ASPECTS OF LIPID-LOWERING THERAPY WITH ATORVASTATIN IN PATIENTS WITH MYOCARDIAL INFARCTION FROM THE PERSPECTIVE OF PERSONALIZED MEDICINE

<p><strong>Aim.</strong> To analyze the impact of the SLCO1B1*5 (c.521T> C) and LIPC (C514T) genes polymorphisms on the efficacy of atorvastatin therapy and the incidence of the combined endpoint in patients after myocardial infarction (MI).</p><p><strong>Mater...

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Main Authors: M. V. Solodun (Author), S. S. Yakushin (Author)
Format: Book
Published: Столичная издательская компания, 2015-09-01T00:00:00Z.
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001 doaj_cebaa056ecb84b4aab542c08965f04d1
042 |a dc 
100 1 0 |a M. V. Solodun  |e author 
700 1 0 |a S. S. Yakushin  |e author 
245 0 0 |a ASPECTS OF LIPID-LOWERING THERAPY WITH ATORVASTATIN IN PATIENTS WITH MYOCARDIAL INFARCTION FROM THE PERSPECTIVE OF PERSONALIZED MEDICINE 
260 |b Столичная издательская компания,   |c 2015-09-01T00:00:00Z. 
500 |a 1819-6446 
500 |a 2225-3653 
500 |a 10.1234/1819-6446-2015-1-31-35 
520 |a <p><strong>Aim.</strong> To analyze the impact of the SLCO1B1*5 (c.521T> C) and LIPC (C514T) genes polymorphisms on the efficacy of atorvastatin therapy and the incidence of the combined endpoint in patients after myocardial infarction (MI).</p><p><strong>Material and methods.</strong> 121 patients with MI aged 45-75 years were included into the study. All patients were prescribed atorvastatin. A group of 65 people in whom lipid levels were studied at baseline and after 3 months of atorvastatin treatment was formed to evaluate the efficacy of statin therapy. Genetic polimorphism of SLCO1B1*5 (c.521T> C) and LIPC (C514T) was determined using polimerase chain reaction. The prognosis was assessed by clinical outcomes after 3 months of follow-up, based on the achievement of the combined endpoint MACE (Major Adverse Cardiac Events), which included cardiovascular deaths, recurrent MI, hospitalization for progressive angina, unplanned coronary revascularization.</p><p><strong>Results.</strong> Patients with SLCO1B1 c.521СC genotype had no significant reduction in the levels of atherogenic lipids (p>0.05), while patients with TT and TC genotypes demonstrated significant reduction in atherogenic cholesterol fractions (p<0.05). Allelic polymorphism of LIPC (C514T) gene has no influence on the atorvastatin treatment efficacy. The SLCO1B1 and LIPC (C514T) genes polymorphism has no impact on the three-month prognosis after MI.</p><p><strong>Conclusion.</strong> The SLCO1B1 polymorphism should be taken into consideration while personalised prescribing of atorvastatin to patients with MI.</p> 
546 |a EN 
546 |a RU 
690 |a полиморфизм генов 
690 |a фармакогенетика 
690 |a аторвастатин 
690 |a прогноз после инфаркта миокарда 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
690 |a Diseases of the circulatory (Cardiovascular) system 
690 |a RC666-701 
655 7 |a article  |2 local 
786 0 |n Рациональная фармакотерапия в кардиологии, Vol 11, Iss 1, Pp 31-35 (2015) 
787 0 |n http://www.rpcardio.ru/jour/article/view/53 
787 0 |n https://doaj.org/toc/1819-6446 
787 0 |n https://doaj.org/toc/2225-3653 
856 4 1 |u https://doaj.org/article/cebaa056ecb84b4aab542c08965f04d1  |z Connect to this object online.