Endoplasmic reticulum stress and expression of nitric oxide synthases in heart failure with preserved and with reduced ejection fraction - pilot study.

Karol Momot, Małgorzata Wojciechowska, Kamil Krauz, Katarzyna Czarzasta, Liana Puchalska, Maciej Zarębiński, Agnieszka Cudnoch-Jędrzejewska
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Abstract

Background: Unfolded Protein Response (UPR), endoplasmic reticulum (ER) stress, and inducible nitric oxide synthase (iNOS) overexpression have been found to influence heart failure with preserved ejection fraction (HFpEF) pathogenesis. Their importance in heart failure with reduced ejection fraction (HFrEF) is not entirely established; there is little data involving a detailed comparison between HFpEF and HFrEF from this perspective. This pilot study aimed to compare circulating levels of Glucose-regulated protein 78kDa (GRP78) (ER - stress marker) and all NOS isoforms between both HFpEF and HFrEF and to analyze the correlation between these markers and the clinical characteristics of the patients.

Methods: Forty-two patients with HFpEF and thirty-eight with HFrEF were involved in this study. Clinical characteristics and echocardiographic data were obtained. Basic laboratory tests were performed and ELISA tests for iNOS, endothelial NOS (eNOS), neuronal NOS (nNOS), and GRP78.

Results: Patients with HFpEF had lower circulating levels of GRP78 and higher iNOS concentrations when compared to HFrEF patients (P = 0.023, P < 0.0001, accordingly). The subgroup of the HFpEF population with eGFR < 60 mL/min/1.73m2 had higher nNOS and eNOS levels than HFpEF patients with normal GFR (P = 0.049, P = 0.035, respectively). In the HFrEF subgroup, patients with coexistent diabetes mellitus had elevated concentrations of nNOS compared to the subpopulation without diabetes mellitus (P = 0.041). There was a positive correlation between eNOS and nNOS concentrations (ρ = 0.86, P < 0.0001).

Conclusions: In HFpEF, there is a more intensified iNOS overexpression, while in HFrEF, ER stress is more prominent.

保留射血分数和减少射血分数的心力衰竭患者的内质网应激和一氧化氮合酶的表达--试点研究。
背景:已发现折叠蛋白反应(UPR)、内质网(ER)应激和诱导型一氧化氮合酶(iNOS)过表达会影响射血分数保留型心力衰竭(HFpEF)的发病机制。它们在射血分数减低型心力衰竭(HFrEF)中的重要性尚未完全确定;从这个角度对 HFpEF 和 HFrEF 进行详细比较的数据很少。这项试验性研究旨在比较 HFpEF 和 HFrEF 之间葡萄糖调节蛋白 78kDa (GRP78)(ER-应激标志物)和所有 NOS 同工酶的循环水平,并分析这些标志物与患者临床特征之间的相关性:本研究涉及 42 名 HFpEF 患者和 38 名 HFrEF 患者。方法:42 名高频低氧血症患者和 38 名高频低氧血症患者参与了这项研究,并获得了临床特征和超声心动图数据。进行了基本实验室检测,并对 iNOS、内皮 NOS(eNOS)、神经元 NOS(nNOS)和 GRP78 进行了 ELISA 检测:与 HFrEF 患者相比,HFpEF 患者循环中的 GRP78 水平较低,iNOS 浓度较高(P = 0.023,P < 0.0001)。与 GFR 正常的 HFpEF 患者相比,eGFR < 60 mL/min/1.73m2 的 HFpEF 亚组的 nNOS 和 eNOS 水平更高(分别为 P = 0.049 和 P = 0.035)。在 HFrEF 亚组中,与无糖尿病的亚组相比,合并糖尿病的患者 nNOS 浓度更高(P = 0.041)。eNOS和nNOS浓度之间呈正相关(ρ = 0.86,P < 0.0001):结论:在高频前房颤中,iNOS过度表达更为严重,而在高频后房颤中,ER应激更为突出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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