INVESTIGATION OF FIVE POLYMORPHIC DNA MARKERS ASSOCIATED WITH LATE ONSET ALZHEIMER DISEASE

INVESTIGATION OF FIVE POLYMORPHIC DNA MARKERS ASSOCIATED WITH LATE ONSET ALZHEIMER DISEASE


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نویسندگان: مریم رضازاده , جلال قره سوران , سید مجتبی محدث اردبیلی

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نشریه: 12605 , 2 , 45 , 2013

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نویسنده ثبت کننده مقاله مریم رضازاده
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده پزشکی
کد مقاله 67478
عنوان فارسی مقاله INVESTIGATION OF FIVE POLYMORPHIC DNA MARKERS ASSOCIATED WITH LATE ONSET ALZHEIMER DISEASE
عنوان لاتین مقاله INVESTIGATION OF FIVE POLYMORPHIC DNA MARKERS ASSOCIATED WITH LATE ONSET ALZHEIMER DISEASE
ناشر 3
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ خیر
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح دو – PubMed
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Investigation of five polymorphic DNA markers associated with late onset Alzheimer disease . Genetika, Vol 45, No. 2, 503-514. Alzheimer's disease is a complex neurodegenerative disorder characterized by memory and cognitive impairment and is the leading cause of dementia in the elderly. The aim of our study was to examine the polymorphic DNA markers CCR2 (+190 G/A), CCR5∆32, TNF-α (-308 G/A), TNF-α (-863 C/A) and CALHM1 (+394 C/T) to determine the relationship between these polymorphisms and the risk of late onset Alzheimer's disease in the population of Eastern Azerbaijan of Iran. A total of 160 patient samples and 163 healthy controls were genotyped by PCR-RFLP and the results confirmed using bidirectional sequencing. Statistical analysis of obtained data revealed non-significant difference between frequency of CCR5∆32 in case and control groups. The same result was observed for TNF-α (-863 C/A) genotype and allele frequencies. Contrary to above results, significant differences were detected in frequency of TNF-α (-308 G/A) and CCR2-64I genotypes between the cases and healthy controls. A weak significant difference observed between allele and genotype frequencies of rs2986017 in CALHM1 (+394 C/T; P86L) in patient and control samples. It can be concluded that the T allele of P86L variant in CALHM1 & +190 G/A allele of CCR2 have a protective role against abnormal clinical features of Alzheimer's disease. Eastern Azerbaijan. INTRODUCTION Alzheimer's disease (AD), originally described by Alois Alzheimer in 1907, is the most common cause of dementia in the elderly. According to age at onset, two major types of AD are

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نویسنده نفر چندم مقاله
مریم رضازادهدوم
جلال قره سوراناول
سید مجتبی محدث اردبیلیسوم

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