J?liaKar?dyMDabThomasMayrhoferPhDacMarosFerencikMD, PhD, MCRadJohn T.NagurneyMD, MPHeJames E.UdelsonMDfAndreas A.KammerlanderMD, PhDagJerome L.FlegMDhW. FrankPeacockMDiJames L.JanuzziJr.MDjWolfgangKoenigMD, PhDklmUdoHoffmannMD, MPHa
doi : 10.1016/j.jacc.2021.01.046
Volume 77, Issue 12, 30 March 2021, Pages 1487-1499
High-sensitivity cardiac troponin (hs-cTn) assays have different analytic characteristics.
Joseph S.AlpertMDaAllanJaffeMDbKristian A.ThygesenMD, DScc
doi : 10.1016/j.jacc.2021.02.031
Volume 77, Issue 12, 30 March 2021, Pages 1500-1502
PaaladineshThavendiranathanMD, SMa?LiliZhangMD, ScMb?AmnaZafarMDcZsofia D.DrobniMDcdSyed S.MahmoodMD, MPHeMarcellaCabralMDfMagidAwadallaMDcgAnjuNohriaMD, MSchDaniel A.ZlotoffMD, PhDcgFranckThunyMD, PhDijkLucie M.HeinzerlingMD, MPHlmAnaBaracMD, PhDnRyan J.SullivanMDoCarol L.ChenMDpDiptiGuptaMD, MPHpMichael C.KirchbergerMDlSarah E.HartmannBScJonathan W.WeinsaftMDep…Tomas G.NeilanMD, MPHcg
doi : 10.1016/j.jacc.2021.01.050
Volume 77, Issue 12, 30 March 2021, Pages 1503-1516
Myocarditis is a potentially fatal complication of immune checkpoint inhibitor (ICI) therapy. Data on the utility of cardiovascular magnetic resonance (CMR) T1 and T2 mapping in ICI myocarditis are limited.
Christopher M.KramerMDabChristopher A.HansonMDa
doi : 10.1016/j.jacc.2021.01.043
Volume 77, Issue 12, 30 March 2021, Pages 1517-1519
FilippaJuulMS, PhDaGeorgetaVaideanMD, MPH, PhDbcYongLinPhDdeAndrea L.DeierleinMS, MPH, PhDfgNiyatiParekhMS, PhD, RDfgh
doi : 10.1016/j.jacc.2021.01.047
Volume 77, Issue 12, 30 March 2021, Pages 1520-1531
Ultra-processed foods provide 58% of total energy in the U.S. diet, yet their association with cardiovascular disease (CVD) remains understudied.
Robert J.OstfeldMD, MScaKathleen E.AllenMS, RDb
doi : 10.1016/j.jacc.2021.02.003
Volume 77, Issue 12, 30 March 2021, Pages 1532-1534
Daniel P.AnderssonMD, PhDaLauraLanducciMDbYlva TrolleLagerrosMD, PhDcdAlessandraGrottaPhDeRinoBelloccoScDefMikaelLehtihetMD, PhDaMartin J.HolzmannMD, PhDcg
doi : 10.1016/j.jacc.2021.01.045
Volume 77, Issue 12, 30 March 2021, Pages 1535-1550
Phosphodiesterase 5 inhibitor (PDE5i) treatment is associated with reduced mortality compared with no treatment for erectile dysfunction after myocardial infarction (MI).
RenkeMaasMDaRoman N.RodionovMD, PHDbc
doi : 10.1016/j.jacc.2021.02.021
Volume 77, Issue 12, 30 March 2021, Pages 1551-1553
AndreasStangMD, MPHabMarkusDeckertaSusanneStolpeMSca
doi : 10.1016/j.jacc.2021.01.031
Volume 77, Issue 12, 30 March 2021, Pages 1554-1561
In 2016, the American Statistical Association stated that the use of statistical significance leads to distortion of the scientific process. The principal alternative to significance or null hypothesis testing (NHT) is estimation with point estimates and confidence intervals (CIs).
Jan G.P.TijssenPhD
doi : 10.1016/j.jacc.2021.02.004
Volume 77, Issue 12, 30 March 2021, Pages 1562-1563
Nick S.NurmohamedMDabAnn MarieNavarMD, PhDcJohn J.P.KasteleinMD, PhDa
doi : 10.1016/j.jacc.2020.11.079
Volume 77, Issue 12, 30 March 2021, Pages 1564-1575
Adding to the foundation of statins, ezetimibe and proprotein convertase subtilisin–kexin type 9 inhibitors (PCSK9i), novel, emerging low-density lipoprotein cholesterol (LDL-C)–lowering therapies are under development for the prevention of cardiovascular disease. Inclisiran, a small interfering RNA molecule that inhibits PCSK9, only needs to be dosed twice a year and has the potential to help overcome current barriers to persistence and adherence to lipid-lowering therapies. Bempedoic acid, which lowers LDL-C upstream from statins, provides a novel alternative for patients with statin intolerance. Angiopoetin-like 3 protein (ANGPTL3) inhibitors have been shown to provide potent LDL-C lowering in patients with homozygous familial hypercholesterolemia without major adverse effects as seen with lomitapide and mipomersen, and may reduce the need for apheresis. Finally, CETP inhibitors may yet be effective with the development of obicetrapib. These novel agents provide the clinician the tools to effectively lower LDL-C across the entire range of LDL-C–induced elevation of cardiovascular risk, from primary prevention and secondary prevention to null-null homozygous familial hypercholesterolemia patients.
SotiriosTsimikasMDaPatrick M.MoriartyMDbErik S.StroesMD, PhDc
doi : 10.1016/j.jacc.2021.01.051
Volume 77, Issue 12, 30 March 2021, Pages 1576-1589
Lipoprotein(a) [Lp(a)] has risen to the level of an accepted cardiovascular disease risk factor, but final proof of causality awaits a randomized trial of Lp(a) lowering. Inhibiting apolipoprotein(a) production in the hepatocyte with ribonucleic acid therapeutics has emerged as an elegant and effective solution to reduce plasma Lp(a) levels. Phase 2 clinical trials have shown that the antisense oligonucleotide pelacarsen reduced mean Lp(a) levels by 80%, allowing 98% of subjects to reach on-treatment levels of <125 nmol/l (?50 mg/dl). The phase 3 Lp(a)HORIZON (Assessing the Impact of Lipoprotein(a) Lowering With TQJ230 on Major Cardiovascular Events in Patients With CVD) outcomes trial is currently enrolling approximately 7,680 patients with history of myocardial infarction, ischemic stroke, and symptomatic peripheral arterial disease and controlled low-density lipoprotein cholesterol to pelacarsen versus placebo. The co-primary endpoints are major adverse cardiovascular events in subjects with Lp(a) >70 mg/dl and >90 mg/dl, in which either of the two being positive will lead to a successful trial. Additional ribonucleic acid–targeted therapies to lower Lp(a) are in preclinical and clinical development. The testing of the Lp(a) hypothesis will provide proof whether Lp(a)-mediated risk can be abolished by potent Lp(a) lowering.
MahmoudAbdelnabiMDYehiaSalehMDAhmedFareedMD, PhDAlexanderNossikofMDLingWangPhDMahmoudMorsiMDNouranEshakMDOlaAbdelkarimMDHaithamBadranMD, PhDAbdallahAlmaghrabyMD
doi : 10.1016/j.jacc.2021.01.049
Volume 77, Issue 12, 30 March 2021, Pages 1590-1592
CathevineYangMDTakuInoharaMDMesferAlfadhelMDCameronMcAlisterMDAndrewStarovoytovMDDexterChoiBHScG.B. JohnManciniMDEveAymongMDJacquelineSawMD
doi : 10.1016/j.jacc.2021.01.048
Volume 77, Issue 12, 30 March 2021, Pages 1592-1594
HeinerLatusMDChristianApitzMD
doi : 10.1016/j.jacc.2020.12.066
Volume 77, Issue 12, 30 March 2021, Pages 1594-1595
AriCedarsMDAlexanderOpotowskyMD, MMScRyan J.TedfordMDDanielBurkhoffMD, PhD
doi : 10.1016/j.jacc.2021.01.036
Volume 77, Issue 12, 30 March 2021, Pages 1595-1596
Alexander C.EgbeMBBS, MPHBarry A.BorlaugMD
doi : 10.1016/j.jacc.2021.01.037
Volume 77, Issue 12, 30 March 2021, Pages 1596-1597
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