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- Publisher Website: 10.1002/ajmg.b.20150
- Scopus: eid_2-s2.0-12144290388
- PMID: 15048655
- WOS: WOS:000220607300017
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Article: Serotonergic Polymorphisms and Psychotic Disorders in Populations from North Spain
Title | Serotonergic Polymorphisms and Psychotic Disorders in Populations from North Spain |
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Authors | |
Keywords | 5-HT2A 5-HTT Psychoses Schizophrenia Serotonin |
Issue Date | 2004 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.interscience.wiley.com/jpages/0148-7299:1/ |
Citation | American Journal Of Medical Genetics - Neuropsychiatric Genetics, 2004, v. 126 B n. 1, p. 88-94 How to Cite? |
Abstract | There is strong biological evidence relating alterations in the serotonergic system with mental disorders. These alterations may be originated at the DNA level by sequence mutations that alter the functioning of serotonin receptors and transporter. To test this hypothesis we investigated three genetic variants of the 5-HT2A receptor (-1438G/A, 102T/C and His452Tyr) and two variants of the serotonin transporter (a VNTR in the second intron and a 44 bp insertion/delition in the promoter region of the gene) in a clinical sample recruited in a human isolate and in surrounding areas in Northern Spain (N = 257) and in ethnically matched controls (N = 334). No clear association was found between 5-HT2A variants and psychosis. However, marginal associations were observed between the 5-HTT LPR and VNTR variants and psychosis (P ≤ 0.05) indicating a minor contribution to psychosis of genetic alterations in this gene. © 2003 Wiley-Liss, Inc. |
Persistent Identifier | http://hdl.handle.net/10722/175902 |
ISSN | 2023 Impact Factor: 1.6 2023 SCImago Journal Rankings: 1.228 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Mata, I | en_US |
dc.contributor.author | Arranz, MJ | en_US |
dc.contributor.author | Patiño, A | en_US |
dc.contributor.author | Lai, T | en_US |
dc.contributor.author | Beperet, M | en_US |
dc.contributor.author | Sierrasesumaga, L | en_US |
dc.contributor.author | Clark, D | en_US |
dc.contributor.author | PerezNievas, F | en_US |
dc.contributor.author | Richards, L | en_US |
dc.contributor.author | Ortuño, F | en_US |
dc.contributor.author | Sham, P | en_US |
dc.contributor.author | Kerwin, RW | en_US |
dc.date.accessioned | 2012-11-26T09:02:20Z | - |
dc.date.available | 2012-11-26T09:02:20Z | - |
dc.date.issued | 2004 | en_US |
dc.identifier.citation | American Journal Of Medical Genetics - Neuropsychiatric Genetics, 2004, v. 126 B n. 1, p. 88-94 | en_US |
dc.identifier.issn | 1552-4841 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/175902 | - |
dc.description.abstract | There is strong biological evidence relating alterations in the serotonergic system with mental disorders. These alterations may be originated at the DNA level by sequence mutations that alter the functioning of serotonin receptors and transporter. To test this hypothesis we investigated three genetic variants of the 5-HT2A receptor (-1438G/A, 102T/C and His452Tyr) and two variants of the serotonin transporter (a VNTR in the second intron and a 44 bp insertion/delition in the promoter region of the gene) in a clinical sample recruited in a human isolate and in surrounding areas in Northern Spain (N = 257) and in ethnically matched controls (N = 334). No clear association was found between 5-HT2A variants and psychosis. However, marginal associations were observed between the 5-HTT LPR and VNTR variants and psychosis (P ≤ 0.05) indicating a minor contribution to psychosis of genetic alterations in this gene. © 2003 Wiley-Liss, Inc. | en_US |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.interscience.wiley.com/jpages/0148-7299:1/ | en_US |
dc.relation.ispartof | American Journal of Medical Genetics - Neuropsychiatric Genetics | en_US |
dc.subject | 5-HT2A | - |
dc.subject | 5-HTT | - |
dc.subject | Psychoses | - |
dc.subject | Schizophrenia | - |
dc.subject | Serotonin | - |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Case-Control Studies | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Genetics, Population | en_US |
dc.subject.mesh | Haplotypes - Genetics | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Minisatellite Repeats - Genetics | en_US |
dc.subject.mesh | Polymorphism, Genetic - Genetics | en_US |
dc.subject.mesh | Promoter Regions, Genetic - Genetics | en_US |
dc.subject.mesh | Psychotic Disorders - Genetics | en_US |
dc.subject.mesh | Receptor, Serotonin, 5-Ht2a - Genetics | en_US |
dc.subject.mesh | Spain - Epidemiology | en_US |
dc.title | Serotonergic Polymorphisms and Psychotic Disorders in Populations from North Spain | en_US |
dc.type | Article | en_US |
dc.identifier.email | Sham, P: pcsham@hku.hk | en_US |
dc.identifier.authority | Sham, P=rp00459 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/ajmg.b.20150 | - |
dc.identifier.pmid | 15048655 | - |
dc.identifier.scopus | eid_2-s2.0-12144290388 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-12144290388&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 126 B | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 88 | en_US |
dc.identifier.epage | 94 | en_US |
dc.identifier.isi | WOS:000220607300017 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Mata, I=9638989000 | en_US |
dc.identifier.scopusauthorid | Arranz, MJ=7006010757 | en_US |
dc.identifier.scopusauthorid | Patiño, A=7004235894 | en_US |
dc.identifier.scopusauthorid | Lai, T=8089161300 | en_US |
dc.identifier.scopusauthorid | Beperet, M=18134905100 | en_US |
dc.identifier.scopusauthorid | Sierrasesumaga, L=7004703567 | en_US |
dc.identifier.scopusauthorid | Clark, D=7404789238 | en_US |
dc.identifier.scopusauthorid | PerezNievas, F=8089160900 | en_US |
dc.identifier.scopusauthorid | Richards, L=8089161500 | en_US |
dc.identifier.scopusauthorid | Ortuño, F=7003786852 | en_US |
dc.identifier.scopusauthorid | Sham, P=34573429300 | en_US |
dc.identifier.scopusauthorid | Kerwin, RW=7102904567 | en_US |
dc.identifier.issnl | 1552-4841 | - |