Article: Do COMT, BDNF and NRG1 polymorphisms influence P50 sensory gating in psychosis?
| Title | Do COMT, BDNF and NRG1 polymorphisms influence P50 sensory gating in psychosis? | ||||||||||||||
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| Authors | Shaikh, M Hall, MH3 Schulze, K Dutt, A Walshe, M Williams, I Constante, M Picchioni, M1 Toulopoulou, T Collier, D Rijsdijk, F2 Powell, J Arranz, M Murray, RM Bramon, E | ||||||||||||||
| Keywords | BDNF COMT NRG1 P50 psychosis | ||||||||||||||
| Issue Date | 2011 | ||||||||||||||
| Publisher | Cambridge University Press. The Journal's web site is located at http://journals.cambridge.org/action/displayJournal?jid=PSM | ||||||||||||||
| Citation | Psychological Medicine, 2011, v. 41 n. 2, p. 263-276 [How to Cite?] DOI: http://dx.doi.org/10.1017/S003329170999239X | ||||||||||||||
| Abstract | Background Auditory P50 sensory gating deficits correlate with genetic risk for schizophrenia and constitute a plausible endophenotype for the disease. The well-supported role of catechol-O-methyltransferase (COMT), brain-derived neurotrophic factor (BDNF) and neuregulin 1 (NRG1) genes in neurodevelopment and cognition make a strong theoretical case for their influence on the P50 endophenotype.Method The possible role of NRG1, COMT Val 158Met and BDNF Val 66Met gene polymorphisms on the P50 endophenotype was examined in a large sample consisting of psychotic patients, their unaffected relatives and unrelated healthy controls using linear regression analyses.Results Although P50 deficits were present in patients and their unaffected relatives, there was no evidence for an association between NRG1, COMT Val 158Met or BDNF Val 66Met genotypes and the P50 endophenotype.Conclusions The evidence from our large study suggests that any such association between P50 indices and NRG1, COMT Val 158Met or BDNF Val 66Met genotypes, if present, must be very subtle. © 2010 Cambridge University Press. | ||||||||||||||
| ISSN | 0033-2917 2011 Impact Factor: 6.159 2011 SCImago Journal Rankings: 0.269 | ||||||||||||||
| DOI | http://dx.doi.org/10.1017/S003329170999239X | ||||||||||||||
| ISI Accession Number ID | WOS:000286072900004
Funding Information: We are grateful to all those who participated in our research study. This study was funded by the Wellcome Trust, the Schizophrenia Research Fund, the National Alliance for Research on Schizophrenia and Depression, the British Medical Association and the Psychiatry Research Trust. We also thank the National Institute for Health Research (NIHR) Biomedical Research Centre for financial support. | ||||||||||||||
| References | References in Scopus |
| dc.contributor.author | Shaikh, M | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| dc.contributor.author | Hall, MH | ||||||||||||||
| dc.contributor.author | Schulze, K | ||||||||||||||
| dc.contributor.author | Dutt, A | ||||||||||||||
| dc.contributor.author | Walshe, M | ||||||||||||||
| dc.contributor.author | Williams, I | ||||||||||||||
| dc.contributor.author | Constante, M | ||||||||||||||
| dc.contributor.author | Picchioni, M | ||||||||||||||
| dc.contributor.author | Toulopoulou, T | ||||||||||||||
| dc.contributor.author | Collier, D | ||||||||||||||
| dc.contributor.author | Rijsdijk, F | ||||||||||||||
| dc.contributor.author | Powell, J | ||||||||||||||
| dc.contributor.author | Arranz, M | ||||||||||||||
| dc.contributor.author | Murray, RM | ||||||||||||||
| dc.contributor.author | Bramon, E | ||||||||||||||
| dc.date.accessioned | 2011-09-27T03:02:37Z | ||||||||||||||
| dc.date.available | 2011-09-27T03:02:37Z | ||||||||||||||
| dc.date.issued | 2011 | ||||||||||||||
| dc.description.abstract | Background Auditory P50 sensory gating deficits correlate with genetic risk for schizophrenia and constitute a plausible endophenotype for the disease. The well-supported role of catechol-O-methyltransferase (COMT), brain-derived neurotrophic factor (BDNF) and neuregulin 1 (NRG1) genes in neurodevelopment and cognition make a strong theoretical case for their influence on the P50 endophenotype.Method The possible role of NRG1, COMT Val 158Met and BDNF Val 66Met gene polymorphisms on the P50 endophenotype was examined in a large sample consisting of psychotic patients, their unaffected relatives and unrelated healthy controls using linear regression analyses.Results Although P50 deficits were present in patients and their unaffected relatives, there was no evidence for an association between NRG1, COMT Val 158Met or BDNF Val 66Met genotypes and the P50 endophenotype.Conclusions The evidence from our large study suggests that any such association between P50 indices and NRG1, COMT Val 158Met or BDNF Val 66Met genotypes, if present, must be very subtle. © 2010 Cambridge University Press. | ||||||||||||||
| dc.description.nature | link_to_subscribed_fulltext | ||||||||||||||
| dc.identifier.citation | Psychological Medicine, 2011, v. 41 n. 2, p. 263-276 [How to Cite?] DOI: http://dx.doi.org/10.1017/S003329170999239X | ||||||||||||||
| dc.identifier.doi | http://dx.doi.org/10.1017/S003329170999239X | ||||||||||||||
| dc.identifier.eissn | 1469-8978 | ||||||||||||||
| dc.identifier.epage | 276 | ||||||||||||||
| dc.identifier.isi | WOS:000286072900004
Funding Information: We are grateful to all those who participated in our research study. This study was funded by the Wellcome Trust, the Schizophrenia Research Fund, the National Alliance for Research on Schizophrenia and Depression, the British Medical Association and the Psychiatry Research Trust. We also thank the National Institute for Health Research (NIHR) Biomedical Research Centre for financial support. | ||||||||||||||
| dc.identifier.issn | 0033-2917 2011 Impact Factor: 6.159 2011 SCImago Journal Rankings: 0.269 | ||||||||||||||
| dc.identifier.issue | 2 | ||||||||||||||
| dc.identifier.scopus | eid_2-s2.0-79952819313 | ||||||||||||||
| dc.identifier.spage | 263 | ||||||||||||||
| dc.identifier.uri | http://hdl.handle.net/10722/141823 | ||||||||||||||
| dc.identifier.volume | 41 | ||||||||||||||
| dc.language | eng | ||||||||||||||
| dc.publisher | Cambridge University Press. The Journal's web site is located at http://journals.cambridge.org/action/displayJournal?jid=PSM | ||||||||||||||
| dc.publisher.place | United Kingdom | ||||||||||||||
| dc.relation.ispartof | Psychological Medicine | ||||||||||||||
| dc.relation.references | References in Scopus | ||||||||||||||
| dc.subject | BDNF | ||||||||||||||
| dc.subject | COMT | ||||||||||||||
| dc.subject | NRG1 | ||||||||||||||
| dc.subject | P50 | ||||||||||||||
| dc.subject | psychosis | ||||||||||||||
| dc.title | Do COMT, BDNF and NRG1 polymorphisms influence P50 sensory gating in psychosis? | ||||||||||||||
| dc.type | Article |
- King's College London
- Medical Research Council
- McLean Hospital

