:::

詳目顯示

回上一頁
題名:分子生物技術對精神醫學的影響
書刊名:臺灣精神醫學
作者:洪成志
作者(外文):Hong, Chen-jee
出版日期:1999
卷期:13:2
頁次:頁3-16
主題關鍵詞:分子生物技術精神疾病遺傳諮詢基因GeneGenetic counselingMolecular biotechnologyPsychiatric disorders
原始連結:連回原系統網址new window
相關次數:
  • 被引用次數被引用次數:期刊(4) 博士論文(0) 專書(0) 專書論文(0)
  • 排除自我引用排除自我引用:3
  • 共同引用共同引用:0
  • 點閱點閱:41
     分子生物技術從1970年代中期起展現其強大的威力,影響遍及農業、環保、海洋 生技、水產養殖、製造產程、基礎研究、醫藥衛生與精神醫學。Gusella et al. 以 DNA 標 記做基因連鎖分析,發現 Huntington's disease 的基因,隨後又有躁鬱症、精神分裂症及 失智症與某些基因座連鎖的研究報告,於是跳過組織生化的層面,利用分子生物技術直接尋 找精神疾病基因的位置,成為另一股研究的風潮。眾多候選基因亞型、次亞型及多型性的陸 續出現,使研究者可以從各種臨床分類檢視疾病與基因的關係;基因移轉動物使科學家可以 直接觀察到個別基因對動物行為的影響,進而推測人類精神疾病與行為的基因基礎;也可以 利用這種技術將己知的人類突變基因移轉到其他動物,以了解該基因的功能與疾病的生理生 化機轉,進而開發可以改變或控制疾病的藥物。失智症的基因逐一被找出來之後,晚發型遺 傳疾病的諮詢將逐漸成為精神科醫師的一大挑戰。筆者相信科學家會在未來的幾年內就找出 一部份精神分裂症或躁鬱症的基因,屆時精神科醫師在臨床上所面臨的問題,如:「我有沒 有精神分裂症的基因?」,「我的子女將來會不會得躁鬱症?」,「我的未婚妻(夫)的家 族有沒有精神疾病的基因?」等,將非常嚴肅卻難以迴避。
     Advances in molecular genetics and progress in mapping and sequencing the human genome has lead to an ever increasing role of molecular biotechnology in psychiatry. Although the use of DNA markers to hunt for genes associated with specific psychiatric diseases is a relatively new field of research, functional variations in a number of susceptibility genes have already been extensively explored. Several popular theories now assume that complex psychiatric disorders are likely to be associated with common polymorphisms. The use of transgenic techniques in animal studies have allowed molecular biology to be integrated with whole-animal physiology, creating an invaluable resource for understanding the molecular regulation of complex physiology and behavior. Progress in this area has been so rapid that treatments involving gene transfer have been undertaken in many somatic diseases. Effective animal models which mimick abnormal human behaviors may soon be available. Molecular insights into the pathogenesis of Alzheimer's disease and other neurodegenerative conditions have led to new therapeutic strategies. In the future comprehensive genotypic analysis, presymptomatic diagnosis, and advice on preventive measures may be advocated. Gene chips and cDNA subtraction are powerful tools which enable gene expression indicative of different psychiatric conditions to be differentiated. Genes that direct the development of the brain are being mapped, and many of them might serve as a new reservoir of candidate genes for psychiatric disorders. The hunt for genes that influence susceptibility to mental disorders is just one step toward improved clinical care. Advances in treatment will depend on understanding the ways in which these genes actually influence behavior and brain function. Problems related to genetic discrimination, misinterpretation of genetic data, genetic screening and the misuse of genetics for eugenic purpose are emerging and will exert a great impact on the legal, ethical and cultural organization of human society. The development of convenient techniques to perform mass screening for human genes will present a challenging issue of genetic counseling for late onset genetic diseases. Psychiatrists should prepare themselves to face the coming era of molecular psychiatry and molecular medicine.
期刊論文
1.Reilly, J. G.、Thomas, C. A.(1980)。Length polymorphisms, restriction site variation, and maternal inheritance of mitochondrial DNA of Drosophila melanogaster。Plasmid,3,109-115。  new window
2.Gusella, J. F.、Wexler, N. S.、Conneally, P. M.(1983)。A polymorphic DNA marker genetically linked to Huntington's disease。Nature,306,234-238。  new window
3.George-Hyslop, P. H.、Tanzi, R. E.、Polinsky, R. J.(1987)。The genetic defect causing familial Alzheimer’s disease maps on chromosome 21。Science,235,885-890。  new window
4.Egeland, J. A.、Gerhard, D. S.、Pauls, D. L.(1987)。Bipolar affective disorders linked to DNA markers on chromosome 11。Nature,325,783-787。  new window
5.Bassett, A. S.(1988)。Partial trisomy chromosome 5 cosegregating with schizophrenia。Lancet,1,799-801。  new window
6.Sherrington, R.(1988)。Localization of a susceptibility locus for schizophrenia on chromosome 5。Nature,336,164-167。  new window
7.Kendler, K. S.(1982)。Psychiatric illness in first-degree relatives of schizophrenia and surgical control patients。Arch Gen Psychiatry,42,770-779。  new window
8.Karayiorgou, M.、Gogos, J. A.、Galke, B. L.(1996)。Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus。Cold Spring Harbor Symposia on Quantitative Biology,61,835-843。  new window
9.Coon, H.、Holik, J.、Hoff, M.(1994)。Analysis of chromosome 22 markers in nine schizophrenia pedigrees。Am J Med Genet,54,72-79。  new window
10.Pulver, A. E.、Nestadt, G.、Goldberg, R.(1994)。Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives。J Nerv Ment Dis,182,476-478。  new window
11.Thomson, G.(1986)。Determining the mode of inheritance of RFLP-associated diseases using the affected sib-pair method。Am J Hum Genet,39,207-221。  new window
12.Hwu, H. G.、Hong, C. J.、Lee, Y. L.、Lee, P. C.、Lee, S. F.(1998)。Dopamine D4 receptor gene polymorphisms and neuroleptic response in schizophrenia。Biol Psychiatry,44,483-487。  new window
13.Hong, C. J.、Lee, Y. L.、Sim, C. B.、Hwu, H. G.(1997)。Dopamine D4 receptor variants in Chinese sporadic and familial schizophrenics。Am J Med Gene,74,412-415。  new window
14.Kamboh, M. I.、Sanghera, D. K.、Ferrell, R. E.、De-Kosky, S. T.(1995)。APOE* 4-associated Alzheimer’s disease risk is modified by alpha 1-antichymotrypsin polymorphism。Nat Genet,10,486-488。  new window
15.Williams, J.、Spurlock, G.、McGuffin, P.(1996)。Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene。Lancet,347,1294-1296。  new window
16.Wang, Y. C.、Liu, T. Y.、Liu, H. C.。No Association between 1-Antichymotrypsin Polymorphism and Alzheimer's Disease in Chinese。Neuropsychobiology。  new window
17.Lin, C. H.、Tsai, S. J.、Yu, Y. W. Y.(1999)。No evidence for association of sertonin-2A receptor variant (102T/C) with schizophrenia and clozapine response in Chinese schizophrenia。Neuroreport,10,57-60。  new window
18.Corder, E. H.、Saunders, A. M.、Strittmatter, W. J.(1993)。Gene Dose of Apolipoprotein E type 4 allele and the risk of Alzheimer's Disease in Late Onset Families。Science,261(5123),921-923。  new window
19.Hong, C. J.、Liu, T. Y.、Liu, H. C.(1996)。4 Allele of Apolipoprotein E Increases Risk of Alzheimer's Disease in a Chinese Population。Neurology,46,1749-1751。  new window
20.Chen, C. H.、Lee, Y. R.、Wei, F. C.、Koong, F. J.、Hwu, H. G.、Hsiao, K. J.(1997)。Association study of NlaⅢ and MspⅠ genetic polymorphisms of catechol -O-methyltransferase gene and susceptibility to schizophrenia。Biol Psychiat,41,985-987。  new window
21.Chen, C. H.、Wei, F. C.、Koong, F. J.、Hsiao, K. J.(1997)。Association of TaqⅠ A polymorphism of dopamine D2 receptor gene and tardive dyskinesia in schizophrenia。Biol Psychiatry,41,827-829。  new window
22.Hsu, Y. P.、Seow, S. V.、Loh, E. W.(1998)。Search for mutations near the alternatively spliced 8-amino-acid exon in the GABAA receptor gamma 2 subunit gene and lack of allelic association with alcoholism among four aboriginal groups and Han Chinese in Taiwan。Brain Research. Mol Brain Res,56,284-286。  new window
23.Chen, W. J.、Chen, C. C.、Yu, J. M.、Cheng, A. T.(1998)。Self-reported flushing and genotypes of ALDH2, ADH2, and ADH3 among Taiwanese Han。Alcoh Clin Exp Res,22,1048-1052。  new window
24.Lu, R. B.、Ko, H. C.、Chang, F. M.(1996)。No association between alcoholism and multiple polymorphisms at the dopamine D2 receptor gene (DRD2) in three distinct Taiwanese populations。Biol Psychiat,39,419-429。  new window
25.Chang, F. M.、Ko, H. C.、Lu, R. B.、Pakstis, A. J.、Kidd, K. K.(1997)。The dopamine D4 receptor gene (DRD4) is not associated with alcoholism in three Taiwanese populations: six polymorphisms tested separately and as haplotypes。Biol Psychiatry,41,394-405。  new window
26.Hamer, D.、Hu, H.、Magnuson, S.(1993)。A linkage between DNA markers on the X chromosome and male sexual orientation。Science,261,321-327。  new window
27.Ebstein, R. P.、Novick, O.、Umansky, R.(1996)。Dopamine D4 receptor (D4DR) exon Ⅲ polymorphism associated with the human personality trait of novelty seeking。Nat Genet,12,78-80。  new window
28.Benjamin, J.、Li, L.、Patterson, C.、Greenberg, B. D.、Murphy, D. L.、Hamer, D. H.(1996)。Population and familial association between the D4 dopamine receptor gene and measures of novelty seeking。Nat Genet,12,81-84。  new window
29.Lesch, K. P.、Bengel, D.、Heils, A.(1996)。Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region。Science,274,1527-1531。  new window
30.Duman, R. S.、Heninger, G. R.、Nestler, E. J.(1997)。A molecular and cellular theory of depression。Arch. Gen. Psychiatry,54,597-606。  new window
31.Hyman, S. E.、Nestler, E. J.(1996)。Initiation and adaptation: a paradigm for understanding psychotropic drug action。Am J Psychiatry,153,151-162。  new window
32.Harrison, P. J.、Burnet, P. W.、Falkai, P.、Bogerts, B.、Eastwood, S. L.(1997)。Gene expression and neuronal activity in schizophrenia: a study of polyadenylated mRNA in the hippocampal formation and cerebral cortex。Schizophr Res,26,93-102。  new window
33.Damask, S. P.、Bovenkerk, K. A.、Pena, G.(1996)。Differential effects of clozapine and haloperidol on dopamine receptor mRNA expression in rat striatum and cortex。Mol Brain Res,41,241-249。  new window
34.Breier, A.、Su, T. P.、Saunders, R.(1997)。Schizophrenia is associated with elevated amphetamine-induced synaptic dopamine concentrations: evidence from a novel positron emission tomography method。Proceedings of the National Academy of Sciences of the United States of America,94,2569-2574。  new window
35.Su, T.-P.、Malhotra, A. K.、Hadd, K.、Breier, A.、Pickar, D.(1997)。D2 dopamine receptor occupancy: a crossover comparison of risperidone with clozapine therapy in schizophrenic patients。Arch Gen Psychiatry,54,972 -973。  new window
36.Holcomb, H. H.、Cascella, N. G.、Thaker, G. K.、Medoff, D. R.、Dannals, R. F.、Tamminga, C. A.(1996)。Functional sites of neuroleptic drug action in the human brain: PET/FDG studies with and without haloperidol。Am J Psychiatry,153,41-49。  new window
37.Schena, M.、Shalon, D.、Davis, R. W.、Brown, P. O.(1995)。Quantitative monitoring of gene expression patterns with a complementary DNA microarray。Science,270,467-470。  new window
38.Schena, M.、Shalon, D.、Heller, R.、Chai, A.、Brown, P. O.、Davis, R. W.(1996)。Parallel human genome analysis: microarray-based expression monitoring of 1000 genes。Proc Nat Acad Sci,93,10614-10619。  new window
39.Heller, R. A.、Schena, M.、Chai, A.(1997)。Discovery and analysis of inflammatory diseaserelated genes using cDNA microarrays。Proc Nat Acad Sci,94,2150-2155。  new window
40.Shalon, D.、Smith, S. J.、Brown, P. O.(1996)。A DNA microarray system for analyzing complex DNA samples using two-color fluorescent probe hybridization。Genome Res,6,639-645。  new window
41.Debouck, Christine、Goodfellow, Peter N.(1999)。DNA microarrays in drug discovery and development。Nature genetics,21(1 supplement),48-50。  new window
42.Sargent, T. D.、David, I. B.(1983)。Differential gene expression in the gastrula of Xenopus laevis。Science,222,135-139。  new window
43.Wang, Z.、Brown, D. D.(1991)。A gene expression screen。Proc Natl Acad Sci,88,11505-11509。  new window
44.Serova, L.、Sabban, E. L.、Zangen, A.、Overstreet, D. H.、Yadid, G.(1998)。Altered gene expression for catecholamine biosynthetic enzymes and stress response in rat genetic model of depression。Brain Research Molecular Brain Research,63,133-138。  new window
45.Brinster, R. L.、Chen, H. Y.、Trumbauer, M.、Senear, A. W.、Warren, R.、Palmiter, R. D.(1981)。Somatic expression of herpes thymidine kinase in mice following injection of a fusion gene into eggs。Cell,27,223-231。  new window
46.Zhou, Q. Y.、Palmiter, R. D.(1995)。Dopamine-deficient mice are severely hypoactive, adipsic, and aphagic。Cell,83,1197-1209。  new window
47.Nelson, R. J.、Demas, G. E.、Huang, P. L.(1995)。Behavioural abnormalities in male mice lacking neuronal nitric oxide synthase。Nature,378,383-386。  new window
48.Dash, P. K.、Hochner, B.、Kandel, E. R.(1990)。Injection of the cAMP-responsive element into the nucleus of Aplysia sensory neurons blocks long-term facilitation。Nature,345,718-721。  new window
49.Tully, T.(1994)。Genetic dissection of consolidated memory in Drosophila。Cell,79,35-47。  new window
50.Yin, J. C.、Wallach, J. S.、Del Vecchio, M.(1994)。Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila。Cell,79,49-58。  new window
51.Yin, J. C.、Del Vecchio, M.、Zhou, H.、Tully, T.(1995)。CREB as a memory modulator: induced expression of a dCREB2 activator isoform enhances long-term memory in Drosophila。Cell,81,107-115。  new window
52.Bourtchuladze, R.、Frenguelli, B.、Blendy, J.、Cioffi, D.、Schutz, G.、Silva, A. J.(1994)。Deficient longterm memory in mice with a targeted mutation of the cAMP-responsive element-binding protein。Cell,79,59-68。  new window
53.Boer, T.(1995)。The effects of mirtazapine on central noradrenergic and serotonergic neurotransmission。Int Clin Psychopharm,10,19-24。  new window
54.Tomita, T.、Maruyama, K.、Saido, T. C.(1997)。The presenilin 2 mutation (N141I) linked to familial Alzheimer disease (Volga German families) increases the secretion of amyloid beta protein ending at the 42nd (or 43rd) residue。Proc Nat Acad Sci,94,2025-2030。  new window
55.Citron, M.、Westaway, D.、Xia, W.(1997)。Mutant presenilins of Alzheimer's disease increase production of 42-residue amyloid beta-protein in both transfected cells and transgenic mice。Nature Med,3,67-72。  new window
56.Lesch, K. P.(1999)。Gene transfer to the brain: emerging therapeutic strategy in psychiatry。Biol Psychiatry,45,247-253。  new window
57.Pai, J. T.、Tsai, S. F.、Hong, C. J.(1994)。Absence of FMR-1 gene expression can be detected with RNA extracted from dried blood specimens。Hum Genet,93,488-493。  new window
58.Hong, C. J.、Song, H. L.、Lai, H. C.、Tsai, S. J.、Hsiao, K. J.(1999)。Methanol/Acetone treatment helps the amplification of FMR1 CGG repeat fragment in dried blood spots from Guthrie cards。Lancet,353-354。  new window
59.Tibben, A.、Frets, P. G.、Kamp, J. J.(1993)。Presymptomatic DNA-testing for Huntington disease: Pretest attitudes and expectations of applicants and their partners in the Dutch program。Am J Med Genet,48,10-16。  new window
60.Smith, L. B.、Sapers, B.、Reus, V. I.、Freimer, N. B.(1996)。Attitudes towards bipolar disorder and predictive genetic testing among patients and providers。J Med Genet,33,544-549。  new window
61.Jamison, K. R.(1998)。Stigma of manic depression: a psychologist's view。Lancet,352,105。  new window
62.Trippitelli, C. L.、Jamison, K. R.、Folstein, M. F.、Barko, J. J.、Paulo, J. R.(1998)。Pilot study on patients’ and spouses' attitudes toward potential genetic testing for bipolar disorder。Am J Psychiatry,155,899-904。  new window
圖書
1.Gottesman, I. I.、Shields, J.(1982)。Schizophrenia: the epigenetic puzzle。Cambridge:Cambridge University Press。  new window
圖書論文
1.Tully, T.(1991)。Genetic dissection of learning and memory in Drosophila melanogaster。Neurobiology of learning, Emotion, and Affect。New York:Raven。  new window
 
 
 
 
第一頁 上一頁 下一頁 最後一頁 top
QR Code
QRCODE