PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 20493430-1 2010 OBJECTIVE: In a previous study involving 18 hypertensive patients with type 2 diabetes mellitus, we found that replacement of valsartan and candesartan by telmisartan significantly improved insulin sensitivity and significantly increased serum adiponectin levels in the patients. candesartan 140-151 adiponectin, C1Q and collagen domain containing Homo sapiens 244-255 20505674-10 2010 The M value, visfatin and ADN increased with candesartan, whereas no significant variations were observed with olmesartan. candesartan 45-56 adiponectin, C1Q and collagen domain containing Homo sapiens 26-29 19059660-8 2010 Ramipril and candesartan therapies improved FMD and increased adiponectin levels and insulin sensitivity to a greater extent than atenolol or thiazide therapies (P<0.001 and P<0.015 by ANOVA). candesartan 13-24 adiponectin, C1Q and collagen domain containing Homo sapiens 62-73 17483542-4 2007 Ramipril, candesartan, or combination therapy reduced blood pressure, improved flow-mediated dilation, and increased plasma adiponectin levels when compared with baseline values. candesartan 10-21 adiponectin, C1Q and collagen domain containing Homo sapiens 124-135 20823643-9 2010 CONCLUSION: Switching from candesartan to telmisartan in obese subjects increases serum adiponectin and improves both insulin resistance and oxidative stress, while these effects were not statistically apparent in the total patient population. candesartan 27-38 adiponectin, C1Q and collagen domain containing Homo sapiens 88-99 17483542-7 2007 There were correlations between percent changes in adiponectin levels and percent changes in insulin sensitivity (determined by QUICKI) (r = 0.319, P = 0.066) following ramipril therapy, percent changes in QUICKI (r = 0.374, P = 0.029) following combination therapy, and percent changes in QUICKI (r = 0.607, P < 0.001) following candesartan therapy. candesartan 333-344 adiponectin, C1Q and collagen domain containing Homo sapiens 51-62 16940715-7 2006 Plasma adiponectin level increased from 12.5 to 18.8 microg/ml (p < 0.05) by candesartan and decreased again to 14.4 microg/ml (p < 0.05) after discontinuation. candesartan 80-91 adiponectin, C1Q and collagen domain containing Homo sapiens 7-18 16443859-12 2006 Fenofibrate, combined therapy, and candesartan significantly increased plasma adiponectin levels and insulin sensitivity relative to baseline measurements. candesartan 35-46 adiponectin, C1Q and collagen domain containing Homo sapiens 78-89 16246439-9 2006 Compared with placebo, candesartan therapy significantly lowered fasting insulin levels (P=0.011) and increased plasma levels of adiponectin by 15+/-4% (P=0.012) and increased QUICKI by 8+/-2% (P=0.007). candesartan 23-34 adiponectin, C1Q and collagen domain containing Homo sapiens 129-140 16246439-11 2006 CONCLUSIONS: Candesartan therapy significantly reduced inflammation and increased adiponectin levels and improved insulin sensitivity in hypertensive patients. candesartan 13-24 adiponectin, C1Q and collagen domain containing Homo sapiens 82-93 16940715-9 2006 CONCLUSION: Candesartan increases plasma adiponectin level in association with the reduction of oxidative stress in peritoneal dialysis patients. candesartan 12-23 adiponectin, C1Q and collagen domain containing Homo sapiens 41-52 12796280-8 2003 Treatment with temocapril or candesartan significantly decreased blood pressure and increased M value and adiponectin concentrations but did not affect BMI and HDL cholesterol. candesartan 29-40 adiponectin, C1Q and collagen domain containing Homo sapiens 106-117 25418492-9 2014 Treatment with high doses of the ARB, candesartan, is associated with significantly reduced LAR and marginally increased circulating adiponectin levels in hypertensive patients with multiple cardiovascular risk factors. candesartan 38-49 adiponectin, C1Q and collagen domain containing Homo sapiens 133-144