TY - JOUR
T1 - Unraveling the Mechanisms of Valvular Heart Disease to Identify Medical Therapy Targets
T2 - A Scientific Statement from the American Heart Association
AU - Small, Aeron M.
AU - Yutzey, Katherine E.
AU - Binstadt, Bryce A.
AU - Voigts Key, Kaitlin
AU - Bouatia-Naji, Nabila
AU - Milan, David
AU - Aikawa, Elena
AU - Otto, Catherine M.
AU - St. Hilaire, Cynthia
N1 - Publisher Copyright:
© 2024 American Heart Association, Inc.
PY - 2024/8/6
Y1 - 2024/8/6
N2 - Valvular heart disease is a common cause of morbidity and mortality worldwide and has no effective medical therapy. Severe disease is managed with valve replacement procedures, which entail high health care-related costs and postprocedural morbidity and mortality. Robust ongoing research programs have elucidated many important molecular pathways contributing to primary valvular heart disease. However, there remain several key challenges inherent in translating research on valvular heart disease to viable molecular targets that can progress through the clinical trials pathway and effectively prevent or modify the course of these common conditions. In this scientific statement, we review the basic cellular structures of the human heart valves and discuss how these structures change in primary valvular heart disease. We focus on the most common primary valvular heart diseases, including calcific aortic stenosis, bicuspid aortic valves, mitral valve prolapse, and rheumatic heart disease, and outline the fundamental molecular discoveries contributing to each. We further outline potential therapeutic molecular targets for primary valvular heart disease and discuss key knowledge gaps that might serve as future research priorities.
AB - Valvular heart disease is a common cause of morbidity and mortality worldwide and has no effective medical therapy. Severe disease is managed with valve replacement procedures, which entail high health care-related costs and postprocedural morbidity and mortality. Robust ongoing research programs have elucidated many important molecular pathways contributing to primary valvular heart disease. However, there remain several key challenges inherent in translating research on valvular heart disease to viable molecular targets that can progress through the clinical trials pathway and effectively prevent or modify the course of these common conditions. In this scientific statement, we review the basic cellular structures of the human heart valves and discuss how these structures change in primary valvular heart disease. We focus on the most common primary valvular heart diseases, including calcific aortic stenosis, bicuspid aortic valves, mitral valve prolapse, and rheumatic heart disease, and outline the fundamental molecular discoveries contributing to each. We further outline potential therapeutic molecular targets for primary valvular heart disease and discuss key knowledge gaps that might serve as future research priorities.
KW - AHA Scientific Statements
KW - aortic valve stenosis
KW - bicuspid aortic valve disease
KW - cellular structures
KW - heart valve diseases
KW - mitral valve prolapse
KW - rheumatic heart disease
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U2 - 10.1161/cir.0000000000001254
DO - 10.1161/cir.0000000000001254
M3 - Review article
C2 - 38881493
AN - SCOPUS:85200746490
SN - 0009-7322
VL - 150
SP - e109-e128
JO - Circulation
JF - Circulation
IS - 6
ER -