No association between tryptophan hydroxylase gene polymorphism and Alzheimer's disease

被引:12
|
作者
Wang, YC
Tsai, SJ
Liu, TY
Liu, HC
Hong, CJ
机构
[1] Vet Gen Hosp Tapei, Dept Psychiat, Taipei 11217, Taiwan
[2] Yu Li Vet Hosp, Sect Psychiat, Hualien, Taiwan
[3] Vet Gen Hosp, Dept Med Res & Educ, Taipei 11217, Taiwan
[4] Vet Gen Hosp, Dept Neurol, Taipei 11217, Taiwan
[5] Natl Yang Ming Univ, Sch Med, Taipei 112, Taiwan
关键词
Alzheimer's disease; association study; polymorphism; serotonin; tryptophan hydroxylase;
D O I
10.1159/000054856
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Serotonergic dysfunction is implicated in Alzheimer's disease (AD) on the basis of studies of serotonin and its metabolite in postmortem specimens and CSF, There were also reports on association of a tryptophan hydroxylase (TPH) intron 7 variant and CSF 5-hydroxyindoleacetic acid concentrations. These suggested TPH might be a candidate to study for possible involvement in AD. Using a case-control association approach, we studied the TPH polymorphism in 150 subjects with AD and 100 controls. There were no significant differences in genotype or allele frequencies between controls and AD patients. The negative findings suggested that this TPH polymorphism has no major effect on the development of AD. However, the genetic variation of the TPH gene related to the symptomatology of AD deserves further investigation. Copyright (C) 2001 S. Karger AG. Basel.
引用
收藏
页码:1 / 4
页数:4
相关论文
共 50 条
  • [31] Allelic variation at the A218C tryptophan hydroxylase polymorphism influences agitation and aggression in Alzheimer's disease
    Craig, D
    Hart, DJ
    Carson, R
    McIlroy, SP
    Passmore, AP
    NEUROSCIENCE LETTERS, 2004, 363 (03) : 199 - 202
  • [32] Alleleic variation at the A218C tryptophan hydroxylase polymorphism influences agitation and aggression in Alzheimer's disease
    Craig, D
    Hart, DJ
    Carson, R
    McIlroy, SP
    Passmore, P
    NEUROBIOLOGY OF AGING, 2004, 25 : S491 - S491
  • [33] Association between Tph2 gene polymorphism, brain tryptophan hydroxylase activity and aggressiveness in mouse strains
    Kulikov, AV
    Osipova, DV
    Naumenko, VS
    Popova, NK
    GENES BRAIN AND BEHAVIOR, 2005, 4 (08) : 482 - 485
  • [34] Association between smoking habits and tryptophan hydroxylase gene C218A polymorphism among the Japanese population
    Mizuno, S
    Ito, H
    Hamajima, N
    Tamakoshi, A
    Hirose, K
    Tajima, K
    JOURNAL OF EPIDEMIOLOGY, 2004, 14 (03) : 94 - 99
  • [35] Association between apolipoprotein E polymorphism and Alzheimer's disease in Koreans
    Kim, KW
    Jhoo, JH
    Lee, KU
    Lee, DY
    Lee, JH
    Youn, JY
    Lee, BJ
    Han, SH
    Woo, JI
    NEUROSCIENCE LETTERS, 1999, 277 (03) : 145 - 148
  • [36] Association between angiotensin-converting enzyme gene polymorphism and Alzheimer's disease in a Chinese population
    Zhang, JW
    Li, XQ
    Zhang, ZX
    Chen, D
    Zhao, HL
    Wu, YN
    Qu, QM
    DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2005, 20 (01) : 52 - 56
  • [37] No evidence of association between apolipoprotein E gene regulatory region polymorphism and Alzheimer's disease in Japanese
    Kimura, M
    Matsushita, S
    Arai, H
    Matsui, T
    Yuzuriha, T
    Higuchi, S
    JOURNAL OF NEURAL TRANSMISSION, 2000, 107 (12) : 1449 - 1456
  • [38] Association between an angiotensin-converting enzyme gene polymorphism and Alzheimer's disease in a Tunisian population
    Fekih-Mrissa, Najiba
    Bedoui, Ines
    Sayeh, Aycha
    Derbali, Hajer
    Mrad, Meriem
    Mrissa, Ridha
    Nsiri, Brahim
    ANNALS OF GENERAL PSYCHIATRY, 2017, 16
  • [39] Association between an angiotensin-converting enzyme gene polymorphism and Alzheimer’s disease in a Tunisian population
    Najiba Fekih-Mrissa
    Ines Bedoui
    Aycha Sayeh
    Hajer Derbali
    Meriem Mrad
    Ridha Mrissa
    Brahim Nsiri
    Annals of General Psychiatry, 16
  • [40] No association between the neuronal nitric oxide synthase gene polymorphism and Alzheimer disease
    Liou, YJ
    Hong, CJ
    Liu, HC
    Liu, CY
    Liu, TY
    Chen, IC
    Tsai, SJ
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (06): : 687 - 688