Division of Cardiology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Division of Cardiology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Am J Cardiol. 2019 Sep 1;124(5):756-762. doi: 10.1016/j.amjcard.2019.05.056. Epub 2019 Jun 6.
Lymphatic flow is augmented in states of chronic heart failure (cHF). However, the biological mechanism driving increased lymphatic flow capacity (lymphangiogenesis) in cHF is unknown. Recent studies have indicated that vascular endothelial growth factors (VEGF-A, -C, and -D) are involved in lymphangiogenesis. This study examined the association between VEGF-A, -C, and -D levels, invasively measured hemodynamics, and heart failure symptoms. Subjects who underwent clinically indicated right heart catheterization at Medical University of South Carolina between 12/2016 and 7/2018 were eligible for inclusion. These subjects underwent clinical assessment of cHF severity (including 6MWT and KCCQ), hemodynamic assessment with right heart catheterization, laboratory studies including B-type natriuretic peptide, and concomitant measurement of VEGF-A, -C, and -D. Fifty-six patients were included for analysis. Subjects with elevated pulmonary artery wedge pressure (PAWP) had significantly higher VEGF-D levels (263 ± 415 pg/ml vs 65 ± 101 pg/ml; p = 0.02). PAWP was not associated with VEGF-A or VEGF-C levels. When stratified by VEGF-D, subjects with elevated VEGF-D had clinical and hemodynamic characteristics associated with worse HF severity (lower ejection fraction, higher b-type natriuretic peptide, higher PAWP, lower cardiac output), but were not more symptomatic by Kansas City Cardiomyopathy Questionnaire scores and had similar 6-minute walk test distance compared with subjects with lower VEGF-D. Subjects with an elevated VEGF-D were more likely to have a diagnosis of heart failure for >3 years. In conclusion, VEGF-D is associated with elevated PAWP in cHF, and elevated VEGF-D may mitigate cHF symptoms.
在慢性心力衰竭 (cHF) 状态下,淋巴液流动增加。然而,导致 cHF 中淋巴液流动能力增加(淋巴管生成)的生物学机制尚不清楚。最近的研究表明,血管内皮生长因子 (VEGF-A、-C 和 -D) 参与了淋巴管生成。本研究探讨了 VEGF-A、-C 和 -D 水平与侵入性测量血流动力学和心力衰竭症状之间的关系。在 2016 年 12 月至 2018 年 7 月期间,南卡罗来纳医科大学进行临床指征性右心导管检查的患者有资格入选。这些患者接受了心力衰竭严重程度的临床评估(包括 6MWT 和 KCCQ)、右心导管血流动力学评估、实验室研究包括 B 型利钠肽和同时测量 VEGF-A、-C 和 -D。对 56 例患者进行了分析。肺动脉楔压 (PAWP) 升高的患者 VEGF-D 水平明显升高(263 ± 415 pg/ml 比 65 ± 101 pg/ml;p=0.02)。PAWP 与 VEGF-A 或 VEGF-C 水平无关。根据 VEGF-D 分层,VEGF-D 升高的患者具有与心力衰竭严重程度恶化相关的临床和血流动力学特征(射血分数较低、B 型利钠肽水平较高、PAWP 较高、心输出量较低),但根据堪萨斯城心肌病问卷评分,症状并不更严重,6 分钟步行试验距离与 VEGF-D 较低的患者相似。VEGF-D 升高的患者更有可能被诊断为心力衰竭超过 3 年。总之,VEGF-D 与 cHF 中的 PAWP 升高相关,而 VEGF-D 升高可能减轻 cHF 症状。