ANTIATHEROGENIC AND PLEIOTROPIC ACTIVITY OF VARIOUS DOSES OF ATORVASTATIN IN PATIENTS WITH ISCHEMIC STROKE

Aim. To study the effects of various atorvastatin doses on blood lipids, hemostatic parameters, endothelial function, renin-angiotensinaldosterone (RAAS) system, and circadian profile of blood pressure (BP) in patients with ischemic stroke (IS).Material and methods. The study included 34 IS patients...

Full description

Bibliographic Details
Main Authors: M. G. Bubnova, E. G. Semenova, D. M. Aronov, T. T. Batysheva
Format: Article
Language:Russian
Published: «SILICEA-POLIGRAF» LLC 2013-08-01
Series:Кардиоваскулярная терапия и профилактика
Subjects:
Online Access:https://cardiovascular.elpub.ru/jour/article/view/212
_version_ 1797882519786356736
author M. G. Bubnova
E. G. Semenova
D. M. Aronov
T. T. Batysheva
author_facet M. G. Bubnova
E. G. Semenova
D. M. Aronov
T. T. Batysheva
author_sort M. G. Bubnova
collection DOAJ
description Aim. To study the effects of various atorvastatin doses on blood lipids, hemostatic parameters, endothelial function, renin-angiotensinaldosterone (RAAS) system, and circadian profile of blood pressure (BP) in patients with ischemic stroke (IS).Material and methods. The study included 34 IS patients (mean age 58,0±6,6 years) with serum levels of low-density lipoprotein cholesterol (LDL-CH) >2,5 mmol/l, arterial hypertension (AH), and BP levels <160/100 mm Hg. All participants were randomised into Groups I and II, which received atorvastatin in daily doses of 10 and 40 mg, respectively, for 12 weeks. The atorvastatin effects on lipid profile, hemostatic parameters, nitric oxide (NO) end products, endothelin-1 (ET-1), angiotensin (AT) II, blood serotonin, and BP dynamics were assessed.Results. After 12 weeks, the patients receiving 10 and 40 mg/d of atorvastatin demonstrated a significant reduction in total CH (by 26,6% (p<0,001) and 33% (p<0,001), respectively), LDL-CH (by 32% (p<0,001) and 44% (p<0,001), respectively), and triglycerides (TG) (by 14% (p<0,001) and 24% (p<0,001), respectively). In both groups, there was no marked dynamics in the initially elevated levels of fibrinogen. In Group I, spontaneous platelet aggregation (PA) reduced by 22,6% (p<0,05). Moreover, in Group I, ADP-induced PA decreased by 16,7% (p<0,05) and 67,2% (p<0,01) for 0,5 and 2 μM of ADP, respectively. In Group II, the respective figures were 30,1% (p<0,05) and 31,6% (p<0,01). The concentration of NO end products increased in both Group I (+15% (p<0,05) after 12 weeks) and Group II (+7,7% (p<0,05) after 6 weeks; +15,5% (p<0,01) after 12 weeks). In all participants (Groups I and II; n=34), atorvastatin therapy was associated with a reduction in ET-1 levels by 4,8% (p<0,05). In Group II, there was a significant reduction in the levels of AT II (-7,1%; p<0,05; n=17) and serotonin (-28,6%; p<0,05; n=11). These changes were accompanied by reduced BP variability, time BP index, and area BP index.Conclusion. In IS patients with hyperlipidemia and AH, atorvastatin demonstrated a dose-dependent lipid-lowering effect on LDL-CH and TG, as well as a dose-dependent pleiotropic activity.
first_indexed 2024-04-10T03:37:03Z
format Article
id doaj.art-31ca553d7c4e4f60a04ceacfd00bd546
institution Directory Open Access Journal
issn 1728-8800
2619-0125
language Russian
last_indexed 2024-04-10T03:37:03Z
publishDate 2013-08-01
publisher «SILICEA-POLIGRAF» LLC
record_format Article
series Кардиоваскулярная терапия и профилактика
spelling doaj.art-31ca553d7c4e4f60a04ceacfd00bd5462023-03-13T07:23:22Zrus«SILICEA-POLIGRAF» LLCКардиоваскулярная терапия и профилактика1728-88002619-01252013-08-01124415010.15829/1728-8800-2013-4-41-50212ANTIATHEROGENIC AND PLEIOTROPIC ACTIVITY OF VARIOUS DOSES OF ATORVASTATIN IN PATIENTS WITH ISCHEMIC STROKEM. G. Bubnova0E. G. Semenova1D. M. Aronov2T. T. Batysheva3ФГБУ “Государственный научно-исследовательский центр профилактической медицины” Минздрава РоссииГБУЗ “Московский научно-практический центр медицинской реабилитации, восстановительной и спортивной медицины” филиал № 6 Департамента Здравоохранения г. МосквыФГБУ “Государственный научно-исследовательский центр профилактической медицины” Минздрава РоссииГБОУ ВПО “Московский государственный медико-стоматологический университет им. А. И. Евдокимова” Минздрава России, МоскваAim. To study the effects of various atorvastatin doses on blood lipids, hemostatic parameters, endothelial function, renin-angiotensinaldosterone (RAAS) system, and circadian profile of blood pressure (BP) in patients with ischemic stroke (IS).Material and methods. The study included 34 IS patients (mean age 58,0±6,6 years) with serum levels of low-density lipoprotein cholesterol (LDL-CH) >2,5 mmol/l, arterial hypertension (AH), and BP levels <160/100 mm Hg. All participants were randomised into Groups I and II, which received atorvastatin in daily doses of 10 and 40 mg, respectively, for 12 weeks. The atorvastatin effects on lipid profile, hemostatic parameters, nitric oxide (NO) end products, endothelin-1 (ET-1), angiotensin (AT) II, blood serotonin, and BP dynamics were assessed.Results. After 12 weeks, the patients receiving 10 and 40 mg/d of atorvastatin demonstrated a significant reduction in total CH (by 26,6% (p<0,001) and 33% (p<0,001), respectively), LDL-CH (by 32% (p<0,001) and 44% (p<0,001), respectively), and triglycerides (TG) (by 14% (p<0,001) and 24% (p<0,001), respectively). In both groups, there was no marked dynamics in the initially elevated levels of fibrinogen. In Group I, spontaneous platelet aggregation (PA) reduced by 22,6% (p<0,05). Moreover, in Group I, ADP-induced PA decreased by 16,7% (p<0,05) and 67,2% (p<0,01) for 0,5 and 2 μM of ADP, respectively. In Group II, the respective figures were 30,1% (p<0,05) and 31,6% (p<0,01). The concentration of NO end products increased in both Group I (+15% (p<0,05) after 12 weeks) and Group II (+7,7% (p<0,05) after 6 weeks; +15,5% (p<0,01) after 12 weeks). In all participants (Groups I and II; n=34), atorvastatin therapy was associated with a reduction in ET-1 levels by 4,8% (p<0,05). In Group II, there was a significant reduction in the levels of AT II (-7,1%; p<0,05; n=17) and serotonin (-28,6%; p<0,05; n=11). These changes were accompanied by reduced BP variability, time BP index, and area BP index.Conclusion. In IS patients with hyperlipidemia and AH, atorvastatin demonstrated a dose-dependent lipid-lowering effect on LDL-CH and TG, as well as a dose-dependent pleiotropic activity.https://cardiovascular.elpub.ru/jour/article/view/212аторвастатинишемический мозговой инсультгиперлипидемияартериальная гипертонияплейотропные эффекты
spellingShingle M. G. Bubnova
E. G. Semenova
D. M. Aronov
T. T. Batysheva
ANTIATHEROGENIC AND PLEIOTROPIC ACTIVITY OF VARIOUS DOSES OF ATORVASTATIN IN PATIENTS WITH ISCHEMIC STROKE
Кардиоваскулярная терапия и профилактика
аторвастатин
ишемический мозговой инсульт
гиперлипидемия
артериальная гипертония
плейотропные эффекты
title ANTIATHEROGENIC AND PLEIOTROPIC ACTIVITY OF VARIOUS DOSES OF ATORVASTATIN IN PATIENTS WITH ISCHEMIC STROKE
title_full ANTIATHEROGENIC AND PLEIOTROPIC ACTIVITY OF VARIOUS DOSES OF ATORVASTATIN IN PATIENTS WITH ISCHEMIC STROKE
title_fullStr ANTIATHEROGENIC AND PLEIOTROPIC ACTIVITY OF VARIOUS DOSES OF ATORVASTATIN IN PATIENTS WITH ISCHEMIC STROKE
title_full_unstemmed ANTIATHEROGENIC AND PLEIOTROPIC ACTIVITY OF VARIOUS DOSES OF ATORVASTATIN IN PATIENTS WITH ISCHEMIC STROKE
title_short ANTIATHEROGENIC AND PLEIOTROPIC ACTIVITY OF VARIOUS DOSES OF ATORVASTATIN IN PATIENTS WITH ISCHEMIC STROKE
title_sort antiatherogenic and pleiotropic activity of various doses of atorvastatin in patients with ischemic stroke
topic аторвастатин
ишемический мозговой инсульт
гиперлипидемия
артериальная гипертония
плейотропные эффекты
url https://cardiovascular.elpub.ru/jour/article/view/212
work_keys_str_mv AT mgbubnova antiatherogenicandpleiotropicactivityofvariousdosesofatorvastatininpatientswithischemicstroke
AT egsemenova antiatherogenicandpleiotropicactivityofvariousdosesofatorvastatininpatientswithischemicstroke
AT dmaronov antiatherogenicandpleiotropicactivityofvariousdosesofatorvastatininpatientswithischemicstroke
AT ttbatysheva antiatherogenicandpleiotropicactivityofvariousdosesofatorvastatininpatientswithischemicstroke