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

2026年9月15日 更新者: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.

調査の概要

状態

積極的、募集していない

条件

詳細な説明

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.

研究の種類

観察的

入学 (推定)

50

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

      • Istanbul、トルコ(Türkiye)
        • Istanbul University Cerrahpasa Institute of Cardiology

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

サンプリング方法

非確率サンプル

調査対象母集団

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.

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Risk reclassification rate after incorporation of multimodality imaging-derived RV characteristics into established non-invasive PAH risk models
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Number of Participants Experiencing Composite Clinical Worsening
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Aybüke Geylan, MD、Istanbul University Cerrahpasa Institute of Cardiology
  • スタディチェア:Umit Yasar Sinan, Professor、Istanbul University Cerrahpasa Institute of Cardiology

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年5月11日

一次修了 (推定)

2027年2月1日

研究の完了 (推定)

2027年5月1日

試験登録日

最初に提出

2026年6月6日

QC基準を満たした最初の提出物

2026年6月19日

最初の投稿 (実際)

2026年6月25日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月18日

QC基準を満たした最後の更新が送信されました

2026年9月15日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 2026/171

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

IPD プランの説明

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.

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