TY - JOUR
T1 - Experimental Models of Hypertrophic Cardiomyopathy
T2 - A Systematic Review
AU - van den Dolder, Floor W.
AU - Dinani, Rafeeh
AU - Warnaar, Vincent A. J.
AU - Vučković, Sofija
AU - Passadouro, Adriana S.
AU - Nassar, Ali A.
AU - Ramsaroep, Azhaar X.
AU - Burchell, George B.
AU - Schoonmade, Linda J.
AU - van der Velden, Jolanda
AU - Goversen, Birgit
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/4/1
Y1 - 2025/4/1
N2 - To advance research in hypertrophic cardiomyopathy (HCM), and guide researchers in choosing the optimal model to answer their research questions, we performed a systematic review of all models investigating HCM induced by gene variants ranging from animal models to human induced pluripotent stem cell–derived cardiomyocytes (hiPSC-CMs). Our research question entailed: which experimental models of HCM have been created thus far, and which major hallmarks of HCM do they present? Out of the 603 included papers, the majority included animal models, though a clear transition to hiPSC-CM is visible since 2010. Our review showed that only 36 mouse models showed minimal 4 out of 6 HCM disease markers (cell/cardiac hypertrophy, disarray, fibrosis, diastolic dysfunction, and arrhythmias), while only 17 hiPSC-CM models showed 3 out of 4 HCM cell characteristics. Our review emphasizes the need to better report data on sample size, sex, age, and relevant disease-specific characteristics.
AB - To advance research in hypertrophic cardiomyopathy (HCM), and guide researchers in choosing the optimal model to answer their research questions, we performed a systematic review of all models investigating HCM induced by gene variants ranging from animal models to human induced pluripotent stem cell–derived cardiomyocytes (hiPSC-CMs). Our research question entailed: which experimental models of HCM have been created thus far, and which major hallmarks of HCM do they present? Out of the 603 included papers, the majority included animal models, though a clear transition to hiPSC-CM is visible since 2010. Our review showed that only 36 mouse models showed minimal 4 out of 6 HCM disease markers (cell/cardiac hypertrophy, disarray, fibrosis, diastolic dysfunction, and arrhythmias), while only 17 hiPSC-CM models showed 3 out of 4 HCM cell characteristics. Our review emphasizes the need to better report data on sample size, sex, age, and relevant disease-specific characteristics.
KW - animal models
KW - human iPSC-derived cardiomyocytes
KW - hypertrophic cardiomyopathy
KW - stem cells
KW - systematic review
UR - https://www.scopus.com/pages/publications/105002582384
U2 - 10.1016/j.jacbts.2024.10.017
DO - 10.1016/j.jacbts.2024.10.017
M3 - Review article
C2 - 40306862
SN - 2452-302X
VL - 10
SP - 511
EP - 546
JO - JACC. Basic to translational science
JF - JACC. Basic to translational science
IS - 4
ER -