The redox state of human serum albumin (HSA) is reported to be an oxidative stress
biomarker; however, its clinical use in cardiac disease has not yet been examined.
This study aimed to investigate the relation between the redox state of HSA and exercise
capacity, which is a robust prognostic factor, in patients with cardiovascular disease.
This cross-sectional study included outpatients with cardiac disease. Exercise capacity
was assessed by peak oxygen consumption (peakVO2) measured using symptom-limited cardiopulmonary exercise testing. The high-performance
liquid chromatography postcolumn bromocresol green method was used to part HSA into
human nonmercaptalbumin (oxidized form) and human mercaptalbumin (HMA, reduced form).
The fraction of human mercaptalbumin found in HSA (f[HMA]) was calculated as an indicator
of the redox state of HSA. The association between peakVO2 and f(HMA) was examined using the Spearman correlation coefficient and multivariate
linear regression analysis. A total of 70 patients were included (median age 76 years;
44 men; median peakVO2 15.5 ml/kg/min). The f(HMA) was positively correlated with peakVO2 (r = 0.38, p <0.01). Even after controlling for potential confounders, this association
remained in the multivariate linear regression analysis (standardized beta = 0.24,
p <0.05). We found a positive association between f(HMA) and peakVO2, independent of potential confounders in patients with cardiac disease, suggesting
that f(HMA) may be a novel biomarker related to exercise capacity in cardiac disease.
Longitudinal studies are required to further examine the prognostic capability of
f(HMA), the responsiveness to clinical intervention, and the association between f(HMA)
and cardiac disease.
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References
- A change of heart: oxidative stress in governing muscle function?.Biophys Rev. 2015; 7: 321-341
- Vascular endothelial dysfunction and mortality risk in patients with chronic heart failure.Circulation. 2005; 111: 310-314
- Skeletal muscle abnormalities in heart failure.Int Heart J. 2015; 56: 475-484
- Cys34-cysteinylated human serum albumin is a sensitive plasma marker in oxidative stress-related chronic diseases.PLoS One. 2014; 9: e85216
- A lower level of reduced albumin induces serious cardiovascular incidence among peritoneal dialysis patients.Clin Exp Nephrol. 2012; 16: 629-635
- Association between redox state of human serum albumin and exercise capacity in older women: a cross-sectional study.Geriatr Gerontol Int. 2020; 20: 256-260
- ATS/ACCP Statement on cardiopulmonary exercise testing.Am J Respir Crit Care Med. 2003; 167: 211-277
- Exercise standards. A statement for healthcare professionals from the American Heart Association. Writing Group.Circulation. 1995; 91: 580-615
- Albumin: pathophysiologic basis of its role in the treatment of cirrhosis and its complications.Hepatology. 2013; 58: 1836-1846
- Oxidative stress is enhanced in correlation with renal dysfunction: examination with the redox state of albumin.Kidney Int. 2004; 66: 1988-1993
- Improvement of the fraction of human mercaptalbumin on hemodialysis treatment using hydrogen-dissolved hemodialysis fluid: a prospective observational study.Ren Replace Ther. 2016; 2: 1-8
- The redox states of serum and synovial fluid of patients with temporomandibular joint disorders.Jpn J Physiol. 2003; 53: 351-355
- Oxidized human serum albumin as a possible correlation factor for atherosclerosis in a rural Japanese population: the results of the Yakumo Study.Environ Health Prev Med. 2018; 23: 1
- Skeletal muscle function and its relation to exercise tolerance in chronic heart failure.J Am Coll Cardiol. 1997; 30: 1758-1764
- Estimation of reduced walking speed using simple measurements of physical and psychophysiological function in community-dwelling elderly people: a cross-sectional and longitudinal study.Aging Clin Exp Res. 2019; 31: 59-66
- Albumin levels predict survival in patients with systolic heart failure.Am Heart J. 2008; 155: 883-889
- Prognostic significance and determinants of the 6-min walk test in patients with heart failure and preserved ejection fraction.JACC Heart Fail. 2015; 3: 459-466
- Factors related to physical functioning decline after cardiac surgery in older patients: a multicenter retrospective study.J Cardiol. 2019; 74: 279-283
- Clinical characteristics and outcomes of hospitalized patients with heart failure from the large-scale Japanese registry of acute decompensated heart failure (JROADHF).Circ J. 2021; 85: 1438-1450
- Breathing during exercise.N Engl J Med. 1978; 298: 780-785
- Endothelial function and oxidative stress in cardiovascular diseases.Circ J. 2009; 73: 411-418
- Oxidative stress and heart failure.Am J Physiol Heart Circ Physiol. 2011; 301: H2181-H2190
- Making the case for skeletal myopathy as the major limitation of exercise capacity in heart failure.Circ Heart Fail. 2010; 3: 537-546
- Systemic oxidative stress is associated with lower aerobic capacity and impaired skeletal muscle energy metabolism in heart failure patients.Sci Rep. 2021; 11: 2272
- Oral branched-chain amino acid granules improve structure and function of human serum albumin in cirrhotic patients.J Gastroenterol. 2017; 52: 754-765
- Redox state of human serum albumin in terms of cysteine-34 in health and disease.Methods Enzymol. 2010; 474: 181-195
- Establishment of a stable sampling method to assay mercaptoalbumin/non-mercaptoalbumin and reference ranges.Pract Lab Med. 2019; 17: e00132
Article info
Publication history
Published online: December 09, 2022
Received in revised form:
October 10,
2022
Received:
June 21,
2022
Footnotes
Funding: This work was supported by the grant No.: 17-005) from the Suzuken Memorial Foundation (Nagoya, Aichi, Japan) (The sponsor played no role in the collection, analysis, and interpretation of data; in writing the report; and in the decision to submit the article for publication.)
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