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Association between obsessive–compulsive disorder and a variable number of tandem repeats polymorphism in intron 2 of the serotonin transporter gene
Pharmacological studies indicate a dysregulation of the serotonergic system in obsessive–compulsive disorder (OCD). A variable number tandem repeats (VNTR) polymorphism with three alleles (Stin2.9, Stin2.10, Stin2.12) has been described in intron 2 of the serotonin transporter (5-HTT) gene. This pol...
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Published in: | Progress in neuro-psychopharmacology & biological psychiatry 2007-03, Vol.31 (2), p.416-420 |
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container_title | Progress in neuro-psychopharmacology & biological psychiatry |
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creator | Baca-Garcia, Enrique Vaquero-Lorenzo, Concepcion Diaz-Hernandez, Montserrat Rodriguez-Salgado, Beatriz Dolengevich-Segal, Helen Arrojo-Romero, Manuel Botillo-Martin, Carlota Ceverino, Antonio Piqueras, Jose Fernandez Perez-Rodriguez, M. Mercedes Saiz-Ruiz, Jeronimo |
description | Pharmacological studies indicate a dysregulation of the serotonergic system in obsessive–compulsive disorder (OCD). A variable number tandem repeats (VNTR) polymorphism with three alleles (Stin2.9, Stin2.10, Stin2.12) has been described in intron 2 of the serotonin transporter (5-HTT) gene. This polymorphism has been associated with unipolar depression, bipolar disorder, schizophrenia, and anxiety disorders including OCD.
The association between OCD and the polymorphism is examined in 97 OCD patients, 578 psychiatric controls and 406 healthy controls, all Spanish Caucasians.
Genotype frequencies for the polymorphism were significantly different in OCD patients, psychiatric patients and controls. There was a significant excess of 12/12 and 12/10 genotypes in OCD patients compared to psychiatric patients and controls.
Our results indicate a possible association between the Stin2.12 allele of the VNTR polymorphism and OCD. |
doi_str_mv | 10.1016/j.pnpbp.2006.10.016 |
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The association between OCD and the polymorphism is examined in 97 OCD patients, 578 psychiatric controls and 406 healthy controls, all Spanish Caucasians.
Genotype frequencies for the polymorphism were significantly different in OCD patients, psychiatric patients and controls. There was a significant excess of 12/12 and 12/10 genotypes in OCD patients compared to psychiatric patients and controls.
Our results indicate a possible association between the Stin2.12 allele of the VNTR polymorphism and OCD.</description><identifier>ISSN: 0278-5846</identifier><identifier>EISSN: 1878-4216</identifier><identifier>DOI: 10.1016/j.pnpbp.2006.10.016</identifier><identifier>PMID: 17174018</identifier><identifier>CODEN: PNPPD7</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Adult and adolescent clinical studies ; Alleles ; Anxiety disorders. Neuroses ; Biological and medical sciences ; Gene Frequency ; Genetic polymorphism ; Genetic Predisposition to Disease ; Humans ; Intron 2 ; Introns ; Medical sciences ; Minisatellite Repeats - genetics ; Neuropharmacology ; Obsessive-Compulsive Disorder - genetics ; Obsessive-compulsive disorders ; Obsessive–compulsive disorder ; Pharmacology. Drug treatments ; Polymorphism, Genetic - genetics ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Serotonin Plasma Membrane Transport Proteins - genetics ; Serotonin transporter ; Variable number tandem repeats</subject><ispartof>Progress in neuro-psychopharmacology & biological psychiatry, 2007-03, Vol.31 (2), p.416-420</ispartof><rights>2006 Elsevier Inc.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-323e5782c186403f03888d9ccd8082710e876300e7a0d46ab27cbe8bea8eb553</citedby><cites>FETCH-LOGICAL-c418t-323e5782c186403f03888d9ccd8082710e876300e7a0d46ab27cbe8bea8eb553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18534373$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17174018$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baca-Garcia, Enrique</creatorcontrib><creatorcontrib>Vaquero-Lorenzo, Concepcion</creatorcontrib><creatorcontrib>Diaz-Hernandez, Montserrat</creatorcontrib><creatorcontrib>Rodriguez-Salgado, Beatriz</creatorcontrib><creatorcontrib>Dolengevich-Segal, Helen</creatorcontrib><creatorcontrib>Arrojo-Romero, Manuel</creatorcontrib><creatorcontrib>Botillo-Martin, Carlota</creatorcontrib><creatorcontrib>Ceverino, Antonio</creatorcontrib><creatorcontrib>Piqueras, Jose Fernandez</creatorcontrib><creatorcontrib>Perez-Rodriguez, M. Mercedes</creatorcontrib><creatorcontrib>Saiz-Ruiz, Jeronimo</creatorcontrib><title>Association between obsessive–compulsive disorder and a variable number of tandem repeats polymorphism in intron 2 of the serotonin transporter gene</title><title>Progress in neuro-psychopharmacology & biological psychiatry</title><addtitle>Prog Neuropsychopharmacol Biol Psychiatry</addtitle><description>Pharmacological studies indicate a dysregulation of the serotonergic system in obsessive–compulsive disorder (OCD). A variable number tandem repeats (VNTR) polymorphism with three alleles (Stin2.9, Stin2.10, Stin2.12) has been described in intron 2 of the serotonin transporter (5-HTT) gene. This polymorphism has been associated with unipolar depression, bipolar disorder, schizophrenia, and anxiety disorders including OCD.
The association between OCD and the polymorphism is examined in 97 OCD patients, 578 psychiatric controls and 406 healthy controls, all Spanish Caucasians.
Genotype frequencies for the polymorphism were significantly different in OCD patients, psychiatric patients and controls. There was a significant excess of 12/12 and 12/10 genotypes in OCD patients compared to psychiatric patients and controls.
Our results indicate a possible association between the Stin2.12 allele of the VNTR polymorphism and OCD.</description><subject>Adult and adolescent clinical studies</subject><subject>Alleles</subject><subject>Anxiety disorders. Neuroses</subject><subject>Biological and medical sciences</subject><subject>Gene Frequency</subject><subject>Genetic polymorphism</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Intron 2</subject><subject>Introns</subject><subject>Medical sciences</subject><subject>Minisatellite Repeats - genetics</subject><subject>Neuropharmacology</subject><subject>Obsessive-Compulsive Disorder - genetics</subject><subject>Obsessive-compulsive disorders</subject><subject>Obsessive–compulsive disorder</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Serotonin Plasma Membrane Transport Proteins - genetics</subject><subject>Serotonin transporter</subject><subject>Variable number tandem repeats</subject><issn>0278-5846</issn><issn>1878-4216</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkctq3DAUhkVpaaZpn6BQtGl2M5Us25IXXYTQGwS6yV5I8nGjwZZcHXlKdnmHQh8wT1I5M5BdCwJJ__nOhfMT8pazHWe8_bDfzWG2865irC3KrmjPyIYrqbZ1xdvnZMOq8m5U3Z6RV4h7xhgXTLwkZ1xyWTOuNuTPJWJ03mQfA7WQfwEEGi0Coj_Aw_1vF6d5GdcP7T3G1EOiJvTU0INJ3tgRaFgmW9Q40FwiMNEEM5iMdI7j3RTTfOtxoj6Uk1NpUz2it0ARUswxlEhOJuAcUy51fkCA1-TFYEaEN6f7nNx8_nRz9XV7_f3Lt6vL662rucpbUQlopKocV23NxMCEUqrvnOsVU5XkDJRsBWMgDevr1thKOgvKglFgm0ack4tj2TnFnwtg1pNHB-NoAsQFdau6Tlaq_i_IO1Xm6EQBxRF0KSImGPSc_GTSneZMr7bpvX60Ta-2rWLRSta7U_nFTtA_5Zx8KsD7E2DQmXEo63IenzjViFrItf3HIwdlaQcPSaPzEBz0PoHLuo_-n4P8BYkHu1Y</recordid><startdate>20070330</startdate><enddate>20070330</enddate><creator>Baca-Garcia, Enrique</creator><creator>Vaquero-Lorenzo, Concepcion</creator><creator>Diaz-Hernandez, Montserrat</creator><creator>Rodriguez-Salgado, Beatriz</creator><creator>Dolengevich-Segal, Helen</creator><creator>Arrojo-Romero, Manuel</creator><creator>Botillo-Martin, Carlota</creator><creator>Ceverino, Antonio</creator><creator>Piqueras, Jose Fernandez</creator><creator>Perez-Rodriguez, M. Mercedes</creator><creator>Saiz-Ruiz, Jeronimo</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070330</creationdate><title>Association between obsessive–compulsive disorder and a variable number of tandem repeats polymorphism in intron 2 of the serotonin transporter gene</title><author>Baca-Garcia, Enrique ; Vaquero-Lorenzo, Concepcion ; Diaz-Hernandez, Montserrat ; Rodriguez-Salgado, Beatriz ; Dolengevich-Segal, Helen ; Arrojo-Romero, Manuel ; Botillo-Martin, Carlota ; Ceverino, Antonio ; Piqueras, Jose Fernandez ; Perez-Rodriguez, M. 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Drug treatments</topic><topic>Polymorphism, Genetic - genetics</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Serotonin Plasma Membrane Transport Proteins - genetics</topic><topic>Serotonin transporter</topic><topic>Variable number tandem repeats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baca-Garcia, Enrique</creatorcontrib><creatorcontrib>Vaquero-Lorenzo, Concepcion</creatorcontrib><creatorcontrib>Diaz-Hernandez, Montserrat</creatorcontrib><creatorcontrib>Rodriguez-Salgado, Beatriz</creatorcontrib><creatorcontrib>Dolengevich-Segal, Helen</creatorcontrib><creatorcontrib>Arrojo-Romero, Manuel</creatorcontrib><creatorcontrib>Botillo-Martin, Carlota</creatorcontrib><creatorcontrib>Ceverino, Antonio</creatorcontrib><creatorcontrib>Piqueras, Jose Fernandez</creatorcontrib><creatorcontrib>Perez-Rodriguez, M. Mercedes</creatorcontrib><creatorcontrib>Saiz-Ruiz, Jeronimo</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Progress in neuro-psychopharmacology & biological psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baca-Garcia, Enrique</au><au>Vaquero-Lorenzo, Concepcion</au><au>Diaz-Hernandez, Montserrat</au><au>Rodriguez-Salgado, Beatriz</au><au>Dolengevich-Segal, Helen</au><au>Arrojo-Romero, Manuel</au><au>Botillo-Martin, Carlota</au><au>Ceverino, Antonio</au><au>Piqueras, Jose Fernandez</au><au>Perez-Rodriguez, M. Mercedes</au><au>Saiz-Ruiz, Jeronimo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between obsessive–compulsive disorder and a variable number of tandem repeats polymorphism in intron 2 of the serotonin transporter gene</atitle><jtitle>Progress in neuro-psychopharmacology & biological psychiatry</jtitle><addtitle>Prog Neuropsychopharmacol Biol Psychiatry</addtitle><date>2007-03-30</date><risdate>2007</risdate><volume>31</volume><issue>2</issue><spage>416</spage><epage>420</epage><pages>416-420</pages><issn>0278-5846</issn><eissn>1878-4216</eissn><coden>PNPPD7</coden><abstract>Pharmacological studies indicate a dysregulation of the serotonergic system in obsessive–compulsive disorder (OCD). A variable number tandem repeats (VNTR) polymorphism with three alleles (Stin2.9, Stin2.10, Stin2.12) has been described in intron 2 of the serotonin transporter (5-HTT) gene. This polymorphism has been associated with unipolar depression, bipolar disorder, schizophrenia, and anxiety disorders including OCD.
The association between OCD and the polymorphism is examined in 97 OCD patients, 578 psychiatric controls and 406 healthy controls, all Spanish Caucasians.
Genotype frequencies for the polymorphism were significantly different in OCD patients, psychiatric patients and controls. There was a significant excess of 12/12 and 12/10 genotypes in OCD patients compared to psychiatric patients and controls.
Our results indicate a possible association between the Stin2.12 allele of the VNTR polymorphism and OCD.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>17174018</pmid><doi>10.1016/j.pnpbp.2006.10.016</doi><tpages>5</tpages></addata></record> |
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subjects | Adult and adolescent clinical studies Alleles Anxiety disorders. Neuroses Biological and medical sciences Gene Frequency Genetic polymorphism Genetic Predisposition to Disease Humans Intron 2 Introns Medical sciences Minisatellite Repeats - genetics Neuropharmacology Obsessive-Compulsive Disorder - genetics Obsessive-compulsive disorders Obsessive–compulsive disorder Pharmacology. Drug treatments Polymorphism, Genetic - genetics Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Serotonin Plasma Membrane Transport Proteins - genetics Serotonin transporter Variable number tandem repeats |
title | Association between obsessive–compulsive disorder and a variable number of tandem repeats polymorphism in intron 2 of the serotonin transporter gene |
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