Pioglitazone induces regression of coronary atherosclerotic plaques in patients with type 2 diabetes mellitus or impaired glucose tolerance: A randomized prospective study using intravascular ultrasound

被引:27
作者
Nakayama, Takashi [2 ]
Komiyama, Nobuyuki [1 ]
Yokoyama, Masaki [2 ]
Namikawa, Susumu [2 ]
Kuroda, Nakabumi [2 ]
Kobayashi, Yoshio [2 ]
Komuro, Issei [2 ]
机构
[1] Saitama Med Univ, Int Med Ctr, Dept Cardiol, Hidaka, Saitama 3501298, Japan
[2] Chiba Univ, Grad Sch Med, Dept Cardiovasc Sci & Med, Chiba, Japan
关键词
Vascular pharmacology; Intravascular imaging; PPAR-gamma agonist; Coronary plaque stabilization; LIPID-LOWERING THERAPY; INSULIN-RESISTANCE SYNDROME; INTIMA-MEDIA THICKNESS; MYOCARDIAL-INFARCTION; CARDIOVASCULAR-DISEASE; GLYCEMIC CONTROL; ARTERY-DISEASE; MICROVASCULAR COMPLICATIONS; STENT IMPLANTATION; GENE-EXPRESSION;
D O I
10.1016/j.ijcard.2008.08.031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: A large clinical trial clarified that pioglitazone reduces cardiovascular events in diabetic patients. However, effects of pioglitazone on structure of coronary atherosclerotic plaques have not been demonstrated. We examined whether pioglitazone reduces volumes of coronary atherosclerotic plaques using intravascular ultrasound (IVUS). Methods: Twenty-six consecutive patients with type 2 diabetes mellitus (DM) or impaired glucose tolerance (IGT) undergoing percutaneous coronary intervention (PCI) were enrolled. Echolucent plaques without significant stenosis were selected in IVUS video images at non-PCI-influenced coronary segments and volumetric analysis of the targeted plaques was performed. The patients were randomly assigned into 2 groups: pioglitazone group consisted of 13 patients taking pioglitazone 15 mg/day for initial 14 days after PCI and subsequent 30 mg/day during 6-month follow-up, and control group with 13 patients as control. The plaque volumes and some parameters such as plasma lipid profiles and high-sensitive C-reacting protein (hs-CRP) levels were compared between baseline and the follow-up in those groups. Results: In the pioglitazone group after 6 months, the plaque volume was significantly reduced (101.3 +/- 32.1 to 94.6 +/- 33.6 mm(3), -7.2%; p=0.0023), plasma triglyceride was significantly decreased (-14.9%) and high density lipoprotein cholesterol was substantially increased (+20.0%) without any significant change in low density lipoprotein cholesterol (LDL-C). Also, hs-CRP level tended to be decreased. However, no significant change in plaque volumes and those parameters was observed in the control group. Conclusions: Pioglitazone may induce regression of coronary atherosclerotic plaques without LDL-C reduction in patients with DM and IGT. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:157 / 165
页数:9
相关论文
共 58 条
  • [1] Association of systolic blood pressure with macrovascular and microvascular complications of type 2 diabetes (UKPDS 36): prospective observational study
    Adler, AI
    Stratton, IM
    Neil, HAW
    Yudkin, JS
    Matthews, DR
    Cull, CA
    Wright, AD
    Turner, RC
    Holman, RR
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2000, 321 (7258): : 412 - 419
  • [2] Pioglitazone enhances cytokine-induced apoptosis in vascular smooth muscle cells and reduces intimal hyperplasia
    Aizawa, Y
    Kawabe, J
    Hasebe, N
    Takehara, N
    Kikuchi, K
    [J]. CIRCULATION, 2001, 104 (04) : 455 - 460
  • [3] *AM COLL CARD CLIN, 2001, EUR J ECHOCARDIOGR, V4, P299
  • [4] [Anonymous], AM J MED
  • [5] Pioglitazone hydrochloride monotherapy improves glycemic control in the treatment of patients with type 2 diabetes - A 6-month randomized placebo-controlled dose-response study
    Aronoff, S
    Rosenblatt, S
    Braithwaite, S
    Egan, JW
    Mathisen, AL
    Schneider, RL
    [J]. DIABETES CARE, 2000, 23 (11) : 1605 - 1611
  • [6] PPAR-γ dependent and independent effects on macrophage-gene expression in lipid metabolism and inflammation
    Chawla, A
    Barak, Y
    Nagy, L
    Liao, D
    Tontonoz, P
    Evans, RM
    [J]. NATURE MEDICINE, 2001, 7 (01) : 48 - 52
  • [7] Ethical authorship and publishing
    Coats, Andrew J. S.
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2009, 131 (02) : 149 - 150
  • [8] Primary prevention of cardiovascular disease with atorvastatin in type 2 diabetes in the Collaborative Atorvastatin Diabetes Study (CARDS): multicentre randomised placebo-controlled trial
    Colhoun, HM
    Betteridge, DJ
    Durrington, PN
    Hitman, GA
    Neil, HAW
    Livingstone, SJ
    Thomason, MJ
    Mackness, MI
    Charlton-Menys, V
    Fuller, JH
    [J]. LANCET, 2004, 364 (9435) : 685 - 696
  • [9] Pioglitazone and rosiglitazone have different effects on serum lipoprotein particle concentrations and sizes in patients with type 2 diabetes and dyslipidemia
    Deeg, Mark A.
    Buse, John B.
    Goldberg, Ronald B.
    Kendall, David M.
    Zagar, Anthony J.
    Jacober, Scott J.
    Khan, Mehmood A.
    Perez, Alfonzo T.
    Tan, Meng H.
    [J]. DIABETES CARE, 2007, 30 (10) : 2458 - 2464
  • [10] Secondary prevention of macrovascular events in patients with type 2 diabetes in the PROactive Study (PROspective pioglitAzone Clinical Trial In macroVascular Events):: a randomised controlled trial
    Dormandy, JA
    Charbonnel, B
    Eckland, DJA
    Erdmann, E
    Massi-Benedetti, M
    Kmoules, IK
    Skene, AM
    Tan, MH
    Lefébvre, PJ
    Murray, GD
    Standl, E
    Wilcox, RG
    Wlhelmsen, L
    Betteridge, J
    Birkeland, K
    Golay, A
    Heine, RJ
    Korányi, L
    Laakso, M
    Mokán, M
    Norkus, A
    Pirags, V
    Podar, T
    Scheen, A
    Scherbaum, W
    Schernthaner, G
    Schmitz, O
    Skrha, J
    Smith, U
    Taton, J
    [J]. LANCET, 2005, 366 (9493) : 1279 - 1289