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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