Hage Camilla, Bjerre Mette, Frystyk Jan, Gu Harvest F, Brismar Kerstin, Donal Erwan, Daubert Jean-Claude, Linde Cecilia, Lund Lars H
Department of Medicine, Cardiology unit, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Medicine, Medical Research Laboratory, Aarhus University, Aarhus, Denmark.
Am J Cardiol. 2018 Jun 15;121(12):1558-1566. doi: 10.1016/j.amjcard.2018.02.041. Epub 2018 Mar 14.
We aimed to characterize of the role of insulin-like growth factor-binding protein 7 (IGFBP-7) in heart failure (HF) pathophysiology. IGFBP-7 has been associated with cardiac hypertrophy and diastolic dysfunction in HF. In 86 patients with HF with a preserved ejection fraction (HFpEF) (ejection fraction [EF] ≥45%) and 79 with HF with a reduced ejection fraction (HFrEF), we assessed concentrations of serum IGFBP-7, correlations between serum IGFBP-7 and clinical data, diastolic function, and associations with outcome. IGFBP-7 was lower in HFpEF than HFrEF (102 vs 152 µg/L, p <0.001) and correlated with New York Heart Association class (HFpEF: r = 0.25, p = 0.020; HFrEF: r = 0.26, p = 0.022), N-terminal pro-brain natriuretic peptide (NT-proBNP) (HFpEF: r = 0.53, p <0.001; HFrEF: r = 0.50, p <0.001), and estimated glomerular filtration rate (eGFR) (HFpEF: r = -0.47, p <0.001; HFrEF: r = -0.45, p <0.001). In HFpEF, IGFBP-7 correlated with E/e' (r = 0.31, p = 0.012) and E/A ratio (r = 0.31, p = 0.011). In HFrEF, but not HFpEF, IGFBP-7 correlated with age (r = 0.29, p = 0.009) and atrial fibrillation (r = 0.34, p = 0.002). IGFBP-7 predicted the outcome in HFpEF (hazard ratio 4.19 [1.01 to 17.35], p = 0.048]) but not in HFrEF (0.72 [0.24 to 2.14], p = 0.554). In conclusion in HFrEF, IGFBP-7 was elevated and associated with HF severity but not prognostic, suggesting a marker of risk. In HFpEF, IGFBP-7 was less elevated but associated with markers of diastolic dysfunction, HF severity, and prognosis. IGFBP-7 may contribute to the progression of HFpEF possibly through inflammation and oxidative stress.
我们旨在明确胰岛素样生长因子结合蛋白7(IGFBP - 7)在心力衰竭(HF)病理生理学中的作用。IGFBP - 7已被证实与HF中的心肌肥厚和舒张功能障碍有关。在86例射血分数保留的心力衰竭(HFpEF)患者(射血分数[EF]≥45%)和79例射血分数降低的心力衰竭(HFrEF)患者中,我们评估了血清IGFBP - 7的浓度、血清IGFBP - 7与临床数据、舒张功能之间的相关性以及与预后的关联。HFpEF患者的IGFBP - 7低于HFrEF患者(102 vs 152 μg/L,p <0.001),且与纽约心脏协会分级相关(HFpEF:r = 0.25,p = 0.020;HFrEF:r = 0.26,p = 0.022)、N末端脑钠肽前体(NT - proBNP)相关(HFpEF:r = 0.53,p <0.001;HFrEF:r = 0.50,p <0.001)以及估算肾小球滤过率(eGFR)相关(HFpEF:r = -0.47,p <0.001;HFrEF:r = -0.45,p <0.001)。在HFpEF中,IGFBP - 7与E/e'(r = 0.31,p = 0.012)和E/A比值(r = 0.31,p = 0.011)相关。在HFrEF中,而非HFpEF中,IGFBP - 7与年龄(r = 0.29,p = 0.009)和心房颤动(r = 0.34,p = 0.002)相关。IGFBP - 7可预测HFpEF的预后(风险比4.19 [1.01至17.35],p = 0.048),但不能预测HFrEF的预后(0.72 [0.24至 2.14],p = 0.554)。总之,在HFrEF中,IGFBP - 7升高且与HF严重程度相关,但与预后无关,提示其为一种风险标志物。在HFpEF中,IGFBP - 7升高程度较低,但与舒张功能障碍标志物、HF严重程度及预后相关。IGFBP - 7可能通过炎症和氧化应激促进HFpEF的进展。