Effects of Insulin Lispro Mix 25 and Insulin Lispro Mix 50 on Postprandial Glucose Excursion in Patients with Type 2 Diabetes: A Prospective, Open-Label, Randomized Clinical Trial

Introduction We compared the effects of insulin lispro mix 25 (LM25) and insulin lispro mix 50 (LM50) on postprandial glucose excursion in patients with type 2 diabetes mellitus (T2DM). Methods In this randomized, open-label, investigator-initiated trial, 81 T2DM patients treated with premixed human...

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Veröffentlicht in:Diabetes therapy 2018-04, Vol.9 (2), p.699-711
Hauptverfasser: Li, Wei, Ping, Fan, Xu, Lingling, Zhou, Meicen, Li, Hongmei, Dong, Yaxiu, Li, Yuxiu
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container_end_page 711
container_issue 2
container_start_page 699
container_title Diabetes therapy
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creator Li, Wei
Ping, Fan
Xu, Lingling
Zhou, Meicen
Li, Hongmei
Dong, Yaxiu
Li, Yuxiu
description Introduction We compared the effects of insulin lispro mix 25 (LM25) and insulin lispro mix 50 (LM50) on postprandial glucose excursion in patients with type 2 diabetes mellitus (T2DM). Methods In this randomized, open-label, investigator-initiated trial, 81 T2DM patients treated with premixed human insulin 70/30 (PHI70/30) for more than 90 days were randomly divided into two groups and received a crossover protocol of either LM25 or LM50 twice daily for 16 weeks. Continuous glucose monitoring (CGM) was performed for 72 h at baseline and at the end of each treatment phase to evaluate glycemic excursions in the subjects. Results The LM50 regimen resulted in significantly smaller postprandial glycemic excursions than the LM25 regimen after breakfast (1.3 ± 2.5 vs. 2.4 ± 2.6 mmol/L, P  = 0.046) and dinner (1.5 ± 2.8 vs. 2.8 ± 2.4 mmol/L, P  = 0.036). Glycosylated hemoglobin levels were similar for the patients on the three regimens. The percentage of patients who achieved their glycosylated hemoglobin target was significantly higher for the LM25 and LM50 regimens than for the PHI70/30 regimen, regardless of whether the target was set at 7.0% or 6.5%. The proportion of the patients who were hypoglycemic for a high percentage (> 10%) of the time was lower for the LM50 regimen than for the LM25 and PHI70/30 regimens. Conclusions LM50 may provide better glycemic excursion control after breakfast and dinner than LM25 in T2DM patients. Trial Registration http://www.chictr.org.cn # ChiCTR-TTRCC-12002516. Funding Lilly Suzhou Pharmaceutical Co., Ltd. (Shanghai Branch, China) and National Key Program of Clinical Science of China (WBYZ 2011-873).
doi_str_mv 10.1007/s13300-018-0398-0
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Methods In this randomized, open-label, investigator-initiated trial, 81 T2DM patients treated with premixed human insulin 70/30 (PHI70/30) for more than 90 days were randomly divided into two groups and received a crossover protocol of either LM25 or LM50 twice daily for 16 weeks. Continuous glucose monitoring (CGM) was performed for 72 h at baseline and at the end of each treatment phase to evaluate glycemic excursions in the subjects. Results The LM50 regimen resulted in significantly smaller postprandial glycemic excursions than the LM25 regimen after breakfast (1.3 ± 2.5 vs. 2.4 ± 2.6 mmol/L, P  = 0.046) and dinner (1.5 ± 2.8 vs. 2.8 ± 2.4 mmol/L, P  = 0.036). Glycosylated hemoglobin levels were similar for the patients on the three regimens. The percentage of patients who achieved their glycosylated hemoglobin target was significantly higher for the LM25 and LM50 regimens than for the PHI70/30 regimen, regardless of whether the target was set at 7.0% or 6.5%. The proportion of the patients who were hypoglycemic for a high percentage (&gt; 10%) of the time was lower for the LM50 regimen than for the LM25 and PHI70/30 regimens. Conclusions LM50 may provide better glycemic excursion control after breakfast and dinner than LM25 in T2DM patients. Trial Registration http://www.chictr.org.cn # ChiCTR-TTRCC-12002516. Funding Lilly Suzhou Pharmaceutical Co., Ltd. (Shanghai Branch, China) and National Key Program of Clinical Science of China (WBYZ 2011-873).</description><identifier>ISSN: 1869-6953</identifier><identifier>EISSN: 1869-6961</identifier><identifier>DOI: 10.1007/s13300-018-0398-0</identifier><identifier>PMID: 29520742</identifier><language>eng</language><publisher>Cheshire: Springer Healthcare</publisher><subject>Blood sugar monitoring ; Cardiology ; ChiCTR-TTRCC ; ChiCTR-TTRCC-12002516 ; Clinical outcomes ; Clinical trials ; Comparative analysis ; Comparative studies ; Dextrose ; Diabetes ; Diabetes therapy ; Drug therapy ; Endocrinology ; Evidence-based medicine ; Glucose ; Glucose monitoring ; Glycosylated hemoglobin ; Hypoglycemia ; Insulin ; Insulin lispro ; Internal Medicine ; Labels ; Medicine ; Medicine &amp; Public Health ; Original Research ; Type 2 diabetes</subject><ispartof>Diabetes therapy, 2018-04, Vol.9 (2), p.699-711</ispartof><rights>The Author(s) 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Diabetes Therapy is a copyright of Springer, (2018). All Rights Reserved.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c537t-c66eb5fb7b0c70d57ff72985181f96186a032890a810602d39184dfd2ec4887c3</citedby><cites>FETCH-LOGICAL-c537t-c66eb5fb7b0c70d57ff72985181f96186a032890a810602d39184dfd2ec4887c3</cites><orcidid>0000-0001-7500-0855</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104282/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104282/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29520742$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Ping, Fan</creatorcontrib><creatorcontrib>Xu, Lingling</creatorcontrib><creatorcontrib>Zhou, Meicen</creatorcontrib><creatorcontrib>Li, Hongmei</creatorcontrib><creatorcontrib>Dong, Yaxiu</creatorcontrib><creatorcontrib>Li, Yuxiu</creatorcontrib><title>Effects of Insulin Lispro Mix 25 and Insulin Lispro Mix 50 on Postprandial Glucose Excursion in Patients with Type 2 Diabetes: A Prospective, Open-Label, Randomized Clinical Trial</title><title>Diabetes therapy</title><addtitle>Diabetes Ther</addtitle><addtitle>Diabetes Ther</addtitle><description>Introduction We compared the effects of insulin lispro mix 25 (LM25) and insulin lispro mix 50 (LM50) on postprandial glucose excursion in patients with type 2 diabetes mellitus (T2DM). Methods In this randomized, open-label, investigator-initiated trial, 81 T2DM patients treated with premixed human insulin 70/30 (PHI70/30) for more than 90 days were randomly divided into two groups and received a crossover protocol of either LM25 or LM50 twice daily for 16 weeks. Continuous glucose monitoring (CGM) was performed for 72 h at baseline and at the end of each treatment phase to evaluate glycemic excursions in the subjects. Results The LM50 regimen resulted in significantly smaller postprandial glycemic excursions than the LM25 regimen after breakfast (1.3 ± 2.5 vs. 2.4 ± 2.6 mmol/L, P  = 0.046) and dinner (1.5 ± 2.8 vs. 2.8 ± 2.4 mmol/L, P  = 0.036). Glycosylated hemoglobin levels were similar for the patients on the three regimens. The percentage of patients who achieved their glycosylated hemoglobin target was significantly higher for the LM25 and LM50 regimens than for the PHI70/30 regimen, regardless of whether the target was set at 7.0% or 6.5%. The proportion of the patients who were hypoglycemic for a high percentage (&gt; 10%) of the time was lower for the LM50 regimen than for the LM25 and PHI70/30 regimens. Conclusions LM50 may provide better glycemic excursion control after breakfast and dinner than LM25 in T2DM patients. Trial Registration http://www.chictr.org.cn # ChiCTR-TTRCC-12002516. Funding Lilly Suzhou Pharmaceutical Co., Ltd. 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Public Health</topic><topic>Original Research</topic><topic>Type 2 diabetes</topic><toplevel>online_resources</toplevel><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Ping, Fan</creatorcontrib><creatorcontrib>Xu, Lingling</creatorcontrib><creatorcontrib>Zhou, Meicen</creatorcontrib><creatorcontrib>Li, Hongmei</creatorcontrib><creatorcontrib>Dong, Yaxiu</creatorcontrib><creatorcontrib>Li, Yuxiu</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetes therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Wei</au><au>Ping, Fan</au><au>Xu, Lingling</au><au>Zhou, Meicen</au><au>Li, Hongmei</au><au>Dong, Yaxiu</au><au>Li, Yuxiu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Insulin Lispro Mix 25 and Insulin Lispro Mix 50 on Postprandial Glucose Excursion in Patients with Type 2 Diabetes: A Prospective, Open-Label, Randomized Clinical Trial</atitle><jtitle>Diabetes therapy</jtitle><stitle>Diabetes Ther</stitle><addtitle>Diabetes Ther</addtitle><date>2018-04-01</date><risdate>2018</risdate><volume>9</volume><issue>2</issue><spage>699</spage><epage>711</epage><pages>699-711</pages><issn>1869-6953</issn><eissn>1869-6961</eissn><abstract>Introduction We compared the effects of insulin lispro mix 25 (LM25) and insulin lispro mix 50 (LM50) on postprandial glucose excursion in patients with type 2 diabetes mellitus (T2DM). Methods In this randomized, open-label, investigator-initiated trial, 81 T2DM patients treated with premixed human insulin 70/30 (PHI70/30) for more than 90 days were randomly divided into two groups and received a crossover protocol of either LM25 or LM50 twice daily for 16 weeks. Continuous glucose monitoring (CGM) was performed for 72 h at baseline and at the end of each treatment phase to evaluate glycemic excursions in the subjects. Results The LM50 regimen resulted in significantly smaller postprandial glycemic excursions than the LM25 regimen after breakfast (1.3 ± 2.5 vs. 2.4 ± 2.6 mmol/L, P  = 0.046) and dinner (1.5 ± 2.8 vs. 2.8 ± 2.4 mmol/L, P  = 0.036). Glycosylated hemoglobin levels were similar for the patients on the three regimens. The percentage of patients who achieved their glycosylated hemoglobin target was significantly higher for the LM25 and LM50 regimens than for the PHI70/30 regimen, regardless of whether the target was set at 7.0% or 6.5%. The proportion of the patients who were hypoglycemic for a high percentage (&gt; 10%) of the time was lower for the LM50 regimen than for the LM25 and PHI70/30 regimens. Conclusions LM50 may provide better glycemic excursion control after breakfast and dinner than LM25 in T2DM patients. Trial Registration http://www.chictr.org.cn # ChiCTR-TTRCC-12002516. Funding Lilly Suzhou Pharmaceutical Co., Ltd. (Shanghai Branch, China) and National Key Program of Clinical Science of China (WBYZ 2011-873).</abstract><cop>Cheshire</cop><pub>Springer Healthcare</pub><pmid>29520742</pmid><doi>10.1007/s13300-018-0398-0</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-7500-0855</orcidid><oa>free_for_read</oa></addata></record>
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subjects Blood sugar monitoring
Cardiology
ChiCTR-TTRCC
ChiCTR-TTRCC-12002516
Clinical outcomes
Clinical trials
Comparative analysis
Comparative studies
Dextrose
Diabetes
Diabetes therapy
Drug therapy
Endocrinology
Evidence-based medicine
Glucose
Glucose monitoring
Glycosylated hemoglobin
Hypoglycemia
Insulin
Insulin lispro
Internal Medicine
Labels
Medicine
Medicine & Public Health
Original Research
Type 2 diabetes
title Effects of Insulin Lispro Mix 25 and Insulin Lispro Mix 50 on Postprandial Glucose Excursion in Patients with Type 2 Diabetes: A Prospective, Open-Label, Randomized Clinical Trial
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