Efficacy of different antidiabetic drugs based on metformin in the treatment of type 2 diabetes mellitus: A network meta-analysis involving eight eligible randomized-controlled trials.


Journal

Journal of cellular physiology
ISSN: 1097-4652
Titre abrégé: J Cell Physiol
Pays: United States
ID NLM: 0050222

Informations de publication

Date de publication:
03 2019
Historique:
received: 12 02 2018
accepted: 29 06 2018
pubmed: 27 8 2018
medline: 21 1 2020
entrez: 27 8 2018
Statut: ppublish

Résumé

Diabetes mellitus is one of the most prevalent metabolic diseases globally and it is increasing in prevalence. It is one of the most expensive diseases with respect to total health care costs per patient as a result of its chronic nature and its severe complications. To provide a more effective treatment of type 2 diabetes mellitus (T2DM), this study aims to compare different efficacies of six kinds of hypoglycemic drugs based on metformin, including glimepiride, pioglitazone, exenatide, glibenclamide, rosiglitazone, and vildagliptin, in T2DM by a network meta-analysis that were verified by randomized-controlled trials (RCTs). Eight eligible RCT in consistency with the aforementioned six hypoglycemic drugs for T2DM were included. The results of network meta-analysis demonstrated that the exenatide + metformin and vildagliptin + metformin regimens presented with better efficacy. Patients with T2DM with unsatisfactory blood glucose control based on diet control, proper exercise, and metformin treatment were included. The original regimen and dose of medication were unchanged, followed by the addition of glimepiride, pioglitazone, exenatide, glibenclamide, rosiglitazone, and vildagliptin. The results of RCTs showed that all these six kinds of drugs reduced the HbA1c level. Compared with other regimens, exenatide + metformin reduced fasting plasma glucose (FPG), fasting plasma insulin (FPI), total cholesterol (TC), and homeostasis model assessment insulin resistance index (HOMA-IR) levels, but increased the high-density lipoprotein (HDL) level; vildagliptin + metformin decreased FPI and low-density lipoprotein (LDL) levels; glibenclamide + metformin decreased the FPG level, but promoted HDL; and glimepiride + metformin decreased the TC level and rosiglitazone + metformin reduced the LDL level. Our findings indicated that exenatide + metformin and vildagliptin + metformin have better efficacy in T2DM since they can improve insulin sensitivity.

Identifiants

pubmed: 30145806
doi: 10.1002/jcp.27097
doi:

Substances chimiques

Blood Glucose 0
Drug Combinations 0
Sulfonylurea Compounds 0
Rosiglitazone 05V02F2KDG
glimepiride 6KY687524K
Metformin 9100L32L2N
Exenatide 9P1872D4OL
Vildagliptin I6B4B2U96P
Glyburide SX6K58TVWC
Pioglitazone X4OV71U42S

Types de publication

Journal Article Meta-Analysis

Langues

eng

Sous-ensembles de citation

IM

Pagination

2795-2806

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Yan Peng (Y)

Department of Endocrinology, Linyi People's Hospital, Linyi, China.

Shu-Hong Chen (SH)

Department of Endocrinology, Linyi People's Hospital, Linyi, China.

Xiao-Nan Liu (XN)

Department of Endocrinology, Linyi People's Hospital, Linyi, China.

Qing-Yun Sun (QY)

Department of Endocrinology, Linyi People's Hospital, Linyi, China.

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Classifications MeSH