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. 2019 Jan 25;10(2):82.
doi: 10.3390/genes10020082.

Analysis of the Association Between TERC and TERT Genetic Variation and Leukocyte Telomere Length and Human Lifespan-A Follow-Up Study

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Analysis of the Association Between TERC and TERT Genetic Variation and Leukocyte Telomere Length and Human Lifespan-A Follow-Up Study

Daniela Scarabino et al. Genes (Basel). .

Abstract

We investigated the possible influence of TERC and TERT genetic variation and leukocyte telomere length (LTL) on human lifespan. Four polymorphisms of TERT and three polymorphisms of TERC were examined in a sample of elderly subjects (70⁻100 years). After nine years of follow-up, mortality data were collected, and sub-samples of long-lived/not long-lived were defined. TERT VNTR MNS16A L/L genotype and TERT rs2853691 A/G or G/G genotypes were found to be associated with a significantly higher risk to die before the age of 90 years, and with a significantly lower age at death. The association between lifespan and LTL at baseline was analyzed in a subsample of 163 subjects. Age at baseline was inversely associated with LTL (p < 0.0001). Mean LTL was greater in the subjects still living than in those no longer living at follow-up (0.79 T/S ± 0.09 vs 0.63 T/S ± 0.08, p < 0.0001). Comparison of age classes showed that, among the 70⁻79-year-olds, the difference in mean LTL between those still living and those no longer living at follow-up was greater than among the 80⁻90-year-olds. Our data provide evidence that shorter LTL at baseline may predict a shorter lifespan, but the reliability of LTL as a lifespan biomarker seems to be limited to a specific age (70⁻79 years).

Keywords: TERC; TERT; genetic variation; human lifespan; leukocyte telomere length.

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Conflict of interest statement

The authors have no competing interests to declare.

Figures

Figure 1
Figure 1
LTL expressed as T/S ratio as a function of age at baseline.

References

    1. Blackburn E.H., Epel E.S., Lin J. Human telomere biology: A contributory and interactive factor in aging, disease risks, and protection. Science. 2015;350:1193–1198. doi: 10.1126/science.aab3389. - DOI - PubMed
    1. Wong J.M.Y., Collins K. Telomere maintenance and disease. Lancet. 2003;362:983–988. doi: 10.1016/S0140-6736(03)14369-3. - DOI - PubMed
    1. Blackburn E.H., Greider C.W., Szostak J.W. Telomeres and telomerase: The path from maize, Tetrahymena and yeast to human cancer and aging. Nat. Med. 2006;12:1133–1138. doi: 10.1038/nm1006-1133. - DOI - PubMed
    1. Cawthon R.M., Smith K.R., O’Brien E., Sivatchenko A., Kerber R.A. Association between telomere length in blood and mortality in people aged 60 years or older. Lancet. 2003;361:393–395. doi: 10.1016/S0140-6736(03)12384-7. - DOI - PubMed
    1. Kimura M., Hjelmborg J.V.B., Gardner J.P., Bathum L., Brimacombe M., Lu X., Christiansen L., Vaupel J.W., Aviv A., Christensen K. Telomere length and mortality: A study of leukocytes in elderly Danish twins. Am. J. Epidemiol. 2008;167:799–806. doi: 10.1093/aje/kwm380. - DOI - PMC - PubMed

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