hematocrit, and higher platelet count and levels of NT-proBNP and C-reactive protein. The prevalence of elevated Lp(a) > 30 mg/dl (75 nmol/l) concentrations was very high in patients with a chronic coronary syndrome (CCS) (52.2% (282/540) vs. 41.5% (607/1461); < 0.001), in patients undergoing PCI during hospitalization (23.9 vs. 19%; = 0.01), and in patients with previous MI (20.6% vs. 14.9%; = 0.0022). In the multivariable analysis, the independent predictors of elevated Lp(a) > 30 mg/dl (75 nmol/l) were only lower Hb values (OR = 0.925; 95% CI: 0.874-0.978; = 0.006) and higher platelet count (1.002; 95%CI: 1.000-1.003; < 0.02).
In Poland, the largest representative of Central and Eastern European countries, 27% of patients at very high cardiovascular risk with established ASCVD experience additional risk related to an elevated Lp(a) level, with every second patient having CCS. Interestingly, only two factors were significantly related to elevated Lp(a) levels: lower Hb values and higher platelet count. However, the clinical relevance of these results needs confirmation.
脂蛋白(a)[Lp(a)]是动脉粥样硬化性心血管疾病(ASCVD)的独立危险因素。Lp(a)浓度升高>30mg/dl(75nmol/l),尤其是>50mg/dl(125nmol/l),可能导致动脉粥样硬化进展更快,是一个重要且未得到充分诊断的心血管残留危险因素。因此,有必要进一步明确目前及随访期间Lp(a)水平高的ASCVD风险患者的临床表型,同时探究地理差异可能产生的影响。
扎布热脂蛋白(a)登记处(Zabrze-Lip(a)R)基于一家三级医院连续收治的2001例心血管风险极高患者的数据建立。作为一项开放标签研究,登记处的患者将至少随访5年,且有可能延长随访时间。将评估全因死亡率和特定病因死亡率、住院情况以及心血管事件,如心肌梗死(MI)和中风。
患者的平均年龄为66.4岁(女性占37.1%)。整个人群的Lp(a)浓度中位数为6.6mg/dl(16.5nmol/l)(平均值:14.3±19.4mg/dl)。540例(27%)患者的Lp(a)水平高于30mg/dl(75nmol/l);他们的年龄显著更大(68.8岁对66.3岁;P=0.04),血红蛋白和血细胞比容显著更低,血小板计数以及NT-proBNP和C反应蛋白水平更高。慢性冠状动脉综合征(CCS)患者中Lp(a)浓度>30mg/dl(75nmol/l)的患病率非常高(52.2%(282/540)对41.5%(607/1461);P<0.001),住院期间接受经皮冠状动脉介入治疗(PCI)的患者中患病率为23.9%对19%;P=0.01),既往有心肌梗死的患者中患病率为20.6%对14.9%;P=0.0022)。在多变量分析中,Lp(a)水平>30mg/dl(75nmol/l)升高的独立预测因素仅为较低的血红蛋白值(OR=0.925;95%CI:0.874-0.978;P=0.006)和较高的血小板计数(1.002;)95%CI:1.000-1.003;P<0.02)。
在作为中东欧国家最大代表的波兰,27%已确诊ASCVD且心血管风险极高的患者存在与Lp(a)水平升高相关的额外风险,其中每两名患者中就有一名患有CCS。有趣的是,仅有两个因素与Lp(a)水平升高显著相关:较低的血红蛋白值和较高的血小板计数。然而,这些结果的临床相关性需要进一步证实。