Hostname: page-component-76fb5796d-45l2p Total loading time: 0 Render date: 2024-04-28T00:27:25.627Z Has data issue: false hasContentIssue false

P0047 - The TAQ1A DRD2 Polymorphism in type II alcoholism: Marker of age at onset or of a familial disease?

Published online by Cambridge University Press:  16 April 2020

E. Pinto
Affiliation:
Department of Psychiatry, University of Liege, Liege, Belgium
J. Reggers
Affiliation:
Department of Psychiatry, University of Liege, Liege, Belgium
P. Gorwood
Affiliation:
INSERM U675, University of Paris, Paris, France
G. Scantamburlo
Affiliation:
Department of Psychiatry, University of Liege, Liege, Belgium
W. Pitchot
Affiliation:
Department of Psychiatry, University of Liege, Liege, Belgium
M. Ansseau
Affiliation:
Department of Psychiatry, University of Liege, Liege, Belgium

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Background and Aims:

Cloninger's type II is a severe, early-onset, male-limited, genetically influenced, impulsive form of alcoholism. We assessed the association of two gene polymorphisms (TaqI A DRD2 and 5-HTTpro) with Cloninger's typology, as defined by age at onset of alcohol-related problems, and family history of alcohol abuse, which is thought to be more frequent in type II alcoholics.

Methods:

58 male alcohol dependent patients were discriminated according to age at onset of alcohol-related problems and interviewed about family history of alcoholism. Genomic DNA was extracted and PCR amplifying the studied polymorphisms were performed. The associations between DRD2 (A1 or A2 alleles), 5-HTTpro (L and S alleles), family history and typology were assessed by Pearson chi2 analyses.

Results:

While typology was not influenced by any of the studied polymorphisms, a higher rate of general family history of alcohol abuse was still observed in type II patients (χ2= 4.53; p = 0.033). Furthermore, the A1 allele of the DRD2 was significantly associated with paternal history of alcoholism (χ2= 4.66; p = 0.031) and male, first-degree, collateral history of alcoholism (χ2= 4.40; p = 0.036).

Conclusions:

Age at onset as main discriminator between type I and type II does not seem to be influenced by TaqI A DRD2 and 5-5HTTpro polymorphisms. However, the A1 allele of the DRD2 may be a marker of male familial alcoholism, which is in line with previous studies showing association between TaqI A DRD2 with some clinical features of type II alcoholism.

Type
Poster Session III: Alcoholism And Addiction
Copyright
Copyright © European Psychiatric Association 2008
Submit a response

Comments

No Comments have been published for this article.