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Association of Alzheimer's Disease With APOE and IL-1α Gene Polymorphisms
Apolipoprotein E (ApoE) gene polymorphisms are thought to be the most important genetic risk factor in the pathogenesis of late onset and sporadic Alzheimer’s disease (AD). Moreover, interleukin-1α (IL-1α) is found to be associated with the pathogenesis of AD. In this research, ∊2, ∊3, and ∊4 polymo...
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Published in: | American journal of Alzheimer's disease and other dementias 2015-12, Vol.30 (8), p.756-761 |
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container_title | American journal of Alzheimer's disease and other dementias |
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creator | Yildiz, Saliha Handan Erdogan, Mujgan Ozdemir Artan, Sevilhan Solak, Mustafa Yaman, Mehmet Ozbabalik, Belgin Demet Terzi, Evrim Suna Arikan |
description | Apolipoprotein E (ApoE) gene polymorphisms are thought to be the most important genetic risk factor in the pathogenesis of late onset and sporadic Alzheimer’s disease (AD). Moreover, interleukin-1α (IL-1α) is found to be associated with the pathogenesis of AD. In this research, ∊2, ∊3, and ∊4 polymorphisms of ApoE gene and C889T polymorphism of IL-1α gene were genotyped in patients with AD and controls. Genotyping was performed by real-time polymerase chain reaction. ∊3/∊3 and ∊3/∊4 genotype frequencies were significantly higher in control and case groups, respectively. While ∊3 allele frequencies were significantly higher in the control group, ∊2 and ∊4 allele frequencies were significantly higher among the cases with AD. No difference was found between the groups according to C889T polymorphism of IL-1α. In conclusion, we demonstrated that there was a strong association between ApoE ∊4 allele and AD, while there was no relation with IL-1α C889T polymorphisms for this study. |
doi_str_mv | 10.1177/1533317512461557 |
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Moreover, interleukin-1α (IL-1α) is found to be associated with the pathogenesis of AD. In this research, ∊2, ∊3, and ∊4 polymorphisms of ApoE gene and C889T polymorphism of IL-1α gene were genotyped in patients with AD and controls. Genotyping was performed by real-time polymerase chain reaction. ∊3/∊3 and ∊3/∊4 genotype frequencies were significantly higher in control and case groups, respectively. While ∊3 allele frequencies were significantly higher in the control group, ∊2 and ∊4 allele frequencies were significantly higher among the cases with AD. No difference was found between the groups according to C889T polymorphism of IL-1α. 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Moreover, interleukin-1α (IL-1α) is found to be associated with the pathogenesis of AD. In this research, ∊2, ∊3, and ∊4 polymorphisms of ApoE gene and C889T polymorphism of IL-1α gene were genotyped in patients with AD and controls. Genotyping was performed by real-time polymerase chain reaction. ∊3/∊3 and ∊3/∊4 genotype frequencies were significantly higher in control and case groups, respectively. While ∊3 allele frequencies were significantly higher in the control group, ∊2 and ∊4 allele frequencies were significantly higher among the cases with AD. No difference was found between the groups according to C889T polymorphism of IL-1α. In conclusion, we demonstrated that there was a strong association between ApoE ∊4 allele and AD, while there was no relation with IL-1α C889T polymorphisms for this study.</description><subject>Aged</subject><subject>Alzheimer Disease - genetics</subject><subject>Apolipoprotein E2 - genetics</subject><subject>Apolipoprotein E3 - genetics</subject><subject>Apolipoprotein E4 - genetics</subject><subject>Humans</subject><subject>Interleukin-1alpha - genetics</subject><subject>Polymorphism, Genetic</subject><subject>Turkey</subject><issn>1533-3175</issn><issn>1938-2731</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1UctKxDAUDaL43ruS7HRTTZqmSVcyjK-RgXGhuAxJ58aJtM2YdAT9K3_EbzIyKiq4uhfO417OQWiPkiNKhTimnDFGBad5UVLOxQrapBWTWS4YXU17grMPfANtxfhASMGlJOtoI2eESUH5JroaxOhrp3vnO-wtHjQvM3AthIOIT10EHQHfuX6GB9eTM6y7KR6NM_r2ii-gA3ztm-fWh_nMxTbuoDWrmwi7n3Mb3Z6f3Qwvs_HkYjQcjLO6YLzPSmNMRfIpLXIrwRIiJc-ttaUlgktTTA1hptClNZbTui4kr0ohhSZlZYBAxbbRydJ3vjAtTGvo-qAbNQ-u1eFZee3Ub6RzM3XvnxQl6VIpZXI4_HQI_nEBsVetizU0je7AL6KigqXkSCHzRCVLah18jAHs9x1K1EcH6m8HSbL_879vwVfoiZAtCVHfg3rwi9ClvP43fAdAYI5_</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Yildiz, Saliha Handan</creator><creator>Erdogan, Mujgan Ozdemir</creator><creator>Artan, Sevilhan</creator><creator>Solak, Mustafa</creator><creator>Yaman, Mehmet</creator><creator>Ozbabalik, Belgin Demet</creator><creator>Terzi, Evrim Suna Arikan</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151201</creationdate><title>Association of Alzheimer's Disease With APOE and IL-1α Gene Polymorphisms</title><author>Yildiz, Saliha Handan ; Erdogan, Mujgan Ozdemir ; Artan, Sevilhan ; Solak, Mustafa ; Yaman, Mehmet ; Ozbabalik, Belgin Demet ; Terzi, Evrim Suna Arikan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-6bbb902d142f8ef008852fff6f0758b4db03b4a6fbf51cc48596787a069be0e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Alzheimer Disease - genetics</topic><topic>Apolipoprotein E2 - genetics</topic><topic>Apolipoprotein E3 - genetics</topic><topic>Apolipoprotein E4 - genetics</topic><topic>Humans</topic><topic>Interleukin-1alpha - genetics</topic><topic>Polymorphism, Genetic</topic><topic>Turkey</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yildiz, Saliha Handan</creatorcontrib><creatorcontrib>Erdogan, Mujgan Ozdemir</creatorcontrib><creatorcontrib>Artan, Sevilhan</creatorcontrib><creatorcontrib>Solak, Mustafa</creatorcontrib><creatorcontrib>Yaman, Mehmet</creatorcontrib><creatorcontrib>Ozbabalik, Belgin Demet</creatorcontrib><creatorcontrib>Terzi, Evrim Suna Arikan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of Alzheimer's disease and other dementias</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Yildiz, Saliha Handan</au><au>Erdogan, Mujgan Ozdemir</au><au>Artan, Sevilhan</au><au>Solak, Mustafa</au><au>Yaman, Mehmet</au><au>Ozbabalik, Belgin Demet</au><au>Terzi, Evrim Suna Arikan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of Alzheimer's Disease With APOE and IL-1α Gene Polymorphisms</atitle><jtitle>American journal of Alzheimer's disease and other dementias</jtitle><addtitle>Am J Alzheimers Dis Other Demen</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>30</volume><issue>8</issue><spage>756</spage><epage>761</epage><pages>756-761</pages><issn>1533-3175</issn><eissn>1938-2731</eissn><abstract>Apolipoprotein E (ApoE) gene polymorphisms are thought to be the most important genetic risk factor in the pathogenesis of late onset and sporadic Alzheimer’s disease (AD). 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subjects | Aged Alzheimer Disease - genetics Apolipoprotein E2 - genetics Apolipoprotein E3 - genetics Apolipoprotein E4 - genetics Humans Interleukin-1alpha - genetics Polymorphism, Genetic Turkey |
title | Association of Alzheimer's Disease With APOE and IL-1α Gene Polymorphisms |
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