Keine Assoziation des - 141C-Ins/Del-Polymorphismus im Gen des Dopaminrezeptor D2 mit Schizophrenie
No Association of the - 141C Ins/Del Polymorphism of the Dopamine D2 Receptor with SchizophreniaThomas Rohrmeier1
, Albert Putzhammer1
, Heino Sartor1
, Michael Knapp2
, Margot Albus3
, Margitta Borrmann-Hassenbach3
, Dirk Lichtermann4
, Dieter Wildenauer4
, Sibylle Schwab4
, Wolfgang Maier4
, Helmfried E. Klein1
, Peter Eichhammer1
1Klinik und Poliklinik für Psychiatrie und Psychotherapie der Universität Regensburg am Bezirksklinikum
2Institut für Medizinische Statistik der Universität Bonn
3Abteilung Forschung und Lehre Bezirkskrankenhaus Haar
4Klinik und Poliklinik für Psychiatrie und Psychotherapie der Universität Bonn
Im Gen des Dopamin-D2-Rezeptors wurde kürzlich der funktionelle - 141C-Ins/Del-Polymorphismus entdeckt, dessen Ins-Allel mit Schizophrenie assoziiert wurde. Die vorliegende Arbeit untersuchte, ob eine Assoziation auch in deutschen Kernfamilien (Trios) nachzuweisen war. 190 Trios von schizophrenen Patienten wurden bezüglich des Ins/Del-Genotyp untersucht. Parallel wurden 268 schizophrene Patienten und 244 Kontrollen analysiert. Weder der Trioansatz (TDT = 0,152, p = 0,696) noch die fallkontrollierte Studie (p = 0,124) wiesen eine Assoziation des Ins-Allels mit Schizophrenie nach. Der - 141C-Ins/Del-Polymorphismus ist kein bedeutender Vulnerabililtätslokus für Schizophrenie.
Abstract
Recently, a putative functional polymorphism (- 141C Ins/Del) in the 5′-flanking region of the dopamine D2 receptor was found. An association of the Ins allele with schizophrenia has been described in a Japanese sample. In the present study this association was examined in a German schizophrenia patient population. In a family based approach 190 German family trios were analyzed for the - 141C Ins/Del genotype. Using the transmission disequilibrium test (TDT) we found no evidence for an association of the Ins allele with schizophrenia (TDT = 0.152, P = 0.696). In parallel, we performed an independent case control study with 268 schizophrenic patients and 244 controls. Again, we did not detect an overrepresentation of the Ins allele in patients (P = 0.124). Thus, our data do not support the hypothesis that the - 141C Ins variant plays a major role in predisposition to schizophrenia. To confirm our conclusion further preferentially family based studies are needed.
Literatur
1
Tsuang M T, Faraone S V.
The genetic epidemiology of schizophrenia.
Compr Ther.
1994;
20 (2)
130-135
3
McGue M, Gottesman I I.
A single dominant gene still cannot account for the transmission of schizophrenia (letter; comment).
Arch Gen Psychiatry.
1989;
46 (5)
478-480
9
Arinami T, Gao M, Hamaguchi H, Toru M.
A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia.
Hum Mol Genet.
1997;
6 (4)
577-582
11 Spitzer R L, Williams J B. Structured clinical interview for DSM-III diagnosis personality disorders. New York; New York State Psychiatric Institute 1985
13
McGuffin P, Farmer A, Harvey I.
A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT system.
Archives of General Psychiatry.
1991;
48 (8)
764-770
15
Spielman R S, McGinnis R E, Ewens W J.
Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).
American Journal of Human Genetics.
1993;
52 (3)
506-516
16
Spielman R S, Ewens W J.
The TDT and other family-based tests for linkage disequilibrium and association.
American Journal of Human Genetics.
1996;
59 (5)
983-989
17
Stöber G, Jatzke S, Heils A. et al .
Insertion/deletion variant (- 141C Ins/Del) in the 5′ regulatory region of the dopamine D2 receptor gene: lack of association with schizophrenia and bipolar affective disorder. Short communication.
J Neural Transm.
1998;
105 (1)
101-109
19
Gelernter J, Kranzler H, Cubells J F, Ichinose H, Nagatsu T.
DRD2 allele frequencies and linkage disequilibria, including the - 141CIns/Del promoter polymorphism, in European-American, African-American, and Japanese subjects.
Genomics.
1998;
51 (1)
21-26
20
Jonsson E G, Nöthen M M, Neidt H. et al .
Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophrenia.
Schizophr Res.
1999;
40 (1)
31-36
21
Inada T, Arinami T, Yagi G.
Association between a polymorphism in the promoter region of the dopamine D2 receptor gene and schizophrenia in Japanese subjects: replication and evaluation for antipsychotic-related features.
Int J Neuropsychopharmcol.
1999;
2 (3)
181-186
22
Ohara K, Nagai M, Tani K, Nakamura Y, Ino A.
Functional polymorphism of - 141C Ins/Del in the dopamine D2 receptor gene promoter and schizophrenia.
Psychiatry Res.
1998;
81 (2)
117-123
23
Hori H, Ohmori O, Shinkai T, Kojima H, Nakamura J.
Association analysis between two functional dopamine D2 receptor gene polymorphisms and schizophrenia.
Am J Med Genet.
2001;
105 (2)
176-178
24
Pohjalainen T, Nagren K, Syvalahti E K, Hietala J.
The dopamine D2 receptor 5′-flanking variant, - 141C Ins/Del, is not associated with reduced dopamine D2 receptor density in vivo.
Pharmacogenetics.
1999;
9 (4)
505-509