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Abstracts of the Invited Speakers<br />

or lamotrigine are listed as recommended medications to prevent recurrent episodes.<br />

NICE Treatment Guidelines: They recommend at least 2 year of maintenance treatment after 1 episode. Long term preventive treatment<br />

should be considered in the following cases: One manic episode with prominent risk factors and negative results and bipolar II cases<br />

with significant functional loss, suicide risk, and frequent recurrent episodes. Lithium, olanzapine, or valproate can be used in long term<br />

maintenance treatment, but valproate should not be used in women with pregnancy potential.<br />

When monotherapy with one of those is not adequate, one of three can be added as a second agent or monotherapy can be tried with a<br />

different agent. Possible combinations are lithium-valproate, lithium-olanzapine, or valproate-olanzapine.<br />

Turkish Psychiatry Association Guidelines: Maintenance treatment is suggested in general after second episode, but it can be started in cases<br />

with risk factors. If a mood stabilizer was initiated during acute phase, it should be continued in maintenance phase, if not, then one should be<br />

started. When a mood stabilizer will be chosen for maintenance phase, it should be lithium. After second episode, whatever the type of episode<br />

was, the same mood stabilizer should be continued if there was one. When there is not adequate response and recurrence occurs a second<br />

mood stabilizer should be added. In cases using lithium as first mood stabilizer, valproate should be given priority as the second mood stabilizer.<br />

In conclusion, even there are similarities in many areas among guidelines, there are also different recommendations regarding treatment options.<br />

Those differences stem from complex clinical presentations of bipolar disorder and different cultural and traditional treatment approaches.<br />

Key words: Bipolar disorder, maintenance phase, guidelines<br />

References:<br />

1. Fountoulakis KN, Vieta E, Sanchez-Moreno J, Kaprinis SG, Goikolea JM, Kaprinis GS. Tretament guidelines for bipolar disorder: A critical review. J Affective Dis 2005;<br />

86: 1-10.<br />

2. Perlis RH. Use of treatment guidelines in clinical decision making in bipolar diorder: a pilot survey of clinicians. Curr Med Res Opin 2007; 23; 467-475.<br />

3. Samalin L, Guillaume S, Auclair C, Llorca PM. J Nerv Ment Dis 2011; 199: 239-243.<br />

Bulletin of Clinical Psychopharmacology 2011;21(Suppl. 2):S99-100<br />

[PS-23]<br />

Symposium Title: Individualized medicine: Focus on pharmacogenetics<br />

Genetics and drugs: From research to clinical studies Turkish perspective<br />

Cem Şengül<br />

Pamukkale University, School of Medicine, Department of Psychiatry, Denizli, Turkey<br />

E-mail: acemsen@gmail.com<br />

Genetic studies in psychiatry are on the rise and they form an important portion of all psychiatric research in last years. The genetic studies<br />

in psychiatry vary from classical association and linkage studies to genome wide association, and copy number variant studies. Genetic<br />

studies were focusing on different dimensions of psychiatric conditions. First of all, associations of target genes with psychiatric disorders<br />

were investigated in majority of studies. Association of drugs and genetics were also studied in many research projects. Genetic drug<br />

association studies consist of studies with efficacy and frequency of side effects of drug on different genetic polymorphisms. Recently,<br />

μ-opiate receptor gene (OPRM1) Asn40Asp single-nucleotide polymorphism was found to be associated with naltrexone drug response in<br />

alcoholic patients. This finding was very important for revealing effect of genetics on drug response. Naltrexone was effective in aspartate<br />

(Asp) 40 allele carriers but drug was ineffective in homozygote asparagine (Asn) carriers. Different genetic polymorphisms of genes<br />

encoding enzymes and receptors that were related to dopaminergic, serotonergic and glutamatergic systems were also associated with<br />

antipsychotic and antidepressant drug response and side effects. For example 5-HT2C receptor 759C/T gene polymorphism was associated<br />

with antipsychotic induced weight gain and T102C polymorphism of 5HT2A receptor gene was associated with response to risperidone.<br />

Genome wide association and copy number variations are new genetic techniques revealing more detailed and reliable results. Studies<br />

using these techniques might be more useful for exploring interactions between drugs and genetics. Studies on association of genetics<br />

with psychiatric disorders were limited and there were only a few studies available on association of genetics with psychiatric drugs in<br />

Turkey. Financial problems and approval speed and requirements of ethics committees are important barriers for conducting studies on<br />

genetic drug interaction. Resolving these issues might increase interest of psychiatrists on this topic.<br />

Key words: Genetics, polymorphism, drug<br />

Bulletin of Clinical Psychopharmacology 2011;21(Suppl. 2):S100<br />

S100 Bulletin of Clinical Psychopharmacology, Vol: 21, Supplement: 2, 2011 - www.psikofarmakoloji.org

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