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   <subfield code="a">10.1007/s10157-010-0343-7</subfield>
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   <subfield code="a">Elevated serum levels of interleukin-18 in patients with overt diabetic nephropathy: effects of miglitol</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Takashi Uzu, Hiroki Yokoyama, Hirofumi Itoh, Daisuke Koya, Atsushi Nakagawa, Makoto Nishizawa, Hiroshi Maegawa, Yukiyo Yokomaku, Shin-ichi Araki, Atsuko Abiko, Masakazu Haneda]</subfield>
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   <subfield code="a">Background: Interleukin-18 (IL-18), a pro-inflammatory cytokine, is a predictor of cardiovascular and renal disease in diabetic patients. Postprandial hyperglycemia is one of the important factors contributing to an increase in the circulating pro-inflammatory cytokine levels. This study investigated the effect of miglitol, an α-glucosidase inhibitor, on postprandial hyperglycemia and IL-18 levels in diabetic patients with nephropathy. Methods: Fifteen Japanese diabetic patients with persistent proteinuria and preserved renal function were recruited. The patients received 50mg miglitol thrice daily after the baseline examinations and were followed up for 12weeks. A meal tolerance test was performed on eight patients at baseline and week 12. The fasting miglitol concentration was measured in seven patients just before the meal tolerance test. Results: There were no changes in the body weight, blood pressure, liver and renal function, and proteinuria from baseline to week 12. However, the levels of glycated hemoglobin and interleukin 18 significantly decreased from baseline to week 12. During the meal tolerance test, plasma glucose was significantly decreased 60min after treatment with miglitol, whereas the serum concentration of insulin was not changed. Fasting and postprandial levels of IL-18 were significantly decreased from baseline to week 12. Serum miglitol concentrations showed a significantly negative correlation with eGFR (r=−0.82, p=0.02). However, the serum miglitol concentrations did not changed during the course of this study. Conclusion: Miglitol improved postprandial hyperglycemia and reduced serum IL-18 levels in patients with stage 3 diabetic nephropathy. Miglitol may therefore prevent atherosclerotic diseases and diabetic micro-vascular complications through decreasing glucose swings and/or the circulating IL-18 level.</subfield>
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   <subfield code="a">Japanese Society of Nephrology, 2010</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Proinflammatory cytokine</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Postprandial</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Hyperglycemia</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Diabetic nephropathy</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">α-Glucosidase inhibitors</subfield>
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   <subfield code="a">Uzu</subfield>
   <subfield code="D">Takashi</subfield>
   <subfield code="u">Department of Medicine, Shiga University of Medical Science, 520-2192, Otsu, Shiga, Japan</subfield>
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   <subfield code="a">Yokoyama</subfield>
   <subfield code="D">Hiroki</subfield>
   <subfield code="u">Internal Medicine, Jiyugaoka Medical Clinic, Obihiro, Hokkaido, Japan</subfield>
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   <subfield code="a">Itoh</subfield>
   <subfield code="D">Hirofumi</subfield>
   <subfield code="u">Internal Medicine, Jiyugaoka Medical Clinic, Obihiro, Hokkaido, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Koya</subfield>
   <subfield code="D">Daisuke</subfield>
   <subfield code="u">Division of Diabetes &amp; Endocrinology, Department of Medicine, Kanazawa Medical University, Kahoku-gun, Ishikawa, Japan</subfield>
   <subfield code="4">aut</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Nakagawa</subfield>
   <subfield code="D">Atsushi</subfield>
   <subfield code="u">Division of Diabetes &amp; Endocrinology, Department of Medicine, Kanazawa Medical University, Kahoku-gun, Ishikawa, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Nishizawa</subfield>
   <subfield code="D">Makoto</subfield>
   <subfield code="u">Division of Diabetes &amp; Endocrinology, Department of Medicine, Kanazawa Medical University, Kahoku-gun, Ishikawa, Japan</subfield>
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   <subfield code="a">Maegawa</subfield>
   <subfield code="D">Hiroshi</subfield>
   <subfield code="u">Department of Medicine, Shiga University of Medical Science, 520-2192, Otsu, Shiga, Japan</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Yokomaku</subfield>
   <subfield code="D">Yukiyo</subfield>
   <subfield code="u">Department of Medicine, Shiga University of Medical Science, 520-2192, Otsu, Shiga, Japan</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Araki</subfield>
   <subfield code="D">Shin-ichi</subfield>
   <subfield code="u">Department of Medicine, Shiga University of Medical Science, 520-2192, Otsu, Shiga, Japan</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Abiko</subfield>
   <subfield code="D">Atsuko</subfield>
   <subfield code="u">Division of Metabolism and Biosystemic Science, Department of Medicine, Asahikawa Medical University, Asahikawa, Hokkaido, Japan</subfield>
   <subfield code="4">aut</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Haneda</subfield>
   <subfield code="D">Masakazu</subfield>
   <subfield code="u">Division of Metabolism and Biosystemic Science, Department of Medicine, Asahikawa Medical University, Asahikawa, Hokkaido, Japan</subfield>
   <subfield code="4">aut</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Clinical and Experimental Nephrology</subfield>
   <subfield code="d">Springer Japan</subfield>
   <subfield code="g">15/1(2011-02-01), 58-63</subfield>
   <subfield code="x">1342-1751</subfield>
   <subfield code="q">15:1&lt;58</subfield>
   <subfield code="1">2011</subfield>
   <subfield code="2">15</subfield>
   <subfield code="o">10157</subfield>
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