Effects of Niacin on Glucose Levels, Coronary Stenosis Progression, and Clinical Events in Subjects With Normal Baseline Glucose Levels (<100 mg/dl): A Combined Analysis of the Familial Atherosclerosis Treatment Study (FATS), HDL-Atherosclerosis Treatment Study (HATS), Armed Forces Regression Study (AFREGS), and Carotid Plaque Composition by MRI During Lipid-Lowering (CPC) Study

Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin’s effects on the glucose levels and atherosclerosis in subjects with normal glucose levels have not been well established. We examined the effect of niacin on the glucose levels, coro...

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Published inThe American journal of cardiology Vol. 111; no. 3; pp. 352 - 355
Main Authors Phan, Binh An P., Muñoz, Luis, Shadzi, Pey, Isquith, Daniel, Triller, Michael, Brown, B. Greg, Zhao, Xue-Qiao
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.02.2013
Elsevier Limited
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Online AccessGet full text
ISSN0002-9149
1879-1913
1879-1913
DOI10.1016/j.amjcard.2012.09.034

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Abstract Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin’s effects on the glucose levels and atherosclerosis in subjects with normal glucose levels have not been well established. We examined the effect of niacin on the glucose levels, coronary stenosis progression using quantitative coronary angiography, and clinical events in 407 subjects who had a baseline glucose level <100 mg/dl and were enrolled in the Familial Atherosclerosis Treatment Study (FATS), HDL-Atherosclerosis Treatment Study (HATS), Armed Forces Regression Study (AFREGS), or Carotid Plaque Composition by MRI during lipid-lowering (CPC) study testing active niacin therapy. Although the fasting glucose levels increased significantly within 3 years in both subjects treated with niacin (from 85.6 ± 9.5 to 95.5 ± 19.7 mg/dl, p <0.001) and without niacin (from 85.2 ± 9.6 to 90 ± 17.9 mg/dl, p = 0.009), those treated with niacin had a significantly larger increase in glucose levels than those not taking niacin (9.88 vs 4.05 mg/dl, p = 0.002). Overall, 29% of subjects developed impaired fasting glucose within 3 years. Incident impaired fasting glucose was significantly more likely to be observed in subjects treated with niacin than in those who were not. However, the frequency of new-onset diabetes mellitus did not differ significantly between the 2 groups (5.6% vs 4.8%, p = 0.5). Niacin-treated subjects compared to untreated subjects had significantly less change in mean coronary stenosis (0.1 ± 0.3% vs 2 ± 12%, p <0.0001) and less major cardiovascular events (8% vs 21%, p = 0.001). In conclusion, the use of niacin for 3 years in subjects with normal baseline glucose levels was associated with an increase in blood glucose levels and the risk of developing impaired fasting glucose, but not diabetes mellitus, and was associated with a significantly reduced incidence of coronary stenosis progression and major cardiovascular events.
AbstractList Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin’s effects on the glucose levels and atherosclerosis in subjects with normal glucose levels have not been well established. We examined the effect of niacin on the glucose levels, coronary stenosis progression using quantitative coronary angiography, and clinical events in 407 subjects who had a baseline glucose level <100 mg/dl and were enrolled in the Familial Atherosclerosis Treatment Study (FATS), HDL-Atherosclerosis Treatment Study (HATS), Armed Forces Regression Study (AFREGS), or Carotid Plaque Composition by MRI during lipid-lowering (CPC) study testing active niacin therapy. Although the fasting glucose levels increased significantly within 3 years in both subjects treated with niacin (from 85.6 ± 9.5 to 95.5 ± 19.7 mg/dl, p <0.001) and without niacin (from 85.2 ± 9.6 to 90 ± 17.9 mg/dl, p = 0.009), those treated with niacin had a significantly larger increase in glucose levels than those not taking niacin (9.88 vs 4.05 mg/dl, p = 0.002). Overall, 29% of subjects developed impaired fasting glucose within 3 years. Incident impaired fasting glucose was significantly more likely to be observed in subjects treated with niacin than in those who were not. However, the frequency of new-onset diabetes mellitus did not differ significantly between the 2 groups (5.6% vs 4.8%, p = 0.5). Niacin-treated subjects compared to untreated subjects had significantly less change in mean coronary stenosis (0.1 ± 0.3% vs 2 ± 12%, p <0.0001) and less major cardiovascular events (8% vs 21%, p = 0.001). In conclusion, the use of niacin for 3 years in subjects with normal baseline glucose levels was associated with an increase in blood glucose levels and the risk of developing impaired fasting glucose, but not diabetes mellitus, and was associated with a significantly reduced incidence of coronary stenosis progression and major cardiovascular events.
Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin's effects on the glucose levels and atherosclerosis in subjects with normal glucose levels have not been well established. We examined the effect of niacin on the glucose levels, coronary stenosis progression using quantitative coronary angiography, and clinical events in 407 subjects who had a baseline glucose level <100 mg/dl and were enrolled in the Familial Atherosclerosis Treatment Study (FATS), HDL-Atherosclerosis Treatment Study (HATS), Armed Forces Regression Study (AFREGS), or Carotid Plaque Composition by MRI during lipid-lowering (CPC) study testing active niacin therapy. Although the fasting glucose levels increased significantly within 3 years in both subjects treated with niacin (from 85.6 ± 9.5 to 95.5 ± 19.7 mg/dl, p <0.001) and without niacin (from 85.2 ± 9.6 to 90 ± 17.9 mg/dl, p = 0.009), those treated with niacin had a significantly larger increase in glucose levels than those not taking niacin (9.88 vs 4.05 mg/dl, p = 0.002). Overall, 29% of subjects developed impaired fasting glucose within 3 years. Incident impaired fasting glucose was significantly more likely to be observed in subjects treated with niacin than in those who were not. However, the frequency of new-onset diabetes mellitus did not differ significantly between the 2 groups (5.6% vs 4.8%, p = 0.5). Niacin-treated subjects compared to untreated subjects had significantly less change in mean coronary stenosis (0.1 ± 0.3% vs 2 ± 12%, p <0.0001) and less major cardiovascular events (8% vs 21%, p = 0.001). In conclusion, the use of niacin for 3 years in subjects with normal baseline glucose levels was associated with an increase in blood glucose levels and the risk of developing impaired fasting glucose, but not diabetes mellitus, and was associated with a significantly reduced incidence of coronary stenosis progression and major cardiovascular events.Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin's effects on the glucose levels and atherosclerosis in subjects with normal glucose levels have not been well established. We examined the effect of niacin on the glucose levels, coronary stenosis progression using quantitative coronary angiography, and clinical events in 407 subjects who had a baseline glucose level <100 mg/dl and were enrolled in the Familial Atherosclerosis Treatment Study (FATS), HDL-Atherosclerosis Treatment Study (HATS), Armed Forces Regression Study (AFREGS), or Carotid Plaque Composition by MRI during lipid-lowering (CPC) study testing active niacin therapy. Although the fasting glucose levels increased significantly within 3 years in both subjects treated with niacin (from 85.6 ± 9.5 to 95.5 ± 19.7 mg/dl, p <0.001) and without niacin (from 85.2 ± 9.6 to 90 ± 17.9 mg/dl, p = 0.009), those treated with niacin had a significantly larger increase in glucose levels than those not taking niacin (9.88 vs 4.05 mg/dl, p = 0.002). Overall, 29% of subjects developed impaired fasting glucose within 3 years. Incident impaired fasting glucose was significantly more likely to be observed in subjects treated with niacin than in those who were not. However, the frequency of new-onset diabetes mellitus did not differ significantly between the 2 groups (5.6% vs 4.8%, p = 0.5). Niacin-treated subjects compared to untreated subjects had significantly less change in mean coronary stenosis (0.1 ± 0.3% vs 2 ± 12%, p <0.0001) and less major cardiovascular events (8% vs 21%, p = 0.001). In conclusion, the use of niacin for 3 years in subjects with normal baseline glucose levels was associated with an increase in blood glucose levels and the risk of developing impaired fasting glucose, but not diabetes mellitus, and was associated with a significantly reduced incidence of coronary stenosis progression and major cardiovascular events.
Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin's effects on the glucose levels and atherosclerosis in subjects with normal glucose levels have not been well established. We examined the effect of niacin on the glucose levels, coronary stenosis progression using quantitative coronary angiography, and clinical events in 407 subjects who had a baseline glucose level <100 mg/dl and were enrolled in the Familial Atherosclerosis Treatment Study (FATS), HDL-Atherosclerosis Treatment Study (HATS), Armed Forces Regression Study (AFREGS), or Carotid Plaque Composition by MRI during lipid-lowering (CPC) study testing active niacin therapy. Although the fasting glucose levels increased significantly within 3 years in both subjects treated with niacin (from 85.6 ± 9.5 to 95.5 ± 19.7 mg/dl, p <0.001) and without niacin (from 85.2 ± 9.6 to 90 ± 17.9 mg/dl, p = 0.009), those treated with niacin had a significantly larger increase in glucose levels than those not taking niacin (9.88 vs 4.05 mg/dl, p = 0.002). Overall, 29% of subjects developed impaired fasting glucose within 3 years. Incident impaired fasting glucose was significantly more likely to be observed in subjects treated with niacin than in those who were not. However, the frequency of new-onset diabetes mellitus did not differ significantly between the 2 groups (5.6% vs 4.8%, p = 0.5). Niacin-treated subjects compared to untreated subjects had significantly less change in mean coronary stenosis (0.1 ± 0.3% vs 2 ± 12%, p <0.0001) and less major cardiovascular events (8% vs 21%, p = 0.001). In conclusion, the use of niacin for 3 years in subjects with normal baseline glucose levels was associated with an increase in blood glucose levels and the risk of developing impaired fasting glucose, but not diabetes mellitus, and was associated with a significantly reduced incidence of coronary stenosis progression and major cardiovascular events.
Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin’s effects on the glucose levels and atherosclerosis in subjects with normal glucose levels have not been well established. We examined the effect of niacin on the glucose levels, coronary stenosis progression using quantitative coronary angiography, and clinical events in 407 subjects who had a baseline glucose level <100 mg/dl and were enrolled in the Familial Atherosclerosis Treatment Study (FATS), HDL-Atherosclerosis Treatment Study (HATS), Armed Forces Regression Study (AFREGS), or Carotid Plaque Composition by MRI during lipid-lowering (CPC) study testing active niacin therapy. Although the fasting glucose levels increased significantly within 3 years in both subjects treated with niacin (from 85.6 – 9.5 to 95.5 – 19.7 mg/dl, p <0.001) and without niacin (from 85.2 – 9.6 to 90 – 17.9 mg/dl, p =0.009), those treated with niacin had a significantly larger increase in glucose levels than those not taking niacin (9.88 vs 4.05 mg/dl, p =0.002). Overall, 29% of subjects developed impaired fasting glucose within 3 years. Incident impaired fasting glucose was significantly more likely to be observed in subjects treated with niacin than in those who were not. However, the frequency of new-onset diabetes mellitus did not differ significantly between the 2 groups (5.6% vs 4.8%, p = 0.5). Niacin-treated subjects compared to untreated subjects had significantly less change in mean coronary stenosis (0.1 – 0.3% vs 2 – 12%, p <0.0001) and less major cardiovascular events (8% vs 21%, p = 0.001). In conclusion, the use of niacin for 3 years in subjects with normal baseline glucose levels was associated with an increase in blood glucose levels and the risk of developing impaired fasting glucose, but not diabetes mellitus, and was associated with a significantly reduced incidence of coronary stenosis progression and major cardiovascular events.
Author Triller, Michael
Phan, Binh An P.
Brown, B. Greg
Muñoz, Luis
Isquith, Daniel
Shadzi, Pey
Zhao, Xue-Qiao
AuthorAffiliation b Division of Cardiology, University of Washington School of Medicine, Seattle, Washington
a Division of Cardiology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois
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Cites_doi 10.1001/jama.1975.03240160024021
10.1146/annurev.pharmtox.48.113006.094746
10.3109/00365519609088812
10.1056/NEJM199011083231901
10.1056/NEJMoa1107579
10.1001/jama.284.10.1263
10.1172/JCI115145
10.7326/0003-4819-142-2-200501180-00008
10.1161/01.CIR.0000148955.19792.8D
10.1056/NEJMoa011090
10.1172/JCI110908
10.2337/diacare.4.4.493
10.1001/archinte.162.14.1568
10.1016/j.amjcard.2004.09.013
10.1016/j.jcmg.2011.06.013
10.1016/j.jacl.2007.05.003
10.1161/circ.106.25.3143
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References Brown, Zhao, Chait, Fisher, Cheung, Morse, Dowdy, Marino, Bolson, Alaupovic, Frohlich, Albers (bib7) 2001; 345
(bib1) 2002; 106
McCulloch, Kahn, Schwartz, Koerker, Palmer (bib13) 1991; 87
Fink, Kolterman, Griffin, Olefsky (bib11) 1983; 71
Canner, Furberg, Terrin, McGovern (bib16) 2005; 95
Whitney, Krasuski, Personius, Michalek, Maranian, Kolasa, Monick, Brown, Gotto (bib8) 2005; 142
DeFronzo (bib10) 1981; 4
Boden, Probstfield, Anderson, Chaitman, Desvignes-Nickens, Koprowicz, McBride, Teo, Weintraub (bib17) 2011; 365
(bib2) 1975; 231
Gille, Bodor, Ahmed, Offermanns (bib12) 2008; 48
Brown, Albers, Fisher, Schaefer, Lin, Kaplan, Zhao, Bisson, Fitzpatrick, Dodge (bib3) 1990; 323
Vittone, Chait, Morse, Fish, Brown, Zhao (bib15) 2007; 1
Zhao, Dong, Hatsukami, Phan, Chu, Moore, Lane, Neradilek, Polissar, Monick, Lee, Underhill, Yuan (bib9) 2011; 4
Alvarsson, Grill (bib14) 1996; 56
Taylor, Sullenberger, Lee, Lee, Grace (bib4) 2004; 110
Elam, Hunninghake, Davis, Garg, Johnson, Egan, Kostis, Sheps, Brinton (bib5) 2000; 284
Grundy, Vega, McGovern, Tulloch, Kendall, Fitz-Patrick, Ganda, Rosenson, Buse, Robertson, Sheehan (bib6) 2002; 162
McCulloch (10.1016/j.amjcard.2012.09.034_bib13) 1991; 87
Whitney (10.1016/j.amjcard.2012.09.034_bib8) 2005; 142
(10.1016/j.amjcard.2012.09.034_bib1) 2002; 106
Elam (10.1016/j.amjcard.2012.09.034_bib5) 2000; 284
Grundy (10.1016/j.amjcard.2012.09.034_bib6) 2002; 162
Fink (10.1016/j.amjcard.2012.09.034_bib11) 1983; 71
Brown (10.1016/j.amjcard.2012.09.034_bib3) 1990; 323
Taylor (10.1016/j.amjcard.2012.09.034_bib4) 2004; 110
Brown (10.1016/j.amjcard.2012.09.034_bib7) 2001; 345
Boden (10.1016/j.amjcard.2012.09.034_bib17) 2011; 365
Gille (10.1016/j.amjcard.2012.09.034_bib12) 2008; 48
Alvarsson (10.1016/j.amjcard.2012.09.034_bib14) 1996; 56
Zhao (10.1016/j.amjcard.2012.09.034_bib9) 2011; 4
(10.1016/j.amjcard.2012.09.034_bib2) 1975; 231
Canner (10.1016/j.amjcard.2012.09.034_bib16) 2005; 95
DeFronzo (10.1016/j.amjcard.2012.09.034_bib10) 1981; 4
Vittone (10.1016/j.amjcard.2012.09.034_bib15) 2007; 1
6345584 - J Clin Invest. 1983 Jun;71(6):1523-35
11757504 - N Engl J Med. 2001 Nov 29;345(22):1583-92
12123399 - Arch Intern Med. 2002 Jul 22;162(14):1568-76
22085343 - N Engl J Med. 2011 Dec 15;365(24):2255-67
18591993 - J Clin Lipidol. 2007 Jul;1(3):203-210
17705685 - Annu Rev Pharmacol Toxicol. 2008;48:79-106
1088963 - JAMA. 1975 Jan 27;231(4):360-81
15642562 - Am J Cardiol. 2005 Jan 15;95(2):254-7
7049632 - Diabetes Care. 1981 Jul-Aug;4(4):493-501
21920335 - JACC Cardiovasc Imaging. 2011 Sep;4(9):977-86
15537681 - Circulation. 2004 Dec 7;110(23):3512-7
10979113 - JAMA. 2000 Sep 13;284(10):1263-70
2215615 - N Engl J Med. 1990 Nov 8;323(19):1289-98
12485966 - Circulation. 2002 Dec 17;106(25):3143-421
8903118 - Scand J Clin Lab Invest. 1996 Oct;56(6):563-70
1826300 - J Clin Invest. 1991 Apr;87(4):1395-401
15657157 - Ann Intern Med. 2005 Jan 18;142(2):95-104
References_xml – volume: 71
  start-page: 1523
  year: 1983
  end-page: 1535
  ident: bib11
  article-title: Mechanisms of insulin resistance in aging
  publication-title: J Clin Invest
– volume: 48
  start-page: 79
  year: 2008
  end-page: 106
  ident: bib12
  article-title: Nicotinic acid: pharmacological effects and mechanisms of action
  publication-title: Annu Rev Pharmacol Toxicol
– volume: 1
  start-page: 203
  year: 2007
  end-page: 210
  ident: bib15
  article-title: Niacin plus simvastatin reduces coronary stenosis progression among patients with metabolic syndrome despite a modest increase in insulin resistance: a subgroup analysis of the HDL-Atherosclerosis Treatment Study (HATS)
  publication-title: J Clin Lipidol
– volume: 323
  start-page: 1289
  year: 1990
  end-page: 1298
  ident: bib3
  article-title: Regression of coronary artery disease as a result of intensive lipid-lowering therapy in men with high levels of apolipoprotein B
  publication-title: N Engl J Med
– volume: 95
  start-page: 254
  year: 2005
  end-page: 257
  ident: bib16
  article-title: Benefits of niacin by glycemic status in patients with healed myocardial infarction (from the Coronary Drug Project)
  publication-title: Am J Cardiol
– volume: 4
  start-page: 493
  year: 1981
  end-page: 501
  ident: bib10
  article-title: Glucose intolerance and aging
  publication-title: Diabetes Care
– volume: 87
  start-page: 1395
  year: 1991
  end-page: 1401
  ident: bib13
  article-title: Effect of nicotinic acid-induced insulin resistance on pancreatic B cell function in normal and streptozocin-treated baboons
  publication-title: J Clin Invest
– volume: 284
  start-page: 1263
  year: 2000
  end-page: 1270
  ident: bib5
  article-title: Effect of niacin on lipid and lipoprotein levels and glycemic control in patients with diabetes and peripheral arterial disease: the ADMIT study: a randomized trial. Arterial Disease Multiple Intervention Trial
  publication-title: JAMA
– volume: 345
  start-page: 1583
  year: 2001
  end-page: 1592
  ident: bib7
  article-title: Simvastatin and niacin, antioxidant vitamins, or the combination for the prevention of coronary disease
  publication-title: N Engl J Med
– volume: 142
  start-page: 95
  year: 2005
  end-page: 104
  ident: bib8
  article-title: A randomized trial of a strategy for increasing high-density lipoprotein cholesterol levels: effects on progression of coronary heart disease and clinical events
  publication-title: Ann Intern Med
– volume: 56
  start-page: 563
  year: 1996
  end-page: 570
  ident: bib14
  article-title: Impact of nicotinic acid treatment on insulin secretion and insulin sensitivity in low and high insulin responders
  publication-title: Scand J Clin Lab Invest
– volume: 365
  start-page: 2255
  year: 2011
  end-page: 2267
  ident: bib17
  article-title: Niacin in patients with low HDL cholesterol levels receiving intensive statin therapy
  publication-title: N Engl J Med
– volume: 110
  start-page: 3512
  year: 2004
  end-page: 3517
  ident: bib4
  article-title: Arterial Biology for the Investigation of the Treatment Effects of Reducing Cholesterol (ARBITER) 2: a double-blind, placebo-controlled study of extended-release niacin on atherosclerosis progression in secondary prevention patients treated with statins
  publication-title: Circulation
– volume: 162
  start-page: 1568
  year: 2002
  end-page: 1576
  ident: bib6
  article-title: Efficacy, safety, and tolerability of once-daily niacin for the treatment of dyslipidemia associated with type 2 diabetes: results of the assessment of diabetes control and evaluation of the efficacy of niaspan trial
  publication-title: Arch Intern Med
– volume: 106
  start-page: 3143
  year: 2002
  end-page: 3421
  ident: bib1
  article-title: Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report
  publication-title: Circulation
– volume: 231
  start-page: 360
  year: 1975
  end-page: 381
  ident: bib2
  article-title: Clofibrate and niacin in coronary heart disease
  publication-title: JAMA
– volume: 4
  start-page: 977
  year: 2011
  end-page: 986
  ident: bib9
  article-title: MR imaging of carotid plaque composition during lipid-lowering therapy a prospective assessment of effect and time course
  publication-title: JACC Cardiovasc Imaging
– volume: 231
  start-page: 360
  year: 1975
  ident: 10.1016/j.amjcard.2012.09.034_bib2
  article-title: Clofibrate and niacin in coronary heart disease
  publication-title: JAMA
  doi: 10.1001/jama.1975.03240160024021
– volume: 48
  start-page: 79
  year: 2008
  ident: 10.1016/j.amjcard.2012.09.034_bib12
  article-title: Nicotinic acid: pharmacological effects and mechanisms of action
  publication-title: Annu Rev Pharmacol Toxicol
  doi: 10.1146/annurev.pharmtox.48.113006.094746
– volume: 56
  start-page: 563
  year: 1996
  ident: 10.1016/j.amjcard.2012.09.034_bib14
  article-title: Impact of nicotinic acid treatment on insulin secretion and insulin sensitivity in low and high insulin responders
  publication-title: Scand J Clin Lab Invest
  doi: 10.3109/00365519609088812
– volume: 323
  start-page: 1289
  year: 1990
  ident: 10.1016/j.amjcard.2012.09.034_bib3
  article-title: Regression of coronary artery disease as a result of intensive lipid-lowering therapy in men with high levels of apolipoprotein B
  publication-title: N Engl J Med
  doi: 10.1056/NEJM199011083231901
– volume: 365
  start-page: 2255
  year: 2011
  ident: 10.1016/j.amjcard.2012.09.034_bib17
  article-title: Niacin in patients with low HDL cholesterol levels receiving intensive statin therapy
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa1107579
– volume: 284
  start-page: 1263
  year: 2000
  ident: 10.1016/j.amjcard.2012.09.034_bib5
  article-title: Effect of niacin on lipid and lipoprotein levels and glycemic control in patients with diabetes and peripheral arterial disease: the ADMIT study: a randomized trial. Arterial Disease Multiple Intervention Trial
  publication-title: JAMA
  doi: 10.1001/jama.284.10.1263
– volume: 87
  start-page: 1395
  year: 1991
  ident: 10.1016/j.amjcard.2012.09.034_bib13
  article-title: Effect of nicotinic acid-induced insulin resistance on pancreatic B cell function in normal and streptozocin-treated baboons
  publication-title: J Clin Invest
  doi: 10.1172/JCI115145
– volume: 142
  start-page: 95
  year: 2005
  ident: 10.1016/j.amjcard.2012.09.034_bib8
  article-title: A randomized trial of a strategy for increasing high-density lipoprotein cholesterol levels: effects on progression of coronary heart disease and clinical events
  publication-title: Ann Intern Med
  doi: 10.7326/0003-4819-142-2-200501180-00008
– volume: 110
  start-page: 3512
  year: 2004
  ident: 10.1016/j.amjcard.2012.09.034_bib4
  article-title: Arterial Biology for the Investigation of the Treatment Effects of Reducing Cholesterol (ARBITER) 2: a double-blind, placebo-controlled study of extended-release niacin on atherosclerosis progression in secondary prevention patients treated with statins
  publication-title: Circulation
  doi: 10.1161/01.CIR.0000148955.19792.8D
– volume: 345
  start-page: 1583
  year: 2001
  ident: 10.1016/j.amjcard.2012.09.034_bib7
  article-title: Simvastatin and niacin, antioxidant vitamins, or the combination for the prevention of coronary disease
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa011090
– volume: 71
  start-page: 1523
  year: 1983
  ident: 10.1016/j.amjcard.2012.09.034_bib11
  article-title: Mechanisms of insulin resistance in aging
  publication-title: J Clin Invest
  doi: 10.1172/JCI110908
– volume: 4
  start-page: 493
  year: 1981
  ident: 10.1016/j.amjcard.2012.09.034_bib10
  article-title: Glucose intolerance and aging
  publication-title: Diabetes Care
  doi: 10.2337/diacare.4.4.493
– volume: 162
  start-page: 1568
  year: 2002
  ident: 10.1016/j.amjcard.2012.09.034_bib6
  article-title: Efficacy, safety, and tolerability of once-daily niacin for the treatment of dyslipidemia associated with type 2 diabetes: results of the assessment of diabetes control and evaluation of the efficacy of niaspan trial
  publication-title: Arch Intern Med
  doi: 10.1001/archinte.162.14.1568
– volume: 95
  start-page: 254
  year: 2005
  ident: 10.1016/j.amjcard.2012.09.034_bib16
  article-title: Benefits of niacin by glycemic status in patients with healed myocardial infarction (from the Coronary Drug Project)
  publication-title: Am J Cardiol
  doi: 10.1016/j.amjcard.2004.09.013
– volume: 4
  start-page: 977
  year: 2011
  ident: 10.1016/j.amjcard.2012.09.034_bib9
  article-title: MR imaging of carotid plaque composition during lipid-lowering therapy a prospective assessment of effect and time course
  publication-title: JACC Cardiovasc Imaging
  doi: 10.1016/j.jcmg.2011.06.013
– volume: 1
  start-page: 203
  year: 2007
  ident: 10.1016/j.amjcard.2012.09.034_bib15
  article-title: Niacin plus simvastatin reduces coronary stenosis progression among patients with metabolic syndrome despite a modest increase in insulin resistance: a subgroup analysis of the HDL-Atherosclerosis Treatment Study (HATS)
  publication-title: J Clin Lipidol
  doi: 10.1016/j.jacl.2007.05.003
– volume: 106
  start-page: 3143
  year: 2002
  ident: 10.1016/j.amjcard.2012.09.034_bib1
  article-title: Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report
  publication-title: Circulation
  doi: 10.1161/circ.106.25.3143
– reference: 2215615 - N Engl J Med. 1990 Nov 8;323(19):1289-98
– reference: 1826300 - J Clin Invest. 1991 Apr;87(4):1395-401
– reference: 12123399 - Arch Intern Med. 2002 Jul 22;162(14):1568-76
– reference: 15642562 - Am J Cardiol. 2005 Jan 15;95(2):254-7
– reference: 17705685 - Annu Rev Pharmacol Toxicol. 2008;48:79-106
– reference: 21920335 - JACC Cardiovasc Imaging. 2011 Sep;4(9):977-86
– reference: 11757504 - N Engl J Med. 2001 Nov 29;345(22):1583-92
– reference: 22085343 - N Engl J Med. 2011 Dec 15;365(24):2255-67
– reference: 7049632 - Diabetes Care. 1981 Jul-Aug;4(4):493-501
– reference: 18591993 - J Clin Lipidol. 2007 Jul;1(3):203-210
– reference: 12485966 - Circulation. 2002 Dec 17;106(25):3143-421
– reference: 10979113 - JAMA. 2000 Sep 13;284(10):1263-70
– reference: 8903118 - Scand J Clin Lab Invest. 1996 Oct;56(6):563-70
– reference: 15537681 - Circulation. 2004 Dec 7;110(23):3512-7
– reference: 1088963 - JAMA. 1975 Jan 27;231(4):360-81
– reference: 15657157 - Ann Intern Med. 2005 Jan 18;142(2):95-104
– reference: 6345584 - J Clin Invest. 1983 Jun;71(6):1523-35
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Snippet Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin’s effects on the glucose levels and...
Although the effect of niacin on the glucose levels in subjects with diabetes mellitus has been investigated, niacin's effects on the glucose levels and...
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StartPage 352
SubjectTerms Blood Glucose - metabolism
Cardiovascular
Cardiovascular disease
Carotid Stenosis - blood
Carotid Stenosis - complications
Carotid Stenosis - drug therapy
Cholesterol
Cholesterol, HDL - blood
Cholesterol, LDL - blood
Coronary Angiography
Coronary Stenosis - diagnosis
Coronary Stenosis - drug therapy
Coronary Stenosis - etiology
Diabetes
Disease Progression
Female
Follow-Up Studies
Glucose
Humans
Hypolipidemic Agents - therapeutic use
Insulin
Lipids - blood
Magnetic Resonance Imaging - methods
Male
Middle Aged
Niacin - therapeutic use
Plaque, Atherosclerotic - blood
Plaque, Atherosclerotic - complications
Plaque, Atherosclerotic - drug therapy
Treatment Outcome
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Title Effects of Niacin on Glucose Levels, Coronary Stenosis Progression, and Clinical Events in Subjects With Normal Baseline Glucose Levels (<100 mg/dl): A Combined Analysis of the Familial Atherosclerosis Treatment Study (FATS), HDL-Atherosclerosis Treatment Study (HATS), Armed Forces Regression Study (AFREGS), and Carotid Plaque Composition by MRI During Lipid-Lowering (CPC) Study
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