Lack of association of CR1, PICALM and CLU gene polymorphisms with Alzheimer disease in a Polish population

2013
journal article
article
23
dc.abstract.enBackground and purpose: Recent genome-wide association studies have indicated 3 new susceptibility loci for Alzheimer disease (AD): complement receptor 1 (CR1), clusterin (CLU), and the phosphatidylinositol-binding clathrin assembly protein (PICALM). We investigated the influence of the rs6656401 single nucleotide polymorphisms (SNP) of the CR1 gene, the rs3851179 SNP of the PICALM gene, and the rs11136000 SNP of the CLU gene on risk of AD in a Polish population. Material and methods: In 253 Caucasian AD patients and 240 controls, analyses identifying the rs6656401, rs3851179 and rs11136000 SNPs and APOE common polymorphisms were performed. Results: No significant differences were observed in the distribution of the rs6656401 of CR1, rs3851179 of PICALM and rs11136000 of CLU SNPs between AD patients and controls. The APOE ε4 common polymorphism was strongly related to the risk of AD. Conclusion: Our results suggest that investigated SNPs are not associated with AD in a Polish population.pl
dc.affiliationWydział Lekarski : Klinika Neurologiipl
dc.affiliationWydział Lekarski : Zakład Neurogenetykipl
dc.cm.date2020-01-07
dc.cm.id58605
dc.contributor.authorKlimkowicz-Mrowiec, Aleksandra - 160111 pl
dc.contributor.authorSado, Małgorzatapl
dc.contributor.authorDziubek, Annapl
dc.contributor.authorDziedzic, Tomasz - 129311 pl
dc.contributor.authorPera, Joanna - 133117 pl
dc.contributor.authorSzczudlik, Andrzej - 133576 pl
dc.contributor.authorSłowik, Agnieszka - 133430 pl
dc.date.accession2021-03-02pl
dc.date.accessioned2020-01-17T07:50:08Z
dc.date.available2020-01-17T07:50:08Z
dc.date.issued2013pl
dc.date.openaccess48
dc.description.accesstimepo opublikowaniu
dc.description.number2pl
dc.description.physical157-160pl
dc.description.points15pl
dc.description.versionostateczna wersja wydawcy
dc.description.volume47pl
dc.identifier.doi10.5114/ninp.2013.33825pl
dc.identifier.eissn1897-4260pl
dc.identifier.issn0028-3843pl
dc.identifier.projectROD UJ / OPpl
dc.identifier.urihttps://ruj.uj.edu.pl/xmlui/handle/item/131398
dc.identifier.weblinkhttps://journals.viamedica.pl/neurologia_neurochirurgia_polska/article/view/60882pl
dc.languageengpl
dc.language.containerengpl
dc.rightsUdzielam licencji. Uznanie autorstwa - Użycie niekomercyjne - Bez utworów zależnych 4.0 Międzynarodowa*
dc.rights.licenceCC-BY-NC-ND
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/legalcode.pl*
dc.share.typeotwarte czasopismo
dc.subject.enAlzheimer diseasepl
dc.subject.enCR1pl
dc.subject.enPICALMpl
dc.subject.enCLUpl
dc.subject.ensingle nucleotide polymorphismpl
dc.subject.plchoroba Alzheimerapl
dc.subject.plCR1pl
dc.subject.plPICALMpl
dc.subject.plCLUpl
dc.subject.plpolimorfizm pojedynczego nukleotydupl
dc.subtypeArticlepl
dc.titleLack of association of CR1, PICALM and CLU gene polymorphisms with Alzheimer disease in a Polish populationpl
dc.title.journalNeurologia i Neurochirurgia Polskapl
dc.typeJournalArticlepl
dspace.entity.typePublication
dc.abstract.enpl
Background and purpose: Recent genome-wide association studies have indicated 3 new susceptibility loci for Alzheimer disease (AD): complement receptor 1 (CR1), clusterin (CLU), and the phosphatidylinositol-binding clathrin assembly protein (PICALM). We investigated the influence of the rs6656401 single nucleotide polymorphisms (SNP) of the CR1 gene, the rs3851179 SNP of the PICALM gene, and the rs11136000 SNP of the CLU gene on risk of AD in a Polish population. Material and methods: In 253 Caucasian AD patients and 240 controls, analyses identifying the rs6656401, rs3851179 and rs11136000 SNPs and APOE common polymorphisms were performed. Results: No significant differences were observed in the distribution of the rs6656401 of CR1, rs3851179 of PICALM and rs11136000 of CLU SNPs between AD patients and controls. The APOE ε4 common polymorphism was strongly related to the risk of AD. Conclusion: Our results suggest that investigated SNPs are not associated with AD in a Polish population.
dc.affiliationpl
Wydział Lekarski : Klinika Neurologii
dc.affiliationpl
Wydział Lekarski : Zakład Neurogenetyki
dc.cm.date
2020-01-07
dc.cm.id
58605
dc.contributor.authorpl
Klimkowicz-Mrowiec, Aleksandra - 160111
dc.contributor.authorpl
Sado, Małgorzata
dc.contributor.authorpl
Dziubek, Anna
dc.contributor.authorpl
Dziedzic, Tomasz - 129311
dc.contributor.authorpl
Pera, Joanna - 133117
dc.contributor.authorpl
Szczudlik, Andrzej - 133576
dc.contributor.authorpl
Słowik, Agnieszka - 133430
dc.date.accessionpl
2021-03-02
dc.date.accessioned
2020-01-17T07:50:08Z
dc.date.available
2020-01-17T07:50:08Z
dc.date.issuedpl
2013
dc.date.openaccess
48
dc.description.accesstime
po opublikowaniu
dc.description.numberpl
2
dc.description.physicalpl
157-160
dc.description.pointspl
15
dc.description.version
ostateczna wersja wydawcy
dc.description.volumepl
47
dc.identifier.doipl
10.5114/ninp.2013.33825
dc.identifier.eissnpl
1897-4260
dc.identifier.issnpl
0028-3843
dc.identifier.projectpl
ROD UJ / OP
dc.identifier.uri
https://ruj.uj.edu.pl/xmlui/handle/item/131398
dc.identifier.weblinkpl
https://journals.viamedica.pl/neurologia_neurochirurgia_polska/article/view/60882
dc.languagepl
eng
dc.language.containerpl
eng
dc.rights*
Udzielam licencji. Uznanie autorstwa - Użycie niekomercyjne - Bez utworów zależnych 4.0 Międzynarodowa
dc.rights.licence
CC-BY-NC-ND
dc.rights.uri*
http://creativecommons.org/licenses/by-nc-nd/4.0/legalcode.pl
dc.share.type
otwarte czasopismo
dc.subject.enpl
Alzheimer disease
dc.subject.enpl
CR1
dc.subject.enpl
PICALM
dc.subject.enpl
CLU
dc.subject.enpl
single nucleotide polymorphism
dc.subject.plpl
choroba Alzheimera
dc.subject.plpl
CR1
dc.subject.plpl
PICALM
dc.subject.plpl
CLU
dc.subject.plpl
polimorfizm pojedynczego nukleotydu
dc.subtypepl
Article
dc.titlepl
Lack of association of CR1, PICALM and CLU gene polymorphisms with Alzheimer disease in a Polish population
dc.title.journalpl
Neurologia i Neurochirurgia Polska
dc.typepl
JournalArticle
dspace.entity.type
Publication
Affiliations

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