Khorram Khorshid Hamid Reza, Gozalpour Elnaz, Saliminejad Kioomars, Karimloo Masood, Ohadi Mina, Kamali Koorosh
1. Genetic Research Centre, University of Social Welfare and Rehabilitation Sciences , Tehran, Iran.
3. Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR , Tehran, Iran.
Iran J Public Health. 2013 Nov;42(11):1253-8.
Late-onset Alzheimer's disease (AD), a genetically heterogeneous neurodegenerative disorder, is the most common form of dementia in people over 65 years old. The role of vitamin D in neuropsychiatric and neurodegenerative disorders such as AD has been supported by epidemiologic investigations and animal models, as well. We examined the association of the vitamin D receptor (VDR) gene polymorphisms and late-onset AD in an Iranian population.
This study was performed in Tehran, Iran from 2007 to 2008. Totally, 145 AD patients and 162 age-matched unrelated healthy controls were included. The genotype and allele frequencies for the VDR polymorphisms, ApaI (G>T; rs7975232) and TaqI (C>T; rs731236), were determined in the case and control subjects PCR-RFLP analysis. Logistic regression analysis was performed to assess the effect of mutant genotype or allele in the study groups.
The statistical analyses showed significant differences neither in genotype nor in allele frequencies of the ApaI and TaqI polymorphisms between the case and control groups.
It seems that the ApaI and TaqI polymorphisms are not associated with the risk of late-onset AD in Iranian population.
晚发性阿尔茨海默病(AD)是一种具有遗传异质性的神经退行性疾病,是65岁以上人群中最常见的痴呆形式。维生素D在神经精神和神经退行性疾病(如AD)中的作用也得到了流行病学调查和动物模型的支持。我们研究了伊朗人群中维生素D受体(VDR)基因多态性与晚发性AD的关联。
本研究于2007年至2008年在伊朗德黑兰进行。共纳入145例AD患者和162例年龄匹配的无血缘关系健康对照。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析确定病例组和对照组中VDR多态性ApaI(G>T;rs7975232)和TaqI(C>T;rs731236)的基因型和等位基因频率。进行逻辑回归分析以评估突变基因型或等位基因在研究组中的作用。
统计分析显示,病例组和对照组之间ApaI和TaqI多态性的基因型和等位基因频率均无显著差异。
似乎ApaI和TaqI多态性与伊朗人群晚发性AD的风险无关。