10 research outputs found
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.
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- Agnelli G.
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- Aidietiene S.
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- Akyea Djamson A.
- Al Saghir Y.
- Al Zoebi A.
- Albina G.
- Albirini A.
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- Alekseeva N.
- Alessi S.
- Alexeeva O.
- Alfieri A.
- Almaguer E.
- Almquist A.
- Altunkeser B.
- Alvarado O.
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- Publication venue
- Publication date
- 01/01/2015
- 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
Use of anticoagulants and antiplatelet agents in stable outpatients with coronary artery disease and atrial fibrillation. International CLARIFY registry
- Author
- A. L. R. Ng
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- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2015
- Field of study
Effects of Anacetrapib in Patients with Atherosclerotic Vascular Disease
- Author
- Aaltonen M
- Abdur Rahman M
- Abell T
- Abide W. Jr
- Acheatel R
- Achiri P
- Acon J
- Adams T
- Affinito S
- Agarwal S
- Aggarwal K
- Aggarwal R
- Ahlström P
- Ahmad A
- Ahmed M
- Aillon C
- Airaksinen A
- Ait-sadi R
- Akers J
- Al-jumaily J
- Albers C
- Albert M
- Alberti A
- Alexander T
- Alford C
- Algotsson L
- Allen T
- Allworth M
- Almond E
- Aloisi A
- Alternburg C
- Alton M
- Amin J
- Amundson A
- Andersen K
- Andersen M
- Anderson E
- Anderson G
- Anderson R
- Anderson T
- Andersson H
- Andersson L
- Andreo J
- Andres C
- Andresen D
- Andrews G
- Andrews L
- Andrews R
- Andrioli V
- Angermann Ce
- Annas T
- Ansell V
- Antonio-drabek C
- Antonishen D
- Antonishen M
- Anuschek V
- Appel Kf
- Appel S
- Appleyard D
- Archer A
- Armitage J
- Armstrong L
- Armstrong M
- Arnesson K
- Arnold M
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- Arp H
- Asbill B
- Ashbrook-raby C
- Ashton L
- Assarsson E
- Audet K
- Augenbraun C
- Aung HNIN THANDA
- Auscher S
- Ausner J
- Aviles R
- Awasty V
- Axelsson U
- Ayers S
- Ayub H
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- Babington G
- Backlund M
- Badal B
- Baggiore C
- Baghiana S
- Bai H
- Bai J
- Baigent C
- Baillargeon G
- Bakbak A
- Baker S
- Baldin Mg
- Baldini E
- Baldwin E
- Ballantyne C
- Baltic A
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- Bang Hansen M
- Banks K
- Bansilal S
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- CARIDAD HERNANDEZ JOSE MANUEL
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- Carlsen H
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- Casey MAEVE ANN
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- Yandamuri S
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- Yang HEE JUNG
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- Yao H
- Yao X
- Yao Y
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- Yedinak S
- Yeh N
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- Yunes R
- Zadra R
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- Zambelli M
- Zbik S
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- Zelenka J
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- Zeuthen E
- Zhai M
- Zhang A
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- Zhang C
- Zhang F
- Zhang H
- Zhang J
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- Zhang R
- Zhang S
- Zhang Ting
- Zhang Wen
- Zhang X
- Zhang Y
- Zhao C
- Zhao JIAYI STELLA
- Zhao L
- Zhao P
- Zhao R
- Zhao Y
- Zheng Y
- Zheng Z
- Zhi Y
- Zhong H
- Zhong R
- Zhou C
- Zhou Juan
- Zhou Xingyu
- Zhou Yingyuan
- Zhu Wangqin
- Zhu X
- Zhu Y
- Ziefle S
- Zilz N
- Zineldine A
- Zlatewa R
- Zoghbi J
- Zong C
- Zong D
- Zong X
- Zuchelkowski A
- Zulauf N
- Ågårdh A
- Öner A
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND:
Patients with atherosclerotic vascular disease remain at high risk for cardiovascular events despite effective statin-based treatment of low-density lipoprotein (LDL) cholesterol levels. The inhibition of cholesteryl ester transfer protein (CETP) by anacetrapib reduces LDL cholesterol levels and increases high-density lipoprotein (HDL) cholesterol levels. However, trials of other CETP inhibitors have shown neutral or adverse effects on cardiovascular outcomes.
METHODS:
We conducted a randomized, double-blind, placebo-controlled trial involving 30,449 adults with atherosclerotic vascular disease who were receiving intensive atorvastatin therapy and who had a mean LDL cholesterol level of 61 mg per deciliter (1.58 mmol per liter), a mean non-HDL cholesterol level of 92 mg per deciliter (2.38 mmol per liter), and a mean HDL cholesterol level of 40 mg per deciliter (1.03 mmol per liter). The patients were assigned to receive either 100 mg of anacetrapib once daily (15,225 patients) or matching placebo (15,224 patients). The primary outcome was the first major coronary event, a composite of coronary death, myocardial infarction, or coronary revascularization.
RESULTS:
During the median follow-up period of 4.1 years, the primary outcome occurred in significantly fewer patients in the anacetrapib group than in the placebo group (1640 of 15,225 patients [10.8%] vs. 1803 of 15,224 patients [11.8%]; rate ratio, 0.91; 95% confidence interval, 0.85 to 0.97; P=0.004). The relative difference in risk was similar across multiple prespecified subgroups. At the trial midpoint, the mean level of HDL cholesterol was higher by 43 mg per deciliter (1.12 mmol per liter) in the anacetrapib group than in the placebo group (a relative difference of 104%), and the mean level of non-HDL cholesterol was lower by 17 mg per deciliter (0.44 mmol per liter), a relative difference of -18%. There were no significant between-group differences in the risk of death, cancer, or other serious adverse events.
CONCLUSIONS:
Among patients with atherosclerotic vascular disease who were receiving intensive statin therapy, the use of anacetrapib resulted in a lower incidence of major coronary events than the use of placebo. (Funded by Merck and others; Current Controlled Trials number, ISRCTN48678192 ; ClinicalTrials.gov number, NCT01252953 ; and EudraCT number, 2010-023467-18 .)
Effect of evolocumab or ezetimibe added to moderate- or high-intensity statin therapy on LDL-C lowering in patients with hypercholesterolemia: the LAPLACE-2 randomized clinical trial.
- Author
- Abdulhakim EE
- Abraham W
- Adamkova V
- Adler L
- Akhras R
- Aronoff S
- Atassi K
- Awasty V
- Bailey K
- Bajnok L
- Barbarash O
- Baron S
- Bear R
- Bertolet B
- Bhagwat R
- Blagden M
- Bod E
- Borgencrantz B
- Borghi C
- Bosson P
- Bous JP
- Bucci M
- Burnier M
- Cattin L
- Cermak O
- Ceska R
- Cha J
- Chehayeb R
- Chilvers M
- Chumakova G
- Clavel S
- Coburn N
- Cohen AA
- Collette R
- Connery L
- Cornelli K
- Curiac D
- D'Costa R
- Dahlén G
- Dauber I
- Davis M
- Davy JM
- De Graaf J
- De Munck L
- Degtyareva E
- Delavaran C
- Demchenko E
- Diederich C
- Donders S
- Dowell A
- Dzongowski P
- Eaton G
- Eberli F
- Falk R
- Fialkow J
- Fialkow J
- Fishbein G
- Fisher M
- Frana P
- French W
- Friedlander I
- Fuchs-Ertman D
- Förster A
- Gallino A
- Gimeno EJ
- Gimilio JF
- Ginsberg D
- Gupta A
- Hagan M
- Hage-Korban E
- Hala T
- Halperin F
- Halpern S
- Hamilton A
- Harcsa E
- Hart R
- Hassanin H
- Heaton K
- Helder D
- Henderson D
- Henein S
- Horacek T
- Horvathova V
- Houser P
- Iannuzzi A
- Ibrahim H
- Imholz B
- Jennings W
- Joubert M
- Kanani S
- Kasperk C
- Kellnerova I
- Kerrane J
- Kivitz A
- Klessens-Godfroy F
- Kohler E
- Kooy A
- Kornder J
- Kotelnikov M
- Kozlowski L
- Krogsaa A
- Lamy A
- Lau EM
- Laufs U
- Legg JC
- Lehman R
- Lindholm CJ
- Lippai J
- Litvin A
- Loh I
- Lukyanov Y
- Mach F
- Machkova M
- Mackay J
- Malone M
- Mansourati J
- McConnehey B
- McCormack T
- McCullum K
- McKinnon C
- Meissner G
- Miccoli R
- Miller M
- Mohacsi A
- Napoli M
- Nedergaard BS
- Nedergaard BS
- Nelson P
- Neutel J
- Neutel JM
- Nuñez-Cortes JM
- OMahony M
- Oyesile B
- Palinkas A
- Pandey A
- Passaro A
- Pavel-Knox I
- Petrzelkova J
- Pintus P
- Pirro M
- Pojsl S
- Poor F
- Prieto JM
- Probst V
- Proietto J
- Purdy D
- Qureshi M
- Ramstad D
- Ramstad D
- Raoof T
- Raya PM
- Reichman A
- Rich K
- Rickli H
- Robinson J
- Robinson JG
- Rogers W
- Rogers WJ
- Ros E
- Sabe-Affaki G
- Sala XP
- Salazar J
- Schenkenberger I
- Scott R
- Shaoulian E
- Shvarts Y
- Simons L
- Sirtori C
- Somaratne R
- Soran H
- St Maurice F
- Stankova V
- Stoessel J
- Stringer J
- Stroes E
- Susekov A
- Szakal I
- Sziegl Z
- Tarleton G
- Thomas H
- Throne M
- Trenk D
- Treshkur T
- Vaclavik J
- Van Leendert R
- Vantroyen
- Verges B
- Vermeersch L
- Viergever P
- Vileyn G
- Vincent H
- Wasserman SM
- Webb C
- Weiss R
- Weiss R
- Wermuth S
- Widmer F
- Winkler K
- Wiseman A.
- Yakhontova P
- Yeung CY
- Zambon S
- Zemanek J
- Publication venue
- 'American Medical Association (AMA)'
- Publication date
- 01/01/2014
- Field of study
Importance In phase 2 studies, evolocumab, a fully human monoclonal antibody to PCSK9, reduced LDL-C levels in patients receiving statin therapy.
Objective To evaluate the efficacy and tolerability of evolocumab when used in combination with a moderate- vs high-intensity statin.
Design, Setting, and Patients Phase 3, 12-week, randomized, double-blind, placebo- and ezetimibe-controlled study conducted between January and December of 2013 in patients with primary hypercholesterolemia and mixed dyslipidemia at 198 sites in 17 countries.
Interventions Patients (n = 2067) were randomized to 1 of 24 treatment groups in 2 steps. Patients were initially randomized to a daily, moderate-intensity (atorvastatin [10 mg], simvastatin [40 mg], or rosuvastatin [5 mg]) or high-intensity (atorvastatin [80 mg], rosuvastatin [40 mg]) statin. After a 4-week lipid-stabilization period, patients (n = 1899) were randomized to compare evolocumab (140 mg every 2 weeks or 420 mg monthly) with placebo (every 2 weeks or monthly) or ezetimibe (10 mg or placebo daily; atorvastatin patients only) when added to statin therapies.
Main Outcomes and Measures Percent change from baseline in low-density lipoprotein cholesterol (LDL-C) level at the mean of weeks 10 and 12 and at week 12.
Results Evolocumab reduced LDL-C levels by 66% (95% CI, 58% to 73%) to 75% (95% CI, 65% to 84%) (every 2 weeks) and by 63% (95% CI, 54% to 71%) to 75% (95% CI, 67% to 83%) (monthly) vs placebo at the mean of weeks 10 and 12 in the moderate- and high-intensity statin-treated groups; the LDL-C reductions at week 12 were comparable. For moderate-intensity statin groups, evolocumab every 2 weeks reduced LDL-C from a baseline mean of 115 to 124 mg/dL to an on-treatment mean of 39 to 49 mg/dL; monthly evolocumab reduced LDL-C from a baseline mean of 123 to 126 mg/dL to an on-treatment mean of 43 to 48 mg/dL. For high-intensity statin groups, evolocumab every 2 weeks reduced LDL-C from a baseline mean of 89 to 94 mg/dL to an on-treatment mean of 35 to 38 mg/dL; monthly evolocumab reduced LDL-C from a baseline mean of 89 to 94 mg/dL to an on-treatment mean of 33 to 35 mg/dL. Adverse events were reported in 36%, 40%, and 39% of evolocumab-, ezetimibe-, and placebo-treated patients, respectively. The most common adverse events in evolocumab-treated patients were back pain, arthralgia, headache, muscle spasms, and pain in extremity (all <2%).
Conclusions and Relevance In this 12-week trial conducted among patients with primary hypercholesterolemia and mixed dyslipidemia, evolocumab added to moderate- or high-intensity statin therapy resulted in additional LDL-C lowering. Further studies are needed to evaluate the longer-term clinical outcomes and safety of this approach for LDL-C lowering.
Trial Registration clinicaltrials.gov Identifier: NCT0176386
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.
- Anderson J.
- Andrews R.
- Angelova I.
- Antonios N.
- Antonishen M.
- Anusauskiene J.
- Archibald J.
- Arkhipov M.
- Aron G.
- Aroney G.
- Arouni A.
- Artis A.
- Arzola F.
- Ashchi M.
- Ata N.
- Avezum A.
- Awan N.
- Ayala-Paredes F.
- Bacon J.
- Baek S.
- Balaguer J.
- Ballyzek M.
- Balparda C.
- Banerjee S.
- Banker D.
- Banos Velasco A.
- Baranov A.
- Baranova E.
- Barbarash O.
- Barbarich V.
- Barber A.
- Barreto Filho J.
- Basart D.
- Basri H.
- Batalla E.
- Bath P.
- Batushkin V.
- Bauknecht C.
- Baumgartner R.
- Bayat J.
- Becker R.
- Becker R. C.
- Bedwell N.
- Behrens-Humbold S.
- Behrens-Spandau S.
- Belber A.
- Belenky D.
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- Yan X.
- Yang J.
- Yang K.
- Yang T.
- Yarokhno N.
- Yarows S.
- Yavuzgil O.
- Yeh H.
- Yeh H.
- Yellen L.
- Yena L.
- Yilmaz O.
- Yin W.
- Yin Y.
- Yordanova V.
- Yu B.
- Yu C.
- Yuan Z.
- Yusof Z.
- Zadionchenko V.
- Zakhary B.
- Zamolyi K.
- Zateyshchikov D.
- Zdravkov N.
- Zebrack J.
- Zelenka J.
- Zeng Z.
- Zhao Y.
- Zheleznyy V.
- Zhurba S.
- Ziada K.
- Zidkova E.
- Ziegler F.
- Zimerman L.
- Zimetbaum P.
- Zimlichman R.
- Zimmermann S.
- Zolty R.
- Zrazhevsky K.
- Zuber M.
- 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
Angiotensin receptor neprilysin inhibition compared with enalapril on the risk of clinical progression in surviving patients with heart failure.
- Author
- Abhyankar A
- Accini J
- Adamson P
- Adelberger V
- Agarwal D K
- Ageev F
- Aggarwal R
- Aguilera M
- Ahlström P
- Ahmad W
- Ahmed F
- Akimov A
- Akinboboye O
- Aktoz M
- Akyea-Djamson A
- Al-Zoebi A
- Albisu J
- Albornoz F
- Alegre R
- Alexeeva-Kovalchuk A
- Almanzar A
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- Arango Juan Luis
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- Willems F
- Williams C
- Witherow F
- Wojciechowska C
- Woldman S
- Wollaert B
- Wong R
- Wronska D
- Wu L
- Wyss F
- Xu G
- Yakhontov D
- Yakovlev A
- Yan B
- Yang K
- Yannick N
- Yao L
- Yavdosyuk A
- Yavuzgil O
- Yenigun M
- Yeo D
- Yigit Z
- Yilmaz A
- Yilmaz M B
- Yip G
- Yokusoglu M
- Yoo B-S
- Yotov Y
- Yousef Z
- Yovaniniz P
- Yuan Z Y
- Yugandhar B
- Zaidman C
- Zannad F
- Zateyshchikova A
- Zebrack J
- Zeh W
- Zemek S
- Zemmrich C
- Zethson-Halldén M
- Zhang J
- Zhao R P
- Zharkov O
- Zhelev V
- Zhilyaev E
- Zilahi Z
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- Zo J-H
- Zotov D
- Zotz R
- Zrazhevsky K
- Zuraw B
- Zámolyi K
- Édes I
- Šuch S
- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 06/01/2015
- Field of study
Evolocumab and clinical outcomes in patients with cardiovascular disease
- Author
- Abelson M.
- Aboufakher R.
- Abrahamsen T. E.
- Accini Mendoza J. L.
- Acheatel R.
- Ackermann D.
- Adamkova V.
- Adams M.
- Adlam D.
- Aggarwal R.
- Aggarwal S.
- Ahsan A.
- Ainsworth P.
- Airody Govinda R.
- Akai A.
- Ako J.
- Al-Bahrani A.
- Al-Joundi T.
- Aldegather J.
- Aldrete Velasco J. A.
- Alfieri A.
- Alt I.
- Alzohaili O.
- Amerena J.
- Amin J.
- Amoedo R.
- Amuchastegui M.
- Anderson T.
- Andreka P.
- Andreotti F.
- Angoulvant D.
- Ansell B.
- Antalik L.
- Antkowiak-Piatyszek K.
- Appel K.
- Arakawa T.
- Arana Londoño C.
- Ardissino D.
- Ardito W. R.
- Arkhipov M.
- Arsenescu-Georgescu C.
- Asamoah N.
- Ascaso Gimilio J. F.
- Atar S.
- Atassi K.
- Athyros V.
- Auerbach E.
- Awtry E.
- Baass A.
- Badariene J.
- Badat A.
- Badila E.
- Bae J.
- Baigent C.
- Bain S.
- Baird I.
- Baker J.
- Balbay Y.
- Baldari D.
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- Bammert A.
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- Bandh S.
- Banerjee S.
- Banik M.
- Banikova A.
- Barbarash O.
- Barcinas R.
- Barnum O.
- Barroso de Souza W. K.
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- Barton J.
- Bata I.
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- Beer H. J.
- Begg A.
- Beltrame J.
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- Publication venue
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- Publication date
- 01/01/2017
- Field of study
peer reviewedBACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets. © 2017 Massachusetts Medical Society
Apixaban versus warfarin in patients with atrial fibrillation
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- V Zadionchenko
- Veli Pekka Harjola
- Verheugt F. W. A.
- W Bowden
- W Cabrera
- W Haught
- W Haverkamp
- W Heddle
- W Henry 3rd
- W Herzog
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- W Kufs
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- W Ridsdill Smith
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- W Smith
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- Wallentin L. Collaborators ARISTOTLE Committees and Investigators: Christopher B Granger
- Witold Ruzyllo
- X Albert
- X Chen
- X Jiang
- X Wang
- X Yang
- Y Atsushi
- Y Burmak
- Y Chandrashekhar
- Y Chen
- Y Cohen
- Y Higashi
- Y K Chan
- Y K Wong
- Y Karpov
- Y Kawase
- Y Kobayashi
- Y Koretsune
- Y Mostovoy
- Y N Kim
- Y Nakamura
- Y Pozdnyakov
- Y Sato
- Y Shubik
- Y Tsubokou
- Y Turgeman
- Y Yin
- Y Zhang
- Z Kiedrowicz
- Z László
- Z Meneghelo
- Z Q Li
- Z Sizova
- Z Telyatnikova
- Z Yousef
- Z Yousef
- Z Yusof
- Zhu J.
- Zubin Eapen
- Á Illés
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2011
- Field of study
BACKGROUND: Vitamin K antagonists are highly effective in preventing stroke in patients with atrial fibrillation but have several limitations. Apixaban is a novel oral direct factor Xa inhibitor that has been shown to reduce the risk of stroke in a similar population in comparison with aspirin. METHODS: In this randomized, double-blind trial, we compared apixaban (at a dose of 5 mg twice daily) with warfarin (target international normalized ratio, 2.0 to 3.0) in 18,201 patients with atrial fibrillation and at least one additional risk factor for stroke. The primary outcome was ischemic or hemorrhagic stroke or systemic embolism. The trial was designed to test for noninferiority, with key secondary objectives of testing for superiority with respect to the primary outcome and to the rates of major bleeding and death from any cause. RESULTS: The median duration of follow-up was 1.8 years. The rate of the primary outcome was 1.27% per year in the apixaban group, as compared with 1.60% per year in the warfarin group (hazard ratio with apixaban, 0.79; 95% confidence interval [CI], 0.66 to 0.95; P<0.001 for noninferiority; P = 0.01 for superiority). The rate of major bleeding was 2.13% per year in the apixaban group, as compared with 3.09% per year in the warfarin group (hazard ratio, 0.69; 95% CI, 0.60 to 0.80; P<0.001), and the rates of death from any cause were 3.52% and 3.94%, respectively (hazard ratio, 0.89; 95% CI, 0.80 to 0.99; P = 0.047). The rate of hemorrhagic stroke was 0.24% per year in the apixaban group, as compared with 0.47% per year in the warfarin group (hazard ratio, 0.51; 95% CI, 0.35 to 0.75; P<0.001), and the rate of ischemic or uncertain type of stroke was 0.97% per year in the apixaban group and 1.05% per year in the warfarin group (hazard ratio, 0.92; 95% CI, 0.74 to 1.13; P = 0.42). CONCLUSIONS: In patients with atrial fibrillation, apixaban was superior to warfarin in preventing stroke or systemic embolism, caused less bleeding, and resulted in lower mortality. Copyright © 2011 Massachusetts Medical Society. All rights reserved
Evolocumab and clinical outcomes in patients with cardiovascular disease
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- Abelson M
- Aboufakher R
- Abrahamsen Te
- Accini Mendoza Jl
- Acheatel R
- Ackermann D
- Adamkova V
- Adams M
- Adlam D
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- Ahsan A
- Ainsworth P
- Airody Govinda R
- Akai A
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- Al-Bahrani A
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- Aldegather J
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- Alfieri A
- Alt I
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- Arana Londoño C
- Ardissino D
- Ardito Wr
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- Arsenescu-Georgescu C
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- Ascaso Gimilio Jf
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- Athyros V
- Auerbach E
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- Sever Peter S.
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- Shifrin G.
- Shimizu M
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- Shinozaki T
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- Shutemova E
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- Sime I
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- Tereshenko S
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- Trenk D
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- Tsoukas G
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- Tyagi S
- Tydén P
- Tyszecka G
- Tzekova M
- Tziakas D
- Uehara H
- Uemura O
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- Uhliar R
- Ulla Mr
- Urbach D
- Urgeova L
- Vaclavik J
- Vakaliuk I
- Valdes Chavarri M
- Vally T
- Valter I
- Van Beek E
- van de Borne P
- van de Wal R
- van der Walt E
- van der Zwaan C
- Van Gaal W
- Van Hessen M
- Van Zyl L
- Vanbelle E
- Vandekerckhove H
- Vasco Salgado A
- Vawda G
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- Venceviciene L
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- Vertes G
- Veze I
- Vida Gutierrez M
- Vidotti Mh
- Viigimaa M
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- Vikman S
- Vinanska D
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- Violante Ortiz Rm
- Vishnevsky A
- Visman A
- Vita J
- Voevoda M
- Vogel Dr
- Volkov V
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- von Hodenberg E
- Vora K
- Vorpahl M
- Wada A
- Wagner S
- Wan Ahmad Wa
- Wang D
- Wang Huei
- Wang J
- Wasserman Scott M.
- Waxman F
- Webel R
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- Weinberg B
- Weinstein D
- Welker J
- Wermuth S
- Westendorp I
- Weyland K
- Whitney R
- Wierzbicka K
- Wilhoit G
- Wilson S
- Wise J
- Wiseman A
- Witt N
- Wittert G
- Wiviott Stephen D.
- Wnetrzak-Michalska R
- Wollaert B
- Wood Sk
- Wozakowska-Kaplon B
- Wozniak I
- Wu C
- Wyatt N
- Wöhrle J
- Xu P
- Xue L
- Yakhontova P
- Yamamoto K
- Yamashita K
- Yan J
- Yang E
- Yang P
- Yang X
- Yang Y
- Yang Z
- Yao Z
- Yasumura Y
- Yataco A
- Yeh H
- Yena L
- Yeoman G
- Yigit Z
- Yilmaz Mb
- Yokoya K
- Yoshimichi G
- Yotov Y
- Youngman D
- Younis L
- Yuge M
- Zabowka M
- Zahn L
- Zamorano Gomez Jl
- Zarich S
- Zateyshchikov D
- Zdrenghea D
- Zechowicz T
- Zeig S
- Zemanek J
- Zeng X
- Zhang L
- Zhang X
- Zhao S
- Zheng Y
- Zheng Z
- Zhou C
- Zhu Y
- Zhurba S
- Zidkova E
- Zieba B
- Ziegler O
- Zilahi Z
- Zrazhevskiy K
- Östergren J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets
Apixaban compared with warfarin in patients with atrial fibrillation and previous stroke or transient ischaemic attack: A subgroup analysis of the ARISTOTLE trial
- Author
- A Agarwal
- A Ahsan
- A Ajala
- A Al-Mudamgha
- A Alexander
- A Alfieri
- A Alings
- A Alwail
- A Bakhai
- A Barsotti
- A Bartkowiak
- A Bauer
- A Bazylevych
- A Bazzi
- A Bethencourt González
- A Bharani
- A Bittersohl
- A Boruczkowska-Kaszkowiak
- A Boyle
- A Bragina
- A Bredero
- A Brockmyre
- A Budaj
- A Buxton
- A Caccavo
- A Cassettari
- A Chhabra
- A Chmielinski
- A Cohen
- A Cooke
- A Cziraki
- A D'Angelo
- A De Paola
- A Dharmadhikari
- A Dowell
- A Francis
- A Gabito
- A Galicia
- A Ghirarduzzi
- A Golovach
- A Gordienko
- A Govorin
- A Hamad
- A Hershson
- A Hetzel
- A Hrabar
- A Ivleva
- A Jacob
- A Jones
- A Kabour
- A Kastanayan
- A Katona
- A Kelly
- A Koniakhin
- A Kovács
- A Lebowitz
- A Levin
- A Liu
- A Lorga Filho
- A Lowy
- A MacKinnon
- A Magnano
- A Marmor
- A Matsushima
- A Meholick
- A Mirode
- A Mohácsi
- A Moriarty
- A Muniz
- A Mügge
- A Mügge
- A Naik
- A Nambiar
- A Obrezan
- A Ocicka-Kozakiewicz
- A Pandey
- A Papp
- A Parkhomenko
- A Patel
- A Peeters
- A Pálinkás
- A Quick
- A Rabelo Alves Jr
- A Reyes
- A Rodriguez
- A Roman
- A Rubin
- A Salacata
- A Salajan
- A Samal
- A Sanchez
- A Schaap
- A Sinopalnikov
- A Skolnick
- A Solomon
- A Svistov
- A Ugarriza
- A Utech
- A Vértes
- A Wade
- A Warner
- A Weiss
- A Wellford
- A Yagensky
- Aldo Maggione
- Alexander J. H.
- Alexander Parkhomenko
- Ali Zomorodi
- Alings M.
- Alvaro Albrecht
- Alvaro Avezum
- Andreas Terent
- Anna Stenborg
- Antonio Carlos Lopes
- Antonio G Hermosillo
- Antonio M W Alings
- Axel Akerblom
- B Bachhuber
- B Beanblossom
- B Blue
- B Bruneel
- B Bryhni
- B Coutu
- B Garbelini Jr
- B Gervais
- B Gorenek
- B Griewing
- B H Oh
- B Hattler
- B Iteld
- B Jackson
- B Kowalski
- B Lachterman
- B Lasko
- B Lewis
- B Malipeddi
- B McClements
- B Peart
- B Pieske
- B Platt
- B Podogrodzka
- B Ramagiri
- B Ramjattan
- B Schifferdecker
- B Sidorenko
- B Srinivasasastry
- B Stockins
- B Winkelmann
- B Wollaert
- B Yu
- B Øie
- Bahit M. C.
- Basil S Lewis
- Bernard J Gersh
- Bradley Kolls
- Byung-Hee Oh
- C Arean Martinez
- C Arsenescu Georgescu
- C Beneitez
- C Bredlau
- C Calvo Vargas
- C Chavez
- C Christersson
- C Corder
- C Cuneo
- C D Tseng
- C Dézsi
- C East
- C Erol
- C Fortin
- C G Fierbinteanu-Braticevici
- C Gonzalez Juanatey
- C Hassel
- C Höglund
- C J Lindholm
- C JerJes-Sanchez
- C Kaoru Indio do Brasil
- C Levin
- C Lovell
- C Massey
- C McPherson
- C Mihaela Tanaseanu
- C Muratore
- C Olivieri
- C Pincetti
- C Pop
- C Powers
- C Poy
- C Raffo
- C Riojas
- C Rios Vasquez
- C Rodriguez-Fierro
- C Russo
- C Sofley
- C Sotolongo
- C Toftager Larsen
- C Torp-Pedersen
- C Tuxen
- C Van der Zwaan
- C W Lee
- C Weimar
- C Y Rhim
- C Yu
- C Zaidman
- Carlo Lombardi
- Cetin Erol
- Cheryl Bushnell
- Christoph Varenhorst
- Claes Held
- D Agarwal
- D Albuquerque
- D Ashby
- D Belenky
- D Borts
- D Brieger
- D Chiu
- D Clark
- D Colan
- D Cross
- D De Jong
- D Dohan
- D Donovan
- D Duplyakov
- D Dutka
- D El Allaf
- D Fell
- D Fischer
- D G Shin
- D Gaita
- D Garcia
- D Goldscher
- D Gottlieb
- D Gupta
- D Hassman
- D Humiston
- D Isaza
- D J Choi
- D Jiang
- D Kelbe
- D Kereiakes
- D Lighezan
- D Linden
- D Lok
- D Mercado
- D Mishkel
- D Morales
- D Moreira
- D Murdoch
- D O'Keefe
- D Perloff
- D Piskorz
- D Precoma
- D Rhodes
- D Riff
- D Rupka
- D Santos
- D Spence
- D Stapleton
- D Travis
- D Tudor Zdrenghea
- D Van Hamersveld
- D Vinereanu
- D Vogel
- D Walters
- D Young
- D Zotov
- Dan Atar
- Daniel Isaza
- David Garcia
- Denis Xavier
- Diener H. -C. ARISTOTLE Committees and Investigators: Christopher B Granger
- Dipen Parikh
- Dragos Vinereanu
- E Ball
- E Blumberg
- E Carasca
- E Engeron
- E Flores
- E Galve
- E Gomez
- E Hasbani
- E Haskel
- E Julian Chuquiure-Valenzuela
- E Klainman
- E Kosinski
- E Lopez Rosas
- E Manenti
- E Mazur
- E Morales-Palomares
- E Mouhayar
- E Panchenko
- E Pelloso
- E Privalova
- E Ramos
- E Retyk
- E Richiardi
- E Rivera
- E Sabbah
- E Schwarz
- E Sivkova
- E Suprun.
- E van Nieuwenhuizen
- E von Hodenberg
- E Zemtsovsky
- E Zidkova
- Easton J. D.
- Elaine M Hylek
- Elaine M Hylek
- Emil Hagstrom
- Erik Lundstrom
- F Agnone
- F Al-Khalili
- F Al-Khalili
- F Albrecht
- F Bai
- F Collado
- F Collado
- F De Leon
- F de Looze
- F de Looze
- F de Looze
- F de Looze
- F Dunn
- F Grondin
- F Kouichi
- F Lakatos
- F Maislos
- F Medina
- F Olías de la Cruz
- F Provenier
- F Rolandi
- F Schlachetzki
- F St Maurice
- F Stockenhuber
- F Stögbauer
- F Verheugt
- F Villaça Guimaraes Filho
- F Zhang
- Fernando Lanas
- Freek W A Verheugt
- G Andrei Dan
- G Arutyunov
- G Aycock
- G Boxho
- G Brooks
- G Bustamante
- G Casolo
- G Dzyak
- G Feldman
- G Filonenko
- G Ford
- G Gojanur
- G Hanovich
- G Ignatenko
- G Jensen
- G Kahrmann
- G Kamalov
- G Kania
- G Lavabre
- G Lip
- G Lu
- G Lupkovics
- G Lysenko
- G Mairesse
- G McInnes
- G Noble
- G Oliveira
- G Popik
- G Rasmanis
- G Reis
- G Rogelio
- G Sabe-Affaki
- G Sosa-Suarez
- G Stenzel
- G Syan
- George Wyse
- Goto S.
- Granger C. B.
- Greg Flaker
- Greg Stashenko
- H B Gowdappa
- H Colombo
- H F Vöhringer
- H Hamer
- H Ikeda
- H Jure
- H Kadr
- H Karunaratne
- H Kihara
- H Kultursay
- H Lastiri
- H Li
- H Li
- H Luciardi
- H Michels
- H Moore
- H Murata
- H Nachtergaele
- H Parikka
- H Po
- H Poppert
- H Punatar
- H Ramos
- H Reis
- H Salem
- H Striekwold
- H Takagi
- H Tan
- H Weich
- H Yoshii
- Hanna M.
- Hans-Christoph Diener
- Helio Guimaraes
- I Aisiku
- I Benedek
- I Bereznyakov
- I Chernichka
- I Chopey
- I Findlay
- I Friedlander
- I Gordeev
- I Hernandez Santamaria
- I Khomazjuk
- I Klimov
- I Kovalsky
- I Kraiz
- I Libov
- I Mackinnon
- I Mangat
- I Manitiu
- I Morales Gonzalez
- I Niazi
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- I Podpera
- I Szakál
- I Vykhovanyuk
- I Z Abidin
- J A Wang
- J Agaiby
- J Alejandro Cordero-Cabra
- J Amerena
- J Amin
- J Anderson
- J Arneja
- J Bakai
- J Berlingieri
- J Brachmann
- J Bruguera
- J Camm
- J Cannon
- J Cebe
- J Cervantes-Escarcega
- J Cha
- J Cobos
- J Cooke
- J Cordero-Sepulveda
- J Counsell
- J Cuadrado
- J Davies
- J Dean
- J Donald Easton
- J Duggal
- J E Otterstad
- J Egido Herrero
- J Estepo
- J F Saraiva
- J Flather
- J Fleming
- J Foley
- J Galizia
- J Garcia Pulido
- J Gerber
- J Gois
- J Gonzalez Guerra
- J Gonzalez Hermosillo
- J Graff
- J Griffin
- J H Bae
- J H Gómez Gómez
- J H Sung
- J Harenberg
- J Healey
- J Hemphill
- J Herlitz
- J Horowitz
- J Hysing
- J Ilvento
- J Ip
- J J V McMurray
- J Jaber
- J Jorge
- J Joseph
- J Jung
- J Kappler
- J Kasprzak
- J Kobayashi
- J Kramer
- J L Aziz
- J L Corbelli
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- J Lang
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- J P Pan
- J Phillips
- J Plomp
- J Porterfield
- J Quartner
- J Ricci
- J Rogers
- J Roos
- J Roquer
- J Roth
- J Schmedtje Jr
- J Seger
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- Wallentin L.
- Witold Ruzyllo
- Wojdyla D. M.
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- Y Yin
- Y Zhang
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- Z Q Li
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- Z Telyatnikova
- Z Yousef
- Z Yousef
- Z Yusof
- Zubin Eapen
- Á Illés
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2012
- Field of study
Background: In the ARISTOTLE trial, the rate of stroke or systemic embolism was reduced by apixaban compared with warfarin in patients with atrial fibrillation (AF). Patients with AF and previous stroke or transient ischaemic attack (TIA) have a high risk of stroke. We therefore aimed to assess the efficacy and safety of apixaban compared with warfarin in prespecified subgroups of patients with and without previous stroke or TIA. Methods: Between Dec 19, 2006, and April 2, 2010, patients were enrolled in the ARISTOTLE trial at 1034 clinical sites in 39 countries. 18 201 patients with AF or atrial flutter were randomly assigned to receive apixaban 5 mg twice daily or warfarin (target international normalised ratio 2·0-3·0). The median duration of follow-up was 1·8 years (IQR 1·4-2·3). The primary efficacy outcome was stroke or systemic embolism, analysed by intention to treat. The primary safety outcome was major bleeding in the on-treatment population. All participants, investigators, and sponsors were masked to treatment assignments. In this subgroup analysis, we estimated event rates and used Cox models to compare outcomes in patients with and without previous stroke or TIA. The ARISTOTLE trial is registered with ClinicalTrials.gov, number NTC00412984. Findings: Of the trial population, 3436 (19%) had a previous stroke or TIA. In the subgroup of patients with previous stroke or TIA, the rate of stroke or systemic embolism was 2·46 per 100 patient-years of follow-up in the apixaban group and 3·24 in the warfarin group (hazard ratio [HR] 0·76, 95% CI 0·56 to 1·03); in the subgroup of patients without previous stroke or TIA, the rate of stroke or systemic embolism was 1·01 per 100 patient-years of follow-up with apixaban and 1·23 with warfarin (HR 0·82, 95% CI 0·65 to 1·03; p for interaction=0·71). The absolute reduction in the rate of stroke and systemic embolism with apixaban versus warfarin was 0·77 per 100 patient-years of follow-up (95% CI -0·08 to 1·63) in patients with and 0·22 (-0·03 to 0·47) in those without previous stroke or TIA. The difference in major bleeding with apixaban compared with warfarin was 1·07 per 100 patient-years (95% CI 0·09-2·04) in patients with and 0·93 (0·54-1·32) in those without previous stroke or TIA. Interpretation: The effects of apixaban versus warfarin were consistent in patients with AF with and without previous stroke or TIA. Owing to the higher risk of these outcomes in patients with previous stroke or TIA, the absolute benefits of apixaban might be greater in this population. Funding: Bristol-Myers Squibb and Pfizer. © 2012 Elsevier Ltd