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Association between Neurocognitive Impairment and the Short Allele of the 5-HTT Promoter Polymorphism in Depression: A Pilot Study
Author(s) -
Hely Kalska,
Ullamari Pesonen,
Sanna Lehikoinen,
JanHenry Stenberg,
Jari Lipsanen,
Jussi Niemi-Pynttäri,
Arja Tuunainen
Publication year - 2012
Publication title -
psychiatry journal
Language(s) - English
Resource type - Journals
eISSN - 2314-4335
pISSN - 2314-4327
DOI - 10.1155/2013/849346
Subject(s) - neurocognitive , major depressive disorder , allele , serotonin transporter , cognition , depression (economics) , neuropsychology , psychology , 5 httlpr , genotype , polymorphism (computer science) , medicine , psychiatry , oncology , genetics , biology , gene , macroeconomics , economics
Depression has been shown to be associated with cognitive deficits in various cognitive domains. However, it is still unclear which factors contribute to cognitive impairment. The objective of this study was to find out whether a functional polymorphism in the promoter region of the serotonin transporter (5-HTTLPR) gene is associated with the impairment of cognitive functioning among depressed patients. In a pilot study, a sample of 19 patients with major depressive disorder (MDD) and 19 healthy controls was investigated with an extensive psychiatric and neuropsychological examination. All participants were genotyped for 5-HTTLPR. Depressed patients with the short allele of the 5-HTT promoter region exhibited inferior cognitive performance compared to patients with the long allele polymorphism. In healthy controls, no association between genotype and cognitive performance was found. The result suggests that in MDD patients with the short allele of the 5-HTTLPR polymorphism the vulnerability to cognitive impairment is increased compared to MDD patients without the short allele inheritance. These preliminary findings need to be confirmed in a larger cohort of MDD patients.

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