| Literature DB >> 25887122 |
Jacob J E Koopman1, Maarten P Rozing2, Anneke Kramer3, José M Abad4, Patrik Finne5, James G Heaf6, Andries J Hoitsma7, Johan M J De Meester8, Runolfur Palsson9, Maurizio Postorino10, Pietro Ravani11, Christoph Wanner12, Kitty J Jager3, David van Bodegom13, Rudi G J Westendorp14.
Abstract
The rate of senescence can be inferred from the acceleration by which mortality rates increase over age. Such a senescence rate is generally estimated from parameters of a mathematical model fitted to these mortality rates. However, such models have limitations and underlying assumptions. Notably, they do not fit mortality rates at young and old ages. Therefore, we developed a method to calculate senescence rates from the acceleration of mortality directly without modeling the mortality rates. We applied the different methods to age group-specific mortality data from the European Renal Association-European Dialysis and Transplant Association Registry, including patients with end-stage renal disease on dialysis, who are known to suffer from increased senescence rates (n = 302,455), and patients with a functioning kidney transplant (n = 74,490). From age 20 to 70, senescence rates were comparable when calculated with or without a model. However, when using non-modeled mortality rates, senescence rates were yielded at young and old ages that remained concealed when using modeled mortality rates. At young ages senescence rates were negative, while senescence rates declined at old ages. In conclusion, the rate of senescence can be calculated directly from non-modeled mortality rates, overcoming the disadvantages of an indirect estimation based on modeled mortality rates.Entities:
Keywords: Acceleration of mortality; Aging; Gompertz model.; Modeling; Senescence; Senescence rate
Mesh:
Year: 2015 PMID: 25887122 DOI: 10.1093/gerona/glv042
Source DB: PubMed Journal: J Gerontol A Biol Sci Med Sci ISSN: 1079-5006 Impact factor: 6.053