Study on the admission levels of circulating cell-free DNA in patients with acute myocardial infarction using different quantification methods

被引:6
|
作者
Agiannitopoulos, Konstantinos [1 ]
Samara, Pinelopi [1 ]
Papadopoulou, Eirini [2 ]
Tsamis, Konstantinos [3 ]
Mertzanos, George [3 ]
Babalis, Dimitrios [3 ]
Lamnissou, Klea [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Dept Biol, Div Genet & Biotechnol, Athens 15784, Greece
[2] Genekor MSA, Mol Oncol & Mol Genet, Athens, Greece
[3] KAT Gen Hosp, Dept Cardiol, Athens, Greece
关键词
Acute myocardial infarction; circulating cell-free DNA; NanoDrop; quantitative PCR; Qubit; 3; 0; BIOMARKER;
D O I
10.1080/00365513.2020.1729400
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Circulating cell-free DNA (cf-DNA) is present in human biological fluids, mainly in plasma and serum, originating from cell death, a process that massively takes place during acute myocardial infarction (AMI). In the present study, cf-DNA was assessed by different quantification techniques, in order to determine its levels in patients admitted with AMI. A total of 130 subjects were included in the study: 80 ST elevation myocardial infarction (STEMI) patients and 50 healthy controls. Cf-DNA extracted from plasma was analyzed by: a) Qubit 3.0 with single (ss) and double (ds) stranded DNA assay kits, b) NanoDrop and c) quantitative PCR (qPCR). Cf-DNA levels were recorded elevated in AMI patients compared to those of healthy individuals. Specifically, Qubit 3.0 ss-DNA kit provided the highest cf-DNA concentration values for all the samples analyzed in comparison with ds-DNA assay kit and NanoDrop, approaching the values obtained by qPCR. Cf-DNA augments in massive cell death settings, including AMI, proposing that the quantification of its levels by novel methodologies could contribute to patient diagnosis and clinical management.
引用
收藏
页码:348 / 350
页数:3
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