Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jacbts.2019.07.008
Title: Seipin Knockout Mice Develop Heart Failure With Preserved Ejection Fraction
Authors: Bai, B.
Yang, W.
Fu, Y.
Foon, H.L.
Tay, W.T.
Yang, K.
Luo, C.
Gunaratne, J.
Lee, P.
Zile, M.R.
Xu, A.
Chin, C.W.L. 
Lam, C.S.P. 
Han, W.
Wang, Y.
Keywords: fibrosis
heart failure with preserved ejection fraction
neutrophil
seipin
titin
Issue Date: 2019
Publisher: Elsevier Inc
Citation: Bai, B., Yang, W., Fu, Y., Foon, H.L., Tay, W.T., Yang, K., Luo, C., Gunaratne, J., Lee, P., Zile, M.R., Xu, A., Chin, C.W.L., Lam, C.S.P., Han, W., Wang, Y. (2019). Seipin Knockout Mice Develop Heart Failure With Preserved Ejection Fraction. JACC: Basic to Translational Science 4 (8) : 924-937. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jacbts.2019.07.008
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: The lean diabetic patients with heart failure with preserved ejection fraction (HFpEF) in Asia suffer from adverse clinical outcomes and poor life quality. The suitable animal models are urgently needed for mechanistic study and therapeutic innovations. Our study reports that lipodystrophic mice with seipin depletion are lean, diabetic, and recapitulate major manifestations of clinical HFpEF, thereby clarifying that lean diabetes per se may produce HFpEF characteristics. We further demonstrate that increased cardiac titin phosphorylation and reactive interstitial fibrosis associated with neutrophil extracellular traps lead to left ventricular stiffness and suggest that both pathways may be potential therapeutic targets in Asian HFpEF patients. © 2019 The Authors
Source Title: JACC: Basic to Translational Science
URI: https://scholarbank.nus.edu.sg/handle/10635/206261
ISSN: 2452-302X
DOI: 10.1016/j.jacbts.2019.07.008
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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