van der Velde A Rogier, Meijers Wouter C, Ho Jennifer E, Brouwers Frank P, Rienstra Michiel, Bakker Stephan J L, Muller Kobold Anneke C, van Veldhuisen Dirk J, van Gilst Wiek H, van der Harst Pim, de Boer Rudolf A
Department of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Cardiovascular Medicine Section, Department of Medicine, Boston University School of Medicine, Boston, USA.
Heart. 2016 Jul 15;102(14):1134-41. doi: 10.1136/heartjnl-2015-308975. Epub 2016 Apr 15.
Lifetime risk for cardiovascular (CV) disease is high but predicting incident events on an individual level remains difficult. Single measurements of galectin-3, a marker of tissue fibrosis, predict mortality and new-onset heart failure (HF). Persistently elevated levels may indicate a clinically silent disease process.
Our aim was to establish the value of serial galectin-3 measurements to predict CV outcomes in the general population.
Plasma galectin-3 was measured in the Prevention of REnal and Vascular ENd-stage Disease (PREVEND) study at baseline and after ∼4 years. Changes in serial galectin-3 were expressed as categorical changes or absolute change from baseline and were related to subsequent outcome.
Serial galectin-3 was measured in 5958 subjects (mean age 49±12 years; 49% female). The median duration of follow-up was 8.3 years. Persistently elevated galectin-3 (defined as highest quartile at baseline and highest quartile during visit 2, n=757 subjects) was associated with a higher risk for new-onset HF, CV mortality, all-cause mortality, new-onset atrial fibrillation and CV events, compared with subjects with non-persistently elevated galectin-3. After multivariable adjustments for baseline characteristics, serial galectin-3 remained an independent predictor of new-onset HF (HR 1.85 (1.10-3.13); p=0.02) but not for other outcomes. Serial measurements provided more accurate prognostic value to predict new-onset HF, compared with a single baseline measurement (Harrell's C: 0.72 (0.68-0.75) vs 0.68 (0.65-0.72); p=0.002, respectively) with significant net reclassification.
Persistently elevated galectin-3 predicts new-onset HF after adjustment for covariates, and serial measurements provide more accurate prognostic information compared with single determination of galectin-3. This may help to identify individuals who are at risk for incident HF and might provide a measure to monitor interventions.
心血管(CV)疾病的终生风险很高,但在个体层面预测发病事件仍然困难。半乳糖凝集素-3是一种组织纤维化标志物,单次测量可预测死亡率和新发心力衰竭(HF)。持续升高的水平可能表明存在临床无症状的疾病进程。
我们的目的是确定连续测量半乳糖凝集素-3对预测普通人群心血管结局的价值。
在预防终末期肾病和血管疾病(PREVEND)研究中,于基线时和大约4年后测量血浆半乳糖凝集素-3。连续半乳糖凝集素-3的变化以分类变化或相对于基线的绝对变化表示,并与随后的结局相关。
对5958名受试者(平均年龄49±12岁;49%为女性)测量了连续半乳糖凝集素-3。中位随访时间为8.3年。与半乳糖凝集素-3非持续升高的受试者相比,半乳糖凝集素-3持续升高(定义为基线时处于最高四分位数且在第2次访视时处于最高四分位数,n = 757名受试者)与新发HF、CV死亡率、全因死亡率、新发心房颤动和CV事件的风险更高相关。在对基线特征进行多变量调整后,连续半乳糖凝集素-3仍然是新发HF的独立预测因子(HR 1.85(1.10 - 3.13);p = 0.02),但对其他结局不是。与单次基线测量相比,连续测量为预测新发HF提供了更准确的预后价值(Harrell's C:分别为0.72(0.68 - 0.75)和0.68(0.65 - 0.72);p = 0.002),具有显著的净重新分类。
在调整协变量后,半乳糖凝集素-3持续升高可预测新发HF,与单次测定半乳糖凝集素-3相比,连续测量可提供更准确的预后信息。这可能有助于识别有发生HF风险的个体,并可能提供一种监测干预措施的方法。