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©2010 Baishideng Publishing Group Co.
World J Diabetes. Sep 15, 2010; 1(4): 116-128
Published online Sep 15, 2010. doi: 10.4239/wjd.v1.i4.116
Published online Sep 15, 2010. doi: 10.4239/wjd.v1.i4.116
Subjects | Treatment | Effects on circulating adipokines | Ref. |
Male New Zealand rabbits with hypercholesterolemia | 6 wk of 2.5 mg/kg per day atorvastatin | Leptin decreased by 38% from 8.9 ± 2.3 to 5.5 ± 2.8 μg/mL (P < 0.05) | [20] |
Humans with T2DMa | 8 wk of 40 mg/d atorvastatin | HMW increased by 42.3% while MMW and LMW decreased by 21% and 23% respectively. Total adiponectin did not change. (2009 article) Leptin decreased by 40% from 20.7 ± 2.3 to 12.5 ± 1.1 ng/mL. Resistin decreased by 20% from 3.5 ± 0.4 to 2.9 ± 0.4 μg/mL | [95] |
Healthy humans | 12 wk of pravastatin (40 mg/d) | No changes in adiponectin or leptin | [21] |
Humans with hypercholesterolemia | 4 mo of pravastatin or atorvastatin (10 mg/d) | Adiponectin increased from 10.7 ± 4.7 to 11.0 ± 5.1 μg/mL in response to atorvastatin (P < 0.05). No change in leptin or resistin. Atorvastatin reduced TNF-α from 2.0 ± 1.0 to 1.7 ± 0.6 (P < 0.05) | [22] |
Humans with hyperlipidemia | 6 mo of simvastatin (10 mg/d) or pitavastatin (2 mg/d) | Adiponectin increased in response to pitavastatin but not in response to simvastatin | [74] |
Humans with increased cardiovascular risk | 12 wk of 10-80 mg/d atorvastatin | Adiponectin increased by 10% with maximal increase (25%) observed at 80 mg/d (P < 0.05) | [75] |
Humans with hypercholesterolemia and CADb | 6 mo of 10-20 mg/d pravastatin | Adiponectin increased by 16.8% from 7.2 to 7.8 μg/mL (P < 0.001) | [76] |
Humans with hypercholesterolemia and ischemic heart disease | 3 mo of 10 mg/d atorvastatin | Adiponectin increased from 9.7 ± 7.4 to 13.9 ± 9.98 μg/mL (P < 0.005) | [77] |
C57BL/6J mice | 0-15 wk of 0.06% of diet as pravastatin | Adiponectin increased (P < 0.01) | [78] |
Men with hypercholesterolemia | 1 year of 40 mg/d pravastatin | Adiponectin increased by 1.47 ± 0.33 μg/mL (P < 0.05) | [78] |
Humans with CADb and IGTc | 6 mo of 20 mg/d pravastatin | Adiponectin increased by 35% from 5.2 to 6.1 μg/mL (P < 0.001) | [79] |
Humans with stable CADb, hypercholesterolemia and hypertriglyceridemia | 6 mo of 10 mg/d atorvastatin | Adiponectin increased by 4 wk (P < 0.05), with further increases by 6 mo (P < 0.01). Atorvastatin decreased TNF-α (P < 0.01) | [80] |
Humans with MetS | 40 mg/d simvastatin for 8 wk | No change in adiponectin | [81] |
Humans at cardiovascular risk | 3 mo of 40 mg simvastatin | Adiponectin decreased from 15.5 ± 12.7 to 11.6 ± 7.0 μg/mL (P < 0.05) | [82] |
Nondiabetic humans with increased cardiovascular risk | 3 mo of simvastatin (40 mg/d) | Adiponectin decreased. No change in RBP4 | [83] |
Humans with hypercholesterolemia | 2 mo of 10-80 mg/d simvastatin | Adiponectin decreased with maximal decrease (10%) observed at 80 mg/d (P < 0.05) | [84] |
Humans with hypercholesterolemia | 2 mo of simvastatin (20 mg/d) or pravastatin (40 mg/d) | Simvastatin decreased adiponectin (5.8 ± 0.8 to 5.2 ± 0.6 μg/mL); pravastatin increased adiponectin (5.6 ± 0.6 to 6.1 ± 0.6 μg/mL) | [85] |
Humans with hypercholesterolemia on fluvastatin plus TLCe and 19 humans with normal cholesterol on TLC alone | 12 wk of 80 mg/d fluvastatin plus TLC (n = 24) or 12 wk of TLC alone (n = 19) | Adiponectin increased from 5.3 ± 1.5 to 6.2 ± 2.2 μg/mL in response to TLC (P < 0.05), but was unchanged in response to fluvastatin | [91] |
Humans with T2DMa and mixed hyperlipoproteinemia | 6 wk of 10 mg/d atorvastatin | No change in adiponectin or resistin | [92] |
Kidney transplant recipients | 12 wk of atorvastatin (10 mg/d) | No change in adiponectin or TNF-α | [93] |
Humans with T2DM or at high risk for T2DM | 12 wk of atorvastatin (20 mg/d) | No effect on adiponectin, resistin or TNF-α | [94] |
Humans with T2DMa | 6 mo of 10 mg/d atorvastatin | Resistin tended to decrease, although not significant (P = 0.11) | [131] |
- Citation: Wanders D, Plaisance EP, Judd RL. Pharmacological effects of lipid-lowering drugs on circulating adipokines. World J Diabetes 2010; 1(4): 116-128
- URL: https://www.wjgnet.com/1948-9358/full/v1/i4/116.htm
- DOI: https://dx.doi.org/10.4239/wjd.v1.i4.116