Impact of autonomic dysfunction on cardiovascular outcomes among patients with ATTR cardiomyopathy: insights from the COMPASS-31.

IF 7.4 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ariel Weinsaft, Sergio Teruya, Alfonsina Mirabal Santos, Stephen Helmke, Karan Wats, Juliana Levy, Dimitrios Bampatsias, Mathew S Maurer
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引用次数: 0

Abstract

Background: ATTR is a systemic disease, causing significant morbidity and mortality, manifesting with symptoms affecting both the heart and nervous system. This study employed the Composite Autonomic Symptom Scale 31 (COMPASS-31) to assess autonomic symptoms in relation to ATTR-CM subtypes and the impact of dysfunction on prognosis.

Methods: This study included contemporary ATTR-CM patients enrolled in an institutional registry from 7/21-6/24. Demographic information, patient-reported outcomes (COMPASS-31 and Kansas City Cardiomyopathy Questionnaire (KCCQ)), 6-min walk test, and clinical data (hospitalisations, mortality) were collected and compared between ATTR-CM sub-types (ATTRwt, ATTRv-Val122Ile, ATTRv-non Val122Ile).

Results: 240 ATTR-CM patients (81% ATTRwt, 11% Val-122Ile, 8% non-Val122Ile) were studied. Following adjustment for age, significant COMPASS-31 score differences were observed between ATTRwt and ATTRv-nonV122I variant patients. "High" COMPASS-31 scores (≥35.42) were associated with later Columbia stage, lower exercise tolerance, and poorer quality of life (QOL) (all p < 0.05). Time-to-event analysis demonstrated higher probability of cardiovascular hospitalisations (CVH) for patients with "High" COMPASS-31 scores (p < 0.01). These patients also had increased CVH risk (HR = 4.26 [95% CI: 1.85-9.83], p = 0.001) independent of age, sex, ATTR type, Columbia Stage and diabetes.

Conclusions: Among ATTR-CM patients, autonomic dysfunction assessed via COMPASS-31 questionnaire was associated with more advanced disease stage and QOL impairment, and independently predicted CVH risk.

自主神经功能障碍对ATTR心肌病患者心血管预后的影响:来自COMPASS-31的见解
背景:ATTR是一种全身性疾病,发病率和死亡率高,表现为累及心脏和神经系统的症状。本研究采用自主神经症状综合量表31 (COMPASS-31)评估自主神经症状与atr - cm亚型的关系以及功能障碍对预后的影响。方法:本研究纳入了7月21日至6月24日在机构登记的当代atr - cm患者。收集了atr - cm亚型(ATTRwt、ATTRv-Val122Ile、ATTRv-non Val122Ile)的人口统计信息、患者报告的结果(compass31和堪萨斯城心肌病问卷(KCCQ))、6分钟步行测试和临床数据(住院、死亡率)。结果:研究了240例atr - cm患者(81%为attrt, 11%为Val-122Ile, 8%为非val122ile)。在年龄调整后,ATTRwt和attrv -非v122i变异患者之间观察到显著的COMPASS-31评分差异。“高”COMPASS-31评分(≥35.42)与较晚的哥伦比亚期、较低的运动耐量和较差的生活质量(QOL)相关(均p p p = 0.001),与年龄、性别、ATTR类型、哥伦比亚期和糖尿病无关。结论:在atr - cm患者中,通过COMPASS-31问卷评估的自主神经功能障碍与更晚期的疾病阶段和生活质量损害相关,并独立预测CVH风险。
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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.
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