Exercise, Sports Participation, and Quality of Life in Young Patients with Heritable Thoracic Aortic Disease.

IF 4.1 2区 医学 Q1 SPORT SCIENCES Medicine and Science in Sports and Exercise Pub Date : 2025-02-01 Epub Date: 2024-10-01 DOI:10.1249/MSS.0000000000003570
Theodore J Millette, Randy K Ramcharitar, Oliver J Monfredi, Matthew J Thomas, Mark R Conaway, Peter N Dean
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Abstract

Introduction: Patients with heritable thoracic aortic disease (HTAD) are often restricted from sports and certain types of exercise. This study was designed to investigate the effect of lifetime exercise exposure and competitive sports participation on quality of life (QOL) in patients 15-35 yr old with syndromic (Marfan syndrome, Loeys-Dietz syndrome, and vascular Ehlers-Danlos syndrome) and nonsyndromic HTAD (nsHTAD).

Methods: This cross-sectional study used questionnaires to assess lifetime exercise exposure and utilized the PedsQL QOL Inventory. We developed an exercise exposure score (EES) to quantify lifetime exercise exposure. Questionnaires were completed via telephone with complimentary medical record review.

Results: Forty patients were enrolled. Mean age was 26 yr. The diagnosis was Marfan syndrome in 83%. Despite 88% of patients being restricted by their provider, 65% reported competitive sports participation and 93% reported recreational exercise. Participants with an EES greater than the median had significantly better total QOL scores compared with those below the median (78 vs 65, P = 0.03). There were significant positive correlations between current frequency of exercise and psychosocial QOL (slope = 3.9, 95% CI = 1.2-6.6, P = 0.005), physical QOL (slope = 8.1, 95% CI = 4.1-12, P < 0.001), and total QOL score (slope = 6.0, 95% CI = 3.1-9.0, P < 0.001). We found no difference in aortic size or need for surgical intervention between those above and below the median EES, or between those who did and did not participate in competitive sports.

Conclusions: Despite exercise restrictions, young HTAD patients are physically active. Increased lifetime exercise and current physical activity levels were associated with improved QOL in HTAD patients.

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可遗传性胸主动脉疾病年轻患者的锻炼、运动参与和生活质量。
导言:遗传性胸主动脉疾病(HTAD)患者通常被限制参加体育运动和某些类型的锻炼。本研究旨在调查 15-35 岁综合征[马凡综合征(MFS)、洛伊-迪茨综合征(LDS)、血管性埃勒斯-丹洛斯综合征(vEDS)]和非综合征遗传性胸主动脉疾病(nsHTAD)患者终生运动暴露和竞技体育参与对生活质量(QOL)的影响:这项横断面研究采用了调查问卷来评估终生运动暴露,并使用了 PedsQL QOL Inventory。我们制定了运动暴露评分(EES)来量化终生运动暴露。问卷通过电话填写,并附带病历审查:结果:共招募了 40 名患者。平均年龄为 26 岁。83% 的患者被诊断为 MFS。尽管有 88% 的患者受到其医疗机构的限制,但仍有 65% 的患者表示参加过竞技运动,93% 的患者表示进行过休闲锻炼。EES 值高于中位数的参与者的 QOL 总分明显高于低于中位数的参与者(78 vs 65,p = 0.03)。当前运动频率与社会心理 QOL(斜率 = 3.9,95% CI:(1.2, 6.6),p = 0.005)、身体 QOL(斜率 = 8.1,95% CI:(4.1, 12),p < 0.001)和 QOL 总分(斜率 = 6.0,95% CI:(3.1, 9.0),p < 0.001)之间存在明显的正相关。我们发现,在EES中位数以上和以下的患者之间,或在参加和不参加竞技运动的患者之间,主动脉大小或手术干预需求没有差异:尽管运动受到限制,但年轻的 HTAD 患者仍积极参加体育锻炼。终生运动量和当前运动量的增加与 HTAD 患者 QOL 的改善有关。
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来源期刊
CiteScore
7.70
自引率
4.90%
发文量
2568
审稿时长
1 months
期刊介绍: Medicine & Science in Sports & Exercise® features original investigations, clinical studies, and comprehensive reviews on current topics in sports medicine and exercise science. With this leading multidisciplinary journal, exercise physiologists, physiatrists, physical therapists, team physicians, and athletic trainers get a vital exchange of information from basic and applied science, medicine, education, and allied health fields.
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