Eastin Ella F, Machnik Jannika V, Stiles Lauren E, Larsen Nicholas W, Seliger Jordan, Geng Linda N, Bonilla Hector, Yang Phillip C, Miglis Mitchell G
Department of Neurology and Neurological Sciences, Stanford University, 213 Quarry Road, Stanford, CA, 94304, USA.
Department of Medicine, Stanford University, Stanford, CA, USA.
Clin Auton Res. 2025 Feb 5. doi: 10.1007/s10286-025-01111-1.
Autonomic dysfunction is a common and often debilitating feature of long-COVID (LC), however, studies evaluating frequency and severity of chronic autonomic dysfunction in LC are limited. We utilized an established online cohort of participants with LC to assess duration and severity of autonomic dysfunction, impact on quality of life, risk factors of autonomic diagnoses including postural tachycardia syndrome (POTS), and efficacy of common treatments.
Our international cohort included 526 adults with LC aged 20-65 years who previously completed baseline evaluations of LC symptoms, autonomic symptom burden, and quality of life. Participants repeated survey instruments and completed new instruments assessing risk factors and symptom mitigation strategies. A subset of individuals completed a 10-min active stand test. Multivariable logistic regression identified predictors of autonomic symptom burden and incident autonomic diagnoses including POTS.
A total of 71.9% of participants with LC had a Composite Autonomic Symptom Score-31 (COMPASS-31) score ≥ 20, suggestive of moderate-to-severe autonomic dysfunction. The median symptom duration was 36 [30-40] months, and 37.5% of participants could no longer work or had to drop out of school due to their illness. In addition, 40.5% of individuals with autonomic dysfunction were newly diagnosed with POTS, representing 33% of the total LC cohort. Female sex and joint hypermobility were associated with an increased risk of autonomic dysfunction.
Evidence of chronic moderate-to-severe autonomic dysfunction was seen in most participants with LC in our cohort and was significantly associated with reduced quality of life and functional disability. POTS was the most common post-COVID autonomic diagnosis.
自主神经功能障碍是长期新冠(LC)常见且往往使人衰弱的特征,然而,评估LC中慢性自主神经功能障碍的频率和严重程度的研究有限。我们利用一个既定的LC参与者在线队列,以评估自主神经功能障碍的持续时间和严重程度、对生活质量的影响、自主神经诊断(包括体位性心动过速综合征(POTS))的危险因素以及常用治疗方法的疗效。
我们的国际队列包括526名年龄在20 - 65岁的LC成年患者,他们之前完成了LC症状、自主神经症状负担和生活质量的基线评估。参与者重复使用调查工具,并完成评估危险因素和症状缓解策略的新工具。一部分个体完成了10分钟的主动站立测试。多变量逻辑回归确定了自主神经症状负担和包括POTS在内的自主神经诊断事件的预测因素。
共有71.9%的LC参与者的综合自主神经症状评分-31(COMPASS-31)得分≥20,提示存在中度至重度自主神经功能障碍。症状持续时间的中位数为36[30 - 40]个月,37.5%的参与者因疾病无法再工作或不得不辍学。此外,40.5%的自主神经功能障碍个体新诊断为POTS,占LC总队列的33%。女性和关节过度活动与自主神经功能障碍风险增加相关。
在我们队列中的大多数LC参与者中都发现了慢性中度至重度自主神经功能障碍的证据,并且与生活质量下降和功能残疾显著相关。POTS是新冠后最常见的自主神经诊断。