Effects of pioglitazone in familial combined hyperlipidaemia

被引:10
作者
Abbink, EJ
De Graaf, J
De Haan, JH
Heerschap, A
Stalenhoef, AF
Tack, CJ
机构
[1] Univ Med Ctr Nijmegen, Dept Med, Div Gen Internal Med, NL-6500 HB Nijmegen, Netherlands
[2] Univ Med Ctr Nijmegen, Dept Radiol, NL-6500 HB Nijmegen, Netherlands
关键词
body fat distribution; endothelial function; familial combined hyperlipidaemia; insulin sensitivity; pioglitazone;
D O I
10.1111/j.1365-2796.2005.01579.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. Familial combined hyperlipidaemia (FCH) is associated with insulin resistance. We hypothesized that pioglitazone treatment of FCH patients might increase insulin sensitivity, but may also improve serum lipid levels, body fat distribution, intramyocellular lipids (IMCL) and endothelia function. Design. Double blind, randomized, cross-over study. Subjects. Seventeen FCH patients. Interventions. Sixteen weeks of pioglitazone treatment (30 mg) compared with 16 weeks of placebo. Main outcome measurements. Insulin sensitivity was measured using the hyperinsulinaemic euglycaemic clamp procedure, body fat distribution and IMCL using magnetic resonance techniques and endothelial function using flow-mediated vasodilatation. Results. Pioglitazone improved insulin sensitivity (M value 37.7 +/- 3.6 mu mol min(-1) kg(-1) vs. 33.0 +/- 3.3 mu mol min(-1) kg(-1) during placebo. P < 0.05) and LDL composition by increasing the K value (-0.11 +/- 0.06 vs. -0.20 +/- 0.06 during placebo, P < 0.05). However. pioglitazone did not affect other serum lipid levels. Endothelial function, body fat distribution and IMCL were also not affected. In addition. pioglitazone was associated with a decrease in liver enzymes (alkaline phosphatase). Conclusion. Pioglitazone treatment of FCH patients without type 2 diabetes mellitus increases insulin sensitivity, decreases liver enzymes and improves LDL composition but has a neutral effect on total serum lipid levels. The change in insulin sensitivity might be too small to induce chances in endothelial function. body fat distribution and IMCL.
引用
收藏
页码:107 / 116
页数:10
相关论文
共 47 条
[1]   No role of calcium- and ATP-dependent potassium channels in insulin-induced vasodilation in humans in vivo [J].
Abbink, EJ ;
Walker, AJ ;
van der Sluijs, HA ;
Tack, CJ ;
Smits, P .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2002, 18 (02) :143-148
[2]   USE OF A HEATED SUPERFICIAL HAND VEIN AS AN ALTERNATIVE SITE FOR THE MEASUREMENT OF AMINO-ACID-CONCENTRATIONS AND FOR THE STUDY OF GLUCOSE AND ALANINE KINETICS IN MAN [J].
ABUMRAD, NN ;
RABIN, D ;
DIAMOND, MP ;
LACY, WW .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1981, 30 (09) :936-940
[3]   Decreased plasma adiponectin concentrations are closely related to hepatic fat content and hepatic insulin resistance in pioglitazone-treated type 2 diabetic patients [J].
Bajaj, M ;
Suraamornkul, S ;
Piper, P ;
Hardies, LJ ;
Glass, L ;
Cersosimo, E ;
Pratipanawatr, T ;
Miyazaki, Y ;
Defronzo, RA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (01) :200-206
[4]   Role of the adipocyte, free fatty acids, and ectopic fat in pathogenesis of type 2 diabetes mellitus: Peroxisomal proliferator-activated receptor agonists provide a rational therapeutic approach [J].
Bays, H ;
Mandarino, L ;
DeFronzo, RA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (02) :463-478
[5]  
Boesch C, 2000, ANN NY ACAD SCI, V904, P25
[6]  
Bredie SJH, 1997, ARTERIOSCL THROM VAS, V17, P1465
[7]   Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis on low-density lipoprotein heterogeneity [J].
Bredie, SJH ;
Demacker, PNM ;
Stalenhoef, AFH .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1997, 27 (10) :802-811
[8]   A meta-analysis comparing the effect of thiazolidinediones on cardiovascular risk factors [J].
Chiquette, E ;
Ramirez, G ;
DeFronzo, R .
ARCHIVES OF INTERNAL MEDICINE, 2004, 164 (19) :2097-2104
[9]   CLINICAL IMPLICATIONS OF INSULIN-RESISTANCE SYNDROMES [J].
DAVIDSON, MB .
AMERICAN JOURNAL OF MEDICINE, 1995, 99 (04) :420-426
[10]   Thiazolidinediones: a new class of antidiabetic drugs [J].
Day, C .
DIABETIC MEDICINE, 1999, 16 (03) :179-192