Exhaled breath acetone: a non-invasive marker of disease severity across the spectrum of heart failure.

IF 2.7 4区 医学 Q1 BIOCHEMICAL RESEARCH METHODS
Nicolò De Biase, Silvia Ghimenti, Lavinia Del Punta, Denise Biagini, Alessio Lenzi, Fabio Di Francesco, Stefano Taddei, Pierpaolo Pellicori, Stefano Masi, Tommaso Lomonaco, Nicola Riccardo Pugliese
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Abstract

Background.Increased exhaled breath acetone (EBA) concentrations might reflect impaired myocardial energetics and haemodynamic stress. We investigated the relation of EBA and cardiac structure, function, and exercise capacity in patients with or at risk of heart failure (HF).Methods.We enrolled outpatients with HF and reduced (<50%, HFrEF) or preserved (>50%, HFpEF) left ventricular ejection fraction (LVEF) and subjects with cardiovascular risk factors and/or structural heart disease without established HF. All participants underwent clinical and laboratory evaluation, resting transthoracic echocardiography, and a combined cardiopulmonary-echocardiographic stress test with EBA monitoring at rest (EBArest) and during exercise (EBAex).Results.Patients with HFpEF (n= 62) were older and more often female than those at risk of HF (n= 50) or with HFrEF (n= 41). EBArest(1.5, interquartile range (IQR) 1.0-3.1 vs 0.9, IQR 0.7-1.2 mcg l-1) and EBAex(2.4, IQR 1.5-4.4 vs 1.1, IQR 0.9-2.1 mcg l-1; allp< 0.0001) were significantly higher in patients with HF compared to others. Among HF patients, those in the highest EBAresttertile had lower LVEF, greater echocardiographic signs of congestion, higher NT-proBNP levels, and lower peak oxygen consumption, indicating impaired exercise capacity. In multivariate regression, NT-proBNP (p= 0.0004) and the slope of minute ventilation to carbon dioxide production (p= 0.0013) were independent predictors of EBArest(adjustedR2= 0.458).Conclusions.EBA concentrations are higher in patients with HF compared to those without, regardless of LVEF, and are associated with markers of disease severity. Further studies are needed to determine whether EBA measurement can aid in HF diagnosis and management.

呼气丙酮:一种非侵入性心力衰竭疾病严重程度的标志物。
背景:呼气丙酮(EBA)浓度升高可能反映心肌能量和血流动力学应激受损。我们研究了心力衰竭(HF)患者或有心力衰竭风险的患者EBA与心脏结构、功能和运动能力的关系。方法:我们招募了心力衰竭和左心室射血分数(LVEF)降低(50%,HFpEF)的门诊患者,以及有心血管危险因素和/或没有确定心力衰竭的结构性心脏病的患者。所有参与者都进行了临床和实验室评估,静息时经胸超声心动图,以及在静息(earest)和运动(EBAex)时监测EBA的心肺-超声心动图联合应激试验。结果:HFpEF患者(n=62)比HF (n=50)或HFrEF (n=41)患者年龄更大,女性更多。ebaest(1.5,四分位数范围[IQR] 1.0-3.1 vs 0.9, IQR 0.7-1.2 mcg/L)和EBAex (2.4, IQR 1.5-4.4 vs 1.1, IQR 0.9-2.1 mcg/L);均p结论:无论LVEF如何,HF患者的EBA浓度高于无HF患者,且与疾病严重程度标志物相关。需要进一步的研究来确定EBA测量是否有助于HF的诊断和治疗。
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来源期刊
Journal of breath research
Journal of breath research BIOCHEMICAL RESEARCH METHODS-RESPIRATORY SYSTEM
CiteScore
7.60
自引率
21.10%
发文量
49
审稿时长
>12 weeks
期刊介绍: Journal of Breath Research is dedicated to all aspects of scientific breath research. The traditional focus is on analysis of volatile compounds and aerosols in exhaled breath for the investigation of exogenous exposures, metabolism, toxicology, health status and the diagnosis of disease and breath odours. The journal also welcomes other breath-related topics. Typical areas of interest include: Big laboratory instrumentation: describing new state-of-the-art analytical instrumentation capable of performing high-resolution discovery and targeted breath research; exploiting complex technologies drawn from other areas of biochemistry and genetics for breath research. Engineering solutions: developing new breath sampling technologies for condensate and aerosols, for chemical and optical sensors, for extraction and sample preparation methods, for automation and standardization, and for multiplex analyses to preserve the breath matrix and facilitating analytical throughput. Measure exhaled constituents (e.g. CO2, acetone, isoprene) as markers of human presence or mitigate such contaminants in enclosed environments. Human and animal in vivo studies: decoding the ''breath exposome'', implementing exposure and intervention studies, performing cross-sectional and case-control research, assaying immune and inflammatory response, and testing mammalian host response to infections and exogenous exposures to develop information directly applicable to systems biology. Studying inhalation toxicology; inhaled breath as a source of internal dose; resultant blood, breath and urinary biomarkers linked to inhalation pathway. Cellular and molecular level in vitro studies. Clinical, pharmacological and forensic applications. Mathematical, statistical and graphical data interpretation.
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