Quality of Life and Exercise Capacity in Early Stage and Subclinical Hypertrophic Cardiomyopathy: A Secondary Analysis of the VANISH Trial.

IF 7.8 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Circulation: Heart Failure Pub Date : 2024-08-01 DOI:10.1161/CIRCHEARTFAILURE.124.011663
Catherine G Ireland, Danielle S Burstein, Sharlene M Day, Anna Axelsson Raja, Mark W Russell, Kenneth G Zahka, Alexandre Pereira, Charles E Canter, Richard G Bach, Matthew T Wheeler, Joseph W Rossano, Anjali T Owens, Henning Bundgaard, Luisa Mestroni, Matthew R G Taylor, Amit R Patel, Ivan Wilmot, Jonathan H Soslow, Jason R Becker, Ilya Giverts, E John Orav, Brian Claggett, Kimberly Y Lin, Carolyn Y Ho
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Abstract

Background: The health-related quality of life (HRQOL) and cardiopulmonary exercise testing (CPET) performance of individuals with subclinical and early stage hypertrophic cardiomyopathy (HCM) have not been systematically studied. Improved understanding will inform the natural history of HCM and factors influencing well-being.

Methods: VANISH trial (Valsartan for Attenuating Disease Evolution in Early Sarcomeric HCM) participants with early stage sarcomeric HCM (primary analysis cohort) and subclinical HCM (sarcomere variant without left ventricular hypertrophy comprising the exploratory cohort) who completed baseline and year 2 HRQOL assessment via the pediatric quality of life inventory and CPET were studied. Metrics correlating with baseline HRQOL and CPET performance were identified. The impact of valsartan treatment on these measures was analyzed in the early stage cohort.

Results: Two hundred participants were included: 166 with early stage HCM (mean age, 23±10 years; 40% female; 97% White; and 92% New York Heart Association class I) and 34 subclinical sarcomere variant carriers (mean age, 16±5 years; 50% female; and 100% White). Baseline HRQOL was good in both cohorts, although slightly better in subclinical HCM (composite pediatric quality of life score 84.6±10.6 versus 90.2±9.8; P=0.005). Both cohorts demonstrated mildly reduced functional status (mean percent predicted peak oxygen uptake 73±16 versus 78±12 mL/kg per minute; P=0.18). Percent predicted peak oxygen uptake and peak oxygen pulse correlated with HRQOL. Valsartan improved physical HRQOL in early stage HCM (adjusted mean change in pediatric quality of life score +4.1 versus placebo; P=0.01) but did not significantly impact CPET performance.

Conclusions: Functional capacity can be impaired in young, healthy people with early stage HCM, despite New York Heart Association class I status and good HRQOL. Peak oxygen uptake was similarly decreased in subclinical HCM despite normal left ventricular wall thickness and excellent HRQOL. Valsartan improved physical pediatric quality of life scores but did not significantly impact CPET performance. Further studies are needed for validation and to understand how to improve patient experience.

Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01912534.

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早期和亚临床肥厚型心肌病患者的生活质量和运动能力:VANISH 试验的二次分析。
背景:亚临床和早期肥厚型心肌病(HCM)患者的健康相关生活质量(HRQOL)和心肺运动测试(CPET)表现尚未得到系统研究。加深了解将有助于了解肥厚性心肌病的自然病史和影响健康的因素:VANISH 试验(缬沙坦可减轻早期肉芽肿型 HCM 的疾病演变)的参与者包括早期肉芽肿型 HCM(主要分析队列)和亚临床型 HCM(不伴有左心室肥厚的肉芽肿变异型,为探索性队列),他们通过儿科生活质量清单和 CPET 完成了基线和第二年的 HRQOL 评估。研究确定了与基线 HRQOL 和 CPET 表现相关的指标。在早期队列中分析了缬沙坦治疗对这些指标的影响:结果:共纳入 200 名参与者:166 名早期 HCM 患者(平均年龄为 23±10 岁;40% 为女性;97% 为白人;92% 为纽约心脏协会 I 级)和 34 名亚临床肌纤维变异携带者(平均年龄为 16±5 岁;50% 为女性;100% 为白人)。两组患者的基线 HRQOL 均良好,但亚临床 HCM 患者的 HRQOL 略好(儿科生活质量综合评分 84.6±10.6 对 90.2±9.8;P=0.005)。两组患者的功能状态均有轻度下降(平均预测峰值摄氧量百分比为 73±16 对 78±12 mL/kg/分钟;P=0.18)。预测峰值摄氧量百分比和峰值氧脉搏与 HRQOL 相关。缬沙坦可改善早期HCM患者的身体HRQOL(与安慰剂相比,儿科生活质量评分的调整后平均变化为+4.1;P=0.01),但对CPET表现没有显著影响:结论:年轻、健康的早期 HCM 患者尽管处于纽约心脏协会 I 级和良好的 HRQOL 状态,但其功能能力可能会受损。尽管左心室壁厚度正常且 HRQOL 良好,但亚临床 HCM 患者的峰值摄氧量同样下降。缬沙坦改善了儿科物理生活质量评分,但对 CPET 的表现没有显著影响。需要进一步的研究进行验证,并了解如何改善患者体验:URL: https://www.clinicaltrials.gov; 唯一标识符:NCT01912534。
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来源期刊
Circulation: Heart Failure
Circulation: Heart Failure 医学-心血管系统
CiteScore
12.90
自引率
3.10%
发文量
271
审稿时长
6-12 weeks
期刊介绍: Circulation: Heart Failure focuses on content related to heart failure, mechanical circulatory support, and heart transplant science and medicine. It considers studies conducted in humans or analyses of human data, as well as preclinical studies with direct clinical correlation or relevance. While primarily a clinical journal, it may publish novel basic and preclinical studies that significantly advance the field of heart failure.
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