Prognostic Impact of High-Molecular-Weight von Willebrand Factor Multimer Ratio in Classical Low-Flow Low-Gradient Aortic Stenosis.

IF 1.9 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiology Pub Date : 2024-06-24 DOI:10.1159/000539731
Joerg Kellermair, Hermann Blessberger, Helmut W Ott, Juergen Kammler, Daniel Kiblboeck, Christian Reiter, Michael Grund, Clemens Steinwender, Sahrai Saeed
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引用次数: 0

Abstract

Introduction: High-molecular-weight (HMW) von Willebrand factor (VWF) multimer deficiency occurs in classical low-flow, low-gradient (LF/LG) aortic stenosis (AS) due to shear force-induced proteolysis. The prognostic value of HMW VWF multimer deficiency is unknown. Therefore, we sought to evaluate the impact of HMW VWF multimer deficiency on clinical outcome.

Methods: In this prospective research study, a total of 83 patients with classical LF/LG AS were included. All patients underwent dobutamine stress echocardiography to distinguish true-severe (TS) from pseudo-severe (PS) classical LF/LG AS. HMW VWF multimer ratio was calculated using densitometric Western blot band quantification. The primary endpoint was all-cause mortality.

Results: Mean age was 79 ± 9 years, and TS classical LF/LG AS was diagnosed in 73% (n = 61) and PS classical LF/LG AS in 27% (n = 22) of all patients. Forty-six patients underwent aortic valve replacement (AVR) and 37 were treated conservatively. During a mean follow-up of 27 ± 17 months, 47 deaths occurred. Major bleeding complications after AVR (10/46; 22%) were more common in patients with HMW VWF multimer ratio <1 (8/17; 47%) in comparison to patients with a normal multimer pattern (2/29; 7%) at baseline (p = 0.003). In a multivariable Cox regression analysis, HMW VWF multimer deficiency was a predictor of all-cause mortality (HR: 3.02 [95% CI: 1.31-6.96], p = 0.009) in the entire cohort. This association was driven by higher mortality rates in the AVR group (multivariable-adjusted HR: 9.4; 95% CI 2.0-43.4, p = 0.004).

Conclusions: This is the first study to demonstrate the predictive value of HMW VWF multimer ratio for risk stratification in patients with classical LF/LG AS. HMW VWF multimer deficiency was associated with an increased risk of all-cause mortality and major bleeding complications after AVR.

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高分子量 von Willebrand 因子多聚物比率对典型低流量低梯度主动脉瓣狭窄的预后影响。
导言:高分子量(HMW)von Willebrand因子(VWF)多聚体缺乏症发生在典型的低流量、低梯度(LF/LG)主动脉狭窄(AS)中,这是由于剪切力引起的蛋白水解所致。HMW VWF 多聚体缺乏症的预后价值尚不清楚。因此,我们试图评估 HMW VWF 多聚体缺乏对临床预后的影响:在这项前瞻性研究中,共纳入了 83 例经典 LF/LG AS 患者。所有患者均接受了多巴酚丁胺应激超声心动图检查,以区分真性重度(TS)和假性重度(PS)LF/LG AS。HMW VWF多聚体比率通过密度计Western印迹条带定量计算得出。主要终点是全因死亡率:所有患者的平均年龄为 79 ± 9 岁,73%(n=61)的患者被诊断为 TS 经典型 LF/LG AS,27%(n=22)的患者被诊断为 PS 经典型 LF/LG AS。46名患者接受了主动脉瓣置换术(AVR),37名患者接受了保守治疗。在平均 27 ± 17 个月的随访期间,47 例患者死亡。与基线多聚酶模式正常的患者(2/29;7%)相比,HMW VWF多聚酶比值为<1(8/17;47%)的患者在主动脉瓣置换术后更容易出现大出血并发症(10/46;22%)(P=0.003)。在多变量 Cox 回归分析中,HMW VWF 多聚酶缺乏是整个队列中全因死亡率的预测因子(HR:3.02 [95% CI:1.31-6.96],p=0.009)。AVR组的死亡率更高(多变量调整后的HR:9.4;95%CI 2.0-43.4,P=0.004)导致了这种关联:该研究首次证明了HMW VWF多聚酶比值对经典LF/LG强直性脊柱炎患者风险分层的预测价值。HMW VWF多聚酶缺乏与全因死亡率和动静脉瓣膜置换术后大出血并发症的风险增加有关。
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来源期刊
Cardiology
Cardiology 医学-心血管系统
CiteScore
3.40
自引率
5.30%
发文量
56
审稿时长
1.5 months
期刊介绍: ''Cardiology'' features first reports on original clinical, preclinical and fundamental research as well as ''Novel Insights from Clinical Experience'' and topical comprehensive reviews in selected areas of cardiovascular disease. ''Editorial Comments'' provide a critical but positive evaluation of a recent article. Papers not only describe but offer critical appraisals of new developments in non-invasive and invasive diagnostic methods and in pharmacologic, nutritional and mechanical/surgical therapies. Readers are thus kept informed of current strategies in the prevention, recognition and treatment of heart disease. Special sections in a variety of subspecialty areas reinforce the journal''s value as a complete record of recent progress for all cardiologists, internists, cardiac surgeons, clinical physiologists, pharmacologists and professionals in other areas of medicine interested in current activity in cardiovascular diseases.
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