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Published on: July 12, 2012
DNA methylation stability in cardiac tissues kept at different temperatures and time intervals
Brando Poggiali1, Mikkel Eriksen Dupont2, Stine Bøttcher Jacobsen2
1Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. brando.poggiali@sund.ku.dk.
DNA methylation (DNAm) in cardiac tissue is stable for at least 28 days at 4°C and 1 day at 22°C, enabling reliable epigenetic analysis in cardiovascular disease research even with suboptimal sample storage.
Area of Science:
- Epigenetics
- Cardiovascular Research
- Genomics
Background:
- DNA methylation (DNAm) analysis is crucial for understanding cardiovascular diseases (CVDs).
- Cardiac biopsies collected during surgery may face storage delays due to resource limitations.
- Assessing DNAm stability under suboptimal conditions is essential for practical application.
Purpose of the Study:
- To investigate the stability of genome-wide DNAm in human cardiac tissues stored at different temperatures and durations.
- To determine the impact of delayed storage on DNAm integrity for future epigenetic studies.
Main Methods:
- Human cardiac tissues were stored at 4°C and 22°C for up to 28 days.
- DNA methylation was analyzed using the Illumina Infinium MethylationEPIC v1.0 BeadChip Array.
- Correlations and differentially methylated positions (DMPs) were assessed.
Main Results:
- High correlations (R² > 0.992) were observed between immediately analyzed and stored samples.
- No significant DNAm changes occurred at 4°C for 28 days or 22°C for 1 day.
- Significant DMPs emerged at 22°C after 7, 14, and 28 days, with thousands of changes observed.
Conclusions:
- Cardiac tissue DNAm is remarkably stable at 4°C for extended periods (28 days).
- Short-term storage at room temperature (22°C for 1 day) also preserves DNAm integrity.
- These findings support the feasibility of DNAm analysis from cardiac samples stored suboptimally post-surgery.
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