Fimasartan increases glucose-stimulated insulin secretion in patients with type 2 diabetes and hypertension compared with amlodipine

被引:7
作者
Yang, Ye Seul [1 ]
Lim, Min Hyuk [2 ]
Lee, Seong Ok [1 ]
Roh, Eun [1 ]
Ahn, Chang Ho [1 ]
Kwak, Soo Heon [1 ]
Cho, Young Min [1 ]
Kim, Sungwan [2 ]
Mari, Andrea [3 ]
Park, Kyong Soo [1 ,4 ]
Jung, Hye Seung [1 ,4 ]
机构
[1] Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea
[2] Seoul Natl Univ, Dept Biomed Engn, Coll Med, Seoul, South Korea
[3] CNR, Inst Neurosci, Padua, Italy
[4] Seoul Natl Univ Hosp, Innovat Res Inst Cell Therapy, Seoul, South Korea
关键词
angiotensin receptor antagonist; beta-cell function; fimasartan; hypertension; insulin secretion; renin-angiotensin system; type; 2; diabetes; BETA-CELL FUNCTION; RENIN-ANGIOTENSIN SYSTEM; RECEPTOR BLOCKADE; ISLET MORPHOLOGY; MOUSE MODEL; TOLERANCE; MELLITUS; INHIBITION; PREVENTION; METAANALYSIS;
D O I
10.1111/dom.13282
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: To study the effects of angiotensin receptor blockers (ARBs) on insulin secretion in hypertensive patients with type 2 diabetes. Materials and methods: A total of 41 patients were enrolled in this open-label, active comparator-controlled, crossover study. After a 2-week run-in period with amlodipine, the participants were assigned to receive either fimasartan (60-120 mg daily) or amlodipine (5-10 mg daily) for 16 weeks. Thereafter, they were treated with the other drug for another 16 weeks. Physical examinations and laboratory tests were performed before and after each treatment. Results: Blood pressure, glycated haemoglobin and oral glucose tolerance test (OGTT) values were similar with each treatment. Fimasartan treatment significantly increased median (range) homeostatic assessment of beta-cell function values (49.9 [22.5-174.4] vs 46.9 [15.6-148.0]), area under the curve of insulin during OGTT (27 284 [9501-94 525] vs 26 818 [8112-76 704] pmol/L x min), insulinogenic index at 60 minutes (19.7 [3.0-131.2] vs 15.0 [2.4-103.8] pmol/mmol) and at 120 minutes (19.1 [1.9-85.5] vs 12.6 [-4.3-178.8] pmol/mmol) compared with those with amlodipine (all P < .05); however, acute insulin response and insulin resistance indices were similar for both agents. Conclusions: Compared with amlodipine, fimasartan increased late-phase glucose-stimulated insulin secretion in patients with type 2 diabetes and hypertension. This finding suggests that ARBs would be more beneficial in such patients compared with other classes of anti-hypertensives.
引用
收藏
页码:1670 / 1677
页数:8
相关论文
共 36 条
  • [1] American Diabetes Association, 2017, Diabetes Care, V40, pS75
  • [2] American Diabetes Association, 2017, Diabetes Care, V40, pS88
  • [3] Classification and Diagnosis of Diabetes
    不详
    [J]. DIABETES CARE, 2015, 38 : S8 - S16
  • [4] Diabetes mellitus as a compelling indication for use of renin angiotensin system blockers: systematic review and meta-analysis of randomized trials
    Bangalore, Sripal
    Fakheri, Robert
    Toklu, Bora
    Messerli, Franz H.
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2016, 352
  • [5] Effects of angiotensin II type 1 receptor blockade on β-cell function in humans
    Bokhari, Syed
    Israelian, Zarmen
    Schmidt, Jonelle
    Brinton, Eliot
    Meyer, Christian
    [J]. DIABETES CARE, 2007, 30 (01) : 181 - 181
  • [6] Oral glucose tolerance test minimal model indexes of β-cell function and insulin sensitivity
    Breda, E
    Cavaghan, MK
    Toffolo, G
    Polonsky, KS
    Cobelli, C
    [J]. DIABETES, 2001, 50 (01) : 150 - 158
  • [7] Angiotensin II and the endocrine pancreas: effects on islet blood flow and insulin secretion in rats
    Carlsson, PO
    Berne, C
    Jansson, L
    [J]. DIABETOLOGIA, 1998, 41 (02) : 127 - 133
  • [8] EVIDENCE FOR AN INTRINSIC ANGIOTENSIN SYSTEM IN THE CANINE PANCREAS
    CHAPPELL, MC
    MILLSTED, A
    DIZ, DI
    BROSNIHAN, KB
    FERRARIO, CM
    [J]. JOURNAL OF HYPERTENSION, 1991, 9 (08) : 751 - 759
  • [9] Combination of the Dipeptidyl Peptidase IV Inhibitor LAF237 [(S)-1-[(3-Hydroxy-1-adamantyl)ammo]acetyl-2-cyano-pyrrolidine] with the Angiotensin II Type 1 Receptor Antagonist Valsartan [N-(1-Oxopentyl)-N-[[2′-(1H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl]methyl]-L-valine] Enhances Pancreatic Islet Morphology and Function in a Mouse Model of Type 2 Diabetes
    Cheng, Qianni
    Law, Pui Ki
    de Gasparo, Marc
    Leung, Po Sing
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2008, 327 (03) : 683 - 691
  • [10] Angiotensin II type 1 receptor blockade improves β-cell function and glucose tolerance in a mouse model of type 2 diabetes
    Chu, KY
    Lau, T
    Carlsson, PO
    Leung, PS
    [J]. DIABETES, 2006, 55 (02) : 367 - 374