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Génétique épidémiologique des troubles de l’humeur: une nouvelle voie de recherches?

Published online by Cambridge University Press:  28 April 2020

M. Leboyer
Affiliation:
INSERM Unité 155, Groupe de recherches en génétique épidémiologique, Château de Longchamp, Bois de Boulogne, 75016Paris Laboratoire de neurobiologie cellulaire et moléculaire, CNRS, 91110Gif-sur-Yvette
T. D’Amato
Affiliation:
Laboratoire de neurobiologie cellulaire et moléculaire, CNRS, 91110Gif-sur-Yvette
A. Malafosse
Affiliation:
Laboratoire de neurobiologie cellulaire et moléculaire, CNRS, 91110Gif-sur-Yvette
D. Campion
Affiliation:
CHSR du Rouvray, 4, rue Paul-Eluard, 76300Sotteville-lès-Rouens
F. Gheysen
Affiliation:
Service du Pr E. Zarifian, CHU Côte-de-Nacre, Centre Esquirol, 14033 Caen, France
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Résumé

Les récents progrès de la biologie moléculaire offrent l’espoir d’une meilleure compréhension de la composante génétique des maladies mentales, la dépression en particulier. L’accès à un nombre quasiment illimité de marqueurs génétiques polymorphes et couvrant le génome, accroît l’efficacité des techniques de liaison génétique (linkage) qui permettent l’étude de la cotransmission des marqueurs génétiques et du trait clinique dans des familles dont plusieurs membres sont malades. D’ores et déjà, en ce qui concerne les troubles de l’humeur, 2 pistes ont été mises en évidence: celle d’une liaison à l’extrémité distale du bras long du chromosome X (Mendlewicz et al., 1987) et celle d’une liaison à l’extrémité du bras court du chromosome 11 (Egeland et al., 1987). Toutefois, ces résultats n’ont pas été constamment répliqués, ce qui soulève le problème de l’hétérogénéité étiologique des troubles dépressifs.

Summary

Summary

Recent developments in molecular biology may elucidate the role of genetic factors in mental disorders, and particularly in depression. The availability of an almost unlimited number of polymorphic genetic markers, covering the whole genome, increases the efficacy of linkage techniques investigating the segregation of genetic markers with the clinical trait in families of affected members. Two chromosomal locations have already been identified in linkage studies of affective disorders: one on the distal end of the long arm of the X chromosome (Mendlewicz et al., 1987) and the other at the distal end of the short arm of chromosome 11 (Egeland et al., 1987). Nevertheless, these results have not always been reproduced, thus suggesting the existence of etiological heterogeneity in major affective disorders.

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Revue
Copyright
Copyright © European Psychiatric Association 1989

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References

Références

Baron, M., Risch, N. & Hamburger, R. (1987) Genetic linkage between X chromosome markers and bipolar affective illness. Nature 326, 289292CrossRefGoogle ScholarPubMed
Bertelsen, A., Harvald, B. & Hauge, M. (1977) A danish twin study of manic-depressive disorders. Br. J. Psychiatry 130, 330351CrossRefGoogle ScholarPubMed
Cadoret, R. (1978) Evidence for genetic inheritance of primary affective disorder in adoptees. Am. J. Psychiatry 135, 4Google ScholarPubMed
Clerget-Darpoux, F., Bonaïti-Pellié, C. & Hochez, J. (1986) Effects of misspecifying genetic parameters in lod score analysis. Biometries 42, 393399CrossRefGoogle ScholarPubMed
Detera-Wadleigh, S., Berettini, W., Goldin, L.R., Boorman, D., Anderson, S. & Gershon, E.S. (1987) Close linkage of C-Harvey-ras and the insulin gene to affective disorders in ruled out in three North American pedigrees. Nature 325, 806807CrossRefGoogle ScholarPubMed
Egeland, J.A., Gerhardt, D.S., Pauls, D.L., Sussex, J.N., Kidd, K.K., Allen, C.R., Hostetter, A.M. & Housman, D.E. (1987) Bipolar affective disorders linked to DNA markers on chromosome 11. Nature 325, 783787CrossRefGoogle ScholarPubMed
Gerhardt, D.S., Egeland, J.A., Pauls, D.L., Kidd, K.K., Kramer, P. & Housman, D.E. (1984) Is a gene for affective disorder located on the short arm of chromosome 11? Am. J. Hum. Genet. 36, Suppl. 35, AbstractGoogle Scholar
Gershon, E.S., Targum, S.D., Matthysse, S. & Bunney, W.E. (1979) Colour blindness not closely linked to bifolar illness. Arch. Gen. Psychiatry 36, 14231430CrossRefGoogle ScholarPubMed
Gershon, E.S., Hamovit, J., Guroff, J., Dibble, E., Leckman, J., Sceery, W., Targum, W., Nurnberger, J., Goldin, L.R. & Bunney, W. (1982) A family study of schizoaffective, bipolar I, bipolar II, unipolar and normal control probands. Arch. Gen. Psychiatry 39, 11571167CrossRefGoogle ScholarPubMed
Goldin, L.R., Cox, N., Pauls, D.A., Gershon, E.S. & Kidd, K.K. (1984) The detection of major loci by segregation and linkage analysis: a simulation study. Genet. Epidemiol. 1, 285296CrossRefGoogle ScholarPubMed
Grima, B., Lamouroux, A., Boni, C., Julien, J.F., Javoy-Agid, F. & Mallet, J. (1987) A single human gene encoding multiple tyrosine hydroxylase with different predicted functional caracteristics. Nature 326, 707711CrossRefGoogle Scholar
Hodgkinson, S., Sherrington, R., Gurling, H., Marchbanks, R., Reeders, S., Mallet, J., Mclnnis, M., Petursson, H. & Brynjolfsson, J. (1987) Molecular genetic evidence of heterogeneity in manie depression. Nature 325, 805806CrossRefGoogle Scholar
Kendler, K. (1985) Psychiatrie illness in first degree relatives of schizophrenia and surgical control patients. Arch. Gen. Psychiatry 42, 770779CrossRefGoogle Scholar
Kendler, K. (1986) A DSMIII family study of the nonschizophrenic psychotic disorder. Am. J. Psychiatry 143, 10981105Google Scholar
Kidd, K.K., Egeland, J.A., Molthan, L., Pauls, D., Kruger, S., Phil, M. & Messner, K. (1984) Amish study, IV: Genetic linkage study of pedigrees of bipolar probands. Am. J. Psychiatry 141, 9, 10421048Google ScholarPubMed
Lathrop, G.M., Lalouel, J.M., Julier, C. & Ott, J. (1985) Multilocus linkage analysis in humans : detection of linkage and estimation of recombination. Am. J. Hum. Genet. 37, 482498Google Scholar
Leckman, J., Gershon, E.S., McGinniss, M.H., Targum, S. D. & Dibble, E.D. (1979) New data do not suggest linkage between the Xg blood group and bipolar illness. Arch. Gen. Psychiatry 36, 14361441CrossRefGoogle Scholar
Mallet, J. & Leboyer, M. (1986) Molecular genetics, bipolar affective disorders and the catecholamine hypothesis. Proc. Symp. lnterdisciplinary Society of Biological Psychiatry, 2731Google Scholar
Mendlewicz, J. & Rainer, J. (1977) Adoption study supporting genetic transmission in manic-depressive illness. Nature 268, 327329CrossRefGoogle ScholarPubMed
Mendlewicz, J., Linkowski, P., Guroff, J.J. & Van Praag, H.M. (1979) Color blindness linkage to bipolar manicdepressive illness : new evidence. Arch. Gen. Psychiatry 36, 14421447CrossRefGoogle Scholar
Mendlewicz, J., Linkowski, P. & Wilmotte, J. (1980) Linkage between glucose-6-phosphate deshydrogenase deficiency and manic-depressive illness: new evidence. Br. J. Psychiatry 137, 337342CrossRefGoogle Scholar
Mendlewicz, J., Simon, P., Sevy, S., Charon, F., Brocas, H., Legros, S. & Vassart, G. (1987) Polymorphie DNA marker on X chromosome and manie depression. Lancet, 12301232CrossRefGoogle Scholar
Morton, N.E. (1955) Sequential tests for the detection of linkage. Am. J. Hum. Genet. 7, 277318Google ScholarPubMed
O’Malley, K. & Rotwein, P. (1986) Human tyrosine hydroxylase and insulin genes are contiguous on chromosome IL Nucleic Acids Res. 1, 285296Google Scholar
Risch, N. & Baron, M. (1982) X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data. Ann. Hum. Genet. 46, 153166CrossRefGoogle ScholarPubMed
Rosenthal, N. (1980) Toward the validation of RDC of schizoaffective disorder. Arch. Gen. Psychiatry 37, 804810CrossRefGoogle ScholarPubMed
Southern, E.M. (1975) Detection of specifie sequences among DNA fragments separated by gel electrophoresis. J. Mol. Biol. 98, 503517CrossRefGoogle Scholar
Tsuang, M. (1980) Morbidity risks of schizophrenia and affective disorders among first degree relatives of patients with schizophrenia, mania, depression and surgical Controls. Br. J. Psychiatry 137, 497504CrossRefGoogle Scholar
Weissman, M. (1984) Psychiatrie disorders in the relatives of probands with affective disorders. Arch. Gen. Psychiatry 41, 1321CrossRefGoogle Scholar
Winokur, G. & Tanna, V. (1969) Possible role of X-linked dominant factor in manic-depressive disease. Dis. Nerv. Syst. 30, 8996Google ScholarPubMed
Xue, F., Kidd, J.R., Pakstis, A., Castiglione, C., Mallet, J. & Kidd, K.K. (1988) Tyrosine hydroxylase maps to the short arm of chromosome 11 near insulin and LIRAS 1 loci. In: Human Gene Mapping, Conf. 9. Cytogenet. Cell. Genet.CrossRefGoogle Scholar
Torgersen, S. (1986) Genetic factors in moderately severe and mild affective disorders. Arch. Gen. Psychiatry 43, 222226CrossRefGoogle ScholarPubMed
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