View Clinical Trial (Medical Research Study)
Remodeling of Chromatin-Based Epigenetic Structures in Development and Aging
| City: |
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Richmond |
| State: |
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Virginia |
| Zip Code: |
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23284 |
| Conditions: |
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Aging |
| Purpose: |
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This study will examine the role of epigenetics (heritable changes in gene function that
occur without a change in DNA sequence) in the aging process. DNA is the primary genetic
material, responsible for transmitting information from one cell to the next or from one
generation to the next. A second layer of heredity is described by the term "epigenetics."
Epigenetic information is reset from one generation to the next. It works in two ways: 1) by
modification of the DNA, like balloons stuck at irregular intervals onto the sides of the
DNA helix that encodes genes, and 2) through specialized protein shells that wrap around
some regions of DNA. As in DNA, these shells can copy themselves and can transmit
instructions. Because they are used to turn genes on and off, errors in their settings cause
critical misinformation to be transmitted.
Aging involves many changes, such as muscle weakening, graying hair, skin wrinkling, and so
forth. There are several current theories of aging, including damage to genes by oxidation,
shortening of tiny structures at the ends of chromosomes called telomeres, and the ability
to stretch lifespan with caloric restrictions. This study will investigate the possible role
of epigenetics in aging by examining and comparing the shell-like epigenetic settings in
skin cells in young adults and older individuals. Preliminary results from earlier studies
show differences in these settings in younger and older people.
Women between the ages of 21 and 30 years and 65 and 90 years who are undergoing breast
reduction or mastectomy at Suburban Hospital in Bethesda, Maryland, may participate in this
study. Tissue removed during surgery for pathological examination will also be used by
researchers in this study to validate the preliminary findings noted above and to continue
studies into the new area of epigenetics and aging.
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| Study Summary: |
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Normal human lifespan is marked by a complex series of developmental events, relative
stability during adulthood, and ultimately a gradual decline in viability. Biological clocks
presumably underlie the developmental events that occur through childhood and adolescence,
but the nature of those clocks has remained obscure. Progress in this area would be of
considerable importance, not only for our understanding of child development, but also
because instability in putative clock-like mechanisms may occur as part of the aging
process. Such instability could well compromise tissue function and contribute to many of
the common degenerative diseases of later life.
We propose to investigate whether developmental clocks and related aspects of the aging
process are attributable in part to age-related epigenome remodeling. Experiments done to
date with cultured human fibroblasts derived from tissue banks provide tentative support for
this hypothesis. To exclude tissue culture-related artifacts and to continue the work, it is
essential to have access to fresh tissue material in the form of surgically obtained skin
specimens that would otherwise be discarded.
Elective breast reduction mammoplasty is a frequently performed surgery at Suburban
Hospital, Bethesda, Maryland. Small skin specimens will be obtained from this procedure, as
well as from normal skin derived from mastectomies. Patients who are to undergo these
procedures will be asked to sign a consent form allowing the specimens, normally discarded,
to be used instead for research on the mechanism of aging. They will be informed that
clinical information will accompany the specimens, including age and known disease
conditions.
Twenty patients in each of two age ranges, 21-30 yr and 65-90 yr, will be enrolled in the
study. The primary outcome will be confirmation of age-related epigenome change in the
chromosome 4q35.2 region, previously documented using tissue bank-derived cultured skin
fibroblasts. Mapping and sampling chromatin from this region revealed higher histone H4
acetylation in young (24-30 yr) than old (80-85 yr) individuals. Confirmation of this change
in primary fibroblasts will be followed by more detailed mapping of chromatin structure and
extension beyond the currently defined limits. Secondary outcomes will include examination
of two areas of epigenome remodeling that appear to occur between birth and adulthood, as
well as searches for additional regions of age-related chromatin change.
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| Criteria: |
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- INCLUSION CRITERIA:
Age 21-30 or 65-90, female or male
Normal liver function, renal function adjusted for age
Written informed consent
EXCLUSION CRITERIA:
Down's or other premature aging syndromes
Mastectomies: skin involvement in the malignant process or damage due to prior radiation
therapy
Active skin infection
Skin damage due to photoaging will be noted but will not be a basis for exclusion
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| NCT ID: |
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NCT00242255 |
| Primary Contact: |
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Principal Investigator
Bruce H Howard, M.D.
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Bruce H Howard, M.D.
Phone: (301) 496-9038
Email: howardb@mail.nih.gov
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| Backup Contact: |
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N/A |
| Location Contact: |
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Richmond, Virginia 23284
United States
There is no listed contact information for this specific location.
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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June 19, 2013 |
| Modifications to this listing: |
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