Literature DB >> 15791170

The apolipoprotein E polymorphism is not associated with response to electroconvulsive therapy in major depressive disorder.

Martti Huuhka1, Sami Anttila, Esa Leinonen, Kaija Huuhka, Riikka Rontu, Kari M Mattila, Heini Huhtala, Terho Lehtimäki.   

Abstract

The apolipoprotein E (APOE) polymorphism is associated with neurodegenerative diseases. Its role regarding psychiatric disorders is controversial. It has been suggested to affect antidepressant treatment response and response to electroconvulsive therapy (ECT). In the present study, the association between APOE polymorphism and response to ECT in 119 patients with major depressive disorder was investigated. Moreover, a relation between APOE polymorphism and the age of onset of depression as well as the cognitive outcome of ECT was studied. In the whole population, no association was found between APOE polymorphism and response to ECT. However, in nonpsychotic patients, the epsilon2 allele tended to be more frequent in responders than nonresponders. Earlier onset of depression was observed in the patients with epsilon4 allele in late-life depression. There was no association between the APOE genotype and the cognitive change caused by ECT in the population as a whole. In women, however, epsilon2 allele may play a protective and epsilon4 allele a deleterious role in cognition during ECT.

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Year:  2005        PMID: 15791170     DOI: 10.1097/01.yct.0000153210.25362.ea

Source DB:  PubMed          Journal:  J ECT        ISSN: 1095-0680            Impact factor:   3.635


  6 in total

1.  Interaction between TPH1 and GNB3 genotypes and electroconvulsive therapy in major depression.

Authors:  S Anttila; K Huuhka; M Huuhka; R Rontu; K M Mattila; E Leinonen; T Lehtimäki
Journal:  J Neural Transm (Vienna)       Date:  2006-10-27       Impact factor: 3.575

2.  Interaction between 5-HT1A and BDNF genotypes increases the risk of treatment-resistant depression.

Authors:  S Anttila; K Huuhka; M Huuhka; R Rontu; M Hurme; E Leinonen; T Lehtimäki
Journal:  J Neural Transm (Vienna)       Date:  2007-03-31       Impact factor: 3.575

3.  Brain-derived neurotrophic factor (BDNF) polymorphisms G196A and C270T are not associated with response to electroconvulsive therapy in major depressive disorder.

Authors:  Kaija Huuhka; Sami Anttila; Martti Huuhka; Esa Leinonen; Riikka Rontu; Kari Mattila; Terho Lehtimäki
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2007-02       Impact factor: 5.270

4.  Association of APOE E2 and low-density lipoprotein with depressive symptoms in Chinese senile schizophrenia inpatients: A cross-sectional study.

Authors:  Wei Li
Journal:  Schizophr Res Cogn       Date:  2020-11-19

5.  ApoE alleles, depression and positive affect in multiple sclerosis.

Authors:  L J Julian; L Vella; D Frankel; S L Minden; J R Oksenberg; D C Mohr
Journal:  Mult Scler       Date:  2009-03       Impact factor: 6.312

Review 6.  The role of APOE-ɛ4 and beta amyloid in the differential rate of recovery from ECT: a review.

Authors:  T A Sutton; H R Sohrabi; S R Rainey-Smith; S M Bird; M Weinborn; R N Martins
Journal:  Transl Psychiatry       Date:  2015-03-31       Impact factor: 6.222

  6 in total

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