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心力衰竭伴射血分数保留患者的合成代谢激素缺乏:患病率及其对抗氧化剂水平和心肌功能障碍的影响。

Anabolic Hormones Deficiencies in Heart Failure With Preserved Ejection Fraction: Prevalence and Impact on Antioxidants Levels and Myocardial Dysfunction.

机构信息

Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome, Italy.

Fondazione Policlinico Universitario a Gemelli IRCCS, Rome, Italy.

出版信息

Front Endocrinol (Lausanne). 2020 May 12;11:281. doi: 10.3389/fendo.2020.00281. eCollection 2020.

DOI:10.3389/fendo.2020.00281
PMID:32477267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7235369/
Abstract

In heart failure with reduced ejection fraction, catabolic mechanisms have a strong negative impact on mortality and morbidity. The relationship between anabolic hormonal deficiency and heart failure with preserved ejection fraction (HFpEF) has still been poorly investigated. On the other hand, oxidative stress is recognized as a player in the pathogenesis of HFpEF. Therefore, we performed a cohort study in HFpEF aimed to (1) define the multi-hormonal deficiency prevalence in HFpEF patients; (2) investigate the relationships between hormonal deficiencies and echocardiographic indexes; (3) explore the modulatory activity of anabolic hormones on antioxidant systems. 84 patients with diagnosis of HFpEF were enrolled in the study. Plasma levels of N-terminal pro-brain natriuretic peptide, fasting glucose, insulin, lipid pattern, insulin-like growth factor-1, dehydroepiandrosterone-sulfate (DHEA-S), total testosterone (T, only in male subjects) were evaluated. Hormonal deficiencies were defined according to T.O.S.C.A. multi-centric study, as previously published. An echocardiographic evaluation was performed. Plasma total antioxidant capacity (TAC) was measured using the system metmyoglobin -HO and the chromogen ABTS, whose radical form is spectroscopically revealed; latency time (LAG) in the appearance of ABTS• is proportional to antioxidants in sample. Multiple deficiencies were discovered. DHEA-S deficiency in 87% of patients, IGF-1 in 67% of patients, T in 42%. Patients with DHEA-S deficiency showed lower levels of TAC expressed by LAG (mean ± SEM 91.25 ± 9.34 vs. 75.22 ± 4.38 s; < 0.05). No differences between TAC in patients with or without IGF-1 deficiency were found. A trend toward high level of TAC in patients without hormonal deficiencies compared with patients with one or multiple deficiencies was found. Regarding echocardiographic parameters, Left Atrial and Left Atrial Volume Index were significantly higher in patients with low IGF-1 values (mean ± SD 90.84 ± 3.86 vs. 72.83 ± 3.78 mL; 51.03 ± 2.33 vs. 40.56 ± 2.46 mL/m, respectively; < 0.05). Our study showed high prevalence of anabolic deficiencies in HFpEF. DHEA-S seems to influence antioxidant levels; IGF-1 deficiency was associated with alteration in parameters of myocardial structure and dysfunction. These data suggest a role of anabolic hormones in the complex pathophysiological mechanisms of HFpEF and could represent the basis for longitudinal studies and investigations on possible benefits of replacement therapy.

摘要

在射血分数降低的心力衰竭中,分解代谢机制对死亡率和发病率有很强的负面影响。激素缺乏与射血分数保留的心力衰竭(HFpEF)之间的关系仍未得到充分研究。另一方面,氧化应激被认为是 HFpEF 发病机制中的一个因素。因此,我们在 HFpEF 患者中进行了一项队列研究,旨在:(1) 确定 HFpEF 患者多激素缺乏的患病率;(2) 研究激素缺乏与超声心动图指标之间的关系;(3) 探讨合成激素对抗氧化系统的调节作用。

研究纳入了 84 例 HFpEF 患者。评估了血浆 N 端脑钠肽前体、空腹血糖、胰岛素、血脂谱、胰岛素样生长因子-1、硫酸脱氢表雄酮(DHEA-S)、总睾酮(仅在男性中)水平。根据 T.O.S.C.A. 多中心研究,按照先前发表的标准,定义了激素缺乏。进行了超声心动图评估。使用 metmyoglobin -HO 和显色剂 ABTS 系统测量血浆总抗氧化能力 (TAC),ABTS•的自由基形式通过光谱法揭示;ABTS•出现的潜伏期 (LAG) 与样品中的抗氧化剂成正比。

发现了多种缺乏。87%的患者存在 DHEA-S 缺乏,67%的患者存在 IGF-1 缺乏,42%的患者存在 T 缺乏。DHEA-S 缺乏的患者表现出 TAC 水平降低,LAG 延长(平均值±SEM 91.25±9.34 vs. 75.22±4.38 s;<0.05)。IGF-1 缺乏患者的 TAC 无差异。与存在一种或多种激素缺乏的患者相比,无激素缺乏的患者 TAC 水平较高。关于超声心动图参数,低 IGF-1 值患者的左心房和左心房容积指数显著升高(平均值±SD 90.84±3.86 vs. 72.83±3.78 mL;51.03±2.33 vs. 40.56±2.46 mL/m;均<0.05)。

我们的研究表明,HFpEF 中存在较高的合成代谢缺乏患病率。DHEA-S 似乎影响抗氧化水平;IGF-1 缺乏与心肌结构和功能障碍参数的改变有关。这些数据表明,合成激素在 HFpEF 的复杂病理生理机制中发挥作用,并可能为替代治疗的纵向研究和调查提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/7235369/2139067a4661/fendo-11-00281-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/7235369/7023305d9dbb/fendo-11-00281-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/7235369/7c3b8b2b5094/fendo-11-00281-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/7235369/2139067a4661/fendo-11-00281-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/7235369/7023305d9dbb/fendo-11-00281-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/7235369/7c3b8b2b5094/fendo-11-00281-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/7235369/2139067a4661/fendo-11-00281-g0003.jpg

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