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1. |
ST-Segment Elevation in an Unresponsive Patient |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 165-166
Glenn Hirsch,
Alan Heldman,
Ilan Wittstein,
Steven Schulman,
Gary Gerstenblith,
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ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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2. |
CirculationAnnouncement Page |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2949-2949
James Willerson,
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PDF (6KB)
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ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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3. |
Should B-Type Natriuretic Peptide Be Measured Routinely to Guide the Diagnosis and Management of Chronic Heart Failure? |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2950-2953
Milton Packer,
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ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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4. |
Apoptosis Inhibitors for Heart Disease |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2954-2956
Keith Webster,
Nanette Bishopric,
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PDF (38KB)
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ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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5. |
Explaining How “High-Grade” Systemic Inflammation Accelerates Vascular Risk in Rheumatoid Arthritis |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2957-2963
Naveed Sattar,
David McCarey,
Hilary Capell,
Iain McInnes,
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摘要:
Abstract—There is intense interest in mechanisms whereby low-grade inflammation could interact with conventional and novel vascular risk factors to promote the atheromatous lesion. Patients with rheumatoid arthritis (RA), who by definition manifest persistent high levels of inflammation, are at greater risk of developing cardiovascular disease. Mechanisms mediating this enhanced risk are ill defined. On the basis of available evidence, we argue here that the systemic inflammatory response in RA is critical to accelerated atherogenesis operating via accentuation of established and novel risk factor pathways. By implication, long-term suppression of the systemic inflammatory response in RA should be effective in reducing risk of coronary heart disease. Early epidemiological observational and clinical studies are commensurate with this hypothesis. By contrast, risk factor modulation with conventional agents, such as statins, may provide unpredictable clinical benefit in the context of uncontrolled systemic inflammatory parameters. Unraveling such complex relationships in which exaggerated inflammation–risk factor interactions are prevalent may elicit novel insights to effector mechanisms in vascular disease generally.
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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6. |
Plasma B-Type Natriuretic Peptide Levels in Ambulatory Patients With Established Chronic Symptomatic Systolic Heart Failure |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2964-2966
W.H. Tang,
John Girod,
Michael Lee,
Randall Starling,
James Young,
Frederick Van Lente,
Gary Francis,
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摘要:
Background—The diagnostic and prognostic values of plasma B-type natriuretic peptide (BNP) testing are established. However, the range of plasma BNP levels present in the setting of chronic, stable systolic heart failure (HF) is unclear.Methods and Results—We followed up 558 consecutive ambulatory patients with chronic, stable systolic HF (left ventricular ejection fraction <50%) treated at a specialized outpatient HF clinic between November 2001 and February 2003. Retrospective chart review was performed to determine clinical and functional data at the time of BNP testing (Biosite Triage). The clinical characteristics of patients with plasma BNP levels <100 pg/mL and those with ≥100 pg/mL were compared. In our cohort, 60 patients were considered asymptomatic, and their plasma BNP levels ranged from 5 to 572 pg/mL (median, 147 pg/mL). Of the remaining 498 symptomatic (NYHA functional class II–III) patients, 106 (21.3%) had plasma BNP levels in the “normal” diagnostic range (<100 pg/mL). Patients in this “normal BNP” subgroup were more likely to be younger, to be female, to have nonischemic pathogenesis, and to have better-preserved cardiac and renal function and less likely to have atrial fibrillation.Conclusions—In the ambulatory care setting, both symptomatic and asymptomatic patients with chronic, stable systolic HF may present with a wide range of plasma BNP levels. In a subset of symptomatic patients (up to 21% in our cohort), plasma BNP levels are below what would be considered “diagnostic” (<100 pg/mL).
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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7. |
Percutaneous Endovascular Repair of Aneurysm After Previous Coarctation Surgery |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2967-2970
Hüseyin Ince,
Michael Petzsch,
Tim Rehders,
Stephan Kische,
Thomas Körber,
Frank Weber,
Christoph Nienaber,
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摘要:
Background—Formation of aortic aneurysm late after surgical repair of coarctation carries a significant risk of rupture and lethal outcome, and repeat surgery is associated with a 14% in-hospital mortality rate and morbidity from paraplegia, injury to the central nervous system, or from bleeding. The potential of nonsurgical endovascular repair by the use of stent-grafts in lieu of repeat surgery for postcoarctation aneurysm is unknown.Methods and Results—The concept of postsurgical endovascular stent-graft placement was evaluated with respect to feasibility and safety in 6 consecutive patients with late aneurysm formation after coarctation repair. All patients had aneurysm formation late after patch aortoplasty; placement of an elephant trunk during surgical repair of secondary type I dissection preceded formation of a local aneurysm in 2 cases. Patient age was 49±12 years, ranging from 31 to 68 years. Transluminal placement of customized stent-grafts was successful, with no 30-day or 1-year intervention-related mortality or morbidity. Follow-up survey of 11 to 47 months revealed optimal reconstruction of the thoracic aorta; 1 patient died 11 months after endovascular repair from cancer.Conclusions—Nonsurgical aortic reconstruction of postsurgical thoracic aneurysms forming late after coarctation repair is safe and feasible; interventional stent-graft placement has the potential to avoid repeat surgery of postsurgical aortic aneurysm.
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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8. |
P2Y12H2 Haplotype Is Associated With Peripheral Arterial DiseaseA Case-Control Study |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2971-2973
Pierre Fontana,
Pascale Gaussem,
Martine Aiach,
Jean-Noël Fiessinger,
Joseph Emmerich,
Jean-Luc Reny,
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摘要:
Background—We recently described a gain-of-function haplotype, called H2, of the adenosine diphosphate (ADP) receptor P2Y12gene associated with increased ADP-induced platelet aggregation ex vivo in healthy volunteers. Because platelets play a key role in atherosclerosis and arterial thrombosis, we tested the possible link between the H2 haplotype and the risk of peripheral arterial disease (PAD) in a case-control study.Methods and Results—We studied 184 consecutive male patients under 70 years of age with PAD and 330 age-matched control subjects free of symptomatic PAD and with no cardiovascular history. Mean age was 57.1±7.2 years (cases) and 56.7±7.6 years (control subjects). The H2 haplotype was more frequent in patients with PAD than in control subjects (30% and 21%, respectively; OR, 1.6; CI, 1.1 to 2.5;P=0.02 in univariate analysis). This association with PAD remained significant in multivariate regression analysis (OR, 2.3; CI, 1.4 to 3.9;P=0.002) after adjustment for diabetes, smoking, hypertension, hypercholesterolemia, and other selected platelet receptor gene polymorphisms.Conclusions—These data point to a role of the H2 haplotype in atherosclerosis and raise the possibility of relative thienopyridine resistance in carriers of the P2Y12H2 haplotype.
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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9. |
Methoxyestradiols Mediate the Antimitogenic Effects of 17&bgr;-EstradiolDirect Evidence From Catechol-O-Methyltransferase–Knockout Mice |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2974-2978
Lefteris Zacharia,
Joseph Gogos,
Maria Karayiorgou,
Edwin Jackson,
Delbert Gillespie,
Federica Barchiesi,
Raghvendra Dubey,
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摘要:
Background—Studies using pharmacological agents suggest but do not prove that the antimitogenic effects of estradiol are caused by conversion of estradiol to hydroxyestradiols (mediated by CYP450s) followed by methylation of hydroxyestradiols to methoxyestradiols (mediated by catechol-O-methyltransferase, COMT).Methods and Results—To test this hypothesis more rigorously, we used aortic smooth muscle cells (SMCs) from mice lacking COMT (COMT-KO). Wild-type (WT) but not COMT-KO SMCs efficiently converted 2-hydroxyestradiol to 2-methoxyestradiol. Both WT and COMT-KO SMCs expressed estrogen receptors. Estradiol and 2-hydroxyestradiol concentration-dependently inhibited serum-induced DNA synthesis, cell numbers, and collagen synthesis in WT but not COMT-KO SMCs. 2-Methoxyestradiol inhibited DNA synthesis, cell numbers, and collagen synthesis in both WT and COMT-KO SMCs.Conclusions—These data provide strong evidence that the vascular antimitogenic effects of estradiol are estrogen receptor–independent and involve the sequential conversion of estradiol to hydroxyestradiols and then to methoxyestradiols.
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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10. |
Impact of Infarct-Related Artery Flow on QT Dynamicity in Patients Undergoing Direct Percutaneous Coronary Intervention for Acute Myocardial Infarction |
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Circulation: Journal of the American Heart Association,
Volume 108,
Issue 24,
2003,
Page 2979-2986
Hendrik Bonnemeier,
Uwe Wiegand,
Frank Bode,
Franz Hartmann,
Volkhard Kurowski,
Hugo Katus,
Gert Richardt,
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摘要:
Background—Complete coronary artery reperfusion in acute myocardial infarction (AMI) has been shown to significantly improve survival. Electrical stability may be the decisive mechanism for this beneficial effect. Because electrical stability is largely dependent on ventricular repolarization, we sought to determine the impact of a modern reperfusion strategy (ie, direct percutaneous coronary intervention [PCI]) on QT dynamicity in AMI and examined its association with infarct-related artery flow.Methods and Results—We prospectively investigated QT dynamicity in 128 patients undergoing direct PCI for a first AMI. Slopes and correlation coefficients of the linear QT/RR regression were determined in the time interval before reperfusion, within the initial hour after reperfusion, and within the remaining recording period from Holter ECG recordings, which were initiated on admission. Subgroup analysis based on TIMI 3 (n=100) and TIMI 2 (n=28) flow after PCI revealed no significant differences in QT/RR slope before PCI (0.145±0.12 versus 0.160±0.19,P=NS). After PCI, QT/RR slopes increased only in the TIMI 2 subgroup (P<0.05). In TIMI 2 patients, QT/RR slopes were significantly steeper in the hour after PCI and in the remaining recording period, respectively (0.155±0.12 versus 0.192±0.15,P<0.05, and 0.159±0.10 versus 0.210±0.17,P<0.01).Conclusions—Alterations of QT dynamicity in patients with incomplete reperfusion may suggest an altered electrical restitution, potentially providing a substrate for serious ventricular arrhythmias. Thus, our findings offer new insights into mechanisms by which complete reperfusion may affect electrical stability.
ISSN:0009-7322
出版商:OVID
年代:2003
数据来源: OVID
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