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Molecular genetic findings in mood disorders

Published online by Cambridge University Press:  18 September 2015

Extract

Traditional methods used to asses genetic effects, such as twins, adoption and family studies, have demonstrated the role genetic vulnerability factors in the etiology of major psychiatric diseases such as affective disorders and schizophrenia. It remains however impossible, using these methods, to specify the genetic variables involved and the exact mode of transmission of these diseases. New genetic approaches in psychiatry include the use of DNA markers in sophisticated strategies to examine families and populations. Genetic linkage (in families) and allelic association (in unrelated subjects) are the most frequent techniques applied searching for genes in psychiatric diseases. Advances in these methods have permitted their application to complex diseases in which the mode of genetic transmission is unknown. Affective disorders and, in particular, bipolar affective disorder (BPAD) have been examined in many molecular genetic studies which have covered a large part of the genome, specific hypotheses such as mutations have also, been studied. Most recent studies indicate that several chromosomal regions may be involved in the aetiology of affective disorders. Large multi-centre and multi-disciplinary projects are currently underway in Europe and in the US and hopefully will improve our understanding of the genetic factors involved in affective disorders. In parallel to these new developments in molecular genetics, the classical genetic epidemiology, represented by twin, adoption and family studies, have been improved, providing validated models to test the gene-environment interactions.

Type
Research Article
Copyright
Copyright © Scandinavian College of Neuropsychopharmacology 1999

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References

Literature

1.Ogilvie, AD, Battersby, S, Bubb, VJ, et al.Polymorphism in serotonin transporter gene associated with susceptibility to major depression. Lancet 1996;347;731–3.CrossRefGoogle ScholarPubMed
2.Gutierrez, B, Pintor, L, Gasto, C, Rosa, A, et al.Variability in the serotonin transporter gene and increased risk for major depression with melancholia. Hum Gen 1998;103;319–22.CrossRefGoogle ScholarPubMed
3.Gutierrez, B, Arranz, MJ, Collier, DA, et al.Serotonin transporter gene and risk for bipolar affective disorder: an association study in Spanish population. Biol Psychiatry 1998;43;843–7.CrossRefGoogle ScholarPubMed
4.Ewald, H, Flint, T, Degn, B, Mors, O, Kruse, TA. A functional variant of the serotonin transporter gene in families with bipolar affective disorder. J affect Disord 1998;48;135–44.CrossRefGoogle ScholarPubMed
5.Smeraldi, E, Zanardi, R, Benedetti, F, et al.Polymorphism within the promoter of the serotonin transporter gene and antidepressant efficacy of fluvoxamine. Mol Psychiat 1998;3;508–11.CrossRefGoogle ScholarPubMed
6.Bellivier, F, Leboyer, M, Courtet, P, et al.Association between the tryptophan hydroxylase gene and manic-depressive illness. Arch gen Psychiatry 1998;55;33–7.CrossRefGoogle ScholarPubMed
7.Mann, JJ, Malone, KM, Nielsen, DA, et al.Possible association of a polymorphism of the tryptophan hydroxylase gene with suicidal behavior in depressed patients. Am J Psychiatry 1997;154;1451–3.Google ScholarPubMed
8.Berrettini, WH, Ferraro, TN, Goldin, LR, et al.Chromosome 18 DNA markers and manic-depressive illness: Evidence for a susceptibility gene. Proc Natl Acad Sci 1994;91;5918–22.CrossRefGoogle ScholarPubMed
9.Stine, C, Xu, J, Koskela, R, et al.Evidence for linkage of bipolar disorder to chromosome 18 with parent-of-origin effect. Am J human Genet 1996;57;1384–94.Google Scholar
10.Gershon, ES, Badner, JA, Detera-Waldeigh, SD, et al.Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees. Am J med Genet (Neuropsychiatric Genetics) 1996;67;202–7.3.0.CO;2-N>CrossRefGoogle ScholarPubMed
11.De Bruyn, A, Souery, D, Mendelbaum, K, et al.Linkage analysis of 2 families with bipolar illness and chromosome 18 markers. Biol Psychiatry; 39: 679–88.CrossRefGoogle Scholar
12.Freimer, N, Reus, V, Escamilla, M. Genetic mapping using haplo-type, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23. Nat Genet 1996; 12:436–41.CrossRefGoogle Scholar
13.Detera-Wadleigh, SD, Badner, JA, Yoshikawa, Tet al.Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 4, 7, 9, 18, 19, 20 and 21q. Am J med Gen (Neuropsychiatric Genetics) 1997;74;254–62.3.0.CO;2-Q>CrossRefGoogle Scholar
14.Souery, D, Papadimitriou, G, Mendlewicz, J. New genetic approaches in affective disorders In: Papadimitriou, GN and Mendlewicz, J. Genetics of Mental Disorders Part I: Theoretical aspects. Bailliere's Clinical Psychiatry, International Practice and Research. London 1996: Bailliere Tindall, Vol. 1, No 1, 97110.Google Scholar
15.Furlong, RA, Rubinsztein, JS, Ho, L, et al.Analysis and metaanalysis of two polymorphisms within the tyrosine hydroxylase gene in bipolar and unipolar affective disorders. Am J med Genet 1999;5;8894.3.0.CO;2-J>CrossRefGoogle Scholar
16.Blackwood, D, He, L, Morris, S, et al.A locus for bipolar affective disorder on chromosome 4p. Nat Gen 1996;12;427–30.CrossRefGoogle ScholarPubMed
17.Coon, H, Jensen, S, Hoff, M, et al.A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance. Am J hum Genet 1993;52;1234–49.Google ScholarPubMed
18.Detera-Wadleigh, SD, Berrettini, WH, Goldin, LR, et al.A systematic search for a bipolar predisposing locus on chromosome 5. Neuropsychopharm 1992;6;219–29.Google ScholarPubMed
19.Souery, D, Lipp, O, Mahieu, B, et al.Association study of bipolar disorder with candidate genes involved in catecholamine neurotransmission: DRD2, DRD3, DAT1 and TH genes. Am J med Genet (Neuropsychiatric Genetics) 1996;67;551–5.3.0.CO;2-K>CrossRefGoogle ScholarPubMed
20.Craddock, N, McGuffin, P, Owen, M. Darier's disease cosegregating with affective disorder. Br J Psychiatry 1994; 165: 272.CrossRefGoogle ScholarPubMed
21.Dawson, E, Parfitt, E, Roberts, Q, et al.Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1. Am J med Genet 1995;24;94102.CrossRefGoogle Scholar
22.Barden, N, Plante, M, Rochette, D, et al.Genome wide microsatellite marker linkage study of bipolar affective disorders in a very large pedigree derived from a homogeneous population in Quebec points to susceptibility locus on chromosome 12. Psychiatr Genet 1996; 6:145–6.CrossRefGoogle Scholar
23.Ewald, H, Degn, B, Mors, O, Kruse, TA. Significant linkage between bipolar affective disorder and chromosome 12q24. Psychiatr Genet 1998;8;131–40.CrossRefGoogle ScholarPubMed
24.Franks, E, Guy, C, Jacobsen, N, et al.Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder. Am J med Genet 1999;5;6770.3.0.CO;2-#>CrossRefGoogle Scholar
25.Straub, RE, Lehner, Th, Luo, Y, et al.A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3. Nat Genet 1994;8;291–6.CrossRefGoogle ScholarPubMed
26.Mendlewicz, J, Simon, P, Sevy, S, et al.Polymorphic DNA marker on chromosome and manicdepression. Lancet 1987;1;1230–2.CrossRefGoogle Scholar
27.Pekkarinen, P, Terwilliger, J, Bredbacka, P-E, Lonnqvist, J, Peltonen, L. Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree. Gen Res 1995;5;105–15.CrossRefGoogle Scholar
28.McInnis, MG, McMahon, FJ, Chase, GA, et al.Anticipation in bipolar affective disorder. Am J hum Genet 1993;53;385–90.Google ScholarPubMed
29.Nyländer, P-O, Engström, C, Chotai, J, Wahlström, J, Adolfsson, R. Anticipation in Swedish Families with Bipolar Affective Disorder. J med Genet 1994;9;686–9.CrossRefGoogle Scholar
30.Engström, C, Johansson, EL, Langström, M, et al.Anticipation in unipolar affective disorder. J affect Dis 1995;35;3140.CrossRefGoogle ScholarPubMed
31.Lindblad, K, Nylander, PO, De Bruyn, A, et al.Expansion of trinucleotide CAG repeats detected in Bipolar Affective Disorder by the RED-(rapid expansion detection) method. Neurobiol Dis 1995;2;5562.CrossRefGoogle Scholar
32.O'Donovan, MC, Guy, C, Craddock, N, et al.Expanded CAG repeats in Schizophrenie and bipolar disorder. Nat Genet 1995;10;380–1.CrossRefGoogle Scholar
33.Oruc, L, Lindblad, K, Verheyen, G, et alCAG expansions in bipolar and unipolar disorders. Am J hum Gen 1997;60;730–2.Google ScholarPubMed
34.Mendlewicz, J, Lipp, O, Souery, D, et al.Possible maternal genomic imprinting on expended trinucleotide CAG repeats in bipolar affective disorder. Biol Psychiatry 1997;42;1115–22.CrossRefGoogle Scholar
35.Lindblad, K, Nylander, P-O, Zander, C, et al. Two commonly expanded CAG/CTG repeat loci: involvment in affective disorders? Mol Psychiatry 1998;3;405–10.CrossRefGoogle ScholarPubMed