Functionally gene-linked polymorphic regions and genetically controlled neurotransmitters metabolism

被引:19
作者
Catalano, M [1 ]
机构
[1] IRCCS, DSNP, Milan, Italy
关键词
pharmacogenetics; mood disorders; panic disorder; neurotransmitters;
D O I
10.1016/S0924-977X(01)00120-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In clinical psychopharmacology, the existence of marked inter-individual differences in both outcome and side effects is a common observation. Consequently, pharmacogenetics has also gained an increasing interest in psychiatry. Recent exciting findings seem to suggest that the growing interest in regulatory regions of candidate genes and neurotransmitters metabolism, together with the application of sophisticated molecular approaches, may offer new opportunities in neuropsychopharmacology. Indeed, quantitative variation of gene expression and/or of neurotransmitters metabolism could better explain both psychopathology and clinical response to psychotropic drugs. Three functional polymorphisms, and their possible relationship with clinical variables, are discussed. The first is the 44-bp insertion/deletion reported in the promoter region of the serotonin transporter gene. A functional repeat polymorphism in the promoter region of the gene encoding for the enzyme monoamine oxidase A represents the second example. The last is a functional polymorphism within the coding region of the gene encoding for the enzyme catechol-O-methyltransferase. (C) 2001 Published by Elsevier Science BY.
引用
收藏
页码:431 / 439
页数:9
相关论文
共 81 条
[51]   The CYP2D6 genotype and plasma concentrations of mianserin enantiomers in relation to therapeutic response to mianserin in depressed Japanese patients [J].
Mihara, K ;
Otani, K ;
Tybring, G ;
Dahl, ML ;
Bertilsson, L ;
Kaneko, S .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1997, 17 (06) :467-471
[52]  
MONTGOMERY SA, 1994, CURRENT INSIGHTS OBS, P215
[53]   Preliminary evidence of an association between bipolar disorder in females and the catechol-O-methyltransferase gene [J].
Mynett-Johnson, LA ;
Murphy, VE ;
Claffey, E ;
Shields, DC ;
McKeon, P .
PSYCHIATRIC GENETICS, 1998, 8 (04) :221-225
[54]   TRANSMISSION-RATIO DISTORTION OF X-CHROMOSOMES AMONG MALE OFFSPRING OF FEMALES WITH SKEWED X-INACTIVATION [J].
NAUMOVA, AK ;
OLIEN, L ;
BIRD, LM ;
SLAMKA, C ;
FONSECA, M ;
VERNER, AE ;
WANG, M ;
LEPPERT, M ;
MORGAN, K ;
SAPIENZA, C .
DEVELOPMENTAL GENETICS, 1995, 17 (03) :198-205
[55]   Pharmacogenetics and pharmacogenomics: why is this relevant to the clinical geneticist? [J].
Nebert, DW .
CLINICAL GENETICS, 1999, 56 (04) :247-258
[56]   Association and linkage of anxiety-related traits with a functional polymorphism of the serotonin transporter gene regulatory region in Israeli sibling pairs [J].
Osher, Y ;
Hamer, D ;
Benjamin, J .
MOLECULAR PSYCHIATRY, 2000, 5 (02) :216-219
[57]   Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles [J].
Palmatier, MA ;
Kang, AM ;
Kidd, KK .
BIOLOGICAL PSYCHIATRY, 1999, 46 (04) :557-567
[58]  
Papolos DF, 1996, AM J PSYCHIAT, V153, P1541
[59]   The medical utility of genomics data in neuropsychiatry: Mutational genetics versus association genetics [J].
Peroutka, SJ .
CURRENT OPINION IN BIOTECHNOLOGY, 1997, 8 (06) :688-691
[60]   A SNPshot: pharmacogenetics and the future of drug therapy [J].
Pfost, DR ;
Boyce-Jacino, MT ;
Grant, DM .
TRENDS IN BIOTECHNOLOGY, 2000, 18 (08) :334-338