Polimorfismos serotoninérgicos y trastorno obsesivo-compulsivo
- P.A. Sáiz 1
- B. Morales 2
- M.P. García-Portilla 1
- M.T. Bascarán 1
- E. Coto 2
- V. Álvarez 2
- J.M. Fernández 1
- M. Bousoño 1
- J. Bobes 1
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1
Universidad de Oviedo
info
- 2 Hospital Central de Asturias
ISSN: 1134-5934
Year of publication: 2001
Volume: 8
Issue: 6
Pages: 219-224
Type: Article
More publications in: Psiquiatría biológica: Publicación oficial de la Sociedad Española de Psiquiatría Biológica
Abstract
Objective: To investigate the possible association between four serotonin gene polymorphisms [T102C, A-1438G, 5-HTTLPR, VNTR5-HTT] and obsessive compulsive disorder (OCD). Patients and methods: We genotyped 41 OCD outpatients (DSM-IV criteria) (mean age: 36.22 [9.62], 31.7% males) and 119 healthy volunteers [blood donors] (mean age: 43.29 [11.28], 75.8% males) from Asturias. Polimorphisms were determined after PCR amplification followed by digestion with restriction enzymes and electrophoresis on an agarose gel. Results: 5-HT2A polymorphisms, both 5-HT2A polymorphisms (T102C and A-1438G) are in complete linkage desequilibrium in our population. T102C or A-1438G (OCD vs Controls): TT or AA: 22.0%, 19.3%; TC or AG: 48.8%, 52,9%; CC or GG: 29.3%, 27.7% (p = 0.908). Serotonin transporter polymorphisms¿ 5HTTLPR (OCD vs Controls): LL: 26.8%, 30.3%; LS: 56.1%, 47.9%; ss: 17.1%, 21.8% (p = 0.648). VNTR-5HTT (OCD vs Controls): 12rep12rep: 53.7%, 39.5%; 12rep10rep: 41.5%, 31.1%; 12rep9rep: 0%, 0.8%; 10rep10rep: 4.9%, 27.7%; 10rep9rep: 0%, 0,8% (p = 0.034). 12rep allele was more frequent in OCD patients; 74.4% vs 55.5%, p = 0.008. However, an analysis according gender shows that these differences only occur in women (p = 0.006 for genotype frequencies and p = 0.001 for allele frequencies). Conclusions: In women polymorphic variations in the VNTR in the serotonin transporter gene might influence susceptibility to OCD. However, larger samples are necessary to confirm or reject the current data.