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EN
Temporal information processing controls many aspects of human mental activity and may be assessed by examining perception of temporal order in the tens of milliseconds time range. Although existing studies suggest an age-related decline in mental abilities, the data on the deterioration of temporal order perception seems inconsistent. Moreover, any evidence on subjects aged over 70 years is lacking. The present experiment aimed to extend the existing data to extremely old people. Temporal order judgment (TOJ) for auditory stimuli was tested across the life span of approx. 80 years, i.e. in young (mean age 22 years), elderly (66 years) and very old (101 years) subjects. Age-related deterioration of performance was observed, with slight changes in elderly subjects and significant deterioration in centenarians which was more distinct in women than in men. The results confirm age-related decrease in temporal resolution which may be explained by slowing of information processing or of a hypothetical internal-timing mechanism. These effects may be influenced by different strategies used in particular age groups.
EN
Analysis of relationships between the ageing cell phenotype and the age of cell donors is one of the ways towards understanding the link between cellular and organismal ageing. Cytogenetically, ageing is associated with a number of gross cellular changes, including altered size and morphology, genomic instability, and changes in expression and proliferation. Genomic instability can be easily assessed by analyzing the level of cytogenetic aberrations. In this review, we focus on the differences in the level and profile of cytogenetic aberrations observed in donors of different age and gender. Centenarians are a small fraction of the population at the extreme of human longevity. Their inclusion in such studies may shed light on one of the basic questions: whether genome stability is better maintained in successfully aged individuals compared to the rest of the population. At the same time, comparing the profile of age-related amount of chromosomal aberrations in men and women may help explaining the commonly observed gender differences in longevity.
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