07.01.2013 Views

Sorted By Test Name - Mayo Medical Laboratories

Sorted By Test Name - Mayo Medical Laboratories

Sorted By Test Name - Mayo Medical Laboratories

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

FPORC<br />

91763<br />

HTT<br />

83302<br />

antidepressant. Individuals homozygous for the IVS2+54538 A allele have improved probability of<br />

response to citalopram, in contrast to individuals homozygous or heterozygous for the IVS2 G allele.<br />

Individuals with major depression disorders are more likely to respond to citalopram if they are<br />

homozygous for the -1438G promoter allele. Guiding treatment choice in individuals who have a<br />

drug-metabolizer phenotype discordant with CYP450 genotypes Identifying patients who may benefit<br />

from treatment with the antipsychotic drug clozapine Identifying those patients receiving atypical<br />

antipsychotic medications with excessive weight gain who may benefit by switching to different<br />

antipsychotic medications<br />

Interpretation: An interpretive report will be provided.<br />

Reference Values:<br />

An interpretive report will be provided.<br />

Clinical References: 1. Malhotra AK, Murphy GM Jr, Kennedy JL: Pharmacogenetics of<br />

psychotropic drug response. Am J Psychiatry 2004;161(5):780-796 2. Murphy GM Jr, Kremer C,<br />

Rodrigues HE, et al: Pharmacogenetics of antidepressants medication intolerance. Am J Psychiatry<br />

2003;160(10):1830-1835 3. Arranz MJ, Murno J, Birkett J, et al: Pharmacogenetic prediction of clozapine<br />

response. Lancet 2000;355(9215):1615-1616 4. Reynolds GP, Zhang ZJ, Zhang XB: Polymorphism of the<br />

promoter region of the serotonin 5-HT2C receptor gene and clozapine-induced weight gain. Am J<br />

Psychiatry 2003;160:677-679 5. Segman RH, Heresco-Levy U, Finkel B, et al: Association between the<br />

serotonin 2A receptor gene and tardive dyskinesia in chronic schizophrenia. Mol Psychiatry<br />

2001;6(2):225-229 6. Segman RH, Heresco-Levy U, Finkel B, et al: Association between the serotonin<br />

2C receptor gene and tardive dyskinesia in chronic schizophrenia: additive contribution of 5-HT2Cser and<br />

DRD3gly alleles to susceptibility. Psychopharmacology 2000;152(4):408-413 7. Choi MJ, Kang RH,<br />

Ham BJ, et al: Serotonin receptor 2A gene polymorphism (-1438A->G) and short-term treatment response<br />

to citalopram. Neuropsychobiology 2005;52:155-162 8. McMahon FJ, Buervenich S, Charney D, et al:<br />

Variation in the gene encoding the serotonin 2A receptor is associated with outcome of antidepressant<br />

treatment. Am J Hum Genet 2006;78:804-814<br />

Serotonin Release Assay, Unfractionated Heparin<br />

Reference Values:<br />

An interpretive comment included with results.<br />

<strong>Test</strong> Performed by: BloodCenter of Wisconsin<br />

638 N. 18th Street<br />

Milwaukee, WI 53233-2121<br />

Serotonin Transporter Genotype, Blood<br />

Clinical Information: Serotonin (5-hydroxytryptamine; 5-HT) is a neurotransmitter. The serotonin<br />

transporter (5-HTT) modulates neurotransmission by facilitating removal of serotonin from the synapse of<br />

serotonergic neurons, resulting in serotonin reuptake into the presynaptic terminus. Other designations for<br />

5-HTT are SLC6A4 (solute carrier family 6 [neurotransmitter transporter, serotonin], member 4), hSERT,<br />

OCD1, SERT, sodium-dependent serotonin transporter, and 5-HT transporter. Selective serotonin<br />

reuptake inhibitors (SSRIs) block the action of the serotonin transporter and are used to treat depression<br />

and other neuropsychiatric disorders. Examples of SSRIs are fluoxetine (Prozac), fluvoxamine (Luvox),<br />

escitalopram oxalate (Lexapro), sertraline (Zoloft), citalopram (Celexa), and paroxetine (Paxil, Paxil CR).<br />

The 5-HTT gene is located at 17q11.1-q12 and is composed of 14 exons spanning 31 kb. A 44-base pair<br />

promoter insertion/deletion polymorphism called LPR, or linked polymorphic region, produces alleles<br />

described as long or short. The short allele is dominant and results in decreased concentration of the<br />

transporter protein and a poorer response to stressful events. While individuals homozygous for the long<br />

allele (l/l) may demonstrate response to SSRI therapy in 3 to 4 weeks, individuals with the short allele (l/s<br />

or s/s) may respond to SSRI therapy more slowly, taking up to 12 weeks.<br />

Useful For: Evaluating patients who have failed therapy with selective serotonin reuptake inhibitors<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 1579

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!