Understanding the Effects of Pulmonary Arterial Hypertension on Lean Muscle Mass (MUSCLE UP-PH)

University of Pennsylvania

Status: Active, not recruiting

Conditions: Pulmonary Hypertension

Treatments: Diagnostic Test: Echocardiogram; Radiation: Dual-Energy X-ray Absorptiometry Scan; Radiation: Chest CT scan; Behavioral: Activity monitoring; Diagnostic Test: Six minute walk test; Diagnostic Test: blood draw; Diagnostic Test: Short Performance Physical Battery; Behavioral: Quality of Life Questionnaire (emPHasis 10); Behavioral: International Physical Activity Questionnaire Short Form (IPAQ-SF); Behavioral: 24 hour diet recall; Diagnostic Test: Grip strength test

Study type: Observational

Funder types: Other; NIH

Identifiers

NCT07132788

R01HL173533 (U.S. NIH Grant/Contract)

856202

Details and patient eligibility

About

Patients with pulmonary arterial hypertension (PAH) are at increased risk of muscle loss and decreased physical activity. This study will aim to (1) understand the way in which muscle loss occurs in PAH, particularly the role of fat surrounding the heart, and (2) look at the impact muscle loss has on quality of life, daily physical activity, and hospitalizations in patients with PAH. The findings from this study could help identify potentially treatable factors that may improve the overall quality of life and physical functioning of patients with PAH.

Subjects will be asked to attend a baseline visit where the following will be performed:

• Measure your vital signs
• Undergo a research blood draw, less than 4 tablespoons
• Provide a urine pregnancy test (if applicable)
• Review demographics, personal history, and medical history
• Review current PAH medications
• Complete questionnaires on how your PAH affects you
• Complete a test of physical performance
• Complete a grip strength test
• Undergo an echocardiogram (Echo)
• Complete a six-minute walk test
• Undergo a Chest CT Scan
• Undergo a scan of your body composition (DXA scan)
• Obtain a weight and body composition measurement on the InBody Scale Subjects will also complete activity moniotring, two 24-hour diet recalls, and participate in remote follow-up visits every 6 months

Enrollment: 150 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Signed informed consent prior to initiation of any study mandated procedure.

• Diagnosis of PAH belonging to one of the following subgroups of Group 1 PH according to the updated clinical classification [Humbert 2022]

  • Idiopathic (IPAH)

  • Heritable (HPAH)

  • Drugs or toxins induced

  • Associated (APAH) with one of the following:

    • Connective tissue disease;
    • Human immunodeficiency virus (HIV) infection;
    • Congenital heart disease; or
    • Portopulmonary hypertension

• Diagnosis of PAH within 6 months of enrollment or diagnosis of PAH and on stable therapy for 3 months prior to enrollment

• Documented hemodynamic diagnosis of PAH by right heart catheterization (RHC), prior to enrollment showing:

  • mPAP > 20 mmHg; and
  • PAWP or LVEDP ≤ 15 mmHg
  • PVR > 2 Wood units

Exclusion criteria

• Prior to enrollment, evidence of moderately severe obstructive ventilator defect with:

  • FEV1/FVC ≤ 5th percentile; and
  • FEV1 z-score < 2.5

• Prior to enrollment, evidence of severe restrictive defect with

  • TLC < 5th percentile
  • FEV1 z-score < 4

• Prior to enrollment, hospitalization (within 1 week) for decompensated right heart failure

• More than moderate aortic or mitral valve disease

• LVEF < 40% within 1 year of screening

• Pregnancy