Evidence map›Paper›PMID 41644091›Full record

Trial reportChest2026

Daily Physical Activity in Pulmonary Arterial Hypertension: Insights From a Multicenter Longitudinal Trial Using Accelerometry.

Jasleen Minhas, Haochang Shou, Nadine Al-Naamani, Rui Feng, Roham Zamanian, Todd Bull, Murali Chakinala, Anna Hemnes, Jude Moutchia, Stephen C Mathai and 3 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Chest, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Jasleen MinhasDivision of Pulmonary, Allergy and Critical Care, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA. Electronic address: jasleen.minhas@pennmedicine.upenn.edu.
Haochang ShouDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA; Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA.
Nadine Al-NaamaniDivision of Pulmonary, Allergy and Critical Care, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA.
Rui FengDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA; Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA.
Roham ZamanianDepartment of Medicine, Stanford University, Stanford, CA.
Todd BullDepartment of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, Pulmonary Vascular Disease, University of Colorado, Denver, CO.
Murali ChakinalaDepartment of Medicine, Washington University in St. Louis, St. Louis, Missouri.
Anna HemnesDepartment of Medicine, Vanderbilt University, Nashville, TN.
Jude MoutchiaDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA.
Stephen C MathaiDepartment of Medicine, Johns Hopkins University, Baltimore, MD.
Susan EllenbergDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA; Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA.
Corey VentetuoloRhode Island Hospital and the Departments of Medicine, Brown University, Providence, RI.
Steven M KawutDivision of Pulmonary, Allergy and Critical Care, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA; Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA.

Funding

Anastrozole in Pulmonary Arterial Hypertension (AIPH2) - CCC (Lead)R01HL134905 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI KAWUT, STEVEN M · 2017 to 2021
$5.5M
Unraveling the systemic manifestations of pulmonary arterial hypertension on lean muscle massR01HL173533 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Nadine Al-Naamani · 2024 to 2026
$2.0M
Anastrozole in Pulmonary Arterial Hypertension (AIPH2) - DCCR01HL134904 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI ELLENBERG, SUSAN S · 2017 to 2021
$990k
Obesity in Pulmonary Arterial HypertensionK23HL141584 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI AL-NAAMANI, NADINE · 2018 to 2022
$970k
Physical activity phenotypes and their association with traditional outcomes in pulmonary arterial hypertensionK23HL169930 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Jasleen Minhas · 2024 to 2026
$575k
NHLBI NIH HHS K23 HL141584NHLBI NIH HHS K23 HL169930NHLBI NIH HHS R01 HL134904NHLBI NIH HHS R01 HL134905NHLBI NIH HHS R01 HL173533
6 · The paper itself

Abstract

backgroundPulmonary arterial hypertension (PAH) is a progressive disease associated with high morbidity and mortality. Traditional assessments such as the 6-minute walk distance (6MWD) may not adequately capture daily physical activity or patient experience in real-world settings. RESEARCH QUESTION: Among patients with PAH, do accelerometer-derived measures of daily physical activity reflect disease severity, functional status, and outcomes over time? STUDY DESIGN AND

methodsPulmonary Hypertension and Anastrozole (PHANTOM), a multicenter randomized controlled trial of anastrozole in PAH, enrolled male patients and postmenopausal female patients with PAH at 7 centers in the United States. Patients completed 4 in-person study visits over 12 months. Participants wore hip-based accelerometers for 7 days at each visit. Mixed-effects models assessed associations between daily physical activity and demographic, clinical, echocardiographic, and environmental variables. Clinical outcomes included: 6MWD; health-related quality of life (HRQoL), assessed by using the emPHasis-10 questionnaire and the 36-item Short Form Health Survey; bone mineral density (BMD); and time to clinical worsening (hospitalization, treatment escalation, or death). Cox models were used to examine associations between activity and time to clinical worsening.

resultsEighty-four participants were enrolled (mean age 61 years; 67% female). Device adherence was high across visits. Activity declined over time and was lower in patients with World Health Organization functional class III, worse right ventricular function, and connective tissue disease-associated PAH. Lower daily activity was associated with worse HRQoL, worse baseline 6MWD, and worse baseline femoral/hip BMD. Lower baseline activity was associated with increased risk of clinical worsening (hazard ratio, 1.06 per hour/week less active; P < .01).

interpretationOur results suggest that accelerometer-derived physical activity reflects disease severity and is associated with HRQoL, BMD, and clinical worsening in PAH. These metrics may offer a dynamic, patient-centered complement to traditional assessments.

Indexed as

AccelerometryExercisePulmonary Arterial HypertensionAgedFemaleHumansLongitudinal StudiesMaleMiddle AgedQuality of LifeSeverity of Illness IndexWalk Testaccelerometryactigraphyoutcomesphysical activitypulmonary arterial hypertensionquality of life

Identifiers

PMID41644091
PMCPMC12919715

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.