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'); Reports of Biochemistry and Molecular Biology rbmb.net Basic Sciences http://rbmb.net 1 admin 2322-3480 2322-3480 10.61882/rbmb en jalali 1398 10 1 gregorian 2020 1 1 8 4 online 1 fulltext
en Investigation of Aneusomy of Chromosome 21 in the Micronuclei of 13 Patients with Early Onset Alzheimer’s Disease Using Fluorescence in Situ Hybridization: A Pilot Study زیست شناسی ملکولی Molecular Biology مقالات اصلی Original Article <div style="text-align: justify;"><strong><em>Background:</em></strong> Alzheimer&rsquo;s disease is one of the most common neurodegenerative and dementia disorders in people between the ages of 30 and 65. When symptoms appear in this age group, the disease is referred to as early-onset Alzheimer&rsquo;s disease (EOAD). Unfortunately, the symptoms are progressive and no current treatments are effective.<br> <br> <strong><em>Methods:</em></strong> In this research, 13 patients, aged 37 to 65 years with symptoms of early-onset Alzheimer&rsquo;s disease, were studied. First, patient lymphocytes were isolated and cultured in RPMI 1640 medium using a special micronucleus (MN) culture method. Next, the lymphocytes were harvested and prepared on slides. The slides were then examined by fluorescent microscopy using a unique FISH protocol specific for MNs. The patients were divided into groups aged 30-39, 40-49, and 50-65.<br> <br> <strong><em>Results</em></strong><strong><em>:</em></strong> We found that 19.76% of the MNs from our EOAD patients originated in chromosome 21. Micronuclei originated in chromosome 21 in 21.20 and 16.52% of patients without and with family histories of Alzheimer&rsquo;s, respectively. This difference was not significant. Also, the percentage of micronuclei originating in chromosome 21 was not dependent on the patient age at the time of the study, or symptom onset age or duration.<br> <br> <strong><em>Conclusions:</em></strong> This study shows that the rate of micronuclei with the origin of chromosome 21 is high in these patients. However, the micronucleus increased has no significant relationship with age and duration of disease or family history of it.</div> Early-onset Alzheimer’s disease (EOAD), Chromosomal instability, Fluorescence in Situ Hybridization (FISH), Neurodegenerative diseases, Micronucleus (MN). 446 453 http://rbmb.net/browse.php?a_code=A-10-299-1&slc_lang=en&sid=1 Sajjad Biglari s1369b@yahoo.com 100319475328460017451 100319475328460017451 No Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. Koorosh Kamali kkamali81@yahoo.com 100319475328460017452 100319475328460017452 No Department of Public Health ,School of Public Health ,Zanjan University of Medical Sciences Sousan Banihashemi Subanihashemi55@yahoo.com 100319475328460017453 100319475328460017453 No Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. Arash Faal Sezavari ArashFaalSezavari@yahoo.com 100319475328460017454 100319475328460017454 No Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. Seyed Mohsen Aghajanpour-Mir mohsenaghajanpour56@gmail.com 100319475328460017455 100319475328460017455 No Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran & Cellular & Molecular Biology Research Center, Health Institute, Babol University of Medical Sciences, Babol, Iran. Farkhondeh Behjati fbehjati@gmail.com 100319475328460017456 100319475328460017456 Yes Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.