The Utility of Circulating and Imaging Biomarkers Alone and in Combination in Heart Failure

被引:1
|
作者
Jaltotage, Biyanka [1 ]
Dwivedi, Girish [1 ,2 ,3 ,4 ]
Ooi, Daryl Eng Lee [5 ,6 ]
Mahadavan, Gnanadevan [5 ,7 ]
机构
[1] Fiona Stanley Hosp, Dept Cardiol, Murdoch, WA, Australia
[2] Univ Ottawa, Heart Inst, Div Cardiol, Fac Med, Ottawa, ON, Canada
[3] Univ Western Australia, Sch Med, Perth, Australia
[4] Harry Perkins Inst Med Res, Nedlands, WA, Australia
[5] Univ Adelaide, Discipline Med, Adelaide, SA 5005, Australia
[6] Northern Adelaide Local Hlth Network, Lyell McEwin Hosp, Cardiol Unit, Haydown Rd, Elizabeth Vale, SA 5112, Australia
[7] Cent Adelaide Local Hlth Network, Queen Elizabeth Hosp, Cardiol Unit, 28 Woodville Rd,South, Woodville, SA 5011, Australia
关键词
Circulating and imaging biomarkers; heart failure; cardiac mortality; myocardial injury; CMR; ECG; C-REACTIVE PROTEIN; CARDIAC MAGNETIC-RESONANCE; LATE GADOLINIUM ENHANCEMENT; BRAIN-NATRIURETIC PEPTIDE; VENTRICULAR EJECTION FRACTION; DIFFUSE MYOCARDIAL FIBROSIS; SENSITIVITY TROPONIN-T; TUMOR-NECROSIS-FACTOR; SURROGATE END-POINTS; LEFT ATRIAL FUNCTION;
D O I
10.2174/1573403X17666210525103512
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Clinical trials in the treatment of heart failure have relied on the use of a composite of hard clinical endpoints to evaluate the efficacy of the treatment arm. This has led to prolonged trials requiring large patient cohorts and extensive funding to reach statistical significance. In this paper, we have explored the potential of currently available circulating and imaging biomarkers associated with heart failure as a surrogate for hard clinical end points in clinical trials. This would be expected to result in shorter trials, smaller patient cohorts and limited funding required. We have subsequently theorized on combining circulating and imaging biomarkers as a surrogate for clinical end points such as hospitalization from heart failure and cardiac mortality.
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收藏
页数:13
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