Michael H. Davidson
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Michael H. Davidson has a total of 208 co-authors. Here are the top co-authors by number of shared publications:
Kevin C. Maki
Provident Clinical Research, Glen Ellyn, USA
8 shared publicationsChristie M. Ballantyne
Baylor college of Medicine, Houston, USA
3 shared publications- Douglas Kling
Omthera Pharmaceuticals, Princeton, NJ, USA.
3 shared publications - Eric J. Brandt
Institute for Healthcare Policy and Innovation University of Michigan Ann Arbor Michigan USA
3 shared publications James M. McKenney
3 shared publicationsLane B. Benes
Section of Cardiology, The University of Chicago Medicine, 5841 South Maryland Avenue, MC 6080, Chicago, IL 60637, USA
3 shared publications
Latest Publications
- Open Access
- 16 August 2024
- Published by Elsevier in Journal of the Society for Cardiovascular Angiography & Interventions
- Vol. 3 (10)
Dr George L. Bakris, 1952-2024
- 16 August 2024
- Published by Elsevier in Journal of the Society for Cardiovascular Angiography & Interventions
- Vol. 3 (10)
Open AccessDr George L. Bakris, 1952-2024
- 1 October 2021
- Published by Elsevier in Trends in Cardiovascular Medicine
- Vol. 31 (7) , 419-424
Recent advances and emerging therapies in management of dyslipidemias
- 1 October 2021
- Published by Elsevier in Trends in Cardiovascular Medicine
- Vol. 31 (7) , 419-424
Recent advances and emerging therapies in management of dyslipidemias
- 1 April 2021
- Published by Wolters Kluwer Health in Current Opinion in Lipidology
- Vol. 32 (2) , 151-156
The clinical black, white, and gray lessons
Purpose of review: This review examines recent contradictory large, well-controlled randomized control trials assessing the effects of omega-3 fatty acids and colchicine on cardiovascular (CV) outcomes. Recent findings: The Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (REDUCE-IT) and Statin Residual Risk Reduction with Epanova in high Cardiovascular Risk patients with Hypertriglyceridemia (STRENGTH) trial assessed the CV outcomes using high-dose omega-3 fatty acids in statin-treated patients with moderate hypertriglyceridemia and high-risk for CV disease with differing results. Similarly, Colchicine Cardiovascular Outcomes trial, (COLCOT) second Low Dose Colchicine (LoDoCo2), and Colchicine in patients with Acute Coronary Syndrome (COPS) assessed the CV outcomes using low-dose colchicine in patients with coronary artery disease with inconsistent results. These contradictory findings among studies assessing similar questions with the same drug or a drug within the same class challenge the scientific validity and clinical applicability of the derived conclusions. Summary: A comprehensive review revealed many differences between the trials, which could have contributed to observed divergent results. Consistent findings across multiple trials help strengthen the evidence for specific endpoints or sub-populations, and these findings must be included in guidelines. Large prospective cohort studies with diligent study protocols are warranted in the future to resolve unanswered dilemmas.
- 1 April 2021
- Published by Wolters Kluwer Health in Current Opinion in Lipidology
- Vol. 32 (2) , 151-156
The clinical black, white, and gray lessons
Purpose of review: This review examines recent contradictory large, well-controlled randomized control trials assessing the effects of omega-3 fatty acids and colchicine on cardiovascular (CV) outcomes. Recent findings: The Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (REDUCE-IT) and Statin Residual Risk Reduction with Epanova in high Cardiovascular Risk patients with Hypertriglyceridemia (STRENGTH) trial assessed the CV outcomes using high-dose omega-3 fatty acids in statin-treated patients with moderate hypertriglyceridemia and high-risk for CV disease with differing results. Similarly, Colchicine Cardiovascular Outcomes trial, (COLCOT) second Low Dose Colchicine (LoDoCo2), and Colchicine in patients with Acute Coronary Syndrome (COPS) assessed the CV outcomes using low-dose colchicine in patients with coronary artery disease with inconsistent results. These contradictory findings among studies assessing similar questions with the same drug or a drug within the same class challenge the scientific validity and clinical applicability of the derived conclusions. Summary: A comprehensive review revealed many differences between the trials, which could have contributed to observed divergent results. Consistent findings across multiple trials help strengthen the evidence for specific endpoints or sub-populations, and these findings must be included in guidelines. Large prospective cohort studies with diligent study protocols are warranted in the future to resolve unanswered dilemmas.
- 19 January 2021
- Published by Taylor & Francis in Future Cardiology
- Vol. 17 (7) , 1249-1260
How I Treat statin-associated Side Effects in an Outpatient Setting
Dyslipidemia promotes atherosclerosis and causes cardiovascular diseases. Statins are potent lipid-lowering medications with a cardiovascular mortality benefit. They are generally safe and well tol... Lay abstract Heart and blood vessel diseases are the most common causes of death worldwide. High cholesterol, when left untreated, can increase the risk of these diseases. Statins are potent choles...
- 19 January 2021
- Published by Taylor & Francis in Future Cardiology
- Vol. 17 (7) , 1249-1260
How I Treat statin-associated Side Effects in an Outpatient Setting
Dyslipidemia promotes atherosclerosis and causes cardiovascular diseases. Statins are potent lipid-lowering medications with a cardiovascular mortality benefit. They are generally safe and well tol... Lay abstract Heart and blood vessel diseases are the most common causes of death worldwide. High cholesterol, when left untreated, can increase the risk of these diseases. Statins are potent choles...
- 16 December 2020
- Published by Springer Nature
- p. 1-9
History of Lipidology
- 1 April 2020
- Published by Wolters Kluwer Health in Current Opinion in Lipidology
- Vol. 31 (2) , 108-110
Reducing residual cardiovascular risk with novel therapies
- 1 April 2020
- Published by Wolters Kluwer Health in Current Opinion in Lipidology
- Vol. 31 (2) , 108-110
Reducing residual cardiovascular risk with novel therapies
- 1 February 2020
- Published by Elsevier in Cardiovascular Revascularization Medicine
- Vol. 21 (2) , 200-204
The Role of Genetics in Cardiovascular Risk Reduction: Findings From a Single Lipid Clinic and Review of the Literature
- 1 February 2020
- Published by Elsevier in Cardiovascular Revascularization Medicine
- Vol. 21 (2) , 200-204
The Role of Genetics in Cardiovascular Risk Reduction: Findings From a Single Lipid Clinic and Review of the Literature
- 17 October 2018
- Published by Springer Nature in Current Cardiology Reports
- Vol. 20 (12) , 1-7
How Genomics Is Personalizing the Management of Dyslipidemia and Cardiovascular Disease Prevention
Purpose of the Review To summarize advances in genomic medicine and anticipated future directions to improve cardiovascular risk reduction. Recent Findings Mendelian randomization and genome-wide association studies have given significant insights into the role of genetics in dyslipidemia and cardiovascular disease (CVD), with over 160 gene loci found to be associated with coronary artery disease to date. This has enabled the creation of genetic risk scores that have demonstrated improved risk prediction when added to clinical markers of CVD risk. Summary Incorporation of genomic data into clinical patient care is on the horizon. Genomic medicine is expected to offer improved risk assessment, determination of targeted treatment strategies, and improved detection of lipid disorders causal to CVD development.
- 17 October 2018
- Published by Springer Nature in Current Cardiology Reports
- Vol. 20 (12) , 1-7
How Genomics Is Personalizing the Management of Dyslipidemia and Cardiovascular Disease Prevention
Purpose of the Review To summarize advances in genomic medicine and anticipated future directions to improve cardiovascular risk reduction. Recent Findings Mendelian randomization and genome-wide association studies have given significant insights into the role of genetics in dyslipidemia and cardiovascular disease (CVD), with over 160 gene loci found to be associated with coronary artery disease to date. This has enabled the creation of genetic risk scores that have demonstrated improved risk prediction when added to clinical markers of CVD risk. Summary Incorporation of genomic data into clinical patient care is on the horizon. Genomic medicine is expected to offer improved risk assessment, determination of targeted treatment strategies, and improved detection of lipid disorders causal to CVD development.
- Open Access
- 1 July 2018
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 12 (4) , 898-907.e2
The burden of familial chylomicronemia syndrome: Results from the global IN-FOCUS study
- 1 July 2018
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 12 (4) , 898-907.e2
Open AccessThe burden of familial chylomicronemia syndrome: Results from the global IN-FOCUS study
- 1 May 2018
- Published by Elsevier in Cardiology Clinics
- Vol. 36 (2) , 277-285
Evolution of Omega-3 Fatty Acid Therapy and Current and Future Role in the Management of Dyslipidemia
- 1 May 2018
- Published by Elsevier in Cardiology Clinics
- Vol. 36 (2) , 277-285
Evolution of Omega-3 Fatty Acid Therapy and Current and Future Role in the Management of Dyslipidemia