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Preliminary evidence that allelic variation in the LMX1A gene influences training-related working memory improvement
Stockholm University, Faculty of Social Sciences, Aging Research Center (ARC), (together with KI).
Stockholm University, Faculty of Social Sciences, Aging Research Center (ARC), (together with KI).
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2011 (English)In: Neuropsychologia, ISSN 0028-3932, E-ISSN 1873-3514, Vol. 49, no 7, p. 1938-42Article in journal (Refereed) Published
Abstract [en]

LMX1A is a transcription factor involved in the development of dopamine (DA)-producing neurons in midbrain. Previous research has shown that allelic variations in three LMX1A single nucleotide polymorphisms (SNPs) were related to risk of Parkinson's disease (PD), suggesting that these SNPs may influence the number of mesencephalic DA neurons. Prompted by the established link between striatal DA functions and working memory (WM) performance, we examined two of these SNPs in relation to the ability to benefit from 4 weeks of WM training. One SNP (rs4657412) was strongly associated with the magnitude of training-related gains in verbal WM. The allele linked to larger gains has previously been suggested to be associated with higher dopaminergic nerve cell density. No differential gains of either SNP were observed for spatial WM, and the genotype groups were also indistinguishable in tests of attention, interference control, episodic memory, perceptual speed, and reasoning for both SNPs. This pattern of data is in agreement with previous findings from our group, suggesting that cognitive effects of DA-related genes may be more easily detected in a training context than for single-assessment performance scores.

Place, publisher, year, edition, pages
2011. Vol. 49, no 7, p. 1938-42
Keywords [en]
cognition, aging, leisure time activities, population study, engagement
National Category
Psychology
Identifiers
URN: urn:nbn:se:su:diva-84264DOI: 10.1016/j.neuropsychologia.2011.03.021PubMedID: 21435346OAI: oai:DiVA.org:su-84264DiVA, id: diva2:579383
Available from: 2012-12-20 Created: 2012-12-20 Last updated: 2017-12-06Bibliographically approved

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