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Sample Preparation to Bioinformatics Analysis of DNA Methylation: Association Strategy for Obesity and Related Trait Studies
Published on: May 6, 2022
Mini Nutritional Assessment Scores Indicate Higher Risk for Prospective Mortality and Contrasting Correlation With
Alberto Montesanto1, Patrizia D'Aquila1, Veronica Rossano1
1Department of Biology, Ecology and Earth Sciences (DiBEST), University of Calabria, Rende, Italy.
Malnutrition in older adults correlates with global DNA methylation changes, but not with specific age-related epigenetic markers. This suggests malnutrition is an early sign of frailty, distinct from the epigenetic aging process.
Area of Science:
- Epigenetics
- Gerontology
- Nutritional Science
Background:
- Epigenetic landscapes change throughout life, influenced by environmental factors.
- The Mini Nutritional Assessment (MNA) is a standard tool for evaluating malnutrition in the elderly.
- Previous research linked specific DNA methylation patterns to chronological and biological aging.
Purpose of the Study:
- To investigate the association between nutritional status, assessed by MNA, and epigenetic biomarkers related to aging.
- To determine if malnutrition affects the same DNA methylation sites correlated with aging.
Main Methods:
- Utilized data from previous studies on methylation biomarkers associated with aging.
- Assessed nutritional status using the Mini Nutritional Assessment (MNA) tool.
- Analyzed correlations between MNA scores and global/gene-specific DNA methylation levels.
Main Results:
- Malnutrition showed a positive correlation with global DNA methylation.
- Most gene-specific methylation sites linked to aging were unaffected by malnutrition.
- Some sites showed correlations with malnutrition opposite to those seen with frailty.
Conclusions:
- Malnutrition may be an early indicator of disability and age-related decline, triggering generalized epigenetic remodeling.
- Specific epigenetic changes related to aging appear largely independent of malnutrition.
- Malnutrition is a survival risk in the elderly, partially separate from the molecular aging process.
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