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临床试验/NCT03901534
NCT03901534终止不适用

Assessment of Continuous Positive Airway Pressure Therapy in OSA and ILD

Columbia University4 个研究点 分布在 1 个国家目标入组 2,021 人开始时间: 2023年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
2,021
试验地点
4
主要终点
Surfactant Protein D (SP-D) [Aim 1]

研究概览

简要总结

The purpose of this study is to evaluate whether biomarkers of lung epithelial and endothelial injury are associated with obstructive sleep apnea (OSA) and interstitial lung disease (ILD).

详细描述

This study is comprised of 3 aims:

Aim 1: Determine whether the greater OSA severity is associated with higher levels of serum biomarkers of AEC and endothelial injury and ECM remodeling in community-dwelling adults. This is a retrospective study that will analyze biospecimens from those who participated in the MESA sleep study [Chen et al].

Aim 2: Determine whether CPAP use is associated with reductions in alveolar epithelial cell (AEC) injury and endothelial injury, and extracellular matrix (ECM) remodeling biomarkers in adults with moderate-to-severe OSA. This is a retrospective study that will analyze biospecimens from those who participated in either the HeartBEAT [Gottlieb et al] and BestAIR [Bakker et al] studies.

Revised Aim 3: a) Determine whether untreated OSA promotes AEC and endothelial injury and ECM remodeling biomarkers in adults with ILD and OSA compared with those without OSA; b) Determine prospectively whether clinically-initiated 4-week PAP therapy increases markers of alveolar endothelial lung injury in OSA. Participants will be recruited at Columbia University and be assigned CPAP therapy as an intervention.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

盲法说明

None (Open Label)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Surfactant Protein D (SP-D) [Aim 1]

时间窗: 1 day

SP-D is a marker of alveolar epithelial cell injury. This Outcome is specific to Aim 1 and will only be measured on participants in the Aim 1 phase of the study.

E-selectin [Aim 1]

时间窗: 1 day

This Outcome is specific to Aim 1 and will only be measured on participants in the Aim 1 phase of the study.

Angiopoietin-2 [Aim 1]

时间窗: 1 day

This Outcome is specific to Aim 1 and will only be measured on participants in the Aim 1 phase of the study.

Vascular Endothelial Growth Factor-A (VEGF-A) [Aim 1]

时间窗: 1 day

This Outcome is specific to Aim 1 and will only be measured on participants in the Aim 1 phase of the study.

Angiopoietin-interacting Soluble Tie-2 (sTie2) [Aim 1]

时间窗: 1 day

This Outcome is specific to Aim 1 and will only be measured on participants in the Aim 1 phase of the study.

Change in Serum Matrix Metalloproteinase-7 (MMP-7) Following CPAP [Aim 2]

时间窗: Baseline and post-CPAP follow-up, up to 24 Weeks

The differences between-arms in the longitudinal changes of MMP-7 will be measured. For the purpose of this analysis, all individuals receiving active CPAP in the experimental arm will be compared to all individuals receiving sham CPAP device in the control arm. This Outcome is specific to Aim 2 and will only be measured on participants in the Aim 2 phase of the study.

Change in Serum Surfactant Protein-D (SP-D) Following CPAP [Aim 2]

时间窗: Baseline and post-CPAP follow-up, up to 24 Weeks

The between-arm difference in the longitudinal changes of SP-D will be measured. For the purpose of this analysis, all individuals receiving active CPAP in the experimental arm will be compared to all individuals receiving sham CPAP device in the control arm. This Outcome is specific to Aim 2 and will only be measured on participants in the Aim 2 phase of the study.

Change in Serum Angiopoietin-2 (Ang-2) Following CPAP [Aim 2]

时间窗: Baseline and post-CPAP follow-up, up to 24 Weeks

The between-arm difference in the longitudinal changes of Ang-2 will be measured. For the purpose of this analysis, all individuals receiving active CPAP in the experimental arm will be compared to all individuals receiving sham CPAP device in the control arm. This Outcome is specific to Aim 2 and will only be measured on participants in the Aim 2 phase of the study.

Change in Serum Osteopontin Following CPAP [Aim 2]

时间窗: Baseline and post-CPAP follow-up, up to 24 Weeks

The differences between-arms in the longitudinal changes of Osteopontin will be measured. For the purpose of this analysis, all individuals receiving active CPAP in the experimental arm will be compared to all individuals receiving sham CPAP device in the control arm. This Outcome is specific to Aim 2 and will only be measured on participants in the Aim 2 phase of the study.

Serum Angiopoietin-2 (Ang-2, ng/mL) [Aim 3a]

时间窗: Baseline and 4 weeks

Participants will be treated with CPAP for 4 weeks. Serum Ang-2 levels will be measured at baseline and after CPAP therapy. This Outcome is specific to Aim 3a and will only be measured on participants in the Aim 3a phase of the study.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sanja Jelic

Associate Professor of Medicine

Columbia University

研究点 (4)

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