Paraoxonase 1 (PON1) gene-108C>T and p.Q192R polymorphisms and arylesterase activity of the enzyme in patients with dementia.

作者: Małgorzata Ewa Bednarska-Makaruk , Tomasz Krzywkowski , Alla Graban , Wanda Lipczyńska-Łojkowska , Anna Bochyńska

DOI: 10.5114/FN.2013.35953

关键词:

摘要: Paraoxonase 1 (PON1) activity was determined using phenylacetate as substrate (arylesterase activity) in 304 individuals with dementia--136 recognised probable Alzheimer's disease (AD), 64 dementia of vascular origin (VaD) and 104 mixed (MD) 129 persons without symptoms a good general health. -108C>T polymorphism the PON1 gene promoter p.Q192R coding region were identified. significantly lower demented patients compared controls particularly neurodegenerative character (AD MD). The prevalence PON1-108T allele carriers higher AD group than controls. frequencies genotypes did not differ between investigated groups. An association rare T-R haplotype dementia, type, found. Multivariate regression analysis showed significant polymorphisms. influence only -108C>T, but also on arylesterase observed. One has to admit that this kind does preclude interference enzyme activity. It could be concluded plays an additional role development. seems however dominating risk.

参考文章(27)
Xiao-ming He, Zhen-xin Zhang, Jun-wu Zhang, Yong-tao Zhou, Mou-ni Tang, Cheng-Bin Wu, HONG Zhen, None, Gln192Arg polymorphism in paraoxonase 1 gene is associated with Alzheimer disease in a Chinese Han ethnic population. Chinese Medical Journal. ,vol. 119, pp. 1204- 1209 ,(2006) , 10.1097/00029330-200607020-00013
B N La Du, C M Wyte, H W Eckerson, The human serum paraoxonase/arylesterase polymorphism. American Journal of Human Genetics. ,vol. 35, pp. 1126- 1138 ,(1983)
Barry J. Kitchen, Colin J. Masters, Donald J. Winzor, Effects of lipid removal on the molecular size and kinetic properties of bovine plasma arylesterase. Biochemical Journal. ,vol. 135, pp. 93- 99 ,(1973) , 10.1042/BJ1350093
Olivier Hanon, Vascular risk factors, cognitve decline, and dementia Vascular Health and Risk Management. ,vol. 4, pp. 363- 381 ,(2008) , 10.2147/VHRM.S1839
A. Klimkowicz-Mrowiec, M. Marona, P. Wolkow, A. Witkowski, A. Maruszak, M. Styczynska, M. Barcikowska, A. Szczudlik, A. Slowik, Paraoxonase gene polymorphism and the risk for Alzheimer's disease in the polish population. Dementia and Geriatric Cognitive Disorders. ,vol. 31, pp. 417- 423 ,(2011) , 10.1159/000329571
Aleksandra Stefanović, Jelena Kotur-Stevuljević, Slavica Spasić, Jelena Vekic, Nada Bujisić, Association of oxidative stress and paraoxonase status with PROCAM risk score. Clinical Biochemistry. ,vol. 42, pp. 617- 623 ,(2009) , 10.1016/J.CLINBIOCHEM.2009.01.008
Bharti Mackness, Paul N. Durrington, Michael I. Mackness, Human Serum Paraoxonase General Pharmacology-the Vascular System. ,vol. 31, pp. 329- 336 ,(1998) , 10.1016/S0306-3623(98)00028-7
Valérie Leduc, Louise Théroux, Doris Dea, Yves Robitaille, Judes Poirier, Involvement of paraoxonase 1 genetic variants in Alzheimer's disease neuropathology. European Journal of Neuroscience. ,vol. 30, pp. 1823- 1830 ,(2009) , 10.1111/J.1460-9568.2009.06983.X
Richard Humbert, David A. Adler, Christine M. Disteche, Christopher Hassett, Curtis J. Omiecinski, Clement E. Furlong, The molecular basis of the human serum paraoxonase activity polymorphism. Nature Genetics. ,vol. 3, pp. 73- 76 ,(1993) , 10.1038/NG0193-73