三维超声心动图评估左房室耦合指数:轻链心脏淀粉样变性短期预后的预后指标。

IF 5.2 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Amyloid-Journal of Protein Folding Disorders Pub Date : 2025-03-01 Epub Date: 2025-01-15 DOI:10.1080/13506129.2024.2448435
Fangmin Meng, Jing Li, Rui Zhao, Yuanfeng Wu, Yu Liu, Yiming Yang, Yang Yang, Nianwei Zhou, Lili Dong, Dehong Kong, Haiyan Chen, Xianhong Shu, Peng Liu, Cuizhen Pan
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引用次数: 0

摘要

背景:轻链心脏淀粉样变性(AL-CA)与左心房和左心室的结构和功能改变有关。本研究旨在评估三维超声心动图(3DE)评估的左房室耦合指数(LACI)对AL-CA主要预后的预测价值。方法:对2022年4月至2024年2月活检证实的AL-CA患者进行前瞻性分析。LACI(左房最小容积与左室舒张末期容积之比)采用EchoPAC 204离线计算。主要结局被定义为全因死亡。结果:研究了67例经活检证实的AL-CA患者(年龄:62.98±10.20岁;67%的男性)。中位随访时间为121天(范围:7 ~ 732天)。26例(39%)患者出现全因死亡。多因素Cox回归分析显示,在调整NT-pro BNP、肌钙蛋白T、中度三尖瓣反流、心包和胸腔积液后,LACI有显著相关性(校正HR: 10.58, p = 0.008)。Kaplan-Meier曲线显示基于中位LACI的预后差异(截止值:0.57,p = 0.002)。似然比χ2检验显示,LACI增加了Mayo 2004模型、Mayo 2004欧洲2015修正模型和Mayo 2012模型的预测价值(均p)。结论:基于3de的LACI与AL-CA患者全因死亡率独立相关,并增强了传统分期模型的预后价值。
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Left atrioventricular coupling index assessed with three-dimensional echocardiography: a prognostic marker of short-term outcomes in light-chain cardiac amyloidosis.

Background: Light-chain cardiac amyloidosis (AL-CA) is associated with structural and functional changes in the left atrium and left ventricle. This study aims to assess the value of the left atrioventricular coupling index (LACI) assessed by three-dimensional echocardiography (3DE) for predicting primary outcome in AL-CA.

Methods: Participants with biopsy-confirmed AL-CA from April 2022 to February 2024 were prospectively analysed. LACI, the ratio of left atrial volume min to left ventricular end-diastolic volumes, was calculated offline using EchoPAC 204. The primary outcome was defined as all-cause death.

Results: Sixty-seven biopsy-proven AL-CA patients were studied (age: 62.98 ± 10.20 years; 67% male). The median follow-up was 121 days (range: 7 ∼ 732 days). All-cause mortality occurred in 26 (39%) patients. Multivariate Cox regression revealed a significant association of LACI after adjusting for NT-pro BNP, troponin T, moderate tricuspid regurgitation, pericardial and pleural effusion (adjusted HR: 10.58, p = 0.008). Kaplan-Meier curves displayed prognostic differences based on median LACI (cut-off : 0.57, p = 0.002). The likelihood ratio χ2 test showed that LACI added predictive value to Mayo 2004, European 2015 modification of Mayo 2004, and Mayo 2012 models (All p < 0.001).

Conclusions: 3DE-based LACI is independently associated with all-cause mortality in AL-CA patients and augments prognostic value to traditional staging models.

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来源期刊
Amyloid-Journal of Protein Folding Disorders
Amyloid-Journal of Protein Folding Disorders 生物-生化与分子生物学
CiteScore
10.60
自引率
10.90%
发文量
48
审稿时长
6-12 weeks
期刊介绍: Amyloid: the Journal of Protein Folding Disorders is dedicated to the study of all aspects of the protein groups and associated disorders that are classified as the amyloidoses as well as other disorders associated with abnormal protein folding. The journals major focus points are: etiology, pathogenesis, histopathology, chemical structure, nature of fibrillogenesis; whilst also publishing papers on the basic and chemical genetic aspects of many of these disorders. Amyloid is recognised as one of the leading publications on amyloid protein classifications and the associated disorders, as well as clinical studies on all aspects of amyloid related neurodegenerative diseases and major clinical studies on inherited amyloidosis, especially those related to transthyretin. The Journal also publishes book reviews, meeting reports, editorials, thesis abstracts, review articles and symposia in the various areas listed above.
期刊最新文献
AA amyloidosis in vertebrates: epidemiology, pathology and molecular aspects. A case of the iatrogenic transmission of vascular Aß40 amyloid. Identification of epidermal growth factor-containing fibulin-like extracellular matrix protein 1-derived amyloid deposition in a rhesus macaque. PRX004 in variant amyloid transthyretin (ATTRv) amyloidosis: results of a phase 1, open-label, dose-escalation study. High frequency of occult transthyretin and apolipoprotein AI-type amyloid in aortic valves removed by valve replacement for aortic stenosis.
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