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The Foundation Announces Largest Research Grant in Its History

The Marfan Foundation has awarded its largest research grant in history, the Everest Award, as well as $600,000 in other new grants to physicians/scientists as part of its Research Grant program, bringing current total grant funding to $1,285,500. 

“Research funding from the Foundation has provided critical seed money to established scientists and has successfully enhanced the pipeline of researchers who are interested in genetic aortic and vascular conditions,” said Craig T Basson, MD, PhD, Chair of the Foundation’s Scientific Advisory Board. “We are now at a crucial juncture where we can more strategically focus on transformational science and aim for cures for these conditions. The Everest Award was designed to promote longer, multidisciplinary, collaborative grants that will help us reach these goals.”

The Everest Award is the largest grant mechanism initiated by the Foundation. It can provide up to four years of funding for a total of $880,000 if yearly milestone goals are met.

First Everest Award Recipient

The Foundation presented the Everest Award, to Joseph W. Turek, MD, Ph.D., MBA, an academic pediatric cardiac surgeon at Duke University. Since 2017, Dr. Turek has served as chief of pediatric cardiac surgery and executive co-director of Duke Children’s Pediatric and Congenital Heart Center.

The Foundation awarded his project, TRPC4/ATR1 Dual Antagonism Blocks Marfan Aortopathy, $220,000 for one year. There is an opportunity for additional years of funding based on annual milestone reviews by the Foundation’s Scientific Advisory Board.  

Current medical therapies slow the rate of aortic growth in people with Marfan syndrome, but they do not eliminate the need for surgery. In preliminary work, Dr. Turek and his team demonstrated that a novel pathway is involved in aneurysm formation in people with Marfan. In animal studies, when a critical protein in this pathway is blocked with medication, these aneurysms do not form. Moreover, this critical protein is found in abundance in the aorta of people with Marfan who require surgery, underscoring its relevance to aneurysm formation.

The Marfan Foundation Everest Grant will allow Dr. Turek and his team to characterize this pathway, discover drugs that can effectively block critical protein-preventing aneurysms, and identify biomarkers found in the blood that can evaluate the effectiveness of the drug. Ultimately, Dr. Turek hopes this results in better medical treatment for this devastating complication of Marfan and that people with Marfan can one day avoid surgery altogether.

Additional New Grant Recipients

Career Development Award – $100,000

Marie Billaud, Ph.D., Brigham and Women’s Hospital

Mitochondria – ECM crosstalk in aortic SMCs of Marfan Patients

Career Development Award – $100,000

Jefferson Doyle, MBBChir, Ph.D., Johns Hopkins University

Treatment of Axial Myopia in Marfan Syndrome using Prostaglandin Analogs

Innovators Award – $100,000

Delphine Gomez, Ph.D., University of Pittsburgh

Alteration of H34Kme2 in Marfan syndrome: A driver of aortic dilation

Innovators Award – $100,000

Bart Loeys, MD, Ph.D., University of Antwerp

Exploration of a novel biomarker for thoracic aortic aneurysms and dissections

Innovators Award – $100,000

Enid Neptune, MD, Johns Hopkins University

Defining Alveolar Epithelial Phenotype in Marfan Lung Disease

Victor McKusick Fellowship Award – $100,000

Josephina Meester, Ph.D.; Bart Loeys, MD, Mentor, University of Antwerp

Pathomechanistic Study of Biglycan Mutations in Aortopathy Development

To support research and progress on Marfan, LDS, and VEDS, please click here.

Watch an announcement about the Everest Award from the Foundation’s Chief Science Officer Josephine Grima, Ph.D.:


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The Marfan Foundation is a nonprofit organization that saves lives and improves the quality of life of individuals with genetic aortic and vascular conditions including Marfan, Loeys-Dietz, and Vascular Ehlers-Danlos syndromes. Our vision is a world in which everyone with genetic aortic and vascular conditions can live their best life.


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