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Extracellular Vesicle Dynamics Predicting Vascular Complications and Treatment Response in Systemic Sclerosis (EVOLVE-SSc)

Extracellular Vesicle Dynamics Across the Circulatory System as Predictors of Major Vascular Complications and Therapeutic Response in Systemic Sclerosis Patients

Systemic sclerosis is a multisystem autoimmune disease characterized by vascular dysfunction, immune dysregulation, and progressive tissue fibrosis. Cardiopulmonary complications and peripheral vascular involvement are the principal causes of disability and mortality.

Extracellular vesicles (EVs) have emerged as key mediators of paracrine intercellular communication. Preclinical studies further suggest that EVs mediate long-range inter-organ communication through the circulation. However, the inability to directly track EV trafficking in vivo in humans has limited the understanding of their contribution to systemic inter-organ communication.

The investigators propose that systemic sclerosis provides a unique human model for investigating circulating EV-mediated inter-organ communication in a multisystem disease. The central hypothesis is that arteriovenous differences in the molecular and cellular characteristics of circulating EVs reflect their dynamic exchange between individual organs and the bloodstream, and that these differences are associated with disease severity. Comparison of EVs across the circulation, rather than relying exclusively on peripheral blood samples, enables a more direct assessment of organ-specific EV release and uptake.

Characterizing EV dynamics along the circulatory pathway has the potential to identify novel biomarkers and therapeutic targets for systemic sclerosis while providing fundamental insights into EV-mediated inter-organ communication in humans.

調査の概要

詳細な説明

Systemic sclerosis (SSc) is a multi-organ disease characterized by vascular, immune, and fibrotic changes. Vascular complications significantly contribute to mortality, disability, and healthcare costs in patients with SSc. These include digital ulcers (DUs) and associated conditions such as gangrene and osteomyelitis, as well as pulmonary arterial hypertension (PAH), all of which continue to have poor outcomes despite treatment advances. Notably, severe vascular disease increases the risk of cardiac and peripheral atherosclerosis, even in the absence of symptoms or overt risk factors. Timely management improves outcomes, but screening and prognostic stratification tools for SSc remain limited. Evidence supporting personalized treatment selection among currently available therapies is lacking.

Extracellular vesicles (EVs) are subcellular particles that facilitate the transfer of proteins, nucleic acids, and lipids between cells. They have been explored as biomarkers, therapeutic targets, and drug carriers across a wide range of diseases.

The investigators hypothesize that EVs play a direct and distinct role in the pathophysiology of multiorgan complications in SSc, particularly PAH and DUs. This hypothesis is supported by preclinical evidence demonstrating the involvement of EVs in endothelial dysfunction, intimal proliferation, immune dysregulation, and fibrosis, which are key processes in SSc pathogenesis. In mouse models, intravenously administered EVs are primarily taken up by the lungs, and PAH can be induced in healthy mice by injecting EVs isolated from pulmonary hypertensive animals. In humans, circulating EVs in the peripheral blood of patients with PAH are more abundant and exhibit distinct proteomic and transcriptomic profiles compared with those of healthy controls. Preliminary evidence further suggests that EV profiles in the venous blood of patients with SSc may correlate with disease severity and activity, although data specifically addressing vascular complications remain limited.

EVs exert biological effects through their protein, nucleic acid, and lipid cargo, as well as their ability to reach and interact with target cells. Recent studies in transgenic zebrafish have demonstrated that endogenous EVs can extravasate to distant target tissues in vivo. However, direct tracking of EVs in humans remains technically unfeasible with current methods. As a surrogate for in vivo tracking, the investigators propose characterizing circulating EVs at specific vascular locations accessible through acral vessels and during clinically indicated procedures such as right heart catheterization (RHC) and coronary angiography. These procedures, recommended for the assessment of PAH in patients with SSc, are consistent with international guidelines and pose no additional risk, making SSc an ideal model for investigating EV dynamics in humans.

This study aims to map EV characteristics across the circulatory system by evaluating changes at key anatomical sites. Sampling locations include the pulmonary artery and ascending aorta, reflecting pulmonary circulation and cardiac EV exchange, and the peripheral radial artery and cephalic vein, representing EV exchange within the acral circulation. EV profiles at these locations are expected to differ as a result of intravasation, extravasation, and collateral blood flow. Current approaches, which rely exclusively on peripheral venous sampling, lack this regional specificity and capture only the aggregate EV output.

The investigators further propose a comprehensive structural and functional evaluation of the cardiopulmonary and peripheral vascular systems to address the complex and heterogeneous nature of SSc complications. Pulmonary hypertension (PH) may arise from pulmonary vascular disease, including PAH or, less commonly, pulmonary veno-occlusive disease (group 1 PH); SSc-associated cardiac disease, including myocarditis, microvascular dysfunction, or accelerated coronary artery disease (group 2 PH); interstitial lung disease (group 3 PH); or, less frequently, chronic thromboembolic disease (group 4 PH). Similarly, DUs may result from microcirculatory failure or accelerated peripheral atherosclerotic disease. Defining the contribution of these overlapping mechanisms in individual patients is essential for interpreting and generalizing EV-related findings.

The unique characteristics of SSc among human diseases may provide broader insights into EV dynamics within the human circulatory system, potentially informing future research on other vascular and multiorgan diseases.

研究の種類

介入

入学 (推定)

60

段階

  • 適用できない

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

はい

説明

Inclusion Criteria:

Male and female patients aged 45-75 years Diagnosis of systemic sclerosis according to the 2013 ACR/EULAR classification criteria High risk of pulmonary arterial hypertension based on the DETECT algorithm Stable treatment with vasoactive, vasodilator, and immunosuppressive therapies for at least 3 months prior to blood sampling

Exclusion Criteria:

Previous diagnosis of pulmonary arterial hypertension confirmed by right heart catheterization Interstitial lung involvement affecting more than 10% of the lung parenchyma Left-sided heart failure (NYHA class 3-4) Evidence of chronic thromboembolic pulmonary disease on contrast-enhanced CT scan Major contraindications to right heart catheterization or coronary angiography Inability to provide informed consent

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

  • 主な目的:他の
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Diagnosis of systemic sclerosis according to the 2013 ACR/EULAR classification criteria.
  • Male and female patients aged 45-75 years.
  • Diagnosis of systemic sclerosis according to the 2013 ACR/EULAR classification criteria.
  • High risk of pulmonary arterial hypertension based on the DETECT algorithm.
  • Stable treatment with vasoactive, vasodilator, and immunosuppressive therapies for at least 3 months prior to blood sampling.
Blood collection during right heart catheterization

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
Transcardiopulmonary extracellular vesicle gradient
時間枠:Periprocedural (during right heart catheterization).

Arteriovenous differences between the pulmonary artery and the ascending aorta in extracellular vesicle characteristics, including particle concentration, size distribution, protein expression profile, and RNA expression profile.

Treatment failure in patients with pulmonary arterial hypertension at 24 weeks, defined as the occurrence of at least one of the following events: an improvement of less than 30 meters in the 6-minute walk distance (6MWD); a reduction in NT-proBNP of less than 30% in patients with baseline levels >300 pg/mL; worsening of World Health Organization (WHO) functional class; or death due to complications of pulmonary arterial hypertension.

Treatment failure in patients with recurrent digital ulcers, defined as the development of new digital ulcers or gangrene at sites previously affected by digital ulcers.

Periprocedural (during right heart catheterization).
Peripheral extracellular vesicle gradient
時間枠:Periprocedural.
Arteriovenous differences between the cephalic vein and the radial artery in extracellular vesicle characteristics, including particle concentration, size distribution, protein expression profile, and RNA expression profile.
Periprocedural.

二次結果の測定

結果測定
メジャーの説明
時間枠
Treatment failure in participants with pulmonary arterial hypertension.
時間枠:24 weeks.
Treatment failure, defined as the occurrence of at least one of the following: improvement in 6-minute walk distance of less than 30 meters; reduction in NT-proBNP of less than 30% in participants with baseline NT-proBNP >300 pg/mL; worsening of World Health Organization functional class; or death related to pulmonary arterial hypertension.
24 weeks.
Treatment failure in participants with recurrent digital ulcers.
時間枠:24 weeks.
Development of new digital ulcers or gangrene at sites previously affected by digital ulcers.
24 weeks.

協力者と研究者

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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 (推定)

2026年9月1日

一次修了 (推定)

2027年9月1日

研究の完了 (推定)

2028年9月1日

試験登録日

最初に提出

2026年7月9日

QC基準を満たした最初の提出物

2026年7月16日

最初の投稿 (実際)

2026年7月21日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月21日

QC基準を満たした最後の更新が送信されました

2026年7月16日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

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?

いいえ

IPD プランの説明

All data will be shared, excluding the patient's first and last name.

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いいえ

米国FDA規制機器製品の研究

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