64 research outputs found
Low fertility and population replacement in Scotland
It has been argued that Scotland faces population ageing and decline that will have potentially serious economic and social consequences, and that the origin of these processes lie in its low and declining fertility rates. After considering alternatives to the total period rate measure of fertility, empirical evidence and theoretical argument about low fertility and its consequences is briefly reviewed. The paper argues that low fertility in general may not be the problem it is often purported to be, that Scotland has relatively high fertility, and that pro-natalist policies are neither desirable nor necessary. It suggests that low fertility and population ageing may be viewed as positive developments, and that within Europe, Scotland is distinguished more by its excess of early deaths than by any shortage of births.Peer reviewe
Neuropsychological Correlates of Transcription Factor AP-2Beta, and Its Interaction with COMT and MAOA in Healthy Females
Background: The transcription factor AP-2β has been shown
to impact clinical and neuropsychological properties. Apparently, it regulates the transcription of genes that code for
molecules which are part of the catecholaminergic transmission system. This investigation focuses on possible effects of
the transcription factor AP-2β intron 2 polymorphism on
cognitive performance parameters. Methods: This hypothesis-driven investigation examined the effects and interactions of the transcription factor AP-2β intron 2 polymorphism, the Val158Met catechol- O -methyltransferase (COMT)
polymorphism, and the variable number of tandem repeat
polymorphism of monoamine oxidase A (MAOA) on cognitive performance parameters within a group of 200 healthy
women (age: mean ± SD, 23.93 ± 3.33 years). Results: The
AP-2β polymorphism significantly influenced cognitive performance (in particular, the Trail Making Test part B), whereas the MAOA and COMT polymorphisms did not. However,
there was an interaction effect of the AP-2β × MAOA × COMT
genotypes on the decision bias β of the degraded-stimulus version of the continuous performance task. Only the Val158Met COMT polymorphism showed an influence on
personality questionnaires (openness and self-transcendence; NEO Five-Factor Inventory, Temperament and Character Inventory). Conclusion: The transcription factor AP-2β
intron 2 polymorphism had more influence on cognition
than the MAOA and COMT polymorphisms. Possibly, the AP2β genotype might influence cognition through pathways
other than those that regulate MAOA and COMT transcription. Interactions of transcription factor AP-2β, COMT, and
MAOA polymorphisms suggest higher leverage effects of
transcription factor AP-2β in subjects with high dopamine
availability
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