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Apolipoprotein E genetic variation and statin therapy appointment

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dc.contributor.author Kassenova, A.
dc.contributor.author Kossumov, A.
dc.contributor.author Nurgozhin, T.
dc.contributor.author Supiyev, A.
dc.date.accessioned 2016-05-30T05:10:29Z
dc.date.available 2016-05-30T05:10:29Z
dc.date.issued 2016-05
dc.identifier.citation A. Kassenova, A. Kossumov, T. Nurgozhin, and A. Supiyev. 2016. Apolipoprotein E genetic variation and statin therapy appointment. Abstract book. 4 th International Scientific Conference “Regenerative medicine & healthy aging”. National Laboratory Astana, Nazarbayev University. http://nur.nu.edu.kz/handle/123456789/1503 ru_RU
dc.identifier.uri http://nur.nu.edu.kz/handle/123456789/1503
dc.description.abstract Dyslipidemia is an important risk factor for cardiovascular disease due to the significant influence of cholesterol on atherosclerosis. Several genetic variants in genes related with triglyceride (TG) metabolism has been described, including LPL, apolipoprotein A5 and apolipoprotein E (Apo E) are associated with dyslipidemia by involvement to lipid metabolism. The combined analysis of these polymorphisms could produce clinically meaningful complementary information. Changes in TG levels are now considered an independent cardiovascular risk factor; hence, the study of combined variants in genes involved in TG metabolism may help explain part of the risk for CVD. The most informative polymorphisms within the Apo E gene are the Arg158Cys (rs7412) and Cys112Arg (rs429358) which define Apo E gene alleles, epsilon2, 3 and 4 (£2, £3 and £4). ru_RU
dc.language.iso en ru_RU
dc.rights Attribution-NonCommercial-ShareAlike 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/3.0/us/ *
dc.subject Dyslipidemia ru_RU
dc.subject apolipoprotein ru_RU
dc.subject genotype ru_RU
dc.subject statin therapy ru_RU
dc.title Apolipoprotein E genetic variation and statin therapy appointment ru_RU
dc.type Abstract ru_RU


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