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WEDNESDAY • MAY 18 393<br />

Objectives<br />

At the conclusion of this session, the participant will be able to:<br />

• learn about current deep-phenotyping of PH;<br />

• understand and learn pediatrics PH registry;<br />

• learn about the national biorepository of PH patient samples for PH research.<br />

Pulmonary hypertension (PH) currently has no cure, thus PH research remains a<br />

high priority for NHLBI. Recently, NHLBI launched several major multi-center<br />

clinical studies of PH including: Redefining Pulmonary Hypertension through<br />

Pulmonary Vascular Disease Phenomics (PVDOMICS); and Pulmonary<br />

Hypertension Breakthrough Initiative (PHBI), which will help us understand the<br />

molecular mechanisms of PH in adult patients, and provide phenotypic data and<br />

biomarkers for future clinical trials and measures of disease severity. Data Fusion:<br />

A Sustainable, Scalable, Open Source Registry Advancing PVD Research using a<br />

novel biomedical informatics approach will develop computable phenotypes of<br />

pediatric pulmonary vascular diseases. This session will introduce these programs<br />

and present data from these studies<br />

Chairing: L. Xiao, MD, PhD, Bethesda, MD<br />

C.J. Blaisdell, MD, Bethesda, MD<br />

12:15 NHLBI PVDOMICS <strong>Program</strong> Overview<br />

S.C. Erzurum, MD, Cleveland, OH<br />

12:25 PVDOMICS Study Design and Update<br />

J.H. Newman, MD, Nashville, TN<br />

12:35 Data Fusion: A Sustainable, Open Source Registry Advancing<br />

Pediatric Pulmonary Vascular Disease Research - Part I<br />

S.H. Abman, MD, Aurora, CO<br />

12:45 Data Fusion: A Sustainable, Open Source Registry Advancing<br />

Pediatric Pulmonary Vascular Disease Research - Part II<br />

K. Mandl, MD, MPH, Boston, MA<br />

12:55 Pulmonary Hypertension Breakthrough Initiative (PHBI) Update<br />

M. Geraci, MD, Indianapolis, IN<br />

1:05 National Biological Sample and Data Repository for Pulmonary<br />

Arterial Hypertension<br />

W. Nichols, PhD, Cincinnati, OH<br />

L27<br />

NATIONAL HEART, LUNG, AND BLOOD INSTITUTE,<br />

DIVISION OF LUNG DISEASES, NIH<br />

OXIDANT STRESS IN HIV-RELATED CHRONIC<br />

LUNG DISEASE<br />

12:15 p.m. - 1:15 p.m. MOSCONE CENTER<br />

Room 2016/2018 (West Building, Level 2)<br />

Target Audience<br />

Providers of lung health; medical fellows in training; graduate post-doctoral<br />

fellows; established scientists in basic research on lung biology, HIV<br />

pathogenesis and infection disease.<br />

Objectives<br />

At the conclusion of this session, the participant will be able to:<br />

• understand the role of oxidative stress in the onset of lung diseases<br />

associated with HIV infection in the HAART era;<br />

• improve target possibilities for treating lung inflammatory diseases such as<br />

pulmonary hypertension in HAART treated HIV patients;<br />

• learn new findings about the role of oxidative stress in the onset of lung<br />

complications in HIV (+) patients undergoing ART.<br />

HIV-infected patients on antiretroviral therapy (ART) have now a longer life<br />

expectancy, but as a consequence chronic diseases are increasingly becoming<br />

a major cause of morbidity and death. Many pulmonary conditions, including<br />

PAH, and COPD are more prevalent in HIV infected individuals under treatment<br />

but the mechanisms by which HIV and ART induce cellular dysfunction that may<br />

trigger these pathologies are largely unknown. One such pathway is oxidative<br />

stress (OS), which results from excessive free radical production, and<br />

exceeding endogenous antioxidant defense mechanisms, which can damage a<br />

wide variety of cellular components. The session will address current research<br />

and results in this area and will give an overview of current HIV research on the<br />

oxidative stress role in HIV infection. Presenters will delineate current<br />

knowledge of lung complications in relationship to OS, and describe latest<br />

results and techniques utilized in their projects.<br />

Chairing: H.L. Twigg, MD, Indianapolis, IN<br />

E. Caler, PhD, Bethesda, MD<br />

12:15 HIV Proteins and Pulmonary Hypertension<br />

S. Flores, PhD, Aurora, CO<br />

12:30 Oxidative Stress in HIV Associated COPD<br />

B.D. Medoff, MD, Boston, MA<br />

12:45 Redox Stress and Chronic Lung Disease in HIV<br />

J. Roman, MD, Louisville, KY<br />

1:00 HIV+ Alveolar Macrophage Oxidant-Mediated Apoptosis of<br />

Pulmonary Endothelium<br />

M.R. Staudt, PhD, New York, NY<br />

NATIONAL HEART, LUNG, AND BLOOD INSTITUTE,<br />

DIVISION OF LUNG DISEASES, NIH<br />

L28 NHLBI PETAL CLINICAL TRIAL NETWORK:<br />

PREVENTION AND EARLY TREATMENT OF ACUTE<br />

LUNG INJURY<br />

12:15 p.m. - 1:15 p.m. MOSCONE CENTER<br />

Room 2020/2022 (West Building, Level 2)<br />

Target Audience<br />

Practicing critical care and emergency medicine clinicians and clinical<br />

researchers would benefit from this session. This includes fellows, students,<br />

nurses, and other medical professionals. Persons interested in clinical trial<br />

design and conduct would also benefit from this session.<br />

Objectives<br />

At the conclusion of this session, the participant will be able to:<br />

• understand the goals and structure of the PETAL network<br />

• understand the questions being addressed in PETAL and outreach efforts of the<br />

network<br />

• have a better understanding of PETAL trial design and conduct including<br />

utilization of a central IRB<br />

WEDNESDAY MID-DAY<br />

ATS 2016 • San Francisco

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