Scott D. Solomon

ORCID: 0000-0003-3698-9597
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About
Contact & Profiles
Research Areas
  • Cardiovascular Function and Risk Factors
  • Heart Failure Treatment and Management
  • Cardiac pacing and defibrillation studies
  • Diabetes Treatment and Management
  • Cardiac Imaging and Diagnostics
  • Cardiac electrophysiology and arrhythmias
  • Blood Pressure and Hypertension Studies
  • Atrial Fibrillation Management and Outcomes
  • Cardiac Arrhythmias and Treatments
  • Potassium and Related Disorders
  • Hormonal Regulation and Hypertension
  • Acute Myocardial Infarction Research
  • Cardiovascular Disease and Adiposity
  • Cardiac Structural Anomalies and Repair
  • Pancreatic function and diabetes
  • Health Systems, Economic Evaluations, Quality of Life
  • Cardiomyopathy and Myosin Studies
  • Cardiovascular Health and Risk Factors
  • Cardiac Valve Diseases and Treatments
  • Influenza Virus Research Studies
  • Erythropoietin and Anemia Treatment
  • Metabolism, Diabetes, and Cancer
  • Heart Rate Variability and Autonomic Control
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Dialysis and Renal Disease Management

Brigham and Women's Hospital
2016-2025

Harvard University
2016-2025

Baim Institute for Clinical Research
2022-2024

Massachusetts General Hospital
1995-2024

University of Glasgow
2014-2024

Duke University Hospital
2004-2024

Oregon Health & Science University
2015-2024

University of Michigan
2008-2024

National Heart Centre Singapore
2017-2024

British Heart Foundation
2011-2024

We compared the angiotensin receptor-neprilysin inhibitor LCZ696 with enalapril in patients who had heart failure a reduced ejection fraction. In previous studies, improved survival such patients.In this double-blind trial, we randomly assigned 8442 class II, III, or IV and an fraction of 40% less to receive either (at dose 200 mg twice daily) 10 daily), addition recommended therapy. The primary outcome was composite death from cardiovascular causes hospitalization for failure, but trial...

10.1056/nejmoa1409077 article EN New England Journal of Medicine 2014-08-30

This trial was designed to determine whether cardiac-resynchronization therapy (CRT) with biventricular pacing would reduce the risk of death or heart-failure events in patients mild cardiac symptoms, a reduced ejection fraction, and wide QRS complex.During 4.5-year period, we enrolled followed 1820 ischemic nonischemic cardiomyopathy, an fraction 30% less, duration 130 msec more, New York Heart Association class I II symptoms. Patients were randomly assigned 3:2 ratio receive CRT plus...

10.1056/nejmoa0906431 article EN New England Journal of Medicine 2009-09-02

Angiotensin-converting–enzyme (ACE) inhibitors such as captopril reduce mortality and cardiovascular morbidity among patients with myocardial infarction complicated by left ventricular systolic dysfunction, heart failure, or both. In a double-blind trial, we compared the effect of angiotensin-receptor blocker valsartan, ACE inhibitor captopril, combination two on in this population patients.

10.1056/nejmoa032292 article EN New England Journal of Medicine 2003-11-12

Mineralocorticoid-receptor antagonists improve the prognosis for patients with heart failure and a reduced left ventricular ejection fraction. We evaluated effects of spironolactone in preserved fraction.In this randomized, double-blind trial, we assigned 3445 symptomatic fraction 45% or more to receive either (15 45 mg daily) placebo. The primary outcome was composite death from cardiovascular causes, aborted cardiac arrest, hospitalization management failure.With mean follow-up 3.3 years,...

10.1056/nejmoa1313731 article EN New England Journal of Medicine 2014-04-09

RAAS Inhibitors in Patients with Covid-19 The effects of renin–angiotensin–aldosterone system blockers on angiotensin-converting enzyme 2 levels and activity humans are uncertain. authors hy...

10.1056/nejmsr2005760 article EN New England Journal of Medicine 2020-03-30

Selective cyclooxygenase-2 (COX-2) inhibitors have come under scrutiny because of reports suggesting an increased cardiovascular risk associated with their use. Experimental research that these drugs may contribute to a prothrombotic state provides support for this concern.We reviewed all potentially serious events among 2035 patients history colorectal neoplasia who were enrolled in trial comparing two doses celecoxib (200 mg or 400 twice daily) placebo the prevention adenomas. All deaths...

10.1056/nejmoa050405 article EN New England Journal of Medicine 2005-02-15

Cardiovascular morbidity and mortality are higher among patients with type 2 diabetes, particularly those concomitant cardiovascular diseases, than in most other populations. We assessed the effects of lixisenatide, a glucagon-like peptide 1-receptor agonist, on outcomes diabetes who had recent acute coronary event.We randomly assigned myocardial infarction or been hospitalized for unstable angina within previous 180 days to receive lixisenatide placebo addition locally determined standards...

10.1056/nejmoa1509225 article EN New England Journal of Medicine 2015-12-02

Anemia is associated with an increased risk of cardiovascular and renal events among patients type 2 diabetes chronic kidney disease. Although darbepoetin alfa can effectively increase hemoglobin levels, its effect on clinical outcomes in these has not been adequately tested.

10.1056/nejmoa0907845 article EN New England Journal of Medicine 2009-10-31

The presence of coexisting conditions has a substantial effect on the outcome acute myocardial infarction. Renal failure is associated with one highest risks, but influence milder degrees renal impairment less well defined.As part Valsartan in Acute Myocardial Infarction Trial (VALIANT), we identified 14,527 patients infarction complicated by clinical or radiologic signs heart failure, left ventricular dysfunction, both, and documented serum creatinine measurement. Patients were randomly...

10.1056/nejmoa041365 article EN New England Journal of Medicine 2004-09-22

In some randomized trials comparing revascularization strategies for patients with diabetes, coronary-artery bypass grafting (CABG) has had a better outcome than percutaneous coronary intervention (PCI). We sought to discover whether aggressive medical therapy and the use of drug-eluting stents could alter approach diabetes multivessel artery disease.In this trial, we assigned disease undergo either PCI or CABG. The were followed minimum 2 years (median among survivors, 3.8 years). All...

10.1056/nejmoa1211585 article EN New England Journal of Medicine 2012-11-04

Abstract Making a firm diagnosis of chronic heart failure with preserved ejection fraction (HFpEF) remains challenge. We recommend new stepwise diagnostic process, the ‘HFA–PEFF algorithm’. Step 1 (P=Pre-test assessment) is typically performed in ambulatory setting and includes assessment for HF symptoms signs, typical clinical demographics (obesity, hypertension, diabetes mellitus, elderly, atrial fibrillation), laboratory tests, electrocardiogram, echocardiography. In absence overt...

10.1093/eurheartj/ehz641 article EN European Heart Journal 2019-08-27

This study was undertaken to determine whether use of the direct renin inhibitor aliskiren would reduce cardiovascular and renal events in patients with type 2 diabetes chronic kidney disease, or both.In a double-blind fashion, we randomly assigned 8561 (300 mg daily) placebo as an adjunct angiotensin-converting-enzyme angiotensin-receptor blocker. The primary end point composite time death first occurrence cardiac arrest resuscitation; nonfatal myocardial infarction; stroke; unplanned...

10.1056/nejmoa1208799 article EN New England Journal of Medicine 2012-11-03

Hereditary transthyretin amyloidosis is caused by pathogenic single-nucleotide variants in the gene encoding (TTR) that induce misfolding and systemic deposition of amyloid. Progressive amyloid accumulation leads to multiorgan dysfunction death. Inotersen, a 2′-O-methoxyethyl–modified antisense oligonucleotide, inhibits hepatic production transthyretin.

10.1056/nejmoa1716793 article EN New England Journal of Medicine 2018-07-04

Studies showing that drugs inhibit cyclooxygenase-2 (COX-2) reduce the number of colorectal adenomas in animals and patients with familial adenomatous polyposis suggest COX-2 inhibitors may also prevent sporadic neoplasia.We randomly assigned who had removed before study entry to receive placebo (679 patients) or 200 mg (685 400 (671 celecoxib twice daily. Randomization was stratified for use low-dose aspirin. Follow-up colonoscopies were performed at one three years after randomization. The...

10.1056/nejmoa061355 article EN New England Journal of Medicine 2006-08-30

Overexpression of cyclooxygenase 2 (COX-2) has been associated with colorectal adenomatous polyps and cancer, prompting researchers to propose its inhibition as a chemopreventive intervention.The Prevention Colorectal Sporadic Adenomatous Polyps trial was randomized, placebo-controlled, double-blind study the COX-2 inhibitor celecoxib given daily in single 400-mg dose. At 107 centers 32 countries, we randomly assigned 1561 subjects who had adenomas removed before enrollment receive (933...

10.1056/nejmoa061652 article EN New England Journal of Medicine 2006-08-30

Phase I clinical studies have demonstrated the feasibility of implanting autologous skeletal myoblasts in postinfarction scars. However, they failed to determine whether this procedure was functionally effective and arrhythmogenic.This multicenter, randomized, placebo-controlled, double-blind study included patients with left ventricular (LV) dysfunction (ejection fraction < or = 35%), myocardial infarction, indication for coronary surgery. Each patient received either cells grown from a...

10.1161/circulationaha.107.734103 article EN Circulation 2008-02-20
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