Department of Cardiology, Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Circ Heart Fail. 2013 Mar;6(2):219-26. doi: 10.1161/CIRCHEARTFAILURE.112.000129. Epub 2013 Feb 8.
In several cross-sectional analyses, circulating baseline levels of galectin-3, a protein involved in myocardial fibrosis and remodeling, have been associated with increased risk for morbidity and mortality in patients with heart failure (HF). The importance and clinical use of repeated measurements of galectin-3 have not yet been reported.
Plasma galectin-3 was measured at baseline and at 3 months in patients enrolled in the Controlled Rosuvastatin Multinational Trial in Heart Failure (CORONA) trial (n=1329), and at baseline and at 6 months in patients enrolled in the Coordinating Study Evaluating Outcomes of Advising and Counseling Failure (COACH) trial (n=324). Patient results were analyzed by categorical and percentage changes in galectin-3 level. A threshold value of 17.8 ng/mL or 15% change from baseline was used to categorize patients. Increasing galectin-3 levels over time, from a low to high galectin-3 category, were associated with significantly more HF hospitalization and mortality compared with stable or decreasing galectin-3 levels (hazard ratio in CORONA, 1.60; 95% confidence interval, 1.13-2.25; P=0.007; hazard ratio in COACH, 2.38; 95% confidence interval, 1.02-5.55; P=0.046). In addition, patients whose galectin-3 increased by >15% between measurements had a 50% higher relative hazard of adverse event than those whose galectin-3 stayed within ±15% of the baseline value, independent of age, sex, diabetes mellitus, left ventricular ejection fraction, renal function, medication (β-blocker, angiotensin converting enzyme inhibitor, and angiotensin receptor blocker), and N-terminal probrain natriuretic peptide (hazard ratio in CORONA, 1.50; 95% confidence interval, 1.17-1.92; P=0.001). The impact of changing galectin-3 levels on other secondary end points was comparable.
In 2 large cohorts of patients with chronic and acute decompensated HF, repeated measurements of galectin-3 level provided important and significant prognostic value in identifying patients with HF at elevated risk for subsequent HF morbidity and mortality.
在几项横断面分析中,参与心肌纤维化和重塑的蛋白半乳糖凝集素-3 的循环基础水平与心力衰竭(HF)患者的发病率和死亡率增加相关。然而,尚未报道重复测量半乳糖凝集素-3 的重要性和临床应用。
在参与控制瑞舒伐他汀多国心力衰竭试验(CORONA)的患者中(n=1329),基线和 3 个月时测量血浆半乳糖凝集素-3,在参与协调研究评估咨询和辅导失败的结果(COACH)试验的患者中(n=324),基线和 6 个月时测量血浆半乳糖凝集素-3。通过半乳糖凝集素-3 水平的分类和百分比变化分析患者结果。使用 17.8ng/mL 或 15%的基线变化作为截断值来分类患者。与稳定或降低的半乳糖凝集素-3 水平相比,随着时间的推移,从低半乳糖凝集素-3 水平到高水平的半乳糖凝集素-3 水平增加与 HF 住院和死亡率显著增加相关(CORONA 中的危险比,1.60;95%置信区间,1.13-2.25;P=0.007;COACH 中的危险比,2.38;95%置信区间,1.02-5.55;P=0.046)。此外,与半乳糖凝集素-3 保持在基线值±15%范围内的患者相比,半乳糖凝集素-3 测量值之间增加>15%的患者发生不良事件的相对危险度增加了 50%,这独立于年龄、性别、糖尿病、左心室射血分数、肾功能、药物(β受体阻滞剂、血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂)和 N 末端脑钠肽前体(CORONA 中的危险比,1.50;95%置信区间,1.17-1.92;P=0.001)。改变半乳糖凝集素-3 水平对其他次要终点的影响相当。
在 2 个大型慢性和急性失代偿性 HF 患者队列中,重复测量半乳糖凝集素-3 水平在识别 HF 发病率和死亡率风险增加的 HF 患者方面提供了重要且有意义的预后价值。