PMID- 29951978 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200929 IS - 1869-6953 (Print) IS - 1869-6961 (Electronic) IS - 1869-6961 (Linking) VI - 9 IP - 4 DP - 2018 Aug TI - Contribution of BHG and PPHG to Overall Hyperglycemia in T2DM Patients Treated with LM25 and LM50: Post Hoc Analysis of a Randomized Crossover Trial. PG - 1605-1614 LID - 10.1007/s13300-018-0462-9 [doi] AB - INTRODUCTION: To investigate the relative contribution rates of basal hyperglycemia (BHG) and postprandial hyperglycemia (PPHG) to overall hyperglycemia in patients with type 2 diabetes mellitus (T2DM) treated with insulin lispro mix 25 and 50 (LM25 and LM50) as evaluated by continuous glucose monitoring (CGM). METHODS: Eighty-one T2DM patients treated with premixed human insulin 70/30 (PHI70/30) were randomly divided into two groups and received a crossover protocol. In the first 16-week stage, one group received LM25 twice daily, the other group received LM50 twice daily. In the second 16-week stage, the two groups exchanged therapeutic regimen. Glycosylated hemoglobin (HbA(1c)) measurement and CGM were performed at enrollment and at the end of each treatment stage. RESULTS: BHG's contribution rate increased with increasing HbA(1c) (from 34.5% to 60.8%). PPHG's contribution rates in the LM50 regimen were significantly lower than those in LM25 and PHI70/30 regimens at HbA(1c) levels < 7.5%. Compared with LM50, LM25 shows a significant difference in reducing HbA(1c) in the subgroup with baseline HbA(1c) >/= 8.5% (DeltaHbA(1c) LM25 vs. LM50 - 0.6 +/- 0.1% vs. 0.3 +/- 0.1%, p < 0.05). CONCLUSIONS: For T2DM patients treated with premixed insulin analogues, postprandial hyperglycemia played a major role in the subgroup of patients with HbA(1c) < 8.5%, while fasting hyperglycemia became the major contributor to overall hyperglycemia in the subgroup of patients with HbA(1c) >/= 8.5%. TRIAL REGISTRATION: Chinese Clinical Trial Registry Identifier ChiCTR-TTRCC-12002516. FUNDING: Lilly Suzhou Pharmaceutical Co., Ltd. (Shanghai Branch, China) and National Key Program of Clinical Science of China (WBYZ2011-873). FAU - Li, Wei AU - Li W AD - Department of Endocrinology, Key Laboratory of Endocrinology of National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. FAU - Ping, Fan AU - Ping F AD - Department of Endocrinology, Key Laboratory of Endocrinology of National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. FAU - Xu, Lingling AU - Xu L AD - Department of Endocrinology, Key Laboratory of Endocrinology of National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. FAU - Zhang, Huabing AU - Zhang H AD - Department of Endocrinology, Key Laboratory of Endocrinology of National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. FAU - Dong, Yaxiu AU - Dong Y AD - Department of Endocrinology, Key Laboratory of Endocrinology of National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. FAU - Li, Hongmei AU - Li H AD - Department of Endocrinology, China Meitan General Hospital, Beijing, China. FAU - Sun, Qi AU - Sun Q AD - Department of Endocrinology, Key Laboratory of Endocrinology of National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. FAU - Li, Yuxiu AU - Li Y AUID- ORCID: 0000-0001-7500-0855 AD - Department of Endocrinology, Key Laboratory of Endocrinology of National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. liyx@pumch.cn. LA - eng GR - WBYZ2011-873/National Key Program of Clinical Science of China/ PT - Journal Article DEP - 20180627 PL - United States TA - Diabetes Ther JT - Diabetes therapy : research, treatment and education of diabetes and related disorders JID - 101539025 PMC - PMC6064593 OTO - NOTNLM OT - Insulin lispro OT - PPHG's contribution rate OT - Premixed human insulin OT - Type 2 diabetes mellitus EDAT- 2018/06/29 06:00 MHDA- 2018/06/29 06:01 PMCR- 2018/06/27 CRDT- 2018/06/29 06:00 PHST- 2018/05/12 00:00 [received] PHST- 2018/06/29 06:00 [pubmed] PHST- 2018/06/29 06:01 [medline] PHST- 2018/06/29 06:00 [entrez] PHST- 2018/06/27 00:00 [pmc-release] AID - 10.1007/s13300-018-0462-9 [pii] AID - 462 [pii] AID - 10.1007/s13300-018-0462-9 [doi] PST - ppublish SO - Diabetes Ther. 2018 Aug;9(4):1605-1614. doi: 10.1007/s13300-018-0462-9. Epub 2018 Jun 27.