Recent studies have indicated that epigenetic processes may play
a major role in both cellular and organismal aging. These
epigenetic processes include not only DNA methylation and histone
modifications, but also extend to many other epigenetic mediators
such as the polycomb group proteins, chromosomal position effects,
and noncoding RNA. The topics of this book range from fundamental
changes in DNA methylation in aging to the most recent research on
intervention into epigenetic modifications to modulate the aging
process. The major topics of epigenetics and aging covered in this
book are: 1) DNA methylation and histone modifications in aging; 2)
Other epigenetic processes and aging; 3) Impact of epigenetics on
aging; 4) Epigenetics of age-related diseases; 5) Epigenetic
interventions and aging: and 6) Future directions in epigenetic
aging research.
The most studied of epigenetic processes, DNA methylation, has
been associated with cellular aging and aging of organisms for many
years. It is now apparent that both global and gene-specific
alterations occur not only in DNA methylation during aging, but
also in several histone alterations. Many epigenetic alterations
can have an impact on aging processes such as stem cell aging,
control of telomerase, modifications of telomeres, and epigenetic
drift can impact the aging process as evident in the recent studies
of aging monozygotic twins.
Numerous age-related diseases are affected by epigenetic
mechanisms. For example, recent studies have shown that DNA
methylation is altered in Alzheimer s disease and autoimmunity.
Other prevalent diseases that have been associated with age-related
epigenetic changes include cancer and diabetes. Paternal age and
epigenetic changes appear to have an effect on schizophrenia and
epigenetic silencing has been associated with several of the
progeroid syndromes of premature aging. Moreover, the impact of
dietary or drug intervention into epigenetic processes as they
affect normal aging or age-related diseases is becoming
increasingly feasible.
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