Abstract 15077: Mitochondrial LonP1 Upregulation in End Stage Heart Failure

Abstract only Introduction: Mitochondrial dysfunction is a hallmark of heart failure (HF), where correct mitochondrial proteins’ folding is challenged under mitochondrial stress. To restore mitochondrial proteostasis and homeostasis, the mitochondrial unfolded protein response (UPR mt ) is activated...

Full description

Saved in:
Bibliographic Details
Published inCirculation (New York, N.Y.) Vol. 148; no. Suppl_1
Main Authors Soliman, Saifullah, Ibrahim, Ayman Maher M, Wagdy, Dr. Kerolos, Selwanos, Peter, Khedr, Hadir, MOSTAFA MOSTAFA, SABER, Shah, Ajay M, Yacoub, Magdi, Aguib, Yasmine
Format Journal Article
LanguageEnglish
Published 07.11.2023
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract only Introduction: Mitochondrial dysfunction is a hallmark of heart failure (HF), where correct mitochondrial proteins’ folding is challenged under mitochondrial stress. To restore mitochondrial proteostasis and homeostasis, the mitochondrial unfolded protein response (UPR mt ) is activated, a mechanism not fully elucidated in HF. Purpose: We here investigate the UPR mt induction in advanced/end-stage HF patients requiring Left Ventricular Assist Device (LVAD). In addition, we analyzed the potential influence on clinical outcome. Methods: RNA was extracted from 44 Left Ventricular discs excised during implantation of LVAD from end-stage HF patients and from 5 control LV tissues. Quantitative PCR was performed to assess the relative expression levels of UPR mt machinery ( ATF5, CHOP, mtDNAj, HSP60/10, CLpP and LonP1 ). Immunoblotting was performed to validate mRNA levels. LonP1 subgrouping was performed in reference to LVAD patients’ 3 rd quartile of pre-LVAD Lonp1 mRNA levels. The primary outcome for the Kaplan-Meier survival analysis was all-cause mortality post-LVAD intervention. Results: Gene expression analysis revealed a significant increase in mRNA levels of CHOP and LonP1. Immunoblotting validated the upregulation of CHOP & LonP1 in end-stage HF tissue in comparison to controls. In High-LonP1 patients, we observed a significant increase in left ventricular ejection fraction and blood sodium levels while serum levels of ST-2 and blood urea levels were significantly decreased. High-LonP1 patients had a significantly higher probability of survival post-LVAD intervention and potential to recover myocardial function. Conclusion: This study suggests LonP1 as a potential marker of myocardial recovery and clinical outcome in end-stage heart failure patients treated by LVADs.
ISSN:0009-7322
1524-4539
DOI:10.1161/circ.148.suppl_1.15077