Abstract:
BACKGROUND:Chronic hyperglycemia has an adverse influence on beta-cell function, which is known as 'glucotoxicity'. Sodium-glucose cotransporter-2 (SGLT2) inhibitors lower the blood glucose concentration by enhancing urinary glucose excretion. This study was performed to clarify the influence of the SGLT2 inhibitor ipragliflozin on beta-cell function assessed from the plasma intact proinsulin/C-peptide ratio in Japanese patients with type 2 diabetes. RESEARCH DESIGN AND METHODS:This was a 24-week, prospective, single-center, open-label, single-arm study. The subjects were 19 Japanese patients with type 2 diabetes. After a 4- to 8-week period of lifestyle modification, ipragliflozin (50 mg/d) was added to their existing treatment. At baseline and at 12 and 24 weeks after starting ipragliflozin treatment, a meal test was performed to evaluate the fasting and 2-hour proinsulin/C-peptide ratio. RESULTS:After 24 weeks, the body mass index, fasting plasma glucose, and hemoglobin A1c were all decreased significantly. Both the fasting and 2-hour proinsulin/C-peptide ratio decreased significantly from 25.0 ± 18.9 × 10-3 to 14.3 ± 9.0 × 10-3 and from 23.2 ± 14.9 × 10-3 to 13.7 ± 5.4 × 10-3, respectively (both p < 0.01 vs. baseline). CONCLUSIONS:These findings indicate that ipragliflozin might have a beneficial effect on beta-cells.
journal_name
Expert Opin Pharmacotherjournal_title
Expert opinion on pharmacotherapyauthors
Nagai Y,Ohta A,Sada Y,Kato H,Tanaka Ydoi
10.1080/14656566.2016.1261110subject
Has Abstractpub_date
2017-01-01 00:00:00pages
13-17issue
1eissn
1465-6566issn
1744-7666journal_volume
18pub_type
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