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在主动脉瓣生物瓣置换患者中,循环脂蛋白相关磷脂酶A2与高瓣膜动脉阻抗及低动脉顺应性相关。

Circulating Lp-PLA2 is associated with high valvuloarterial impedance and low arterial compliance in patients with aortic valve bioprostheses.

作者信息

Mahmut Ablajan, Mahjoub Haïfa, Boulanger Marie-Chloé, Dahou Abdellaziz, Bouchareb Rihab, Capoulade Romain, Arsenault Benoît J, Larose Eric, Bossé Yohan, Pibarot Philippe, Mathieu Patrick

机构信息

Laboratoire d'Études Moléculaires des Valvulopathies (LEMV), Groupe de Recherche en Valvulopathies (GRV), Quebec Heart and Lung Institute/Research Center, Department of Surgery, Laval University, Quebec, Canada.

Department of Medicine, Laval University, Québec, Canada.

出版信息

Clin Chim Acta. 2016 Apr 1;455:20-5. doi: 10.1016/j.cca.2016.01.014. Epub 2016 Jan 18.


DOI:10.1016/j.cca.2016.01.014
PMID:26797670
Abstract

BACKGROUND: We previously reported that plasma Lp-PLA2 was associated with aortic valve disease progression and degeneration of bioprostheses. Low systemic arterial compliance and high valvuloarterial impedance (Z(va)) are predictors of poor survival in patients with aortic valve disease. However, the prevalence of high Z(va) after AVR is largely unknown and whether Lp-PLA2 could predict Z(va) has not been documented. We investigated the relationships between plasma lipoprotein-associated phospholipase A2 (Lp-PLA2) mass and activity and valvuloarterial impedance (Z(va)), an index of global LV hemodynamic load, in patients that underwent aortic valve replacement (AVR). METHODS: A total of 195 patients with aortic bioprostheses underwent echocardiographic assessment of the prosthetic aortic valve function 8±3.4 years after AVR. Lp-PLA2 mass and activity were measured. RESULTS: In this group of patients, the mean Z(va) was elevated (5.73±1.21 mm Hg·ml(-1)·m(2)). In univariate analyses, Lp-PLA2 mass (p=0.003) and Lp-PLA2 activity (p=0.046) were associated with Z(va). After adjustment for covariates including age, gender, clinical risk factors, anti-hypertensive medications, body mass index and prosthesis size, Lp-PLA2 mass was associated with high Z(va) (≥4.5 mm Hg·ml(-1)·m(2)) (OR: 1.29, 95%CI: 1.10-1.53; p=0.005) and was inversely related with the systemic arterial compliance (β=-0.01, SEM=0.003; p=0.003). CONCLUSIONS: An increased Z(va), an index of excessive hemodynamic load, was highly prevalent 8-year post-AVR and was independently related to circulating Lp-PLA2.

摘要

背景:我们之前报道过,血浆脂蛋白相关磷脂酶A2(Lp-PLA2)与主动脉瓣疾病进展及生物瓣膜退变相关。低全身动脉顺应性和高瓣膜动脉阻抗(Z(va))是主动脉瓣疾病患者生存不良的预测指标。然而,主动脉瓣置换术(AVR)后高Z(va)的患病率很大程度上未知,且Lp-PLA2是否能预测Z(va)尚未见报道。我们研究了接受主动脉瓣置换术(AVR)患者的血浆脂蛋白相关磷脂酶A2(Lp-PLA2)质量和活性与瓣膜动脉阻抗(Z(va))(左心室整体血流动力学负荷指标)之间的关系。 方法:总共195例植入生物主动脉瓣的患者在AVR术后8±3.4年接受了人工主动脉瓣功能的超声心动图评估。测量了Lp-PLA2质量和活性。 结果:在这组患者中,平均Z(va)升高(5.73±1.21 mmHg·ml(-1)·m(2))。在单因素分析中,Lp-PLA2质量(p = 0.003)和Lp-PLA2活性(p = 0.046)与Z(va)相关。在对包括年龄、性别、临床危险因素、抗高血压药物、体重指数和人工瓣膜尺寸等协变量进行校正后,Lp-PLA2质量与高Z(va)(≥4.5 mmHg·ml(-1)·m(2))相关(OR:1.29,95%CI:1.10 - 1.53;p = 0.005),且与全身动脉顺应性呈负相关(β = -0.01,SEM = 0.003;p = 0.003)。 结论:作为血流动力学负荷过高指标的Z(va)升高在AVR术后8年非常普遍,且与循环Lp-PLA2独立相关。

相似文献

[1]
Circulating Lp-PLA2 is associated with high valvuloarterial impedance and low arterial compliance in patients with aortic valve bioprostheses.

Clin Chim Acta. 2016-4-1

[2]
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J Cardiothorac Vasc Anesth. 2014-12

[3]
Lp-PLA2 is associated with structural valve degeneration of bioprostheses.

Eur J Clin Invest. 2013-11-28

[4]
Impact of plasma Lp-PLA2 activity on the progression of aortic stenosis: the PROGRESSA study.

JACC Cardiovasc Imaging. 2014-11-1

[5]
Lipoprotein-associated phospholipase A2 activity, genetics and calcific aortic valve stenosis in humans.

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[6]
Elevated expression of lipoprotein-associated phospholipase A2 in calcific aortic valve disease: implications for valve mineralization.

J Am Coll Cardiol. 2013-10-23

[7]
Usefulness of the valvuloarterial impedance to predict adverse outcome in asymptomatic aortic stenosis.

J Am Coll Cardiol. 2009-9-8

[8]
Lipoprotein-associated phospholipase A2 is elevated in patients with severe aortic valve stenosis without clinically overt atherosclerosis.

Clin Chem Lab Med. 2012-10-1

[9]
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Arch Cardiovasc Dis. 2010-5-20

[10]
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Clin Chem Lab Med. 2015-6

引用本文的文献

[1]
Mechanisms and Drug Therapies of Bioprosthetic Heart Valve Calcification.

Front Pharmacol. 2022-6-3

[2]
Proteomic Architecture of Valvular Extracellular Matrix: FNDC1 and MXRA5 Are New Biomarkers of Aortic Stenosis.

JACC Basic Transl Sci. 2021-1-13

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