PMID- 27236108 OWN - NLM STAT- MEDLINE DCOM- 20170804 LR - 20170910 IS - 1874-1754 (Electronic) IS - 0167-5273 (Linking) VI - 218 DP - 2016 Sep 1 TI - Effects of intensive glucose lowering in treatment of type 2 diabetes mellitus on cardiovascular outcomes: A meta-analysis of data from 58,160 patients in 13 randomized controlled trials. PG - 50-58 LID - S0167-5273(16)30869-5 [pii] LID - 10.1016/j.ijcard.2016.04.163 [doi] AB - BACKGROUND: Previous trials indicated that intensive glucose lowering in treatment of patients with type 2 diabetes mellitus (T2DM) was associated with a higher incidence of mortality. We therefore conducted a meta-analysis to evaluate the benefits and harms of intensive glucose lowering therapy in treatment of T2DM patients on major cardiovascular outcomes. METHODS: Randomized controlled trials (RCTs) were obtained from searches of PubMed, EmBase, and the Cochrane Library electronic databases until Feb. 2016. Relative risk (RR) was used to measure the treatment effect by random-effect model. Meta-regression, sensitivity analyses, subgroup analyses, and publication biases were also conducted. RESULTS: Thirteen RCTs were included with 58,160 T2DM patients and reported 5719 major cardiovascular events (MACEs), 6569 deaths, 2057 cardiac death cases, 3201 myocardial infarction (MI) cases, 1835 stroke cases, and 1778 congestive heart failure cases. Intensive glucose lowering therapy significantly reduced risk of MACEs (RR: 0.92; 95%CI: 0.85-1.00; P=0.042), and MI (RR: 0.90; 95%CI: 0.82-0.98; P=0.020) compared with conventional glucose control therapy. Furthermore, intensive glucose lowering therapy has no significant effect on the incidence of total mortality (RR: 0.98; 95%CI: 0.91-1.07; P=0.693), cardiac death (RR: 1.00; 95%CI: 0.87-1.04; P=0.999), stroke (RR: 0.94; 95%CI: 0.84-1.06; P=0.333), and congestive heart failure (RR: 1.19; 95%CI: 0.96-1.48; P=0.108). CONCLUSION: T2DM patients who received intensive glucose lowering therapy are associated with a reduced risk of MACEs and MI, whereas it has no significant effect on the risk of total mortality, cardiac death, stroke, and congestive heart failure. These effects might differ when stratified by baseline characteristics in T2DM patients. CI - Copyright (c) 2016 Elsevier Ireland Ltd. All rights reserved. FAU - Fang, Hong-Juan AU - Fang HJ AD - Department of Endocrinology, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China. FAU - Zhou, Yu-Hao AU - Zhou YH AD - Department of Rehabilitation Institute, Shanghai Seventh People's Hospital, Shanghai 200137, China. FAU - Tian, Yong-Ji AU - Tian YJ AD - Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, 6 Tiantan Xili, Dongcheng District, Beijing 100050, China. FAU - Du, Han-Yang AU - Du HY AD - Department of Emergency, Beijing Tiantan Hospital, Capital Medical University, 6 Tiantan Xili, Dongcheng District, Beijing 100050, China. FAU - Sun, Yan-Xia AU - Sun YX AD - Department of Anesthesiolgy, Beijing TongRen Hospital, Capital Medical University, No.2 Chongwenmennei Street, Dongcheng District, Beijing 100730, China. FAU - Zhong, Li-Yong AU - Zhong LY AD - Department of Endocrinology, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China. Electronic address: zhongliyong@126.com. LA - eng PT - Journal Article PT - Meta-Analysis DEP - 20160513 PL - Netherlands TA - Int J Cardiol JT - International journal of cardiology JID - 8200291 RN - 0 (Blood Glucose) RN - 0 (Hypoglycemic Agents) SB - IM MH - Blood Glucose/drug effects/*metabolism MH - Cardiovascular Diseases/*blood/*drug therapy/epidemiology MH - Diabetes Mellitus, Type 2/*blood/*drug therapy MH - Humans MH - Hypoglycemic Agents/pharmacology/therapeutic use MH - Randomized Controlled Trials as Topic/*methods MH - Treatment Outcome OTO - NOTNLM OT - Cardiovascular OT - Intensive glucose lowering OT - Meta-analysis OT - Type 2 diabetes mellitus EDAT- 2016/05/29 06:00 MHDA- 2017/08/05 06:00 CRDT- 2016/05/29 06:00 PHST- 2016/04/08 00:00 [received] PHST- 2016/04/29 00:00 [accepted] PHST- 2016/05/29 06:00 [entrez] PHST- 2016/05/29 06:00 [pubmed] PHST- 2017/08/05 06:00 [medline] AID - S0167-5273(16)30869-5 [pii] AID - 10.1016/j.ijcard.2016.04.163 [doi] PST - ppublish SO - Int J Cardiol. 2016 Sep 1;218:50-58. doi: 10.1016/j.ijcard.2016.04.163. Epub 2016 May 13.