Characterizing HIV-related Diastolic Dysfunction: A Cross Sectional Study Leveraging the NHLBI Heart Failure Clinical Research Network
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 195
- 试验地点
- 12
- 主要终点
- immune activation between HIV+/DD- and HIV+/DD+ subjects
研究概览
简要总结
This is a multicenter clinical trial of a cross section of HIV+ patients with and without diastolic dysfunction. Approximately 200 HAART-treated virally suppressed HIV+ subjects (100 HIV+/DD+ & 100 HIV+/DD-) will be enrolled. This study will evaluate biomarkers, phenomapping, metabolomics, cMRI, echocardiography to determine characteristics unique to this patient population.
详细描述
With the advent of highly active antiretroviral therapy (HAART), human immuno¬deficiency virus (HIV) type 1 infection has become a chronic disease. The proportion of patients expected to survive 5, 10, and 15 years after conversion in the HAART era are 99%, 93% and 89% respectively. With increased life expectancy and decreased morbidity from opportunistic infections, the importance of chronic complications associated with HIV-1 infection, including HF is becoming more evident. The advent of HAART has altered the epidemiology of HIV associated cardiomyopathy evolving from a primarily left ventricular systolic dysfunction to the growing recognition of left ventricular DD. DD is associated with the development of atrial fibrillation and heart failure (HF), and portends higher risk for all-cause mortality. Thus there is a widespread prevalence of cardiac abnormalities in HIV infected individuals that are associated with HF development and may represent a sub-clinical abnormality that may be potentially intervened upon to reduce the risk of subsequent HF. There are little data to understand the natural history and pathogenesis of cardiac abnormalities, specifically DD in HIV+ individuals, which may adversely affect the longevity and quality of life of these individuals.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 40 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age >40 years
- •Willingness and ability to provide informed consent
- •HIV antibody positive
- •On HAART for >6 months (HIV positive cohort only)
- •History of adequate viral suppression as defined by HIV RNA level <200 copies/mL in the past 6 months
- •LVEF >50% -
排除标准
- •Past EF <50%
- •Moderate or severe valve stenosis or regurgitation, or past repair or replacement
- •Percutaneous or surgical revascularization or active angina
- •Persistent atrial fibrillation
- •BP>160mmHg SBP or >100mmHg DBP
- •Comorbid inflammatory disease (e.g. RA or SLE)
- •Active cancer or cancer chemotherapy treatment in the prior year (except skin cancer that did not require chemotherapy or radiation)
- •Chronic use of steroids or anti-inflammatory therapy
- •GFR <30 mL/min
- •Active in a clinical trial with investigational product
- •Pregnant or lactating females
- •Contraindication to cMR or gadolinium injection (such as severe claustrophobia, metal implants, etc.)
结局指标
主要结局
immune activation between HIV+/DD- and HIV+/DD+ subjects
时间窗: baseline visit
Compare immune activation between HIV+/DD- and HIV+/DD+ subjects.
the effect of DD on mechanics of the left atrium in HIV
时间窗: baseline visit
To study the effect of DD on mechanics using left atrial strain during passive leg raise
Perform phenomics of aggregate imaging data to define risk factor phenotype signatures and relate these to HIV+/DD- and HIV+/DD+ subjects
时间窗: baseline visit
imaging data
Perform phenomics of aggregate demographic data to define risk factor phenotype signatures and relate these to HIV+/DD- and HIV+/DD+ subjects
时间窗: baseline visit
inflammation between HIV+/DD- and HIV+/DD+ subjects
时间窗: baseline visit
To compare inflammation between HIV+/DD- and HIV+/DD+
novel mechanisms underlying DD in HIV+ subjects as measured by proteomic and metabolomics panels
时间窗: baseline visit
To study the proteomic and metabolomics panels to enable identification of novel mechanisms underlying DD in HIV+ subjects
persistent inflammation between HIV+/DD- and HIV+/DD+ subjects
时间窗: baseline visit
Compare inflammation between HIV+/DD- and HIV+/DD+ subjects.
myocardial fibrosis by magnetic resonance imaging between HIV+/DD- and HIV+/DD+
时间窗: baseline visit
To compare myocardial fibrosis by magnetic resonance imaging between HIV+/DD- and HIV+/DD+
serum levels of biomarkers
时间窗: baseline visit
To identify systemic determinants (biomarkers) of DD in HIV+ persons
Perform phenomics of aggregate clinical data to define risk factor phenotype signatures and relate these to HIV+/DD- and HIV+/DD+ subjects
时间窗: baseline visit
Clinical data
Perform phenomics of aggregate biomarker data to define risk factor phenotype signatures and relate these to HIV+/DD- and HIV+/DD+ subjects
时间窗: baseline visit
Biomarker data
sub-clinical necrosis in HIV+/DD+ subjects
时间窗: baseline visit
To study the sub-clinical necrosis using Troponin levels in HIV+/DD+ subjects
myocardial stress in HIV+/DD+ subjects
时间窗: baseline visit
To study myocardial stress using NTProBNP levels in HIV+/DD+ subjects
Perform phenomics of aggregate electrocardiogram data to define risk factor phenotype signatures and relate these to HIV+/DD- and HIV+/DD+ subjects
时间窗: baseline visit
electrocardiogram data
次要结局
未报告次要终点