Kevin C. Maki
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
Kevin C. Maki has a total of 137 co-authors. Here are the top co-authors by number of shared publications:
Tia M. Rains
15 shared publicationsMary R. Dicklin
Provident Clinical Research/Biofortis North America, Glen Ellyn, IL
11 shared publicationsMatthew S. Reeves
Provident Clinical Research/Biofortis North America Addison IL USA
11 shared publicationsMarjorie Bell
ClinData Services, Bloomington, Indiana
5 shared publicationsAndrea L. Lawless
Provident Clinical Research and Consulting, Inc., Glen Ellyn, IL; and
4 shared publicationsMaciej Turowski
The Dow Chemical Company, Midland, Michigan, USA
4 shared publications
Latest Publications
- 1 May 2016
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 10 (3) , 700
Effects of Eicosapentaenoic Acid Plus Docosapentaenoic Acid and Eicosapentaenoic Acid Alone on Fasting and Postprandial Lipids
- 1 May 2016
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 10 (3) , 700
Effects of Eicosapentaenoic Acid Plus Docosapentaenoic Acid and Eicosapentaenoic Acid Alone on Fasting and Postprandial Lipids
- 1 May 2015
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 9 (3) , 431
Triglyceride-Lowering Therapies Reduce Cardiovascular Disease Event Risk in Subjects with Hypertriglyceridemia
- 1 May 2015
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 9 (3) , 431
Triglyceride-Lowering Therapies Reduce Cardiovascular Disease Event Risk in Subjects with Hypertriglyceridemia
- 1 July 2012
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 6 (4) , 352-361
A meta-analysis of randomized controlled trials that compare the lipid effects of beef versus poultry and/or fish consumption
- 1 July 2012
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 6 (4) , 352-361
A meta-analysis of randomized controlled trials that compare the lipid effects of beef versus poultry and/or fish consumption
- 1 May 2012
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 6 (3) , 276-277
Favorable Lipid-Altering Effects of a Softgel Plant Sterol/Stanol Dietary Supplement in Men and Women with Primary Hypercholesterolemia
- 1 May 2012
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 6 (3) , 276-277
Favorable Lipid-Altering Effects of a Softgel Plant Sterol/Stanol Dietary Supplement in Men and Women with Primary Hypercholesterolemia
- Open Access
- 1 April 2012
- Published by Elsevier in The Journal of Nutrition
- Vol. 142 (4) , 717-723
Resistant Starch from High-Amylose Maize Increases Insulin Sensitivity in Overweight and Obese Men
This study evaluated the effects of 2 levels of intake of high-amylose maize type 2 resistant starch (HAM-RS2) on insulin sensitivity (SI) in partici
- 1 April 2012
- Published by Elsevier in The Journal of Nutrition
- Vol. 142 (4) , 717-723
Open AccessResistant Starch from High-Amylose Maize Increases Insulin Sensitivity in Overweight and Obese Men
This study evaluated the effects of 2 levels of intake of high-amylose maize type 2 resistant starch (HAM-RS2) on insulin sensitivity (SI) in partici
- Open Access
- 1 March 2012
- Published by Elsevier in The Journal of Nutrition
- Vol. 142 (3) , 626S-629S
Stearidonic Acid Raises Red Blood Cell Membrane Eicosapentaenoic Acid,
The consumption of EPA and DHA has been associated with reduced risk for cardiovascular disease morbidity and mortality. Mean intakes of EPA and DHA
- 1 March 2012
- Published by Elsevier in The Journal of Nutrition
- Vol. 142 (3) , 626S-629S
Open AccessStearidonic Acid Raises Red Blood Cell Membrane Eicosapentaenoic Acid,
The consumption of EPA and DHA has been associated with reduced risk for cardiovascular disease morbidity and mortality. Mean intakes of EPA and DHA
- Open Access
- 1 January 2012
- Published by Taylor & Francis in Vascular Health and Risk Management
- Vol. 8, 31-38
Indicators of the atherogenic lipoprotein phenotype measured with density gradient ultracentrifugation predict changes in carotid intima-media thickness in men and women
Objective: Progression of carotid intima-media thickness (CIMT) is a surrogate indicator for the early stages of atherosclerosis. Methods: The study investigated relationships between baseline lipoprotein cholesterol, triglyceride (TG), and apolipoprotein (Apo) B levels assessed with density gradient ultracentrifugation (DGU) and progression of posterior wall common CIMT in men (45–75 years of age) and women (55–74 years of age) in the control arm of a clinical trial. Participants had baseline posterior wall CIMT 0.7–2.0 mm, without significant stenosis. CIMT was assessed using B-mode ultrasound at baseline, and 12 and ~18 months. A DGU cholesterol panel that assessed the major lipoprotein classes and subclasses, plus triglycerides, lipoprotein (a) cholesterol, low-density lipoprotein (LDL) peak time (inversely related to LDL particle density), and Apo B were performed on fasting baseline samples. Apo B was also measured using an enzyme linked immunosorbent assay. Results: Baseline CIMT was inversely associated (P < 0.001) with CIMT progression. After adjustment for baseline CIMT, significant predictors of posterior wall CIMT progression in linear regression analyses included LDL peak time (inverse, P = 0.045), total high-density lipoprotein cholesterol (HDL-C) (inverse, P = 0.001), HDL2-C (inverse, P = 0.005), HDL3-C (inverse, P = 0.003), very low-density lipoprotein (VLDL)-C (P = 0.037), and VLDL1+2-C (P = 0.016). Conclusion: These data indicate that DGU-derived indicators of the “atherogenic lipoprotein phenotype,” including increased TG-rich lipoprotein cholesterol, lower HDL-C and HDL-C subfractions, and a greater proportion of LDL-C carried by more dense LDL particles, are associated with CIMT progression in men and women at moderate risk for coronary heart disease.
- 1 January 2012
- Published by Taylor & Francis in Vascular Health and Risk Management
- Vol. 8, 31-38
Open AccessIndicators of the atherogenic lipoprotein phenotype measured with density gradient ultracentrifugation predict changes in carotid intima-media thickness in men and women
Objective: Progression of carotid intima-media thickness (CIMT) is a surrogate indicator for the early stages of atherosclerosis. Methods: The study investigated relationships between baseline lipoprotein cholesterol, triglyceride (TG), and apolipoprotein (Apo) B levels assessed with density gradient ultracentrifugation (DGU) and progression of posterior wall common CIMT in men (45–75 years of age) and women (55–74 years of age) in the control arm of a clinical trial. Participants had baseline posterior wall CIMT 0.7–2.0 mm, without significant stenosis. CIMT was assessed using B-mode ultrasound at baseline, and 12 and ~18 months. A DGU cholesterol panel that assessed the major lipoprotein classes and subclasses, plus triglycerides, lipoprotein (a) cholesterol, low-density lipoprotein (LDL) peak time (inversely related to LDL particle density), and Apo B were performed on fasting baseline samples. Apo B was also measured using an enzyme linked immunosorbent assay. Results: Baseline CIMT was inversely associated (P < 0.001) with CIMT progression. After adjustment for baseline CIMT, significant predictors of posterior wall CIMT progression in linear regression analyses included LDL peak time (inverse, P = 0.045), total high-density lipoprotein cholesterol (HDL-C) (inverse, P = 0.001), HDL2-C (inverse, P = 0.005), HDL3-C (inverse, P = 0.003), very low-density lipoprotein (VLDL)-C (P = 0.037), and VLDL1+2-C (P = 0.016). Conclusion: These data indicate that DGU-derived indicators of the “atherogenic lipoprotein phenotype,” including increased TG-rich lipoprotein cholesterol, lower HDL-C and HDL-C subfractions, and a greater proportion of LDL-C carried by more dense LDL particles, are associated with CIMT progression in men and women at moderate risk for coronary heart disease.
- 1 November 2011
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 5 (6) , 483-492
Effects of prescription omega-3-acid ethyl esters, coadministered with atorvastatin, on circulating levels of lipoprotein particles, apolipoprotein CIII, and lipoprotein-associated phospholipase A2 mass in men and women with mixed dyslipidemia
- 1 November 2011
- Published by Elsevier in Journal of Clinical Lipidology
- Vol. 5 (6) , 483-492
Effects of prescription omega-3-acid ethyl esters, coadministered with atorvastatin, on circulating levels of lipoprotein particles, apolipoprotein CIII, and lipoprotein-associated phospholipase A2 mass in men and women with mixed dyslipidemia