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Updated: Jan 22, 2026

Electroeluting DNA Fragments
Published on: September 5, 2010
Circulating cell-free DNA fragment analysis by microchip electrophoresis and its relationship with DNase I in cardiac
Junko Fujihara1, Yoshikazu Takinami2, Misuzu Ueki3
1Department of Legal Medicine, Faculty of Medicine, Shimane University, 89-1 Enya, Izumo, Shimane 693-8501, Japan.
Insights
Circulating cell-free DNA (cfDNA) levels are elevated in cardiac patients. A specific cfDNA fragment ratio shows promise as a novel diagnostic indicator for myocardial infarction (MI).
Area of Science:
- Biochemistry
- Molecular Biology
- Cardiology
Background:
- Circulating cell-free DNA (cfDNA) is linked to various diseases, including cardiovascular conditions.
- Understanding cfDNA characteristics in cardiac patients is crucial for diagnostic advancements.
Purpose of the Study:
- To investigate plasma cfDNA concentrations and fragment distributions in cardiac disease patients.
- To explore the relationship between cfDNA levels, deoxyribonuclease I (DNase I) activity, and myocardial infarction (MI).
Main Methods:
- Plasma cfDNA was extracted from cardiac patients and healthy controls.
- cfDNA fragment analysis was performed using microchip electrophoresis.
- Deoxyribonuclease I (DNase I) activity was measured and correlated with cfDNA concentration.
Main Results:
- Significantly higher cfDNA concentrations were observed in MI and cardiac angina patients compared to controls.
- Cardiac patients exhibited three cfDNA fragments (150-200 bp, 300-400 bp, 500-600 bp), while controls showed a single fragment.
- A 150-200 bp/500-600 bp cfDNA ratio was more prevalent in MI patients, and a positive correlation between DNase I activity and cfDNA concentration was found.
Conclusions:
- Plasma cfDNA in cardiac disease patients may originate from apoptosis.
- The 150-200 bp/500-600 bp cfDNA fragment ratio could serve as a novel diagnostic biomarker for MI.
- DNase I activity is positively correlated with cfDNA concentration in cardiac patients.
Abstract:
Circulating cell-free DNA (cfDNA) has been directly related to cancer, diabetes, stroke, systemic lupus erythematosus, trauma, rheumatoid arthritis, inflammation, infection, and myocardial infarction (MI). In this study, plasma cfDNA was extracted from the plasma of cardiac disease patients and the cfDNA fragment distribution as well as the relationships between cfDNA concentration and deoxyribonuclease I (DNase I) activity enzyme implicated in double-stranded DNA processing were examined. Results revealed that the cfDNA concentrations in patients with MI and cardiac angina were significantly higher than that in healthy control subjects. Microchip electrophoresis of plasma cfDNA revealed a single fragment (150-200 bp) in some healthy control subjects and three fragments (150-200 bp, 300-400 bp, and 500-600 bp) in all cardiac patient samples. Moreover, a cfDNA ratio of 150-200 bp/500-600 bp was significantly more prevalent in MI patients than in patients with other cardiac diseases (chest pain, cardiac angina, atrial fibrillation and cardiac failure). In addition, a positive correlation between DNase I activity and cfDNA concentration was observed. These results suggest that the plasma cfDNA in cardiac disease patients may originate from apoptosis and that the 150-200 bp/500-600 bp ratio for cfDNA may be a novel diagnostic indicator for MI.
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