Assessing Daily Life Physical Activity by Actigraphy in Pulmonary Arterial Hypertension Insights From the Randomized Controlled Study With Selexipag (TRACE)

被引:11
|
作者
Howard, Luke S. [1 ]
Rosenkranz, Stephan [2 ,3 ]
Frantz, Robert P. [4 ,5 ,6 ]
Hemnes, Anna R. [7 ]
Fister, Thomas P. [8 ]
Schmitz, Shu-Fang Hsu [8 ]
Skara, Hall [9 ]
Humbert, Marc [10 ,11 ]
Preston, Ioana R. [12 ]
机构
[1] Hammersmith Hosp, London, England
[2] Imperial Coll Healthcare NHS Trust, London, England
[3] Heart Ctr, Cologne, Germany
[4] Univ Hosp Cologne, Cologne, Germany
[5] Cologne Cardiovasc Res Ctr, Cologne, Germany
[6] Mayo Clin, Rochester, MN USA
[7] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[8] Janssen Pharmaceut Co Johnson & Johnson, Actelion Pharmaceut Ltd, Allschwil, Switzerland
[9] European Pulm Hypertens Assoc PHA Europe, Vienna, Austria
[10] Hop Bicetre, Assistance Publ Hop Paris, Dept Resp & Intens Care Med, Le Kremlin Bicetre, France
[11] Hop Marie Lannelongue, UMR S 999, INSERM, Le Plessis Robinson, France
[12] Tufts Med Ctr, Boston, MA USA
关键词
actigraphy; daily life physical activity; pulmonary arterial hypertension; quality of life; selexipag; UNITED-STATES; SYMPTOMS; IMPACT;
D O I
10.1016/j.chest.2022.08.2231
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: Reduced daily life physical activity (DLPA) in pulmonary arterial hypertension (PAH) contributes to a poor quality of life. RESEARCH QUESTION: Can actigraphy be used to assess changes in DLPA in patients with PAH receiving selexipag or placebo? STUDY DESIGN AND METHODS: Effect of Selexipag on Daily Life Physical Activity of Patients With Pulmonary Arterial Hypertension (TRACE) was a prospective, multicenter, randomized, placebo-controlled, double-blind, exploratory phase 4 study enrolling patients with PAH in World Health Organization functional class II/III, receiving stable endothelin receptor antagonist with/without phosphodiesterase type 5 inhibitor background therapy. Primary end points were change from baseline to Week 24 in actigraphy-assessed DLPA (recorded by using an accelerometer), including daily time spent in nonsedentary physical activity (NSPA), daily time spent in moderate to vigorous physical activity (MVPA), daily volume of activity, and daily number of steps. RESULTS: At baseline, patients (N = 108) were prevalent, on stable background PAH therapy, and at low risk of disease progression. Patients showed high compliance with wear of the accelerometer throughout the study. From baseline to Week 24, mean daily time spent in NSPA increased by 1.1 min and decreased by 16.7 min in the selexipag and placebo groups (treatment difference [95% CI], 17.8 [-6.0, 41.6] min); mean time spent in MVPA increased by 0.3 min and was reduced by 2.0 min in the selexipag and placebo groups (treatment difference [95% CI], 2.3 [-10.8, 15.4] min); and mean number of daily steps decreased by 0.3 and 201.9 in the selexipag and placebo groups (treatment difference [95% CI], 201.6 [-243.0, 646.2]). INTERPRETATION: TRACE enrolled a prevalent population on background therapy and at low risk of disease progression. Changes in DLPA were small and highly variable, with no statistically significant differences between treatment groups. This patient-centric study was the first randomized trial in PAH to capture high-quality actigraphy data and to describe DLPA in terms of mean/median and variability, which may inform the design of future studies.
引用
收藏
页码:407 / 418
页数:12
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