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1 Plan II, The University of Texas at Austin.
2 Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas.
3 Department of Biopathology and Diagnostic Imaging, Tor Vergata University, Rome, Italy.
4 Department of Psychology, The University of Texas at Austin.
Address correspondence to Marc Lewis, PhD, Department of Psychology, The University of Texas at Austin, Austin, Texas, 78703. E-mail: lewis{at}psy.utexas.edu
Segmental progeroid syndromes are those whose phenotypes resemble accelerated aging. Here we analyze those phenotypes and hypothesize that short telomeres produce the same group of symptoms in a variety of otherwise unrelated progeroid syndromes. Specific findings are the following: (a) short telomeres in some progeroid syndromes cause an alopecia/osteoporosis/fingernail-atrophy group of symptoms; (b) fingernail atrophy in progeroid syndromes resembles the natural slowing of nail growth that occurs in normal aging and nail growth velocity, and may be a marker of replicative aging in keratinocyte stem cells; (c) alopecia and reduced hair diameter parallel the nail results; (d) osteoporosis in Dyskeratosis Congenita resembles age-related osteoporosis, but the same is not true of other progerias; and (e) gray hair is associated with short telomeres, but may also involve reactive oxygen species. On the basis of these results, we make several predictions and discuss how the segmental quality of progeroid syndromes may provide insight into normative aging.
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