Journals of Gerontology Series A: Biological Sciences and Medical Sciences Large Type Edition
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The Journals of Gerontology Series A: Biological Sciences and Medical Sciences 56:B27-B32 (2001)
© 2001 The Gerontological Society of America

Age-Associated Accumulation of the Apolipoprotein C-III Gene T-455C Polymorphism C Allele in a Russian Population

Sergey V. Anisimova, Maria V. Volkovaa,b, Lilia V. Lenskayac, Vladimir K. Khavinsond, Dina V. Solovievad and Eugene I. Schwartza,b

a Department of Cardiology, I.P. Pavlov St. Petersburg State Medical University, Russia
b Laboratory of Human Molecular Genetics, St. Petersburg Institute of Nuclear Physics RAS, Gatchina, Russia
c City Geriatric Center, St. Petersburg, Russia
d St. Petersburg Institute of Bioregulation and Gerontology, Russia

Sergey V. Anisimov, Laboratory of Cardiovascular Science, Gerontology Research Center, National Institute on Aging, National Institutes of Health, 5600 Nathan Shock Drive, Baltimore, MD 21224 E-mail: anisimovs{at}grc.nia.nih.gov.

Decision Editor: Jay Roberts, PhD

Apolipoprotein C-III (apoC-III) is the major component of triglyceride-rich lipoproteins. One of six identified polymorphisms in the apoC-III 5'-untranslated region (T-455C) is located within a functional insulin-response element. In a group of 137 elderly individuals (70–106 years old), the allele distribution was analyzed using restriction fragment length polymorphisms. Statistical analysis of allele frequencies was performed on subgroups selected by age and in elderly patients with arterial hypertension or ischemic heart disease. A greater frequency of the apoC-III -455C allele was demonstrated with aging (p < .005). No statistically significant difference in allele distributions was detected between healthy subjects and groups of elderly patients of the same age with either ischemic heart disease or arterial hypertension. The increased incidence of the C allele with advanced age indicates that this variant promoter is associated with longevity. The greater incidence of this allele is detectable only in adults older than 80 years of age.




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