Effects of telmisartan vs olmesartan on metabolic parameters, insulin resistance and adipocytokines in hypertensive obese patients

被引:26
作者
de Luis, D. A.
Conde, R.
Gonzalez-Sagrado, M.
Aller, R.
Izaola, O.
Duenas, A.
Perez Castrillon, J. L.
Romero, E.
机构
[1] Univ Valladolid, RD RETICEF 056 0013, Sch Med, Inst Endocrinol & Nutr,Hosp Rio Hortega, Valladolid 47130, Spain
[2] Univ Valladolid, RD RETICEF 056 0013, Hosp Rio Hortega, Unit Invest, Valladolid 47130, Spain
关键词
Adiponectin; Hypertension; Insulin resistance; Leptin; Olmesartan; Telmisartan; ANGIOTENSIN-II; ADIPOSE-TISSUE; LEPTIN; ADIPONECTIN; SYSTEM; ASSOCIATION; BLOCKADE; RELEASE; ALPHA;
D O I
10.3305/nh.2010.25.2.4545
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Angiotensin II regulates the production of adipokines. The objective was to study the effect of treatment with telmisartan versus olmesartan in hypertensive obese and overweight patients. Subjects: A sample of 65 overweight and obese patients with mild to moderate hypertension was analyzed in a prospective way with a randomized trial. Patients were randomized to telmisartan (80 mg/day) or olmesartan (40 mg/day) for 3 months. Weight, body mass index, blood pressure, basal glucose, insulin, total cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides, HOMA, QUICKI, leptin and adiponectin were determined at basal time and after 3 months of treatment. Results: Sixty five patients gave informed consent and were enrolled in the study. Patients treated with telmisartan had a significative decrease of glucose 1053 mg/dl (CI 95%: 2.6-18.5), insulin 231 mUI/L (CI 95%: 2.07-7.17) and HOMA 1.08 (Cl 95%: 0.39-2.55). Patients treated with olmesartan had a significative decrease of total cholesterol 20.2 mg/dl (CI 95%: 5.8-34.9) and LDL cholesterol 22.6 mg/dl (Cl 95%: 9.7-35.6). Only leptin levels have a significant decrease in telmisartan group 739 ng/ml (CI 95%: 1.47-13.31). Conclusion: Telmisartan improved blood pressure, glucose, insulin, HOMA and leptin in hypertensive diabetic patients. Olmesartan improved blood pressure and lipid levels.
引用
收藏
页码:275 / 279
页数:5
相关论文
共 29 条
[1]   Identification of telmisartan as a unique angiotensin II receptor antagonist with selective PPARγ-modulating activity [J].
Benson, SC ;
Pershadsingh, HA ;
Ho, CI ;
Chittiboyina, A ;
Desai, P ;
Pravenec, M ;
Qi, NN ;
Wang, JM ;
Avery, MA ;
Kurtz, TW .
HYPERTENSION, 2004, 43 (05) :993-1002
[2]   Two compartments for insulin-stimulated exocytosis in 3T3-L1 adipocytes defined by endogenous ACRP30 and GLUT4 [J].
Bogan, JS ;
Lodish, HF .
JOURNAL OF CELL BIOLOGY, 1999, 146 (03) :609-620
[3]   Physiological increase in plasma leptin markedly inhibits insulin secretion in vivo [J].
Cases, JA ;
Gabriely, I ;
Ma, XH ;
Yang, XM ;
Michaeli, T ;
Fleischer, N ;
Rossetti, L ;
Barzilai, N .
DIABETES, 2001, 50 (02) :348-352
[4]   Differential effects of local versus systemic angiotensin II in the regulation of leptin release from adipocytes [J].
Cassis, LA ;
English, VL ;
Bharawaj, K ;
Boustany, CM .
ENDOCRINOLOGY, 2004, 145 (01) :169-174
[5]  
Chalmers J, 1999, J HYPERTENS, V17, P151
[6]   Lack of association of-55CT polymorphism of UCP3 gene with fat distribution in obese patients [J].
de Luis, D. A. ;
Aller, R. ;
Izaola, O. ;
Gonzalez Sagrado, M. ;
Conde, R. ;
Perez Castrillon, J. L. .
ANNALS OF NUTRITION AND METABOLISM, 2007, 51 (04) :374-378
[7]   The adipose-tissue renin-angiotensin-aldosterone system:: role in the metabolic syndrome? [J].
Engeli, S ;
Schling, P ;
Gorzelniak, K ;
Boschmann, M ;
Janke, E ;
Ailhaud, G ;
Teboul, M ;
Massiéra, F ;
Sharma, AA .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2003, 35 (06) :807-825
[8]   Adipose tissue, adipokines, and inflammation [J].
Fantuzzi, G .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2005, 115 (05) :911-919
[9]   Crosstalk between insulin and angiotensin II signalling systems [J].
Folli, F ;
Saad, MJA ;
Velloso, L ;
Hansen, H ;
Carandente, O ;
Feener, EP ;
Kahn, CR .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 1999, 107 (02) :133-139
[10]  
Furuhashi M, 2004, J HYPERTENS, V22, P1977, DOI 10.1097/00004872-200410000-00021