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DOI 10.1016/j.archger.2010.06.006

Медицинская библиотека · Archives of gerontology and geriatrics · 2011

Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).

Marini Sandro, Bagnoli Silvia, Bessi Valentina, Tedde Andrea, Bracco Laura, Sorbi Sandro, Nacmias Benedetta

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Serotonin-transporter-linked polymorphism (5-HTTLPR) is involved in neuropsychiatric diseases and recently the S-isoform has been correlated with a higher risk of developing emotion-induced retrograde amnesia. In order to better clarify the possible role of the 5-HTT S/L polymorphism and its effects on cognitive ability, especially on memory skills, we report here the distributions of the 5-HTT genetic variant and the Apolipoprotein E (ApoE) ɛ-4 allele and their association with neuropsychological measures in older adults reporting problems with everyday memory. Moreover, we verified the presence of a possible association between the S-allele with depression and the personal trait of neuroticism. Our results indicate an association between the 5-HTTLPR S-allele and the risk of developing MCI. No association was found in the other three groups. We found a positive dose-dependent association between the S-allele and the Rey-Osterrieth complex figure test (recall) score. Finally, our data did not find an association between the same allele and depression or neuroticism. This data, in our opinion shows a slight, non-established influence of 5-HTTLPR on memory skills exhibited in challenging memory tests but no influence on other extra-mnesic cognitive abilities.

Для цитирования: Marini Sandro, Bagnoli Silvia, Bessi Valentina, Tedde Andrea, Bracco Laura, Sorbi Sandro, Nacmias Benedetta. Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).. Archives of gerontology and geriatrics. 2011. DOI: 10.1016/j.archger.2010.06.006.

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