Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: A preliminary study

Background and Objectives: This study is designed to understand the pathophysiology of one of the most serious health problems, chronic tension-type headache (CTTH). Two polymorphic sites in serotonin transporter protein gene attracted much interest. These are: the variable number of tandem repeats...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurology India 2008-04, Vol.56 (2), p.156-160
Hauptverfasser: Akcali, Aylin, Tataroglu, Cengiz, Erdal, Emin, Aydin, Neriman, Pehlivan, Sacide
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 160
container_issue 2
container_start_page 156
container_title Neurology India
container_volume 56
creator Akcali, Aylin
Tataroglu, Cengiz
Erdal, Emin
Aydin, Neriman
Pehlivan, Sacide
description Background and Objectives: This study is designed to understand the pathophysiology of one of the most serious health problems, chronic tension-type headache (CTTH). Two polymorphic sites in serotonin transporter protein gene attracted much interest. These are: the variable number of tandem repeats (VNTR) and 5′-flanking promoter region (5-HTTLPR). Materials and Methods: VNTR and 5-HTTLPR polymorphisms were investigated in 126 CTTH patients and 138 healthy control subjects. The patients were being treated with amitripytyline or citalopram or sertraline (SSRI). The polymerase chain reaction (PCR) method was used to investigate the polymorphisms in the serotonin transporter protein gene. Results: There were no statistically significant results based on the 5-HTTLPR gene alleles, however, STin 2.12/12 genotype and STin 2.12 allele were seen to predominate the control group. In order to investigate the combined effect of the two polymorphic loci on the 5-HTT gene expression, samples were separated into nine groups. Genotypes (S/S-12/10) and (L/S-12/10) displayed statistically significant frequency in the CTTH group than in the control group. No significant differences were noticed between the 5-HTTLPR and VNTR haplotype groups and success in treatment. Conclusion: It is possible to make reliable comparisons and hypothesis about the homozygous and/or heterozygous presence of S and STin 12/10 alleles which may be in interaction with CTTH. On the other hand, the presence of homozygous L and STin12 alleles may play a protective role against CTTH. It is also possible that heterogeneity among diseases showing the same clinical research will require a lot of effort for individual identification.
doi_str_mv 10.4103/0028-3886.41993
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_69405765</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A181704362</galeid><sourcerecordid>A181704362</sourcerecordid><originalsourceid>FETCH-LOGICAL-b479t-b410b691ea6e834517247e2559dd780d86fb8475eceeb0be7a7d857d09db5d883</originalsourceid><addsrcrecordid>eNptkdFv1SAUxonRuLvps2-G-OBbNygUqG83i06TJT6oz4SW05WlhQo0y_3vpd7rlpgFwsmB30dOvg-hd5RcckrYFSG1qphSorRty16gXSmq4qSuX6Ld4-sZOk_pvrSM0fo1OqNKKEU52aHpB8SQg3ce52h8WkLMEPEdeMBLmA5ziMvo0pxwIRaTHfic8IPLI-7HWHQ9zuCTC77KhwXwCMaafoRPeI-XCJObnTfxgFNe7eENejWYKcHbU71Av758_nn9tbr9fvPten9bdVy2uZyUdKKlYAQoxhsqay6hbprWWqmIVWLoFJcN9AAd6UAaaVUjLWlt11il2AX6ePx3ieH3Cinr2aUepsl4CGvSouWkkaIp4If_wPuwRl9m0zUT7eaWLFB1hO7MBNr5IRSn-s2haKbgYXDlek8VlYQzURf-8hm-LAuz658VXB0FfQwpRRj0Et1cXNOU6C1mvQWptyD135iL4v1p7rWbwT7xp1yfZuhcmJyHR6KPzuh_l96VTVSZgv0BHme0Gw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>236933127</pqid></control><display><type>article</type><title>Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: A preliminary study</title><source>MEDLINE</source><source>Bioline International</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Akcali, Aylin ; Tataroglu, Cengiz ; Erdal, Emin ; Aydin, Neriman ; Pehlivan, Sacide</creator><creatorcontrib>Akcali, Aylin ; Tataroglu, Cengiz ; Erdal, Emin ; Aydin, Neriman ; Pehlivan, Sacide</creatorcontrib><description>Background and Objectives: This study is designed to understand the pathophysiology of one of the most serious health problems, chronic tension-type headache (CTTH). Two polymorphic sites in serotonin transporter protein gene attracted much interest. These are: the variable number of tandem repeats (VNTR) and 5′-flanking promoter region (5-HTTLPR). Materials and Methods: VNTR and 5-HTTLPR polymorphisms were investigated in 126 CTTH patients and 138 healthy control subjects. The patients were being treated with amitripytyline or citalopram or sertraline (SSRI). The polymerase chain reaction (PCR) method was used to investigate the polymorphisms in the serotonin transporter protein gene. Results: There were no statistically significant results based on the 5-HTTLPR gene alleles, however, STin 2.12/12 genotype and STin 2.12 allele were seen to predominate the control group. In order to investigate the combined effect of the two polymorphic loci on the 5-HTT gene expression, samples were separated into nine groups. Genotypes (S/S-12/10) and (L/S-12/10) displayed statistically significant frequency in the CTTH group than in the control group. No significant differences were noticed between the 5-HTTLPR and VNTR haplotype groups and success in treatment. Conclusion: It is possible to make reliable comparisons and hypothesis about the homozygous and/or heterozygous presence of S and STin 12/10 alleles which may be in interaction with CTTH. On the other hand, the presence of homozygous L and STin12 alleles may play a protective role against CTTH. It is also possible that heterogeneity among diseases showing the same clinical research will require a lot of effort for individual identification.</description><identifier>ISSN: 0028-3886</identifier><identifier>EISSN: 1998-4022</identifier><identifier>DOI: 10.4103/0028-3886.41993</identifier><identifier>PMID: 18688140</identifier><language>eng</language><publisher>India: Medknow Publications on behalf of the Neurological Society of India</publisher><subject>5-flanking promoter region, chronic tension-type headache, haplotypes, serotonin transporter protein gene, a variable number of tandem repeats ; Adolescent ; Adult ; Analysis of Variance ; Chronic Disease ; Chronic illnesses ; Drugs ; Female ; Gene expression ; Gene Frequency ; Genetic aspects ; Genetic polymorphisms ; Genetic Predisposition to Disease ; Genotype ; Genotype &amp; phenotype ; Headaches ; Health aspects ; Humans ; Male ; Middle Aged ; Polymerase chain reaction ; Polymorphism, Genetic - genetics ; Promoter Regions, Genetic - genetics ; Serotonin Plasma Membrane Transport Proteins - genetics ; Serotonin uptake inhibitors ; Studies ; Tension headache ; Tension-Type Headache - genetics ; Young Adult</subject><ispartof>Neurology India, 2008-04, Vol.56 (2), p.156-160</ispartof><rights>Copyright 2008 Neurology India.</rights><rights>COPYRIGHT 2008 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications Apr-Jun 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b479t-b410b691ea6e834517247e2559dd780d86fb8475eceeb0be7a7d857d09db5d883</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,79426</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18688140$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Akcali, Aylin</creatorcontrib><creatorcontrib>Tataroglu, Cengiz</creatorcontrib><creatorcontrib>Erdal, Emin</creatorcontrib><creatorcontrib>Aydin, Neriman</creatorcontrib><creatorcontrib>Pehlivan, Sacide</creatorcontrib><title>Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: A preliminary study</title><title>Neurology India</title><addtitle>Neurol India</addtitle><description>Background and Objectives: This study is designed to understand the pathophysiology of one of the most serious health problems, chronic tension-type headache (CTTH). Two polymorphic sites in serotonin transporter protein gene attracted much interest. These are: the variable number of tandem repeats (VNTR) and 5′-flanking promoter region (5-HTTLPR). Materials and Methods: VNTR and 5-HTTLPR polymorphisms were investigated in 126 CTTH patients and 138 healthy control subjects. The patients were being treated with amitripytyline or citalopram or sertraline (SSRI). The polymerase chain reaction (PCR) method was used to investigate the polymorphisms in the serotonin transporter protein gene. Results: There were no statistically significant results based on the 5-HTTLPR gene alleles, however, STin 2.12/12 genotype and STin 2.12 allele were seen to predominate the control group. In order to investigate the combined effect of the two polymorphic loci on the 5-HTT gene expression, samples were separated into nine groups. Genotypes (S/S-12/10) and (L/S-12/10) displayed statistically significant frequency in the CTTH group than in the control group. No significant differences were noticed between the 5-HTTLPR and VNTR haplotype groups and success in treatment. Conclusion: It is possible to make reliable comparisons and hypothesis about the homozygous and/or heterozygous presence of S and STin 12/10 alleles which may be in interaction with CTTH. On the other hand, the presence of homozygous L and STin12 alleles may play a protective role against CTTH. It is also possible that heterogeneity among diseases showing the same clinical research will require a lot of effort for individual identification.</description><subject>5-flanking promoter region, chronic tension-type headache, haplotypes, serotonin transporter protein gene, a variable number of tandem repeats</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Analysis of Variance</subject><subject>Chronic Disease</subject><subject>Chronic illnesses</subject><subject>Drugs</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Frequency</subject><subject>Genetic aspects</subject><subject>Genetic polymorphisms</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Genotype &amp; phenotype</subject><subject>Headaches</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Polymerase chain reaction</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Serotonin Plasma Membrane Transport Proteins - genetics</subject><subject>Serotonin uptake inhibitors</subject><subject>Studies</subject><subject>Tension headache</subject><subject>Tension-Type Headache - genetics</subject><subject>Young Adult</subject><issn>0028-3886</issn><issn>1998-4022</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>RBI</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkdFv1SAUxonRuLvps2-G-OBbNygUqG83i06TJT6oz4SW05WlhQo0y_3vpd7rlpgFwsmB30dOvg-hd5RcckrYFSG1qphSorRty16gXSmq4qSuX6Ld4-sZOk_pvrSM0fo1OqNKKEU52aHpB8SQg3ce52h8WkLMEPEdeMBLmA5ziMvo0pxwIRaTHfic8IPLI-7HWHQ9zuCTC77KhwXwCMaafoRPeI-XCJObnTfxgFNe7eENejWYKcHbU71Av758_nn9tbr9fvPten9bdVy2uZyUdKKlYAQoxhsqay6hbprWWqmIVWLoFJcN9AAd6UAaaVUjLWlt11il2AX6ePx3ieH3Cinr2aUepsl4CGvSouWkkaIp4If_wPuwRl9m0zUT7eaWLFB1hO7MBNr5IRSn-s2haKbgYXDlek8VlYQzURf-8hm-LAuz658VXB0FfQwpRRj0Et1cXNOU6C1mvQWptyD135iL4v1p7rWbwT7xp1yfZuhcmJyHR6KPzuh_l96VTVSZgv0BHme0Gw</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Akcali, Aylin</creator><creator>Tataroglu, Cengiz</creator><creator>Erdal, Emin</creator><creator>Aydin, Neriman</creator><creator>Pehlivan, Sacide</creator><general>Medknow Publications on behalf of the Neurological Society of India</general><general>Medknow Publications and Media Pvt. Ltd</general><general>Medknow Publications &amp; Media Pvt. Ltd</general><scope>RBI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20080401</creationdate><title>Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: A preliminary study</title><author>Akcali, Aylin ; Tataroglu, Cengiz ; Erdal, Emin ; Aydin, Neriman ; Pehlivan, Sacide</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b479t-b410b691ea6e834517247e2559dd780d86fb8475eceeb0be7a7d857d09db5d883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>5-flanking promoter region, chronic tension-type headache, haplotypes, serotonin transporter protein gene, a variable number of tandem repeats</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Analysis of Variance</topic><topic>Chronic Disease</topic><topic>Chronic illnesses</topic><topic>Drugs</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Frequency</topic><topic>Genetic aspects</topic><topic>Genetic polymorphisms</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Genotype &amp; phenotype</topic><topic>Headaches</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Polymerase chain reaction</topic><topic>Polymorphism, Genetic - genetics</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Serotonin Plasma Membrane Transport Proteins - genetics</topic><topic>Serotonin uptake inhibitors</topic><topic>Studies</topic><topic>Tension headache</topic><topic>Tension-Type Headache - genetics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akcali, Aylin</creatorcontrib><creatorcontrib>Tataroglu, Cengiz</creatorcontrib><creatorcontrib>Erdal, Emin</creatorcontrib><creatorcontrib>Aydin, Neriman</creatorcontrib><creatorcontrib>Pehlivan, Sacide</creatorcontrib><collection>Bioline International</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Neurology India</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akcali, Aylin</au><au>Tataroglu, Cengiz</au><au>Erdal, Emin</au><au>Aydin, Neriman</au><au>Pehlivan, Sacide</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: A preliminary study</atitle><jtitle>Neurology India</jtitle><addtitle>Neurol India</addtitle><date>2008-04-01</date><risdate>2008</risdate><volume>56</volume><issue>2</issue><spage>156</spage><epage>160</epage><pages>156-160</pages><issn>0028-3886</issn><eissn>1998-4022</eissn><abstract>Background and Objectives: This study is designed to understand the pathophysiology of one of the most serious health problems, chronic tension-type headache (CTTH). Two polymorphic sites in serotonin transporter protein gene attracted much interest. These are: the variable number of tandem repeats (VNTR) and 5′-flanking promoter region (5-HTTLPR). Materials and Methods: VNTR and 5-HTTLPR polymorphisms were investigated in 126 CTTH patients and 138 healthy control subjects. The patients were being treated with amitripytyline or citalopram or sertraline (SSRI). The polymerase chain reaction (PCR) method was used to investigate the polymorphisms in the serotonin transporter protein gene. Results: There were no statistically significant results based on the 5-HTTLPR gene alleles, however, STin 2.12/12 genotype and STin 2.12 allele were seen to predominate the control group. In order to investigate the combined effect of the two polymorphic loci on the 5-HTT gene expression, samples were separated into nine groups. Genotypes (S/S-12/10) and (L/S-12/10) displayed statistically significant frequency in the CTTH group than in the control group. No significant differences were noticed between the 5-HTTLPR and VNTR haplotype groups and success in treatment. Conclusion: It is possible to make reliable comparisons and hypothesis about the homozygous and/or heterozygous presence of S and STin 12/10 alleles which may be in interaction with CTTH. On the other hand, the presence of homozygous L and STin12 alleles may play a protective role against CTTH. It is also possible that heterogeneity among diseases showing the same clinical research will require a lot of effort for individual identification.</abstract><cop>India</cop><pub>Medknow Publications on behalf of the Neurological Society of India</pub><pmid>18688140</pmid><doi>10.4103/0028-3886.41993</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0028-3886
ispartof Neurology India, 2008-04, Vol.56 (2), p.156-160
issn 0028-3886
1998-4022
language eng
recordid cdi_proquest_miscellaneous_69405765
source MEDLINE; Bioline International; EZB-FREE-00999 freely available EZB journals
subjects 5-flanking promoter region, chronic tension-type headache, haplotypes, serotonin transporter protein gene, a variable number of tandem repeats
Adolescent
Adult
Analysis of Variance
Chronic Disease
Chronic illnesses
Drugs
Female
Gene expression
Gene Frequency
Genetic aspects
Genetic polymorphisms
Genetic Predisposition to Disease
Genotype
Genotype & phenotype
Headaches
Health aspects
Humans
Male
Middle Aged
Polymerase chain reaction
Polymorphism, Genetic - genetics
Promoter Regions, Genetic - genetics
Serotonin Plasma Membrane Transport Proteins - genetics
Serotonin uptake inhibitors
Studies
Tension headache
Tension-Type Headache - genetics
Young Adult
title Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: A preliminary study
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T02%3A53%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Serotonin%20transporter%20gene%20polymorphisms%20in%20patients%20with%20chronic%20tension-type%20headache:%20A%20preliminary%20study&rft.jtitle=Neurology%20India&rft.au=Akcali,%20Aylin&rft.date=2008-04-01&rft.volume=56&rft.issue=2&rft.spage=156&rft.epage=160&rft.pages=156-160&rft.issn=0028-3886&rft.eissn=1998-4022&rft_id=info:doi/10.4103/0028-3886.41993&rft_dat=%3Cgale_proqu%3EA181704362%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=236933127&rft_id=info:pmid/18688140&rft_galeid=A181704362&rfr_iscdi=true