Page last updated: 2024-10-19

niacin and Arteriosclerosis, Coronary

niacin has been researched along with Arteriosclerosis, Coronary in 101 studies

Niacin: A water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is required by the body for the formation of coenzymes NAD and NADP. It has PELLAGRA-curative, vasodilating, and antilipemic properties.
vitamin B3 : Any member of a group of vitamers that belong to the chemical structural class called pyridines that exhibit biological activity against vitamin B3 deficiency. Vitamin B3 deficiency causes a condition known as pellagra whose symptoms include depression, dermatitis and diarrhea. The vitamers include nicotinic acid and nicotinamide (and their ionized and salt forms).
nicotinic acid : A pyridinemonocarboxylic acid that is pyridine in which the hydrogen at position 3 is replaced by a carboxy group.

Research Excerpts

ExcerptRelevanceReference
"To determine the effect of extended release (ER) niacin on endothelial and vascular function assessed by brachial flow-mediated dilatation (FMD), peak hyperemic velocity (VTiRH) and pulse arterial tonometry (PAT) in patients with established coronary artery disease (CAD), already treated with high dose statins."9.17Niacin improves lipid profile but not endothelial function in patients with coronary artery disease on high dose statin therapy. ( Anderson, TJ; Hillard, D; Hubacek, J; Philpott, AC; Sun, YC, 2013)
"In this study, niacin was added to existing therapy for 3 months in 54 subjects with stable coronary artery disease."9.12Effects of extended-release niacin on lipoprotein particle size, distribution, and inflammatory markers in patients with coronary artery disease. ( Dave, DM; Karas, RH; Kimmelstiel, CD; Kuvin, JT; Mooney, P; Patel, AR; Sliney, KA, 2006)
" In our study, patients were randomized, on average, 6 days after an acute myocardial infarction and/or percutaneous transluminal coronary angioplasty secondary to unstable angina, to pravastatin (combined, when necessary, with cholestyramine and/or nicotinic acid) to achieve low-density lipoprotein cholesterol levels of < or =130 mg/dl (group A, n = 70)."9.09Beneficial effects of pravastatin (+/-colestyramine/niacin) initiated immediately after a coronary event (the randomized Lipid-Coronary Artery Disease [L-CAD] Study). ( Agrawal, R; Arntz, HR; Fischer, F; Schnitzer, L; Schultheiss, HP; Stern, R; Wunderlich, W, 2000)
" The AIM-HIGH (Atherothrombosis Intervention in Metabolic Syndrome With Low HDL/High Triglycerides: Impact on Global Health Outcomes) trial, which compared combined niacin/simvastatin with simvastatin alone, failed to demonstrate an incremental benefit of niacin among patients with atherosclerotic CVD and on-treatment low-density lipoprotein cholesterol values <70 mg/dl, but this study had some limitations."8.88Niacin and statin combination therapy for atherosclerosis regression and prevention of cardiovascular disease events: reconciling the AIM-HIGH (Atherothrombosis Intervention in Metabolic Syndrome With Low HDL/High Triglycerides: Impact on Global Health Ou ( Baer, JT; Blaha, MJ; Blumenthal, RS; Michos, ED; Sibley, CT, 2012)
"The change in logarithmic reactive hyperemia index between 1 month and 12 months was similar in patients receiving ER-niacin vs placebo (0."6.80Effect of Extended-Release Niacin on Carotid Intima Media Thickness, Reactive Hyperemia, and Endothelial Progenitor Cell Mobilization: Insights From the Atherosclerosis Lesion Progression Intervention Using Niacin Extended Release in Saphenous Vein Grafts ( Abdurrahim, G; Banerjee, S; Brilakis, ES; Chao, H; Christopoulos, G; Coleman, A; de Lemos, JA; Guerra, A; Han, H; Kotsia, A; McGuire, DK; Packer, M; Rangan, BV; Roesle, M; Sosa, A; Xu, H, 2015)
"Niacin treatment was without effect on FMD or NMD, respectively, compared to placebo."6.74Effects of oral niacin on endothelial dysfunction in patients with coronary artery disease: results of the randomized, double-blind, placebo-controlled INEF study. ( Blankenberg, S; Elsner, V; Lackner, K; Munzel, T; Ostad, MA; Peetz, D; Schinzel, R; Stieber, F; Walter, U; Warnholtz, A; Wild, P, 2009)
" How safe and well-tolerated is this combination? One hundred sixty patients with CAD, including 25 with diabetes mellitus, with mean low-density lipoprotein cholesterol of 128 mg/dl, HDL cholesterol of < or =35 mg/dl (mean 31), and mean triglycerides of 217 mg/dl were randomized to 4 factorial combinations of antioxidant vitamins or their placebos and simvastatin plus niacin or their placebos."6.71Safety and tolerability of simvastatin plus niacin in patients with coronary artery disease and low high-density lipoprotein cholesterol (The HDL Atherosclerosis Treatment Study). ( Albers, JJ; Brown, BG; Chait, A; DeAngelis, D; Dowdy, AA; Frohlich, J; Heise, N; Morse, JS; Zhao, XQ, 2004)
"To determine the effect of extended release (ER) niacin on endothelial and vascular function assessed by brachial flow-mediated dilatation (FMD), peak hyperemic velocity (VTiRH) and pulse arterial tonometry (PAT) in patients with established coronary artery disease (CAD), already treated with high dose statins."5.17Niacin improves lipid profile but not endothelial function in patients with coronary artery disease on high dose statin therapy. ( Anderson, TJ; Hillard, D; Hubacek, J; Philpott, AC; Sun, YC, 2013)
"To assess effects of niacin on risk factors of atherosclerosis in men with coronary heart disease (CHD) and high lipoprotein(a) [Lp(a)] levels."5.15[Pleiotropic effects of nicotinic acid therapy in men with coronary heart disease and elevated lipoprotein(a) levels]. ( Afanas'eva, MI; Afanas'eva, OI; Ezhov, MV; Liakishev, AA; Pokrovskiĭ, SN; Safarova, MS; Tripoten', MI; Trukhacheva, EP, 2011)
" This study aimed to investigate the effects of combined application of extended-release niacin and atorvastatin on lipid profile modification and the risks of adverse events in patients with coronary artery disease."5.14Combined use of extended-release niacin and atorvastatin: safety and effects on lipid modification. ( Chen, SY; Li, YG; Li, YH; Sang, ZC; Wang, F; Wang, HP; Zhou, Q, 2009)
"In this study, niacin was added to existing therapy for 3 months in 54 subjects with stable coronary artery disease."5.12Effects of extended-release niacin on lipoprotein particle size, distribution, and inflammatory markers in patients with coronary artery disease. ( Dave, DM; Karas, RH; Kimmelstiel, CD; Kuvin, JT; Mooney, P; Patel, AR; Sliney, KA, 2006)
"The HDL Atherosclerosis Treatment Study (HATS) demonstrated a clinical benefit in coronary artery disease patients with low HDL cholesterol (HDL-C) levels treated with simvastatin and niacin (S-N) or S-N plus antioxidants (S-N+A) compared with antioxidants alone or placebo."5.10Impact of simvastatin, niacin, and/or antioxidants on cholesterol metabolism in CAD patients with low HDL. ( Brown, BG; Giovanni, A; Lichtenstein, AH; Matthan, NR; Schaefer, EJ, 2003)
" In our study, patients were randomized, on average, 6 days after an acute myocardial infarction and/or percutaneous transluminal coronary angioplasty secondary to unstable angina, to pravastatin (combined, when necessary, with cholestyramine and/or nicotinic acid) to achieve low-density lipoprotein cholesterol levels of < or =130 mg/dl (group A, n = 70)."5.09Beneficial effects of pravastatin (+/-colestyramine/niacin) initiated immediately after a coronary event (the randomized Lipid-Coronary Artery Disease [L-CAD] Study). ( Agrawal, R; Arntz, HR; Fischer, F; Schnitzer, L; Schultheiss, HP; Stern, R; Wunderlich, W, 2000)
" The AIM-HIGH (Atherothrombosis Intervention in Metabolic Syndrome With Low HDL/High Triglycerides: Impact on Global Health Outcomes) trial, which compared combined niacin/simvastatin with simvastatin alone, failed to demonstrate an incremental benefit of niacin among patients with atherosclerotic CVD and on-treatment low-density lipoprotein cholesterol values <70 mg/dl, but this study had some limitations."4.88Niacin and statin combination therapy for atherosclerosis regression and prevention of cardiovascular disease events: reconciling the AIM-HIGH (Atherothrombosis Intervention in Metabolic Syndrome With Low HDL/High Triglycerides: Impact on Global Health Ou ( Baer, JT; Blaha, MJ; Blumenthal, RS; Michos, ED; Sibley, CT, 2012)
"Combined statin and niacin therapy partially reverses the changes in the protein composition seen in HDL(3) in coronary artery disease subjects."3.74Combined statin and niacin therapy remodels the high-density lipoprotein proteome. ( Brunzell, J; Green, PS; Heinecke, JW; Knopp, RH; Kulstad, JJ; Marcovina, S; Moore, AB; Pennathur, S; Vaisar, T; Zhao, XQ, 2008)
"This report describes a patient with coronary artery disease who was instructed to take extended-release niacin to treat low high-density lipoprotein cholesterol and instead purchased "flush-free niacin" available at the pharmacy."3.73"Flush-free niacin": dietary supplement may be "benefit-free". ( Norris, RB, 2006)
"The change in logarithmic reactive hyperemia index between 1 month and 12 months was similar in patients receiving ER-niacin vs placebo (0."2.80Effect of Extended-Release Niacin on Carotid Intima Media Thickness, Reactive Hyperemia, and Endothelial Progenitor Cell Mobilization: Insights From the Atherosclerosis Lesion Progression Intervention Using Niacin Extended Release in Saphenous Vein Grafts ( Abdurrahim, G; Banerjee, S; Brilakis, ES; Chao, H; Christopoulos, G; Coleman, A; de Lemos, JA; Guerra, A; Han, H; Kotsia, A; McGuire, DK; Packer, M; Rangan, BV; Roesle, M; Sosa, A; Xu, H, 2015)
"Niacin treatment was without effect on FMD or NMD, respectively, compared to placebo."2.74Effects of oral niacin on endothelial dysfunction in patients with coronary artery disease: results of the randomized, double-blind, placebo-controlled INEF study. ( Blankenberg, S; Elsner, V; Lackner, K; Munzel, T; Ostad, MA; Peetz, D; Schinzel, R; Stieber, F; Walter, U; Warnholtz, A; Wild, P, 2009)
" How safe and well-tolerated is this combination? One hundred sixty patients with CAD, including 25 with diabetes mellitus, with mean low-density lipoprotein cholesterol of 128 mg/dl, HDL cholesterol of < or =35 mg/dl (mean 31), and mean triglycerides of 217 mg/dl were randomized to 4 factorial combinations of antioxidant vitamins or their placebos and simvastatin plus niacin or their placebos."2.71Safety and tolerability of simvastatin plus niacin in patients with coronary artery disease and low high-density lipoprotein cholesterol (The HDL Atherosclerosis Treatment Study). ( Albers, JJ; Brown, BG; Chait, A; DeAngelis, D; Dowdy, AA; Frohlich, J; Heise, N; Morse, JS; Zhao, XQ, 2004)
"Progression of coronary artery disease is assumed to be a surrogate end point for clinical coronary events."2.68Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study. ( Azen, SP; Blankenhorn, DH; Cashin-Hemphill, L; Hodis, HN; LaBree, L; Mack, WJ; Selzer, RH; Shircore, AM, 1996)
"Lipid-lowering therapy ameliorates coronary atherosclerosis in patients with raised concentrations of low-density-lipoprotein (LDL) cholesterol."2.67Effect on coronary atherosclerosis of decrease in plasma cholesterol concentrations in normocholesterolaemic patients. Harvard Atherosclerosis Reversibility Project (HARP) Group. ( Gibson, CM; Pasternak, RC; Rosner, B; Sacks, FM; Stone, PH, 1994)
"Niacin has a favorable unique impact on factors affecting the rate of glomerular filtration rate decline, including high-density lipoprotein (HDL) particle number and function, triglyceride levels, oxidant stress, inflammation and endothelial function, and lowering of serum phosphorus levels by reducing dietary phosphorus absorption in the gastrointestinal tract."2.52Niacin and progression of CKD. ( Kalantar-Zadeh, K; Kashyap, ML; Kovesdy, CP; Moradi, H; Streja, DA; Streja, E, 2015)
"Niacin treatment reduces cardiovascular events and the progression of atherosclerosis."2.45Nicotinic acid and the prevention of coronary artery disease. ( Choudhury, RP; Digby, JE; Lee, JM, 2009)
"As the significance of treating coronary artery disease (CAD) remains a high priority in reducing morbidity and mortality worldwide, newer treatment strategies continue to evolve."2.45Novel targets that affect high-density lipoprotein metabolism: the next frontier. ( Davidson, MH; Rosenson, RS, 2009)
"Furthermore, severe hypertriglyceridemia is associated with an increased risk of acute pancreatitis, irrespective of its effect on risk of cardiovascular disease."2.44Hypertriglyceridemia: its etiology, effects and treatment. ( Al-Shali, KZ; Hegele, RA; Yuan, G, 2007)
"Niacin has been shown to regress atherosclerosis when used as monotherapy, in combination with a statin, and in combination with nonstatin therapies (including cholesterol-binding resins) and fibrates."2.44Evidence to support aggressive management of high-density lipoprotein cholesterol: implications of recent imaging trials. ( Taylor, AJ, 2008)
"The metabolic syndrome and type 2 diabetes mellitus are both becoming more prevalent, and both increase the risk of cardiovascular disease."2.43Beyond low-density lipoprotein: addressing the atherogenic lipid triad in type 2 diabetes mellitus and the metabolic syndrome. ( Nesto, RW, 2005)
"Hypertriglyceridemia is commonly embedded in the context of a metabolic syndrome that includes central obesity, insulin resistance, low levels of HDL cholesterol, and often hypertension."2.41A risk factor for atherosclerosis: triglyceride-rich lipoproteins. ( Kane, JP; Malloy, MJ, 2001)
"Treatment of dyslipidemia to prevent CHD depends on the pattern and severity of dyslipidemia, the presence of overt CHD, and the patient's response to diet."2.40Perspectives in the treatment of dyslipidemias in the prevention of coronary heart disease. ( Borgia, MC; Medici, F, 1998)
" Third, lower levels of HDL cholesterol are associated in a dose-response fashion with the severity and number of angiographically documented atherosclerotic coronary arteries."2.40The antiatherogenic role of high-density lipoprotein cholesterol. ( Kwiterovich, PO, 1998)
"Niacin has been studied in 6 major clinical trials with cardiovascular endpoints."2.40Effect of niacin on atherosclerotic cardiovascular disease. ( Guyton, JR, 1998)
"Dyslipidemia is one of the risk factors for the development of coronary atherosclerosis."2.39Number-needed-to-treat analysis of the prevention of myocardial infarction and death by antidyslipidemic therapy. ( Rembold, CM, 1996)
"Ten patients with NIDDM, CAD, and severe LV dysfunction (mean ejection fraction, 29."1.31Myocardial glucose utilization and optimization of (18)F-FDG PET imaging in patients with non-insulin-dependent diabetes mellitus, coronary artery disease, and left ventricular dysfunction. ( Beanlands, RS; deKemp, RA; Ruddy, TD; Vitale, GD; Williams, K, 2001)
"13 patients aged 39 to 60 years with coronary atherosclerosis confirmed at selective coronary angiography combined with primary hyperlipidemia (phenotypes 2a and 2b) received enduracin in a dose 1500 mg/day."1.30[The effect of long-term Enduracin monotherapy on the clinical and biochemical status of patients with ischemic heart disease]. ( Aronskaia, EE; Kukharchuk, VV; Malyshev, PP; Rozhkova, TA; Semenova, OA; Solov'ev, EIu, 1997)

Research

Studies (101)

TimeframeStudies, this research(%)All Research%
pre-19909 (8.91)18.7374
1990's21 (20.79)18.2507
2000's47 (46.53)29.6817
2010's24 (23.76)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Pisarik, P1
Ponce, OJ1
Larrea-Mantilla, L1
Hemmingsen, B1
Serrano, V1
Rodriguez-Gutierrez, R1
Spencer-Bonilla, G1
Alvarez-Villalobos, N1
Benkhadra, K1
Haddad, A1
Gionfriddo, MR1
Prokop, LJ1
Brito, JP1
Murad, MH1
Egom, EE1
Mamas, MA1
Soran, H1
Ylä-Herttuala, S1
Bentzon, JF1
Daemen, M1
Falk, E1
Garcia-Garcia, HM1
Herrmann, J1
Hoefer, I1
Jauhiainen, S1
Jukema, JW1
Krams, R1
Kwak, BR1
Marx, N1
Naruszewicz, M1
Newby, A1
Pasterkamp, G1
Serruys, PW1
Waltenberger, J1
Weber, C1
Tokgözoglu, L1
Gudzune, KA1
Monroe, AK1
Sharma, R1
Ranasinghe, PD1
Chelladurai, Y1
Robinson, KA1
Streja, E1
Kovesdy, CP1
Streja, DA1
Moradi, H1
Kalantar-Zadeh, K1
Kashyap, ML1
Guerra, A1
Rangan, BV1
Coleman, A1
Xu, H1
Kotsia, A1
Christopoulos, G1
Sosa, A1
Chao, H1
Han, H1
Abdurrahim, G1
Roesle, M1
de Lemos, JA1
McGuire, DK1
Packer, M1
Banerjee, S1
Brilakis, ES1
Vavlukis, M1
Mladenovska, K1
Daka, A1
Dimovski, A1
Domazetovska, S1
Kuzmanovska, S1
Kedev, S1
Albers, JJ2
Slee, A1
Fleg, JL1
O'Brien, KD1
Marcovina, SM1
Rembold, CM3
Green, PS1
Vaisar, T1
Pennathur, S1
Kulstad, JJ1
Moore, AB1
Marcovina, S1
Brunzell, J1
Knopp, RH1
Zhao, XQ3
Heinecke, JW1
Warnholtz, A1
Wild, P1
Ostad, MA1
Elsner, V1
Stieber, F1
Schinzel, R1
Walter, U1
Peetz, D1
Lackner, K1
Blankenberg, S1
Munzel, T1
Robinson, JG1
Cooper-DeHoff, RM1
Pacanowski, MA1
Pepine, CJ1
Digby, JE1
Lee, JM1
Choudhury, RP1
Sang, ZC1
Wang, F1
Zhou, Q1
Li, YH1
Li, YG1
Wang, HP1
Chen, SY1
Davidson, MH5
Rosenson, RS1
Riesen, WF1
Duggal, JK1
Singh, M1
Attri, N1
Singh, PP1
Ahmed, N1
Pahwa, S1
Molnar, J1
Singh, S1
Khosla, S1
Arora, R1
Natarajan, P1
Ray, KK1
Cannon, CP1
Devendra, GP1
Whitney, EJ1
Krasuski, RA2
Johansen, CT1
Kathiresan, S1
Hegele, RA2
Safarova, MS1
Trukhacheva, EP1
Ezhov, MV1
Afanas'eva, OI1
Afanas'eva, MI1
Tripoten', MI1
Liakishev, AA1
Pokrovskiĭ, SN1
Custodis, F1
Laufs, U1
Elmallah, W1
Nicholls, SJ1
Michos, ED1
Sibley, CT1
Baer, JT1
Blaha, MJ1
Blumenthal, RS1
Yeboah, J1
Philpott, AC1
Hubacek, J1
Sun, YC1
Hillard, D1
Anderson, TJ1
Matthan, NR1
Giovanni, A1
Schaefer, EJ1
Brown, BG5
Lichtenstein, AH1
Hecht, HS2
Harman, SM2
Ryan, MJ1
Gibson, J1
Simmons, P1
Stanek, E1
Ito, MK1
GOLDSBOROUGH, CE1
POPA, Iu1
ILIESCU, M1
DOMOCOS, G1
IACOBINI, P1
CONSTANTINESCU, S1
ILIESCU, CC1
BUEDINGEN, F1
MOELLER, HC1
Wang, M1
Briggs, MR1
Morse, JS1
Dowdy, AA1
Heise, N2
DeAngelis, D2
Frohlich, J2
Chait, A2
VINOGRADOV, AV1
Ng, DS1
Wierzbicki, AS1
Reasner, CA1
McKenney, JM1
Nesto, RW1
Schwiesow, SJ1
Nappi, JM1
Ragucci, KR1
Norris, RB1
Vogt, A1
Kassner, U1
Hostalek, U1
Peiter, A1
Steinhagen-Thiessen, E1
Kuvin, JT2
Dave, DM1
Sliney, KA1
Mooney, P1
Patel, AR2
Kimmelstiel, CD1
Karas, RH2
Yuan, G1
Al-Shali, KZ1
Yavasoglu, I1
Kadikoylu, G1
Bolaman, Z1
Röggla, G1
Fasan, M1
Kapiotis, S1
Holub, BJ1
Toth, PP1
Ballantyne, CM1
Polonsky, TS1
Taylor, AJ1
Leithäuser, B1
Gerk, U1
Mrowietz, C1
Jung, F1
Park, JW1
Lapuerta, P1
Azen, SP7
LaBree, L3
Sacks, FM1
Pasternak, RC1
Gibson, CM1
Rosner, B1
Stone, PH1
Bays, H1
Dujovne, CA1
Mays, JB1
Mack, WJ6
Cashin-Hemphill, L3
Shircore, AM3
Selzer, RH5
Blankenhorn, DH6
Hodis, HN3
Kukharchuk, VV1
Solov'ev, EIu1
Malyshev, PP1
Rozhkova, TA1
Semenova, OA1
Aronskaia, EE1
Borgia, MC1
Medici, F1
Cheung, M1
Dowdy, A1
Fisher, LD1
Albers, J1
Kwiterovich, PO1
Guyton, JR1
Zambon, A1
Hokanson, JE1
Brunzell, JD1
Xiang, M1
Liu, C1
Arntz, HR1
Agrawal, R1
Wunderlich, W1
Schnitzer, L1
Stern, R1
Fischer, F1
Schultheiss, HP1
Kris-Etherton, PM1
Vitale, GD1
deKemp, RA1
Ruddy, TD1
Williams, K1
Beanlands, RS1
SoRelle, R1
Malloy, MJ2
Kane, JP2
Klungel, OH1
Heckbert, SR1
de Boer, A1
Leufkens, HG1
Sullivan, SD1
Fishman, PA1
Veenstra, DL1
Psaty, BM1
Drown, DJ1
Dalessandri, KM1
Rämet, ME1
Pandian, NG1
Mendelsohn, ME1
Squires, RW1
Allison, TG1
Gau, GT1
Miller, TD1
Kottke, BA1
Crawford, DW1
Pogoda, J1
Lee, PL2
Pogoda, JM2
Szamosi, A1
Shepherd, J1
Simpson, H1
Williamson, CM1
Pringle, S1
MacLean, J1
Lorimer, AR1
Packard, CJ1
Johansson, J1
Carlson, LA1
Ports, TA1
Phillips, NR1
Diehl, JC1
Havel, RJ1
Sanmarco, ME2
Alaupovic, P1
Wickham, E1
Chin, HP1
Witztum, JL1
Nessim, SA1
Johnson, RL1
Tseluĭko, VI1

Clinical Trials (16)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Effect of Extended-Release Niacin on Saphenous Vein Graft Atherosclerosis: The Atherosclerosis Lesion Progression Intervention Using Niacin Extended Release in Saphenous Vein Grafts (ALPINE-SVG) Pilot Trial[NCT01221402]Phase 238 participants (Actual)Interventional2010-10-31Completed
Carotid Plaque Composition by Magnetic Resonance Imaging During Lipid Lowering Therapy[NCT00715273]Phase 4217 participants (Actual)Interventional2001-05-01Completed
FLAT-SUGAR: FLuctuATion Reduction With inSULin and Glp-1 Added togetheR[NCT01524705]Phase 4102 participants (Actual)Interventional2012-08-31Completed
AIM HIGH: Niacin Plus Statin to Prevent Vascular Events[NCT00120289]Phase 33,414 participants (Actual)Interventional2005-09-30Terminated (stopped due to AIM-HIGH was stopped on the recommendation of the DSMB because of lack of efficacy of niacin in preventing primary outcome events.)
Role of Lipoprotein(a) Concentration and Apolipoprotein(a) Phenotype in Prediction of Coronary Events in General Population[NCT02515747]1,400 participants (Actual)Interventional1993-01-31Completed
HDL Modulation and Endothelial Function[NCT00150722]Phase 375 participants (Actual)Interventional2005-09-30Completed
[NCT00000461]Phase 20 participants Interventional1986-12-31Completed
[NCT00000599]Phase 30 participants Interventional1980-06-30Completed
ARBITER 6: ARterial Biology for the Investigation of the Treatment Effects of Reducing Cholesterol 6 - HDL and LDL Treatment Strategies in Atherosclerosis (HALTS)[NCT00397657]Phase 4400 participants (Anticipated)Interventional2006-11-30Terminated (stopped due to Independent steering committee has stopped the trial based on results of a prespecified, blinded interim analysis. It was not stopped due to safety concerns.)
[NCT00005696]0 participants Observational1994-01-31Completed
[NCT00000553]Phase 30 participants Interventional1994-09-30Completed
Niacin Therapy to Improve Endothelial Function in Sickle Cell Disease[NCT00508989]Phase 230 participants (Actual)Interventional2007-07-24Completed
Human Lipoprotein Pathophysiology - Subproject: Genetics of Familial Combined Hyperlipidemia[NCT00005313]450 participants (Actual)Observational2001-04-30Completed
Familial Atherosclerosis Treatment Study[NCT00000512]Phase 3146 participants (Actual)Interventional1984-01-31Completed
Correlates of Angiographic Changes and Coronary Events: The Cholesterol-Lowering Atherosclerosis Study (CLAS)[NCT00005433]188 participants (Actual)Observational1996-04-30Completed
Lipoprotein Metabolism in Normal Volunteers and Dyslipoproteinemic Patients (Stable Isotopes)[NCT00001226]90 participants Observational1987-12-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Annualized LRNC Volume Change in Carotid Plaque Composition, as Assessed by MRI

"The primary endpoint of this study is carotid plaque lipid composition identified by MRI. The determination of plaque lipid content for each carotid artery will be performed using the automated interactive system. These measurements will be performed from the MRI scans at four time points blinded to time sequence of MRI examinations, patient treatment, lipid levels and clinical course.~Volume Measurements: Contours were placed around the lumen, outer-wall boundaries, and plaque features of carotid artery. (Arterial wall area) = (outer-wall area) - (lumen area). Volume calculated as: area x 2 mm (slice thickness). Tissue volume/wall volume x (100%) is presented as percentage. Annualized change presented mm^3/year (for volume) and as percentage change/year." (NCT00715273)
Timeframe: Measured at Years 1, 2, and 3

Interventionmm^3/year (Mean)
1 - Single Therapy Group-4.6
2 - Double Therapy Group-15.1
3 - Triple Therapy Group-9.4

Annualized LRNC and Wall Volume Changes in Carotid Plaque Composition, as Assessed by MRI

"The primary endpoint of this study is carotid plaque lipid composition identified by MRI. The determination of plaque lipid content for each carotid artery will be performed using the automated interactive system. These measurements will be performed from the MRI scans at four time points blinded to time sequence of MRI examinations, patient treatment, lipid levels and clinical course.~Volume Measurements: Contours were placed around the lumen, outer-wall boundaries, and plaque features of carotid artery. (Arterial wall area) = (outer-wall area) - (lumen area). Volume calculated as: area x 2 mm (slice thickness). Tissue volume/wall volume x (100%) is presented as percentage. Annualized change presented mm^3/year (for volume) and as percentage change/year." (NCT00715273)
Timeframe: Measured at Years 1, 2, and 3

,,
Interventionpercentage change/year (Mean)
LRNC changeWall Volume change
1 - Single Therapy Group-1.6-0.6
2 - Double Therapy Group-3.6-1.4
3 - Triple Therapy Group-2.8-1.2

Composite of Cardiovascular Endpoints: Number of Participants With Cardiovascular Disease Death, Non-fatal Heart Attack, Stroke, and Worsening Ischemia Requiring Medical Interventions

Any cardiovascular events such as death from any cause, nonfatal myocardial infarction, stroke, and revascularization procedures (PCI or CABG) due to unstable ischemia will be recorded and verified. (NCT00715273)
Timeframe: Measured at Years 3, 4, and 5

,,
InterventionParticipants (Count of Participants)
Composite Measured at Year 3Composite Measured at Year 4 (cumulative)Composite Measured at Year 5 (cumulative)
1 - Single Therapy Group679
2 - Double Therapy Group61111
3 - Triple Therapy Group799

Coefficient of Variation at 26 Weeks Minus Coefficient of Variation at Baseline

The change in the coefficient of variation (CV) of continuous glucose readings, as assessed by Continuous Glucose Monitoring (CGM) (NCT01524705)
Timeframe: At baseline, 6 months of intervention

Interventionpercentage (Mean)
Insulin Glargine, Metformin, Exenatide-2.43
Insulin Glargine, Metformin, Prandial Insulin0.44

HbA1C Levels

% of glycosylated hemoglobin in whole blood at 26 weeks (NCT01524705)
Timeframe: Baseline vs 26 weeks

Intervention% of HbA1C (Mean)
Insulin Glargine, Metformin, Exenatide7.1
Insulin Glargine, Metformin, Prandial Insulin7.2

Number of Participants With Hypoglycemia

Severe hypoglycemia-documented glucose <50mg/dl (participant journal), and hypoglycemic attacks requiring hospitalization, or treatment by emergency personnel. (NCT01524705)
Timeframe: 26 weeks

InterventionParticipants (Count of Participants)
Insulin Glargine, Metformin, Exenatide0
Insulin Glargine, Metformin, Prandial Insulin0

Weight Change During Trial

Weight in kg at 26 weeks minus weight at baseline. (NCT01524705)
Timeframe: Baseline vs 26 weeks

Interventionkg (Mean)
Insulin Glargine, Metformin, Exenatide-4.8
Insulin Glargine, Metformin, Prandial Insulin0.7

Cardiovascular Mortality

(NCT00120289)
Timeframe: Time to first event measured from date of randomization through last follow-up visit (common termination), for an average of 36 months follow-up, maximum 66 months.

Interventionparticipants (Number)
ERN + Simvastatin45
Placebo + Simvastatin38

Composite End Point of CHD Death, Nonfatal MI, Ischemic Stroke, Hospitalization for Non-ST Segment Elevation Acute Coronary Syndrome (ACS), or Symptom-driven Coronary or Cerebral Revascularization

(NCT00120289)
Timeframe: Time to first event measured from date of randomization through last follow-up visit (common termination) for an average of 36 months follow-up, maximum 66 months.

Interventionparticipants (Number)
ERN + Simvastatin282
Placebo + Simvastatin274

Composite Endpoint of CHD Death, Non-fatal MI, High-risk ACS or Ischemic Stroke

(NCT00120289)
Timeframe: Time to first event measured from date of randomization through last follow-up visit (common termination) for an average of 36 months follow-up, maximum 66 months

Interventionparticipants (Number)
ERN + Simvastatin171
Placebo + Simvastatin158

Composite Endpoint of CHD Death, Non-fatal MI, or Ischemic Stroke

(NCT00120289)
Timeframe: Time to first event measured from date of randomization through last follow-up visit (common termination) for an average of 36 months follow-up, maximum 66 months

Interventionparticipants (Number)
ERN + Simvastatin156
Placebo + Simvastatin138

Reviews

32 reviews available for niacin and Arteriosclerosis, Coronary

ArticleYear
Lipid-Lowering Agents in Older Individuals: A Systematic Review and Meta-Analysis of Randomized Clinical Trials.
    The Journal of clinical endocrinology and metabolism, 2019, 05-01, Volume: 104, Issue:5

    Topics: Aged; Aged, 80 and over; Cardiovascular Diseases; Coronary Artery Disease; Diabetes Mellitus; Fibric

2019
HDL quality or cholesterol cargo: what really matters--spotlight on sphingosine-1-phosphate-rich HDL.
    Current opinion in lipidology, 2013, Volume: 24, Issue:4

    Topics: Animals; Atherosclerosis; Cardiotonic Agents; Cholesterol, HDL; Coronary Artery Disease; Drug Therap

2013
Effectiveness of combination therapy with statin and another lipid-modifying agent compared with intensified statin monotherapy: a systematic review.
    Annals of internal medicine, 2014, Apr-01, Volume: 160, Issue:7

    Topics: Anticholesteremic Agents; Azetidines; Bile Acids and Salts; Cholesterol, LDL; Coronary Artery Diseas

2014
Niacin and progression of CKD.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2015, Volume: 65, Issue:5

    Topics: Comorbidity; Coronary Artery Disease; Disease Progression; Endothelium, Vascular; Humans; Hypolipide

2015
LDL reduction: how low should we go and is it safe?
    Current cardiology reports, 2008, Volume: 10, Issue:6

    Topics: Allylamine; Anticholesteremic Agents; Azetidines; Cholesterol, LDL; Colesevelam Hydrochloride; Coron

2008
Cardiovascular therapies and associated glucose homeostasis: implications across the dysglycemia continuum.
    Journal of the American College of Cardiology, 2009, Feb-03, Volume: 53, Issue:5 Suppl

    Topics: Adrenergic beta-Antagonists; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibit

2009
Nicotinic acid and the prevention of coronary artery disease.
    Current opinion in lipidology, 2009, Volume: 20, Issue:4

    Topics: Cholesterol, HDL; Cholesterol, LDL; Clinical Trials as Topic; Coronary Artery Disease; Humans; Niaci

2009
Novel targets that affect high-density lipoprotein metabolism: the next frontier.
    The American journal of cardiology, 2009, Nov-16, Volume: 104, Issue:10 Suppl

    Topics: Apolipoprotein A-I; Cholesterol Ester Transfer Proteins; Cholesterol, HDL; Clinical Trials as Topic;

2009
Effect of niacin therapy on cardiovascular outcomes in patients with coronary artery disease.
    Journal of cardiovascular pharmacology and therapeutics, 2010, Volume: 15, Issue:2

    Topics: Cardiovascular Diseases; Coronary Artery Disease; Humans; Hypolipidemic Agents; Myocardial Infarctio

2010
High-density lipoprotein and coronary heart disease: current and future therapies.
    Journal of the American College of Cardiology, 2010, Mar-30, Volume: 55, Issue:13

    Topics: Acetyl-CoA C-Acetyltransferase; Animals; Apolipoprotein A-I; Biological Transport; Cholesterol Ester

2010
Genetic determinants of plasma triglycerides.
    Journal of lipid research, 2011, Volume: 52, Issue:2

    Topics: Adaptor Proteins, Signal Transducing; Angiopoietin-Like Protein 3; Angiopoietin-like Proteins; Angio

2011
[Hypertricglyceridemia: prognostic impact and treatment options].
    Deutsche medizinische Wochenschrift (1946), 2011, Volume: 136, Issue:30

    Topics: Adult; Cardiovascular Diseases; Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Diet, R

2011
Niacin and statin combination therapy for atherosclerosis regression and prevention of cardiovascular disease events: reconciling the AIM-HIGH (Atherothrombosis Intervention in Metabolic Syndrome With Low HDL/High Triglycerides: Impact on Global Health Ou
    Journal of the American College of Cardiology, 2012, Jun-05, Volume: 59, Issue:23

    Topics: Aged; Cardiovascular Diseases; Coronary Artery Disease; Drug Therapy, Combination; Female; Follow-Up

2012
Niacin: a powerful adjunct to other lipid-lowering drugs in reducing plaque progression and acute coronary events.
    Current atherosclerosis reports, 2003, Volume: 5, Issue:5

    Topics: Acute Disease; Algorithms; Clinical Trials as Topic; Coronary Artery Disease; Coronary Disease; Diab

2003
HDL: the metabolism, function, and therapeutic importance.
    Chemical reviews, 2004, Volume: 104, Issue:1

    Topics: Animals; Anticholesteremic Agents; Apolipoprotein A-I; ATP-Binding Cassette Transporters; Carrier Pr

2004
Treating low HDL--from bench to bedside.
    Clinical biochemistry, 2004, Volume: 37, Issue:8

    Topics: Animals; Cholesterol; Coronary Artery Disease; Coronary Disease; Endothelium, Vascular; Humans; Hype

2004
Have we forgotten the pivotal role of high-density lipoprotein cholesterol in atherosclerosis prevention?
    Current medical research and opinion, 2005, Volume: 21, Issue:2

    Topics: Arteriosclerosis; Cholesterol, HDL; Clofibric Acid; Coronary Artery Disease; Disease Progression; Hu

2005
Commentary: A new approach to atherogenic dyslipidemia.
    Postgraduate medicine, 2005, Volume: 117, Issue:4

    Topics: Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Humans; Hyperlipidemias; Hypolipidemic

2005
Pharmacologic options for aggressive low-density lipoprotein cholesterol lowering: benefits versus risks.
    The American journal of cardiology, 2005, Aug-22, Volume: 96, Issue:4A

    Topics: Allylamine; Anticholesteremic Agents; Atorvastatin; Azetidines; Cholesterol, LDL; Clinical Trials as

2005
Beyond low-density lipoprotein: addressing the atherogenic lipid triad in type 2 diabetes mellitus and the metabolic syndrome.
    American journal of cardiovascular drugs : drugs, devices, and other interventions, 2005, Volume: 5, Issue:6

    Topics: Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Diabetes Mellitus, Type 2; Diet; Drug T

2005
To statin or to non-statin in coronary disease--considering absolute risk is the answer.
    Atherosclerosis, 2007, Volume: 195, Issue:1

    Topics: Acute Coronary Syndrome; Aspirin; Atherosclerosis; Cholesterol, LDL; Coronary Artery Disease; Diet;

2007
Hypertriglyceridemia: its etiology, effects and treatment.
    CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2007, Apr-10, Volume: 176, Issue:8

    Topics: Clofibric Acid; Coronary Artery Disease; Diet; Exercise; Humans; Hydroxymethylglutaryl-CoA Reductase

2007
High-density lipoprotein metabolism: potential therapeutic targets.
    The American journal of cardiology, 2007, Dec-03, Volume: 100, Issue:11 A

    Topics: Cholesterol, HDL; Cholesterol, LDL; Clofibric Acid; Coronary Artery Disease; Humans; Hydroxymethylgl

2007
Reducing the residual risk of 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibitor therapy with combination therapy.
    The American journal of cardiology, 2008, Apr-17, Volume: 101, Issue:8A

    Topics: Anticholesteremic Agents; C-Reactive Protein; Cholesterol, HDL; Coronary Artery Disease; Drug Therap

2008
Evidence to support aggressive management of high-density lipoprotein cholesterol: implications of recent imaging trials.
    The American journal of cardiology, 2008, Apr-17, Volume: 101, Issue:8A

    Topics: Anticholesteremic Agents; Cholesterol, HDL; Clofibric Acid; Coronary Artery Disease; Disease Progres

2008
Number-needed-to-treat analysis of the prevention of myocardial infarction and death by antidyslipidemic therapy.
    The Journal of family practice, 1996, Volume: 42, Issue:6

    Topics: Coronary Angiography; Coronary Artery Disease; Disease Progression; Female; Humans; Hydroxymethylglu

1996
Perspectives in the treatment of dyslipidemias in the prevention of coronary heart disease.
    Angiology, 1998, Volume: 49, Issue:5

    Topics: Cholesterol; Cholesterol, HDL; Cholesterol, LDL; Combined Modality Therapy; Coronary Artery Disease;

1998
Lipid altering or antioxidant vitamins for patients with coronary disease and very low HDL cholesterol? The HDL-Atherosclerosis Treatment Study Design.
    The Canadian journal of cardiology, 1998, Volume: 14 Suppl A

    Topics: Adult; Aged; Antioxidants; Cholesterol, HDL; Coronary Angiography; Coronary Artery Disease; Coronary

1998
The antiatherogenic role of high-density lipoprotein cholesterol.
    The American journal of cardiology, 1998, Nov-05, Volume: 82, Issue:9A

    Topics: 1-Alkyl-2-acetylglycerophosphocholine Esterase; Animals; Anticholesteremic Agents; Aryldialkylphosph

1998
Effect of niacin on atherosclerotic cardiovascular disease.
    The American journal of cardiology, 1998, Dec-17, Volume: 82, Issue:12A

    Topics: Cerebrovascular Disorders; Coronary Artery Disease; Drug Therapy, Combination; Humans; Hypolipidemic

1998
A risk factor for atherosclerosis: triglyceride-rich lipoproteins.
    Advances in internal medicine, 2001, Volume: 47

    Topics: Coronary Artery Disease; Diabetes Mellitus; Drug Therapy, Combination; Gemfibrozil; Humans; Hydroxym

2001
Current approaches to drug therapy for the hypercholesterolemic patient.
    Circulation, 1989, Volume: 80, Issue:5

    Topics: Anticholesteremic Agents; Cholesterol, LDL; Coronary Artery Disease; Humans; Hydroxymethylglutaryl-C

1989

Trials

27 trials available for niacin and Arteriosclerosis, Coronary

ArticleYear
Effect of Extended-Release Niacin on Carotid Intima Media Thickness, Reactive Hyperemia, and Endothelial Progenitor Cell Mobilization: Insights From the Atherosclerosis Lesion Progression Intervention Using Niacin Extended Release in Saphenous Vein Grafts
    The Journal of invasive cardiology, 2015, Volume: 27, Issue:12

    Topics: Aged; Atherosclerosis; Carotid Arteries; Carotid Intima-Media Thickness; Coronary Artery Disease; De

2015
Relationship of baseline HDL subclasses, small dense LDL and LDL triglyceride to cardiovascular events in the AIM-HIGH clinical trial.
    Atherosclerosis, 2016, Volume: 251

    Topics: Aged; Anticholesteremic Agents; Cardiovascular Diseases; Cardiovascular System; Cholesterol, HDL; Co

2016
Effects of oral niacin on endothelial dysfunction in patients with coronary artery disease: results of the randomized, double-blind, placebo-controlled INEF study.
    Atherosclerosis, 2009, Volume: 204, Issue:1

    Topics: Administration, Oral; Aged; Biomarkers; Blood Glucose; Brachial Artery; Cell Adhesion Molecules; Cho

2009
Combined use of extended-release niacin and atorvastatin: safety and effects on lipid modification.
    Chinese medical journal, 2009, Jul-20, Volume: 122, Issue:14

    Topics: Aged; Anticholesteremic Agents; Apolipoproteins A; Atorvastatin; Cholesterol; Cholesterol, HDL; Chol

2009
Impact of increases in high-density lipoprotein cholesterol on cardiovascular outcomes during the armed forces regression study.
    Journal of cardiovascular pharmacology and therapeutics, 2010, Volume: 15, Issue:4

    Topics: Adult; Aged; Anticholesteremic Agents; Cardiovascular Diseases; Cholesterol, HDL; Cholestyramine Res

2010
The role of niacin in raising high-density lipoprotein cholesterol to reduce cardiovascular events in patients with atherosclerotic cardiovascular disease and optimally treated low-density lipoprotein cholesterol: baseline characteristics of study partici
    American heart journal, 2011, Volume: 161, Issue:3

    Topics: Aged; Anticholesteremic Agents; Azetidines; Cardiovascular Diseases; Cholesterol, HDL; Coronary Arte

2011
[Pleiotropic effects of nicotinic acid therapy in men with coronary heart disease and elevated lipoprotein(a) levels].
    Kardiologiia, 2011, Volume: 51, Issue:5

    Topics: 1-Alkyl-2-acetylglycerophosphocholine Esterase; Atherosclerosis; Atorvastatin; Carotid Arteries; Cor

2011
Niacin improves lipid profile but not endothelial function in patients with coronary artery disease on high dose statin therapy.
    Atherosclerosis, 2013, Volume: 226, Issue:2

    Topics: Aged; Atorvastatin; Coronary Artery Disease; Endothelium, Vascular; Female; Heptanoic Acids; Humans;

2013
Impact of simvastatin, niacin, and/or antioxidants on cholesterol metabolism in CAD patients with low HDL.
    Journal of lipid research, 2003, Volume: 44, Issue:4

    Topics: Antioxidants; Cholesterol; Constriction, Pathologic; Coronary Artery Disease; Desmosterol; Drug Ther

2003
Comparison of effectiveness of statin monotherapy versus statin and niacin combination therapy in primary prevention and effects on calcified plaque burden.
    The American journal of cardiology, 2003, Feb-01, Volume: 91, Issue:3

    Topics: Anti-Infective Agents; Coronary Artery Disease; Drug Therapy, Combination; Female; Fluoroquinolones;

2003
Safety and tolerability of simvastatin plus niacin in patients with coronary artery disease and low high-density lipoprotein cholesterol (The HDL Atherosclerosis Treatment Study).
    The American journal of cardiology, 2004, Feb-01, Volume: 93, Issue:3

    Topics: Blood Glucose; Cholesterol, HDL; Coronary Artery Disease; Double-Blind Method; Drug Therapy, Combina

2004
Effects of extended-release niacin on lipoprotein particle size, distribution, and inflammatory markers in patients with coronary artery disease.
    The American journal of cardiology, 2006, Sep-15, Volume: 98, Issue:6

    Topics: 1-Alkyl-2-acetylglycerophosphocholine Esterase; Biomarkers; C-Reactive Protein; Cholesterol, HDL; Co

2006
Effect on coronary atherosclerosis of decrease in plasma cholesterol concentrations in normocholesterolaemic patients. Harvard Atherosclerosis Reversibility Project (HARP) Group.
    Lancet (London, England), 1994, Oct-29, Volume: 344, Issue:8931

    Topics: Anticholesteremic Agents; Cardiac Catheterization; Cholesterol; Cholesterol, HDL; Cholesterol, LDL;

1994
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Progression of coronary artery disease predicts clinical coronary events. Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study.
    Circulation, 1996, Jan-01, Volume: 93, Issue:1

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Disease; Diet, Fat-Restricted; Follow-Up St

1996
Lipid altering or antioxidant vitamins for patients with coronary disease and very low HDL cholesterol? The HDL-Atherosclerosis Treatment Study Design.
    The Canadian journal of cardiology, 1998, Volume: 14 Suppl A

    Topics: Adult; Aged; Antioxidants; Cholesterol, HDL; Coronary Angiography; Coronary Artery Disease; Coronary

1998
Evidence for a new pathophysiological mechanism for coronary artery disease regression: hepatic lipase-mediated changes in LDL density.
    Circulation, 1999, Apr-20, Volume: 99, Issue:15

    Topics: Aged; Anticholesteremic Agents; Apolipoproteins B; Centrifugation, Density Gradient; Chemical Phenom

1999
Evidence for a new pathophysiological mechanism for coronary artery disease regression: hepatic lipase-mediated changes in LDL density.
    Circulation, 1999, Apr-20, Volume: 99, Issue:15

    Topics: Aged; Anticholesteremic Agents; Apolipoproteins B; Centrifugation, Density Gradient; Chemical Phenom

1999
Evidence for a new pathophysiological mechanism for coronary artery disease regression: hepatic lipase-mediated changes in LDL density.
    Circulation, 1999, Apr-20, Volume: 99, Issue:15

    Topics: Aged; Anticholesteremic Agents; Apolipoproteins B; Centrifugation, Density Gradient; Chemical Phenom

1999
Evidence for a new pathophysiological mechanism for coronary artery disease regression: hepatic lipase-mediated changes in LDL density.
    Circulation, 1999, Apr-20, Volume: 99, Issue:15

    Topics: Aged; Anticholesteremic Agents; Apolipoproteins B; Centrifugation, Density Gradient; Chemical Phenom

1999
Serial quantitative coronary angiography and coronary events.
    American heart journal, 2000, Volume: 139, Issue:6

    Topics: Adult; Cholesterol, LDL; Colestipol; Collateral Circulation; Coronary Angiography; Coronary Artery D

2000
Correlations between measures of atherosclerosis change using carotid ultrasonography and coronary angiography.
    Atherosclerosis, 2000, Volume: 150, Issue:2

    Topics: Adult; Carotid Artery, Common; Carotid Stenosis; Colestipol; Coronary Angiography; Coronary Artery D

2000
Beneficial effects of pravastatin (+/-colestyramine/niacin) initiated immediately after a coronary event (the randomized Lipid-Coronary Artery Disease [L-CAD] Study).
    The American journal of cardiology, 2000, Dec-15, Volume: 86, Issue:12

    Topics: Adult; Aged; Angina, Unstable; Angioplasty, Balloon, Coronary; Anticholesteremic Agents; Chemopreven

2000
Low-dose, time-release nicotinic acid: effects in selected patients with low concentrations of high-density lipoprotein cholesterol.
    Mayo Clinic proceedings, 1992, Volume: 67, Issue:9

    Topics: Cholesterol, HDL; Coronary Artery Disease; Delayed-Action Preparations; Female; Humans; Male; Middle

1992
Comparison of computer- and human-derived coronary angiographic end-point measures for controlled therapy trials.
    Arteriosclerosis and thrombosis : a journal of vascular biology, 1992, Volume: 12, Issue:3

    Topics: Adult; Colestipol; Combined Modality Therapy; Computers; Coronary Angiography; Coronary Artery Disea

1992
Effect of lovastatin or niacin combined with colestipol and regression of coronary atherosclerosis.
    European heart journal, 1992, Volume: 13 Suppl B

    Topics: Apolipoprotein A-I; Apolipoproteins B; Cholesterol, HDL; Cholesterol, LDL; Colestipol; Coronary Angi

1992
[Angiographic regression of coronary atheromatosis].
    Lakartidningen, 1991, Apr-10, Volume: 88, Issue:15

    Topics: Angiography; Anticholesteremic Agents; Coronary Angiography; Coronary Artery Disease; Drug Therapy,

1991
Regression of coronary atherosclerosis during treatment of familial hypercholesterolemia with combined drug regimens.
    JAMA, 1990, Dec-19, Volume: 264, Issue:23

    Topics: Adult; Aged; Cholesterol, HDL; Cholesterol, LDL; Colestipol; Coronary Artery Disease; Drug Therapy,

1990
Beneficial effects of colestipol-niacin on coronary atherosclerosis. A 4-year follow-up.
    JAMA, 1990, Dec-19, Volume: 264, Issue:23

    Topics: Adult; Apolipoproteins; Cholesterol; Colestipol; Coronary Artery Disease; Drug Therapy, Combination;

1990
Beneficial effects of colestipol-niacin on coronary atherosclerosis. A 4-year follow-up.
    JAMA, 1990, Dec-19, Volume: 264, Issue:23

    Topics: Adult; Apolipoproteins; Cholesterol; Colestipol; Coronary Artery Disease; Drug Therapy, Combination;

1990
Beneficial effects of colestipol-niacin on coronary atherosclerosis. A 4-year follow-up.
    JAMA, 1990, Dec-19, Volume: 264, Issue:23

    Topics: Adult; Apolipoproteins; Cholesterol; Colestipol; Coronary Artery Disease; Drug Therapy, Combination;

1990
Beneficial effects of colestipol-niacin on coronary atherosclerosis. A 4-year follow-up.
    JAMA, 1990, Dec-19, Volume: 264, Issue:23

    Topics: Adult; Apolipoproteins; Cholesterol; Colestipol; Coronary Artery Disease; Drug Therapy, Combination;

1990
Prediction of angiographic change in native human coronary arteries and aortocoronary bypass grafts. Lipid and nonlipid factors.
    Circulation, 1990, Volume: 81, Issue:2

    Topics: Apolipoprotein C-III; Apolipoproteins; Apolipoproteins C; Colestipol; Coronary Angiography; Coronary

1990
Beneficial effects of combined colestipol-niacin therapy on coronary atherosclerosis and coronary venous bypass grafts.
    JAMA, 1987, Jun-19, Volume: 257, Issue:23

    Topics: Adult; Clinical Trials as Topic; Colestipol; Coronary Artery Bypass; Coronary Artery Disease; Drug T

1987
Beneficial effects of combined colestipol-niacin therapy on coronary atherosclerosis and coronary venous bypass grafts.
    JAMA, 1987, Jun-19, Volume: 257, Issue:23

    Topics: Adult; Clinical Trials as Topic; Colestipol; Coronary Artery Bypass; Coronary Artery Disease; Drug T

1987
Beneficial effects of combined colestipol-niacin therapy on coronary atherosclerosis and coronary venous bypass grafts.
    JAMA, 1987, Jun-19, Volume: 257, Issue:23

    Topics: Adult; Clinical Trials as Topic; Colestipol; Coronary Artery Bypass; Coronary Artery Disease; Drug T

1987
Beneficial effects of combined colestipol-niacin therapy on coronary atherosclerosis and coronary venous bypass grafts.
    JAMA, 1987, Jun-19, Volume: 257, Issue:23

    Topics: Adult; Clinical Trials as Topic; Colestipol; Coronary Artery Bypass; Coronary Artery Disease; Drug T

1987

Other Studies

43 other studies available for niacin and Arteriosclerosis, Coronary

ArticleYear
Evidence Supporting Niacin Therapy Is More Nuanced Than Article States.
    American family physician, 2018, 12-01, Volume: 98, Issue:11

    Topics: Coronary Artery Disease; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypolipidemic Agent

2018
Stabilization of atherosclerotic plaques: an update.
    European heart journal, 2013, Volume: 34, Issue:42

    Topics: Antihypertensive Agents; Apolipoprotein B-100; Blood Platelets; CCR5 Receptor Antagonists; Chemokine

2013
Effects of Rosuvastatin Versus Atorvastatin, Alone or in Combination, on Lipoprotein (a).
    The Annals of pharmacotherapy, 2016, Volume: 50, Issue:8

    Topics: Apolipoprotein A-I; Atorvastatin; Cholesterol; Coronary Artery Disease; Drug Therapy, Combination; F

2016
To statin or to non-statin in coronary disease-considering absolute risk is the answer.
    Atherosclerosis, 2008, Volume: 200, Issue:2

    Topics: Acute Coronary Syndrome; Atherosclerosis; Cholesterol, LDL; Coronary Artery Disease; Diet; Fatty Aci

2008
What can I do to lower my lipoprotein(a) level?
    Heart advisor, 2008, Volume: 11, Issue:4

    Topics: Cholesterol, LDL; Coronary Artery Disease; Humans; Hypolipidemic Agents; Lipoprotein(a); Niacin; Ris

2008
Combined statin and niacin therapy remodels the high-density lipoprotein proteome.
    Circulation, 2008, Sep-16, Volume: 118, Issue:12

    Topics: Adult; Aged; Amino Acid Sequence; Coronary Artery Disease; Drug Therapy, Combination; Humans; Hydrox

2008
Combined statin and niacin therapy remodels the high-density lipoprotein proteome.
    Circulation, 2008, Sep-16, Volume: 118, Issue:12

    Topics: Adult; Aged; Amino Acid Sequence; Coronary Artery Disease; Drug Therapy, Combination; Humans; Hydrox

2008
Combined statin and niacin therapy remodels the high-density lipoprotein proteome.
    Circulation, 2008, Sep-16, Volume: 118, Issue:12

    Topics: Adult; Aged; Amino Acid Sequence; Coronary Artery Disease; Drug Therapy, Combination; Humans; Hydrox

2008
Combined statin and niacin therapy remodels the high-density lipoprotein proteome.
    Circulation, 2008, Sep-16, Volume: 118, Issue:12

    Topics: Adult; Aged; Amino Acid Sequence; Coronary Artery Disease; Drug Therapy, Combination; Humans; Hydrox

2008
Commentary to factors predicting cardiovascular events in statin-treated diabetic and non-diabetic patients with coronary atherosclerosis.
    Atherosclerosis, 2010, Volume: 208, Issue:2

    Topics: Cholesterol, LDL; Clinical Trials as Topic; Coronary Artery Disease; Diabetes Complications; Diabete

2010
Trial clouds use of niacin with a statin.
    Harvard heart letter : from Harvard Medical School, 2011, Volume: 21, Issue:12

    Topics: Anticholesteremic Agents; Azetidines; Cardiovascular Diseases; Cholesterol, HDL; Clinical Trials as

2011
Therapy and clinical trials.
    Current opinion in lipidology, 2011, Volume: 22, Issue:6

    Topics: Amides; Cholesterol Ester Transfer Proteins; Coronary Artery Disease; Diabetes Mellitus; Drug Therap

2011
Is niacin ineffective? Or did AIM-HIGH miss its target?
    Cleveland Clinic journal of medicine, 2012, Volume: 79, Issue:1

    Topics: Brain Ischemia; Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Dyslipidemias; Female;

2012
High patient compliance with nicacin/laropiprant in large clinical trial: interim safety and tolerability results from HPS-2 THRIVE study released at 2012 ESC congress: drug trends in cardiology.
    Cardiovascular journal of Africa, 2012, Volume: 23, Issue:8

    Topics: Chemical Safety; China; Cholesterol, HDL; Coronary Artery Disease; Europe; Follow-Up Studies; Humans

2012
Targeting specific traditional risk factors to improve cardiovascular outcomes: Sound or flawed?
    Atherosclerosis, 2013, Volume: 226, Issue:2

    Topics: Atorvastatin; Coronary Artery Disease; Endothelium, Vascular; Female; Heptanoic Acids; Humans; Hydro

2013
Effectiveness of aggressive management of dyslipidemia in a collaborative-care practice model.
    The American journal of cardiology, 2003, Jun-15, Volume: 91, Issue:12

    Topics: Adult; Aged; Aged, 80 and over; Biomarkers; Cholesterol, HDL; Cholesterol, LDL; Cohort Studies; Coop

2003
Advances in the understanding and management of dyslipidemia: using niacin-based therapies.
    American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 2003, Jul-01, Volume: 60, Issue:13 Suppl 2

    Topics: Chemistry, Pharmaceutical; Cholesterol, HDL; Coronary Artery Disease; Delayed-Action Preparations; D

2003
Nicotinic acid in the treatment of ischaemic heart-disease.
    Lancet (London, England), 1960, Sep-24, Volume: 2, Issue:7152

    Topics: Coronary Artery Disease; Coronary Disease; Myocardial Ischemia; Niacin; Nicotinic Acids

1960
[The use of nicotinic acid in patients with coronary insufficiency].
    Terapevticheskii arkhiv, 1961, Volume: 33

    Topics: Cardiotonic Agents; Coronary Artery Disease; Coronary Disease; Niacin; Nicotinic Acids

1961
[PROLONGED TREATMENT WITH LARGE DOSES OF NICOTINIC ACID IN CORONARY ARTERIOSCLEROSIS].
    Medicina interna, 1964, Volume: 16

    Topics: Coronary Artery Disease; Coronary Disease; Humans; Hyperlipidemias; Niacin; Nicotinic Acids

1964
[ON THE THERAPY OF CORONARY INSUFFICIENCY].
    Therapie der Gegenwart, 1964, Volume: 103

    Topics: Anticoagulants; Coronary Artery Disease; Coronary Disease; Digitalis Glycosides; Dipyridamole; Drug

1964
Relation of response of subclinical atherosclerosis detected by electron beam tomography to baseline low-density lipoprotein cholesterol levels.
    The American journal of cardiology, 2004, Jan-01, Volume: 93, Issue:1

    Topics: Anticholesteremic Agents; Cholesterol; Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease;

2004
[Use of nicotinic acid in coronary insufficiency].
    Klinicheskaia meditsina, 1950, Volume: 18, Issue:10

    Topics: Coronary Artery Disease; Coronary Vessels; Humans; Niacin; Nicotinic Acids

1950
Assessment of compliance with lipid guidelines in an academic medical center.
    The Annals of pharmacotherapy, 2006, Volume: 40, Issue:1

    Topics: Academic Medical Centers; American Heart Association; Angioplasty, Balloon, Coronary; Cerebrovascula

2006
"Flush-free niacin": dietary supplement may be "benefit-free".
    Preventive cardiology, 2006,Winter, Volume: 9, Issue:1

    Topics: Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Dietary Supplements; Flushing; Humans;

2006
[Safety and tolerability of nicotinic acid. Results of the multicenter, open, prospective NAUTILUS study].
    MMW Fortschritte der Medizin, 2006, May-04, Volume: 148, Issue:18

    Topics: Adverse Drug Reaction Reporting Systems; Anticholesteremic Agents; Cholesterol, HDL; Cholesterol, LD

2006
Treating hypertriglyceridemia.
    CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2007, Sep-11, Volume: 177, Issue:6

    Topics: Adult; Clofibric Acid; Coronary Artery Disease; Diet; Exercise; Heparin; Humans; Hydroxymethylglutar

2007
Treating hypertriglyceridemia.
    CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2007, Sep-11, Volume: 177, Issue:6

    Topics: Clofibric Acid; Coronary Artery Disease; Diet; Exercise; Humans; Hydroxymethylglutaryl-CoA Reductase

2007
Treating hypertriglyceridemia.
    CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2007, Sep-11, Volume: 177, Issue:6

    Topics: Clofibric Acid; Coronary Artery Disease; Diet; Exercise; Fatty Acids, Omega-3; Humans; Hydroxymethyl

2007
Niacin therapy: an evolving paradigm for the management of mixed dyslipidemia and low high-density lipoprotein cholesterol. Introduction.
    The American journal of cardiology, 2008, Apr-17, Volume: 101, Issue:8A

    Topics: Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Dyslipidemias; Humans; Hypolipidemic Ag

2008
Influence of xantinole nicotinic acid on cutaneous microcirculation in patients with coronary artery disease and hyperlipoproteinemia.
    Clinical hemorheology and microcirculation, 2008, Volume: 39, Issue:1-4

    Topics: Aged; Blood Pressure; Capillaries; Coronary Artery Disease; Female; Heart Rate; Humans; Hyperlipopro

2008
Use of neural networks in predicting the risk of coronary artery disease.
    Computers and biomedical research, an international journal, 1995, Volume: 28, Issue:1

    Topics: Adult; Cholesterol; Colestipol; Coronary Artery Disease; Coronary Disease; Diet, Fat-Restricted; Fol

1995
Elevated lipoprotein (a) blood levels as the single treatable atherosclerotic risk factor in patients with coronary artery disease.
    The Journal of the Kentucky Medical Association, 1993, Volume: 91, Issue:11

    Topics: Aged; Coronary Artery Disease; Humans; Lipoprotein(a); Male; Middle Aged; Niacin; Risk Factors

1993
[The effect of long-term Enduracin monotherapy on the clinical and biochemical status of patients with ischemic heart disease].
    Terapevticheskii arkhiv, 1997, Volume: 69, Issue:9

    Topics: Adult; Cardiovascular System; Coronary Artery Disease; Delayed-Action Preparations; Digestive System

1997
Antioxidants blunt high-density lipoprotein response to statin plus niacin therapy.
    Current atherosclerosis reports, 2001, Volume: 3, Issue:6

    Topics: Antioxidants; Cholesterol, HDL; Cholesterol, LDL; Cholesterol, VLDL; Clinical Trials as Topic; Coron

2001
Myocardial glucose utilization and optimization of (18)F-FDG PET imaging in patients with non-insulin-dependent diabetes mellitus, coronary artery disease, and left ventricular dysfunction.
    Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2001, Volume: 42, Issue:12

    Topics: Coronary Artery Disease; Diabetes Mellitus, Type 2; Female; Fluorodeoxyglucose F18; Glucose; Glucose

2001
Niacin-simvastatin combination benefits patients with coronary artery disease.
    Circulation, 2001, Dec-11, Volume: 104, Issue:24

    Topics: Antioxidants; Coronary Artery Disease; Drug Therapy, Combination; Humans; Hypolipidemic Agents; Niac

2001
Lipid-lowering drug use and cardiovascular events after myocardial infarction.
    The Annals of pharmacotherapy, 2002, Volume: 36, Issue:5

    Topics: Cholesterol; Clofibrate; Cohort Studies; Coronary Artery Disease; Coronary Disease; Female; Humans;

2002
The effects of simvastatin-niacin and antioxidant therapy on HDL.
    Progress in cardiovascular nursing, 2002,Spring, Volume: 17, Issue:2

    Topics: Antioxidants; Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Drug Therapy, Combination

2002
Multiple Methods for Reduction of Lipoprotein(a).
    Atherosclerosis, 2002, Volume: 163, Issue:2

    Topics: Ascorbic Acid; Carnitine; Coronary Artery Disease; Diet, Reducing; Estrogens; Exercise; Female; Huma

2002
A novel mechanism for the beneficial vascular effects of high-density lipoprotein cholesterol: enhanced vasorelaxation and increased endothelial nitric oxide synthase expression.
    American heart journal, 2002, Volume: 144, Issue:1

    Topics: Case-Control Studies; Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Endothelium, Vasc

2002
Evaluation of colestipol/niacin therapy with computer-derived coronary end point measures. A comparison of different measures of treatment effect.
    Circulation, 1992, Volume: 86, Issue:6

    Topics: Adult; Colestipol; Coronary Angiography; Coronary Artery Bypass; Coronary Artery Disease; Coronary V

1992
[Antilipemic agents and postprandial lipidemia].
    Klinische Wochenschrift, 1990, Volume: 68 Suppl 22

    Topics: Cholesterol; Chylomicrons; Coronary Artery Disease; Dietary Fats; Diterpenes; Female; Fenofibrate; H

1990
The effects of nicotinic acid treatment on high density lipoprotein particle size subclass levels in hyperlipidaemic subjects.
    Atherosclerosis, 1990, Volume: 83, Issue:2-3

    Topics: Adult; Cholesterol, HDL; Cholesterol, LDL; Coronary Artery Disease; Dose-Response Relationship, Drug

1990
Colestipol-niacin therapy and coronary atherosclerosis.
    JAMA, 1987, Nov-20, Volume: 258, Issue:19

    Topics: Adult; Colestipol; Coronary Artery Disease; Humans; Male; Middle Aged; Niacin; Polyamines; Research

1987
[Blood plasma prostanoids in coronary atherosclerosis patients].
    Vrachebnoe delo, 1986, Issue:8

    Topics: Adult; Aged; Coronary Artery Disease; Drug Evaluation; Female; Hemoperfusion; Humans; Male; Middle A

1986