PMID- 30148851 OWN - NLM STAT- MEDLINE DCOM- 20190207 LR - 20221207 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 13 IP - 8 DP - 2018 TI - Comparison of antidiabetic drugs added to sulfonylurea monotherapy in patients with type 2 diabetes mellitus: A network meta-analysis. PG - e0202563 LID - 10.1371/journal.pone.0202563 [doi] LID - e0202563 AB - AIMS: This study aimed to investigate the efficacy and safety of dual therapy comprising sulfonylurea (SU) plus antidiabetic drugs for the treatment of type 2 diabetes mellitus (T2DM). METHODS: We searched the PubMed, Cochrane library, and Embase databases for randomized clinical trials (>/=24 weeks) published up to December 28, 2017. Subsequently, we conducted pairwise and network meta-analyses to calculate the odds ratios (ORs) and mean differences (MDs) with 95% confidence intervals (CIs) of the outcomes. RESULTS: The final analyses included 24 trials with a total of 10,032 patients. Compared with placebo, all treatment regimens were associated with a significantly higher risk of hypoglycemia, except the combinations of SU plus sodium-glucose co-transporter-2 inhibitor (SGLT-2i) [OR, 1.35 (95% CI: 0.81 to 2.25)] or alpha-glucosidase inhibitor (AGI) [OR, 1.16 (95% CI: 0.55 to 2.44)]. Notably, the combination of SU plus glucagon-like peptide-1 receptor agonist (GLP-1RA) was associated with the most significant increase in the risk of hypoglycemia. Furthermore, all SU-based combination regimens reduced the glycated hemoglobin (HbA1c) and fasting plasma glucose levels (FPG). However, only combinations containing SGLT-2i [MD, -1.00 kg (95% CI: -1.73 to -0.27)] and GLP-1RA [MD, -0.56 kg (95% CI: -1.10 to -0.02)] led to weight loss. CONCLUSIONS: Our findings highlight the importance of considering the risk of hypoglycemia when selecting antidiabetic drugs to be administered concomitantly with SU. Although all classes of antidiabetic drugs improved glucose control when administered in combination with SU, SGLT-2i might be the best option with respect to factors such as hypoglycemia and body weight. FAU - Qian, Dan AU - Qian D AD - Department of Pharmacy, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. FAU - Zhang, Tiantian AU - Zhang T AD - College of Pharmacy, Jinan University, Guangzhou, China. FAU - Tan, Xiangping AU - Tan X AD - Department of Pharmacy, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. FAU - Zheng, Peiying AU - Zheng P AD - Department of Pharmacy, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. FAU - Liang, Zhuoru AU - Liang Z AD - College of Pharmacy, Jinan University, Guangzhou, China. FAU - Xie, Jingmei AU - Xie J AD - College of Pharmacy, Jinan University, Guangzhou, China. FAU - Jiang, Jie AU - Jiang J AD - College of Pharmacy, Jinan University, Guangzhou, China. FAU - Situ, Bing AU - Situ B AUID- ORCID: 0000-0002-1615-1191 AD - Department of Pharmacy, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. LA - eng PT - Journal Article PT - Meta-Analysis DEP - 20180827 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Blood Glucose) RN - 0 (Dipeptidyl-Peptidase IV Inhibitors) RN - 0 (Drug Combinations) RN - 0 (Glycated Hemoglobin A) RN - 0 (Hypoglycemic Agents) RN - 0 (Sulfonylurea Compounds) RN - 9100L32L2N (Metformin) SB - IM MH - Blood Glucose/drug effects MH - Body Weight MH - Diabetes Mellitus, Type 2/blood/*drug therapy/pathology MH - Dipeptidyl-Peptidase IV Inhibitors/therapeutic use MH - Drug Combinations MH - Female MH - Glycated Hemoglobin/drug effects/metabolism MH - Humans MH - Hypoglycemia/blood/*drug therapy/pathology MH - Hypoglycemic Agents/*therapeutic use MH - Male MH - Metformin/therapeutic use MH - Network Meta-Analysis MH - Randomized Controlled Trials as Topic MH - Sulfonylurea Compounds/*therapeutic use MH - Weight Loss/drug effects PMC - PMC6110472 COIS- The authors have declared that no competing interests exist. EDAT- 2018/08/28 06:00 MHDA- 2019/02/08 06:00 PMCR- 2018/08/27 CRDT- 2018/08/28 06:00 PHST- 2018/03/12 00:00 [received] PHST- 2018/08/06 00:00 [accepted] PHST- 2018/08/28 06:00 [entrez] PHST- 2018/08/28 06:00 [pubmed] PHST- 2019/02/08 06:00 [medline] PHST- 2018/08/27 00:00 [pmc-release] AID - PONE-D-18-07621 [pii] AID - 10.1371/journal.pone.0202563 [doi] PST - epublish SO - PLoS One. 2018 Aug 27;13(8):e0202563. doi: 10.1371/journal.pone.0202563. eCollection 2018.