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Lim, Min Hyuk
Intelligence and Control-based BioMedicine Lab
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Fimasartan increases glucose‐stimulated insulin secretion in patients with type 2 diabetes and hypertension compared with amlodipine

Author(s)
Yang, Ye SeulLim, Min HyukLee, Seong OkRoh, EunAhn, Chang HoKwak, Soo HeonCho, Young MinKim, SungwanMari, AndreaPark, Kyong SooJung, Hye Seung
Issued Date
2018-07
DOI
10.1111/dom.13282
URI
https://scholarworks.unist.ac.kr/handle/201301/66033
Fulltext
https://dom-pubs.onlinelibrary.wiley.com/doi/full/10.1111/dom.13282
Citation
DIABETES OBESITY & METABOLISM, v.20, no.7, pp.1670 - 1677
Abstract
AimTo study the effects of angiotensin receptor blockers (ARBs) on insulin secretion in hypertensive patients with type 2 diabetes.Materials and methodsA 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.ResultsBlood pressure, glycated haemoglobin and oral glucose tolerance test (OGTT) values were similar with each treatment. Fimasartan treatment significantly increased median (range) homeostatic assessment of β‐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 × 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.ConclusionsCompared 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.
Publisher
Wiley
ISSN
1462-8902
Keyword (Author)
angiotensin receptor antagonistbeta-cell functionfimasartanhypertensioninsulin secretionrenin-angiotensin systemtype 2 diabetes
Keyword
BETA-CELL FUNCTIONRENIN-ANGIOTENSIN SYSTEMRECEPTOR BLOCKADEISLET MORPHOLOGYMOUSE MODELTOLERANCEMELLITUSINHIBITIONPREVENTIONMETAANALYSIS

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