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<article article-type="research-article" dtd-version="1.0" xml:lang="en" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">jkd</journal-id>
<journal-title-group>
<journal-title>The Journal of Korean Diabetes</journal-title>
<abbrev-journal-title>J Korean Diabetes</abbrev-journal-title>
</journal-title-group>
<issn pub-type="ppub">2233-7431</issn>
<issn pub-type="epub">2714-0547</issn>
<publisher>
<publisher-name>Korean Diabetes Association</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.4093/jkd.2014.15.3.146</article-id>
<article-id pub-id-type="publisher-id">jkd-15-146</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Focused Issue</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Glucose Lowering Effect of SGLT2 Inhibitors: A Review of Clinical Studies</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name name-style="western" xml:lang="en">
<surname>Kim</surname><given-names>Hae Jin</given-names></name>
<xref ref-type="aff" rid="aff1-jkd-15-146"/>
</contrib>
<aff id="aff1-jkd-15-146" xml:lang="en">Department of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, <country>Korea</country></aff>
</contrib-group>
<author-notes>
<corresp id="c1-jkd-15-146">&#xAD50;&#xC2E0;&#xC800;&#xC790;&#x3A;&#x20;&#xAE40;&#xD61C;&#xC9C4;&#x2C;&#x20;&#xACBD;&#xAE30;&#xB3C4;&#x20;&#xC218;&#xC6D0;&#xC2DC;&#x20;&#xC601;&#xD1B5;&#xAD6C;&#x20;&#xC6D4;&#xB4DC;&#xCEF5;&#xB85C;&#x20;&#x32;&#x30;&#x36;&#x20;&#xC544;&#xC8FC;&#xB300;&#xD559;&#xAD50;&#xBCD1;&#xC6D0;&#x20;&#xB0B4;&#xBD84;&#xBE44;&#xB300;&#xC0AC;&#xB0B4;&#xACFC;&#x2C; E-mail: <email>jinkim@ajou.ac.kr</email></corresp>
</author-notes>
<pub-date pub-type="ppub"><month>1</month><year>2014</year></pub-date>
<pub-date pub-type="epub"><day>7</day><month>1</month><year>2014</year></pub-date>
<volume>15</volume><issue>3</issue>
<fpage>146</fpage><lpage>150</lpage>
<permissions>
<copyright-statement>Copyright &#x00A9; 2014 Korean Diabetes Association</copyright-statement>
<copyright-year>2014</copyright-year>
<license><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">http://creativecommons.org/licenses/by-nc/3.0/</ext-link>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license>
</permissions>
<abstract xml:lang="en">
<title>Abstract</title>
<p>There are numerous glucose lowering agents in clinical use for type 2 diabetic patients, yet most do not achieve glycemic targets. Recently, inhibitors of the sodium glucose cotransporter 2 (SGLT2) have been developed, which show great potential of being a novel therapeutic option to treat type 2 diabetes. Many researches have turned their attention to the kidney as a target because renal glucose reabsorption is increased in type 2 DM. SGLT2 is a protein transporter that mediates glucose reabsorption from glomerular filtrates. In an insulin-independent manner, inhibition of SGLT2 increases urinary glucose excretion and decreases plasma glucose levels. To date, there are a few SGLT2 inhibiting agents being clinically studied both as a monotherapy and in combination with other antidiabetic agents. This review will focus on the efficacy of SGLT2 inhibitors based on clinical studies.</p>
</abstract>
<kwd-group xml:lang="en">
<kwd>Hypoglycemic agents</kwd>
<kwd>Sodium glucose cotransporter 2</kwd>
<kwd>Type 2 diabetes mellitus</kwd>
</kwd-group>
</article-meta>
</front>
<back>
<ref-list xml:lang="en">
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<title>Figures</title>
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<caption xml:lang="en"><p>Changes in glycated hemoglobin (HbA1C) in trials with sodium glucose cotransporter 2 inhibitors. PBO, placebo. Adapted from Fujita Y et al. J Diabetes Investig. 2014;5:265-75[3].</p></caption>
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