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Multimodality RV Phenotyping for Risk Stratification and Short-Term Outcomes in Group 1 PAH (MIRROR-PAH)

15 september 2026 bijgewerkt door: Neziha Aybuke Geylan, MD, Istanbul University - Cerrahpasa

Multimodality Imaging-Based Right Ventricular Phenotyping for Risk Stratification and Short-Term Outcomes in Group 1 Pulmonary Arterial Hypertension: The MIRROR-PAH Study

The MIRROR-PAH is a single-center, prospective, observational cohort study evaluating the incremental value of multimodality imaging-derived right ventricular characteristics for risk stratification in patients with Group 1 pulmonary arterial hypertension (PAH). The study aims to determine whether incorporation of echocardiographic and cardiac magnetic resonance (CMR)-derived right ventricular parameters into established non-invasive risk assessment models results in risk reclassification and improves identification of patients at risk for short-term clinical worsening.

Adult patients with established Group 1 PAH undergoing routine follow-up and with available right heart catheterization (RHC) and CMR data will be consecutively enrolled. Clinical, laboratory, echocardiographic, and follow-up data will be prospectively collected over a 6-month period. Associations between multimodality imaging findings, invasive hemodynamic measurements, risk classification, and short-term clinical outcomes will be evaluated.

Studie Overzicht

Gedetailleerde beschrijving

Pulmonary arterial hypertension (PAH) is a progressive disease characterized by pulmonary vascular remodeling, increased pulmonary vascular resistance, and progressive right ventricular (RV) pressure overload. Despite substantial advances in targeted therapies, morbidity and mortality remain high, and patient prognosis is largely determined by the ability of the right ventricle to adapt to the increased afterload imposed by the pulmonary circulation.

Current clinical practice guidelines recommend periodic risk assessment to guide treatment decisions and monitor disease progression. Contemporary non-invasive risk stratification models incorporate clinical, functional, and biochemical parameters, including World Health Organization (WHO) functional class, exercise capacity, and natriuretic peptide levels. Although cardiac imaging provides important information regarding right ventricular structure and function and is widely used during the evaluation and follow-up of patients with PAH, imaging parameters are not routinely incorporated into simplified follow-up risk assessment models. Consequently, a considerable proportion of patients remain classified within intermediate-risk categories, representing a heterogeneous population with variable clinical trajectories and therapeutic needs.

Multimodality cardiac imaging provides comprehensive assessment of right ventricular structure, function, and remodeling. Echocardiography remains the cornerstone imaging modality for routine evaluation and longitudinal follow-up of PAH patients, while cardiac magnetic resonance (CMR) offers highly accurate and reproducible quantification of right ventricular volumes and function. Several imaging-derived parameters have been associated with disease severity and adverse outcomes in PAH. In addition, invasive hemodynamic assessment obtained by right heart catheterization (RHC) provides important prognostic information regarding pulmonary vascular disease and right ventricular adaptation. The integration of imaging and hemodynamic information may therefore provide incremental value beyond conventional non-invasive risk assessment strategies.

The MIRROR-PAH Study (Multimodality Imaging-Based Right Ventricular Phenotyping for Risk Stratification and Short-Term Outcomes in Group 1 Pulmonary Arterial Hypertension) is a single-center, prospective, observational cohort study designed to evaluate the relationship between multimodality imaging-derived right ventricular characteristics, invasive hemodynamic measurements, established risk assessment models, and short-term clinical outcomes in patients with Group 1 PAH.

Adult patients with established Group 1 PAH who are undergoing routine follow-up and have available RHC and CMR examinations will be consecutively enrolled. Baseline clinical, laboratory, echocardiographic, hemodynamic, and CMR data will be collected. Follow-up clinical assessment and transthoracic echocardiography will be performed at 6 months.

The primary objective of the study is to determine whether incorporation of multimodality imaging-derived right ventricular (RV) characteristics into established non-invasive PAH risk assessment models results in risk reclassification at baseline and at 6-month follow-up.

Secondary objectives are to:

  • Evaluate the predictive value of imaging-augmented risk reclassification for composite clinical worsening during follow-up;
  • Assess the incidence of composite clinical worsening, defined as PAH treatment escalation, PAH-related hospitalization, worsening WHO functional class, decline in 6-minute walk distance, or death;
  • Identify multimodality imaging-derived RV characteristics associated with an increased risk of short-term clinical worsening;
  • Evaluate the relationship between multimodality imaging-derived RV characteristics and invasive hemodynamic measurements obtained by right heart catheterization (RHC);
  • Identify multimodality imaging-derived RV characteristics associated with high-risk classification according to established PAH risk stratification models;
  • Evaluate changes in echocardiographic RV characteristics between baseline and 6-month follow-up;
  • Assess the incremental prognostic value of multimodality imaging-derived RV characteristics beyond established non-invasive PAH risk assessment models for predicting clinical worsening.

The study is based on the hypothesis that multimodality assessment of right ventricular structure and function provides clinically relevant information beyond conventional non-invasive risk stratification models and may improve identification of patients at increased risk of disease progression and short-term adverse outcomes. By integrating echocardiographic, CMR, and invasive hemodynamic information, the MIRROR-PAH Study aims to explore the potential role of imaging-enhanced risk assessment in refining prognostic evaluation and supporting clinical decision-making during follow-up of patients with PAH.

Studietype

Observationeel

Inschrijving (Geschat)

50

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Istanbul, Turkije (Türkiye)
        • Istanbul University Cerrahpasa Institute of Cardiology

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Bemonsteringsmethode

Niet-waarschijnlijkheidssteekproef

Studie Bevolking

Adult patients with established Group 1 pulmonary arterial hypertension (PAH) undergoing routine follow-up at a specialized pulmonary hypertension center. Eligible participants will have available right heart catheterization (RHC), transthoracic echocardiography, and cardiac magnetic resonance (CMR) imaging data and will undergo prospective clinical and echocardiographic follow-up for 6 months.

Beschrijving

Inclusion Criteria:

  • Adults aged 18 years or older
  • Diagnosis of Group 1 pulmonary arterial hypertension (PAH) according to ESC/ERS guidelines
  • Followed at the study center with a diagnosis of PAH
  • Availability of right heart catheterization (RHC) and cardiac magnetic resonance (CMR) imaging data obtained within a clinically relevant time interval
  • Availability of analyzable clinical, imaging, and hemodynamic data
  • Willingness to participate in the study and provision of written informed consent

Exclusion Criteria:

  • Age younger than 18 years
  • Pulmonary hypertension groups other than Group 1 PAH (Groups 2-5 PH)
  • Absence of either right heart catheterization or cardiac magnetic resonance imaging data within a clinically relevant time interval
  • Incomplete clinical or imaging data preventing analysis
  • Unavailable follow-up data

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

Cohorten en interventies

Groep / Cohort
Patients with Group 1 Pulmonary Arterial Hypertension
Participants are adult patients with established Group 1 pulmonary arterial hypertension (PAH) undergoing follow-up at a specialized pulmonary hypertension center.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Risk reclassification rate after incorporation of multimodality imaging-derived RV characteristics into established non-invasive PAH risk models
Tijdsspanne: Baseline and 6-month follow-up
The proportion of patients undergoing risk reclassification after incorporation of multimodality imaging-derived right ventricular (RV) characteristics obtained from echocardiography and cardiac magnetic resonance imaging into established non-invasive PAH risk assessment models will be evaluated. Changes in risk category assignment compared with conventional non-invasive risk stratification will be assessed.
Baseline and 6-month follow-up

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Number of Participants Experiencing Composite Clinical Worsening
Tijdsspanne: 6 months
Composite clinical worsening is defined as the occurrence of at least one of the following events during the 6-month follow-up period: pulmonary arterial hypertension (PAH) treatment escalation, PAH-related hospitalization, worsening World Health Organization (WHO) functional class, decline in 6-minute walk distance, or death.
6 months
Change in Predictive Performance for Composite Clinical Worsening After Addition of RV Imaging Characteristics to Conventional PAH Risk Classification
Tijdsspanne: 6 months
The predictive performance of conventional three-strata pulmonary arterial hypertension risk classification for 6-month composite clinical worsening will be compared with the predictive performance of an imaging-augmented risk classification incorporating predefined right ventricular imaging characteristics. Predictive performance will be assessed using the area under the receiver operating characteristic curve.
6 months
RV imaging characteristics associated with clinical worsening
Tijdsspanne: 6 months
Multimodality imaging-derived RV characteristics associated with an increased risk of composite clinical worsening will be identified.
6 months
Agreement Between Cardiovascular Magnetic Resonance-Derived Stroke Volume Index and Right Heart Catheterization-Derived Stroke Volume Index
Tijdsspanne: Baseline
Agreement between stroke volume index (mL/m²) measured by cardiovascular magnetic resonance imaging using ventricular volumetric analysis and stroke volume index (mL/m²) calculated from cardiac output obtained during right heart catheterization will be assessed at baseline using Bland-Altman analysis. The mean difference in stroke volume index (mL/m²) between the two methods will be reported.
Baseline
RV imaging characteristics associated with high-risk status
Tijdsspanne: Baseline and 6-month follow-up
Multimodality imaging-derived RV characteristics associated with high-risk classification according to established PAH risk assessment models will be identified.
Baseline and 6-month follow-up
Change in Right Ventricular Free-Wall Longitudinal Strain From Baseline to 6 Months
Tijdsspanne: Baseline to 6 months
Change in right ventricular free-wall longitudinal strain (%) measured by two-dimensional speckle-tracking echocardiography will be assessed between baseline and the 6-month follow-up. The mean change in right ventricular free-wall longitudinal strain (%) from baseline to 6 months will be reported.
Baseline to 6 months

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Aybüke Geylan, MD, Istanbul University Cerrahpasa Institute of Cardiology
  • Studie stoel: Umit Yasar Sinan, Professor, Istanbul University Cerrahpasa Institute of Cardiology

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

11 mei 2026

Primaire voltooiing (Geschat)

1 februari 2027

Studie voltooiing (Geschat)

1 mei 2027

Studieregistratiedata

Eerst ingediend

6 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

19 juni 2026

Eerst geplaatst (Werkelijk)

25 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

18 september 2026

Laatste update ingediend die voldeed aan QC-criteria

15 september 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

ONBESLIST

Beschrijving IPD-plan

Individual participant data (IPD) sharing plans have not yet been determined. Any future data sharing will be subject to institutional policies, ethical considerations, participant confidentiality requirements, and applicable regulations.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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