Karolinska Institutet, Department of Medicine, Cardiology unit, Stockholm, Sweden.
Translational Science and Experimental Medicine; Research and early Development, Cardiovascular, Renal and Metabolism, Biopharmaceutical R&D, AstraZeneca, Gothenburg, Sweden.
J Card Fail. 2020 Dec;26(12):1050-1059. doi: 10.1016/j.cardfail.2020.07.010. Epub 2020 Aug 1.
Heart failure with preserved ejection fraction (HFpEF) and HF with reduced ejection fraction (HFrEF) are associated with metabolic derangements, which may have different pathophysiological implications.
In new-onset HFpEF (EF of ≥50%, n = 46) and HFrEF (EF of <40%, n = 75) patients, 109 endogenous plasma metabolites including amino acids, phospholipids and acylcarnitines were assessed using targeted metabolomics. Differentially altered metabolites and associations with clinical characteristics were explored. Patients with HFpEF were older, more often female with hypertension, atrial fibrillation, and diabetes compared with patients with HFrEF. Patients with HFpEF displayed higher levels of hydroxyproline and symmetric dimethyl arginine, alanine, cystine, and kynurenine reflecting fibrosis, inflammation and oxidative stress. Serine, cGMP, cAMP, l-carnitine, lysophophatidylcholine (18:2), lactate, and arginine were lower compared with patients with HFrEF. In patients with HFpEF with diabetes, kynurenine was higher (P = .014) and arginine lower (P = .014) vs patients with no diabetes, but did not differ with diabetes status in HFrEF. Decreasing kynurenine was associated with higher eGFR only in HFpEF (P = .020).
Patients with new-onset HFpEF compared with patients with new-onset HFrEF display a different metabolic profile associated with comorbidities, such as diabetes and kidney dysfunction. HFpEF is associated with indices of increased inflammation and oxidative stress, impaired lipid metabolism, increased collagen synthesis, and downregulated nitric oxide signaling. Together, these findings suggest a more predominant systemic microvascular endothelial dysfunction and inflammation linked to increased fibrosis in HFpEF compared with HFrEF.
ClinicalTrials.gov NCT03671122 https://clinicaltrials.gov.
射血分数保留的心力衰竭(HFpEF)和射血分数降低的心力衰竭(HFrEF)与代谢紊乱有关,这些紊乱可能具有不同的病理生理意义。
在新发 HFpEF(EF≥50%,n=46)和 HFrEF(EF<40%,n=75)患者中,使用靶向代谢组学评估了 109 种内源性血浆代谢物,包括氨基酸、磷脂和酰基辅酶 A。探讨了差异改变的代谢物与临床特征的关系。与 HFrEF 患者相比,HFpEF 患者年龄较大,女性更多,患有高血压、心房颤动和糖尿病。HFpEF 患者的羟基脯氨酸和对称二甲基精氨酸、丙氨酸、半胱氨酸和犬尿氨酸水平较高,反映了纤维化、炎症和氧化应激。与 HFrEF 患者相比,丝氨酸、cGMP、cAMP、左旋肉碱、溶血磷脂酰胆碱(18:2)、乳酸和精氨酸水平较低。在伴有糖尿病的 HFpEF 患者中,犬尿氨酸水平较高(P=0.014),精氨酸水平较低(P=0.014),而在 HFrEF 患者中,犬尿氨酸水平与糖尿病状态无关。在 HFpEF 中,降低的犬尿氨酸与更高的 eGFR 相关(P=0.020)。
与新发 HFrEF 患者相比,新发 HFpEF 患者的代谢谱不同,与合并症相关,如糖尿病和肾功能障碍。HFpEF 与炎症和氧化应激增加、脂质代谢受损、胶原蛋白合成增加和一氧化氮信号下调相关。总的来说,这些发现表明,与 HFrEF 相比,HFpEF 中更主要的全身微血管内皮功能障碍和炎症与纤维化增加有关。
ClinicalTrials.gov NCT03671122 https://clinicaltrials.gov.