Polymorphism in Cytochrome P450 2D6, Glutathione S-Transferases Pi 1 Genes, and Organochlorine Pesticides in Alzheimer Disease

Author:

Singh Neeraj Kumar1,Banerjee B. D.2,Bala Kiran3,Basu Mitra4,Chhillar Neelam1

Affiliation:

1. Department of Neurochemistry, Institute of Human Behaviour and Allied Sciences, Dilshad Garden, Delhi, India

2. Department of Biochemistry, Environmental Biochemistry Laboratory, University College of Medical Science & G.T.B. Hospital (University of Delhi), Dilshad Garden, Delhi, India

3. Department of Neurology, Institute of Human Behaviour and Allied Sciences, Dilshad Garden, Delhi, India

4. Health Centre, Institute of Nuclear Medicine and Allied Sciences, DRDO, Delhi, India

Abstract

Objectives: It has been assumed that the association between Alzheimer disease (AD) and pesticides may be stronger among genetically susceptible individuals. The aim of the study was to examine the genetic polymorphism in cytochrome P450 2D6 ( CYP2D6) and glutathione S-transferases pi 1 ( GSTP1) with respect to organochlorine pesticides (OCPs) and metals in AD. Methods: This study included 100 patients with AD and 100 age-matched controls. The genetic polymorphisms were analyzed by restriction fragment length polymorphism. The OCPs and serum metal levels were determined using gas chromatography and an autoanalyzer, respectively. Results: We found a statistically significant association between AD and high levels of β-hexachlorocyclohexane (β-HCH; odds ratio [OR] = 2.064, 95% confidence intervals [95% CIs] = 1.373-3.102, dieldrin [OR = 2.086, 95% CI = 1.224-3.555], and copper [OR = 1.038, 95% CI = 1.012-1.064). The significant low level of magnesium (OR = 0.151, 95% CI = 0.047-0.489) even appears to have a protective role against AD. The GSTP1*B ( P = .009) and GSTP1*C ( P = .011) allelic variants were associated with increase in AD risk. Conclusion: This study demonstrates that the GSTP1*B and *C allelic variants may be considered a candidate gene for AD. It can be suggested that although CYP2D6*4 polymorphism is not a risk of AD, the CYP2D6*4 and GSTP1 polymorphism may interact with β-HCH, dieldrin, and copper to influence the risk of AD.

Publisher

SAGE Publications

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Neurology (clinical)

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