6 research outputs found
Metabolic profile of patients with coronary artery disease and comorbid obesity.
- Publication venue
- Dnipro State Medical University
- Publication date
- 01/01/2018
- Field of study
Cardiovascular diseases (CVD) are the leading cause of death worldwide. Most CVD can be prevented by modification of such risk factors as tobacco use, obesity and unhealthy diet, physical inactivity and harmful use of alcohol. Patients with CVD or who are at high cardiovascular risk due to the presence of risk factors such as dyslipidemia, hypertension, diabetes mellitus type 2, need early detection and management of these states. The article describes differences between metabolic profile of patients with obesity and coronary artery disease. The study included 58 patients. They were divided into 3 groups: 1st - patients with BMI <30 and CAD, 2nd - patients with BMI>30 and CAD, and 3rd - patients with BMI>30. 1st and 2nd group of patients were treated with atorvastatin in the dose of 40 mg for 2 years, 3rd - untreated. The results indicate that significant difference was faund in the lipid profile between groups of patients treated with atorvastatin in the dose of 40 mg . Transaminases and uric acid levels were different but within the reference range. The difference was found in serum glucose, insulin and HOMA-IR between participants of the 2-nd and other groups. We observed significant insulin resistance in the group of patients with coronary heart disease, obesity, treated with atorvastatin. So, administration of atorvastatin to the patients with IHD and obesity may negatively impact carbohydrate exchange and serve as a possible cause of diabetes melitus type 2 development
Varespladib and cardiovascular events in patients with an acute coronary syndrome: the VISTA-16 randomized clinical trial
- Author
- Abraham J
- Abramson B
- Acheatel R
- Ahmed M
- Akhunova S
- Alegret JM
- Alonso-Pulpón L
- Amerena J
- Amkieh A
- Amlani M
- Anand D
- Anderson J
- Antolin JM
- Areses EL
- Arkhipov M
- Aroney C
- Arstall M
- Asfour A
- Ashchi M
- Auguadro C
- Azar R
- Balog C
- Banker D
- Barbarash O
- Barbarich V
- Bash Dianna
- Battaglia J
- Belenky D
- Benczur B
- BERNI Andrea
- Berti S
- Bertolet B
- Biasucci LM
- Black R
- Blanchard A
- Blonder R
- Bokern MJ
- Bosschaert M
- Braun-Dullaeus R
- Breedveld RW
- Brennan Danielle M.
- Brilakis E
- Broadwater S
- Bronisz M
- Bronzwaer PN
- Brown A
- Brown WV
- Browne K
- Burtt D
- Camp A
- Cannon K
- Cavender JB
- Cavender Matthew A.
- Cendon AA
- Cervinka P
- Chandna H
- Chandra S
- Chandrashekhar Y
- Chapidze G
- Chawla K
- Chernick R
- Chronos N
- Chumburidze V
- Collins N
- Constance C
- Corrada E
- Cortés JM
- Crowley S
- Csapo K
- Cuccia C
- Dabrowski M
- Dani S
- Dart A
- Davies C
- Delafontaine P
- Della-Siega A
- DeMets D
- Den Hartog F
- den Hartoog M
- Dengler T
- Denning S
- Derlaga B
- Devlin G
- Dezsi C
- Dinnyes J
- Dobrzycki S
- Doevendans P
- Dorsel T
- Dovgalevskiy Y
- Downes T
- Drenning D
- Drozdz J
- Drzewiecki A
- East C
- Eaton G
- Edes I
- Eich D
- Elliott J
- Ermoshkina L
- Esquivias GB
- Farshid A
- Faynyk A
- Fedele F
- Fernández JD
- Ferrier L
- Feskov O
- Fineschi M
- Franco SN
- French W
- Frey N
- Fulwani M
- Gebel J
- Genth-Zotz S
- Genís AB
- Gessek J
- Gielen S
- Gillespie E
- Gniot J
- Go B
- Goloborodko B
- Goloshchekin B
- González MJ
- Gordeev I
- Gormaz CL
- Gosselin G
- Goswami R
- Goya IL
- Gunalingam B
- Gupta S
- Guseva G
- Haldis T
- Haltern G
- Harding S
- Hart H
- Heckman MJ
- Hengstenberg C
- Henry P
- Hermans W
- Herrman J
- Heuer H
- Horak D
- Horowitz J
- Hubacek J
- Huff C
- Hulinsky V
- Hutyra M
- Huynh T
- Ilmer B
- Ingelmo JM
- Janik M
- Jarne EF
- Jay D
- Jukema J. Wouter
- Kahali D
- Kancz S
- Karpenko O
- Karpenko Y
- Kashou H
- Kastelein John J. P.
- Katerenchuk O
- Katzan I
- Kedhi E
- Keijzers M
- Khaisheva L
- Khintibidze I
- Kie SH
- Kiss R
- Kleiman N
- Klein G
- Klimovic T
- Klimsa Z
- Kmetzo J
- Kobulia B
- Kochmanski M
- Koenig W
- Koenig Wolfgang
- Kokis A
- Kopytsya M
- Korban E
- Kornacewicz-Jach Z
- Kostenko V
- Kovacs Z
- Koval O
- Kozhukhov S
- Kozlowski A
- Kraiz I
- Kreuzer J
- Kukuy E
- Kuznetsov V
- Lago VN
- Lai C
- Lamas G
- Lambert C
- Lapp H
- Lauer M
- Lavi S
- Leithäuser B
- Lenderink T
- Leschke M
- Libis R
- Lieberman S
- Liem A
- Lincoff A. Michael
- Linev K
- Lioy E
- Lochridge S
- Lok D
- Loussararian A
- Lu D
- Lupkovics G
- MacDonald L
- Madej A
- Magagnini E
- Mahar L
- Maly M
- Mamatsashvili M
- Mann J
- Marenzi G
- Markov V
- Marso S
- Martin Mde M
- Martin IH
- Martin L
- Mayer O
- McCullum K
- Megreladze I
- Mennuni M
- Menon Venu
- Merenda R
- Merkely B
- Miekus P
- Mikhin V
- Minisi A
- Miranda JM
- Monhart Z
- Monraats P
- Montero JS
- Moretti L
- Motovska Z
- Movahed M
- Mudra H
- Mukherjee A
- Muller G
- Musial W
- Möllmann H
- Nagy A
- Nambi Vijay
- Nava JS
- Navarro MJ
- Nicholls Stephen J.
- Nierop P
- Nissen
- Nogai K
- Oei F
- Ortiz AI
- Ovcharenko E
- Paradis JM
- Parikh K
- Parker J
- Peñaranda AS
- Pfeffer M
- Piscione F
- Pleva L
- Pluta W
- Polasek P
- Polgar P
- Polk D
- Pollock S
- Ponikowski P
- Prasad C
- Prati F
- Premchand R
- Prokhorov O
- Psuja P
- Pudil R
- Pérez MB
- Rajput R
- Ramaswamy G
- Rassi A
- Reichert P
- Rekosz J
- Rezkalla S
- Richardson J
- Rivera E
- Robertson R
- Rodes-Cabau J
- Roleau J
- Romero AJ
- Romo AI
- Ronaszeki A
- Ronner E
- Rosenberg M
- Rosenson Robert S.
- Rotterova H
- Rubio AM
- Ruda M
- Rudenko L
- Runquist L
- Rynkiewicz A
- Sangiorgi G
- Sanmartín M
- Sanz M
- Sanz RR
- Saucedo J
- Schwartz G
- Schwartz Gregory G.
- Seigel P
- Semenka J
- Senaratne M
- Sereg M
- Shaburishvili T
- Shah A
- Shalnev V
- Shishehbor M
- Shvarts Y
- Silverman P
- Simanenkov V
- Simonyi G
- Skelding K
- Soriano FR
- Speciale G
- Spinar J
- Stellbrink C
- Steven E. Hennekens C
- Stillabower M
- Strain J
- Strasser R
- Sultan P
- Suriano P
- Tans JG
- Testa R
- Thadani U
- Thompson P
- Timofeev A
- Tolerico P.
- Treasure C
- Trip MD
- Trivedi S
- Troquay R
- Uchino K
- Ujda M
- Urbano RH
- Vadaganelli P
- Vakaliuk I
- Valgimigli M
- van de Wetering ML
- van der Heijden R
- van Gaal W
- van Wijk L
- Veen G
- Vertes A
- Vest A
- Vijay N
- Vishnevsky A
- Voehringer HF
- Volkova E
- Wachter R
- Werner N
- White M
- Wiley M
- Wilkins G
- Williams J
- Witkowski A
- Wright R. Scott
- Wysokinski A
- Youssef G
- Zadra R
- Zateyshchikov D
- Zishiri E
- Zubiri JJ
- Publication venue
- 'American Medical Association (AMA)'
- Publication date
- 01/01/2014
- Field of study
IMPORTANCE: Secretory phospholipase A2(sPLA2) generates bioactive phospholipid products implicated in atherosclerosis. The sPLA2inhibitor varespladib has favorable effects on lipid and inflammatory markers; however, its effect on cardiovascular outcomes is unknown. OBJECTIVE: To determine the effects of sPLA2inhibition with varespladib on cardiovascular outcomes. DESIGN, SETTING, AND PARTICIPANTS: A double-blind, randomized, multicenter trial at 362 academic and community hospitals in Europe, Australia, New Zealand, India, and North America of 5145 patients randomized within 96 hours of presentation of an acute coronary syndrome (ACS) to either varespladib (n = 2572) or placebo (n = 2573) with enrollment between June 1, 2010, and March 7, 2012 (study termination on March 9, 2012). INTERVENTIONS: Participants were randomized to receive varespladib (500 mg) or placebo daily for 16 weeks, in addition to atorvastatin and other established therapies. MAIN OUTCOMES AND MEASURES: The primary efficacy measurewas a composite of cardiovascular mortality, nonfatal myocardial infarction (MI), nonfatal stroke, or unstable angina with evidence of ischemia requiring hospitalization at 16 weeks. Six-month survival status was also evaluated. RESULTS: At a prespecified interim analysis, including 212 primary end point events, the independent data and safety monitoring board recommended termination of the trial for futility and possible harm. The primary end point occurred in 136 patients (6.1%) treated with varespladib compared with 109 patients (5.1%) treated with placebo (hazard ratio [HR], 1.25; 95%CI, 0.97-1.61; log-rank P = .08). Varespladib was associated with a greater risk of MI (78 [3.4%] vs 47 [2.2%]; HR, 1.66; 95%CI, 1.16-2.39; log-rank P = .005). The composite secondary end point of cardiovascular mortality, MI, and stroke was observed in 107 patients (4.6%) in the varespladib group and 79 patients (3.8%) in the placebo group (HR, 1.36; 95% CI, 1.02-1.82; P = .04). CONCLUSIONS AND RELEVANCE: In patients with recent ACS, varespladib did not reduce the risk of recurrent cardiovascular events and significantly increased the risk of MI. The sPLA2inhibition with varespladib may be harmful and is not a useful strategy to reduce adverse cardiovascular outcomes after ACS. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01130246. Copyright 2014 American Medical Association. All rights reserved
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Cause of Death and Predictors of All-Cause Mortality in Anticoagulated Patients With Nonvalvular Atrial Fibrillation : Data From ROCKET AF
- Author
- Abadier R.
- Abelson M.
- Abhyankar A.
- Abram N.
- Achimastos A.
- Agacdiken Agir A.
- Agah R.
- Agamasu J.
- Aganauskiene J.
- Ageno W.
- Agnelli G.
- Aguirre A.
- Ahuad Guerrero A.
- Aidietiene S.
- Aiub J.
- Akyea Djamson A.
- Al Saghir Y.
- Al Zoebi A.
- Albina G.
- Albirini A.
- Alcocer Gamba M.
- Alekseeva N.
- Alessi S.
- Alexeeva O.
- Alfieri A.
- Almaguer E.
- Almquist A.
- Altunkeser B.
- Alvarado O.
- Alvarez Garcia P.
- Alvarez Lopez H.
- Alvariqueta A.
- Alzaghrini G.
- Amaram S.
- Amerena J.
- Amosova K.
- Amuchastegui M.
- Anderson C.
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- Angelova I.
- Antonios N.
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- Anusauskiene J.
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- Arkhipov M.
- Aron G.
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- Publication date
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- Field of study
M. Kaste on työryhmän ROCKET AF Steering Comm jäsen.Background-Atrial fibrillation is associated with higher mortality. Identification of causes of death and contemporary risk factors for all-cause mortality may guide interventions. Methods and Results-In the Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation (ROCKET AF) study, patients with nonvalvular atrial fibrillation were randomized to rivaroxaban or dose-adjusted warfarin. Cox proportional hazards regression with backward elimination identified factors at randomization that were independently associated with all-cause mortality in the 14 171 participants in the intention-to-treat population. The median age was 73 years, and the mean CHADS(2) score was 3.5. Over 1.9 years of median follow-up, 1214 (8.6%) patients died. Kaplan-Meier mortality rates were 4.2% at 1 year and 8.9% at 2 years. The majority of classified deaths (1081) were cardiovascular (72%), whereas only 6% were nonhemorrhagic stroke or systemic embolism. No significant difference in all-cause mortality was observed between the rivaroxaban and warfarin arms (P=0.15). Heart failure (hazard ratio 1.51, 95% CI 1.33-1.70, P= 75 years (hazard ratio 1.69, 95% CI 1.51-1.90, P Conclusions-In a large population of patients anticoagulated for nonvalvular atrial fibrillation, approximate to 7 in 10 deaths were cardiovascular, whereasPeer reviewe
Cause of death and predictors of all-cause mortality in anticoagulated patients with nonvalvular atrial fibrillation: Data from ROCKET AF
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- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 01/01/2015
- Field of study
Background-Atrial fibrillation is associated with higher mortality. Identification of causes of death and contemporary risk factors for all-cause mortality may guide interventions. Methods and Results-In the Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation (ROCKET AF) study, patients with nonvalvular atrial fibrillation were randomized to rivaroxaban or dose-adjusted warfarin. Cox proportional hazards regression with backward elimination identified factors at randomization that were independently associated with all-cause mortality in the 14 171 participants in the intentionto- treat population. The median age was 73 years, and the mean CHADS2 score was 3.5. Over 1.9 years of median follow-up, 1214 (8.6%) patients died. Kaplan-Meier mortality rates were 4.2% at 1 year and 8.9% at 2 years. The majority of classified deaths (1081) were cardiovascular (72%), whereas only 6% were nonhemorrhagic stroke or systemic embolism. No significant difference in all-cause mortality was observed between the rivaroxaban and warfarin arms (P=0.15). Heart failure (hazard ratio 1.51, 95% CI 1.33-1.70, P<0.0001) and age 6575 years (hazard ratio 1.69, 95% CI 1.51-1.90, P<0.0001) were associated with higher all-cause mortality. Multiple additional characteristics were independently associated with higher mortality, with decreasing creatinine clearance, chronic obstructive pulmonary disease, male sex, peripheral vascular disease, and diabetes being among the most strongly associated (model C-index 0.677). Conclusions-In a large population of patients anticoagulated for nonvalvular atrial fibrillation, 487 in 10 deaths were cardiovascular, whereas <1 in 10 deaths were caused by nonhemorrhagic stroke or systemic embolism. Optimal prevention and treatment of heart failure, renal impairment, chronic obstructive pulmonary disease, and diabetes may improve survival
Ezetimibe added to statin therapy after acute coronary syndromes
- Author
- Aagnes I
- Aambakk MB
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- Aaser E
- Abdel-Latief A
- Abell T
- Aboufakher R
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- Zweiker R
- Ångman K
- Édes I
- Östberg S
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2015
- Field of study
BACKGROUND: Statin therapy reduces low-density lipoprotein (LDL) cholesterol levels and the risk of cardiovascular events, but whether the addition of ezetimibe, a nonstatin drug that reduces intestinal cholesterol absorption, can reduce the rate of cardiovascular events further is not known. METHODS: We conducted a double-blind, randomized trial involving 18,144 patients who had been hospitalized for an acute coronary syndrome within the preceding 10 days and had LDL cholesterol levels of 50 to 100 mg per deciliter (1.3 to 2.6 mmol per liter) if they were receiving lipid-lowering therapy or 50 to 125 mg per deciliter (1.3 to 3.2 mmol per liter) if they were not receiving lipid-lowering therapy. The combination of simvastatin (40 mg) and ezetimibe (10 mg) (simvastatin-ezetimibe) was compared with simvastatin (40 mg) and placebo (simvastatin monotherapy). The primary end point was a composite of cardiovascular death, nonfatal myocardial infarction, unstable angina requiring rehospitalization, coronary revascularization ( 6530 days after randomization), or nonfatal stroke. The median follow-up was 6 years. RESULTS: The median time-weighted average LDL cholesterol level during the study was 53.7 mg per deciliter (1.4 mmol per liter) in the simvastatin-ezetimibe group, as compared with 69.5 mg per deciliter (1.8 mmol per liter) in the simvastatin-monotherapy group (P<0.001). The Kaplan-Meier event rate for the primary end point at 7 years was 32.7% in the simvastatin-ezetimibe group, as compared with 34.7% in the simvastatin-monotherapy group (absolute risk difference, 2.0 percentage points; hazard ratio, 0.936; 95% confidence interval, 0.89 to 0.99; P = 0.016). Rates of pre-specified muscle, gallbladder, and hepatic adverse effects and cancer were similar in the two groups. CONCLUSIONS: When added to statin therapy, ezetimibe resulted in incremental lowering of LDL cholesterol levels and improved cardiovascular outcomes. Moreover, lowering LDL cholesterol to levels below previous targets provided additional benefit
Edoxaban versus warfarin in patients with atrial fibrillation
- Author
- Abdullakutty J
- Abi-Mansour P
- Abril SB
- Accini J
- Accini M
- Acikel M
- Acikel M
- Adachi C
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- Adamus J
- Adler J
- Adler P
- Agarwal D
- Aggarwal R
- Aggarwal R
- Agirov M
- Agraou B
- Ahmad A
- Ahmadpour H
- Ahuad Guerrero R
- Ajioka M
- Akhter F
- Akihisa U
- Akilli H
- Al-Maliky T
- Al-Zoebi A
- Albert L. Waldo
- Albisu J
- Albulescu P
- Alexander J
- Alexandrova L
- Alexopoulos D
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- Alhakim M
- Aliyar P
- Allall O
- Allison J
- Allman J
- Almaraz SP
- Almeida A
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- Almquist A
- Aloni I
- Alsheikh T
- Altonen D
- Alvarez C
- Alvarez M
- Alvarez RF
- Amarenco P
- Amato Vincenzo de Paola A
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- Ambrovicova V
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- Ameriso S
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- Ŝpinar J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2013
- Field of study
Contains fulltext :
125374.pdf (publisher's version ) (Open Access)BACKGROUND: Edoxaban is a direct oral factor Xa inhibitor with proven antithrombotic effects. The long-term efficacy and safety of edoxaban as compared with warfarin in patients with atrial fibrillation is not known. METHODS: We conducted a randomized, double-blind, double-dummy trial comparing two once-daily regimens of edoxaban with warfarin in 21,105 patients with moderate-to-high-risk atrial fibrillation (median follow-up, 2.8 years). The primary efficacy end point was stroke or systemic embolism. Each edoxaban regimen was tested for noninferiority to warfarin during the treatment period. The principal safety end point was major bleeding. RESULTS: The annualized rate of the primary end point during treatment was 1.50% with warfarin (median time in the therapeutic range, 68.4%), as compared with 1.18% with high-dose edoxaban (hazard ratio, 0.79; 97.5% confidence interval [CI], 0.63 to 0.99; P<0.001 for noninferiority) and 1.61% with low-dose edoxaban (hazard ratio, 1.07; 97.5% CI, 0.87 to 1.31; P=0.005 for noninferiority). In the intention-to-treat analysis, there was a trend favoring high-dose edoxaban versus warfarin (hazard ratio, 0.87; 97.5% CI, 0.73 to 1.04; P=0.08) and an unfavorable trend with low-dose edoxaban versus warfarin (hazard ratio, 1.13; 97.5% CI, 0.96 to 1.34; P=0.10). The annualized rate of major bleeding was 3.43% with warfarin versus 2.75% with high-dose edoxaban (hazard ratio, 0.80; 95% CI, 0.71 to 0.91; P<0.001) and 1.61% with low-dose edoxaban (hazard ratio, 0.47; 95% CI, 0.41 to 0.55; P<0.001). The corresponding annualized rates of death from cardiovascular causes were 3.17% versus 2.74% (hazard ratio, 0.86; 95% CI, 0.77 to 0.97; P=0.01), and 2.71% (hazard ratio, 0.85; 95% CI, 0.76 to 0.96; P=0.008), and the corresponding rates of the key secondary end point (a composite of stroke, systemic embolism, or death from cardiovascular causes) were 4.43% versus 3.85% (hazard ratio, 0.87; 95% CI, 0.78 to 0.96; P=0.005), and 4.23% (hazard ratio, 0.95; 95% CI, 0.86 to 1.05; P=0.32). CONCLUSIONS: Both once-daily regimens of edoxaban were noninferior to warfarin with respect to the prevention of stroke or systemic embolism and were associated with significantly lower rates of bleeding and death from cardiovascular causes. (Funded by Daiichi Sankyo Pharma Development; ENGAGE AF-TIMI 48 ClinicalTrials.gov number, NCT00781391.)