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Introduction: This systematic review aims to verify the efficacy of acarbose monotherapy in treating obese or overweight patients without diabetes.
Methods: In the study, we conducted a systematic search of the Pub-Med, EMBASE, Cochrane and Science Citation Index Expanded databases in search of clinical trials on acarbose treatment, overweight and obesity. The crucial inclusion criteria were as follows: (1) patients were diagnosed as overweight or obese (BMI ≥ 25 kg/m); (2) randomized controlled trials (RCTs); (3) patients had undergone acarbose monotherapy or placebo control; (4) acarbose treatment had been carried out for at least 3 months. Exclusion criteria were as follows: (1) patients diagnosed with diabetes mellitus (DM); (2) patients had received a weight loss medication or surgery in the past 3 months; (3) papers not published in English; (4) repeated research results of the same experiment or repeated published documents.
Results: A total of 7 studies involving 132 in the acarbose group and 137 in placebo group, 269 subjects in total, were included in this meta-analysis. From the selected seven papers, we extracted the following clinical parameters: systolic blood pressure (SBP), diastolic blood pressure (DBP), body weight (BW), body mass index (BMI), triglyceride (TG), total cholesterol (TC), low density lipoprotein (LDL), high density cholesterol (HDL) and fasting plasma glucose (FPG). An important finding of our research is that TG was the only significantly reduced parameter in the acarbose group. Weight mean difference (WMD) was - 0.21 (95% CI - 0.33, - 0.09) mmol/l between acarbose (P = 0.0006) and placebo patients. Reduction of BMI was also greater for acarbose than placebo subjects, although the discrepancy was not statistically significant (P = 0.56). Moreover, no hypoglycemia occurred in either the acarbose group or placebo group. A few subjects experienced gastrointestinal reactions, but these were mild and improved over time. Acarbose has no obvious influence on other metabolic indexes.
Conclusion: Acarbose monotherapy is beneficial in reducing TG levels in obese or overweight patients and will not result in hypoglycemia during medication. The side effects of acarbose are mild.
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http://dx.doi.org/10.1007/s12325-020-01602-9 | DOI Listing |
Int J Biol Macromol
September 2025
Department of Chemistry and Chemical Sciences, Central University of Jammu, Rahya-Suchani (Bagla), District-Samba, Jammu, 181143, J&K, India. Electronic address:
The rise in diabetes complications drives the development of novel drugs targeting α-amylase and α-glucosidase for improving glycaemic control in diabetes management. This review comprehensively summarizes the antidiabetic properties of 3-mercapto-1,2,4-triazoles, based on studies published between 2018 and 2025; extensive research within this period has demonstrated the efficacy of 3-mercapto-1,2,4-triazole scaffolds, particularly when combined with additional heterocyclic ring structures, exhibiting promising dual enzyme inhibition potential. The inhibitory potential of these scaffolds has been evaluated through various parameters, including IC values, percentage inhibition, molecular docking, SAR, and kinetic analyses, consistently showing promising results compared to standard drugs like acarbose.
View Article and Find Full Text PDFJ Enzyme Inhib Med Chem
December 2025
College of Traditional Chinese Medicine Resources, Guangdong Pharmaceutical University, Yunfu, China.
A green ultrasound-assisted deep eutectic solvent (UAEDES) method was optimised for extracting flavonoid enzyme inhibitors from . Optimal conditions (choline chloride-1,4-butanediol 1:3 molar ratio, 43% water content, 50 mL/g liquid-to-solid ratio, 80 °C ultrasound for 48 min) yielded 3.15% total flavonoids, 45.
View Article and Find Full Text PDFArch Pharm (Weinheim)
September 2025
Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore, India.
A series of fifteen 1,2,3-triazole derivatives 6(a-o) were developed and evaluated for their inhibitory effects on carbohydrate-hydrolyzing enzymes implicated in Type 2 diabetes management. The compounds were assessed through in silico studies (including molecular docking and ADME predictions) and in vitro assays such as α-amylase, α-glucosidase, and antioxidant activities. Notably, the compounds 6a, 6d, 6g, 6h, 6k, 6l, and 6n exhibited dual inhibition against both enzymes.
View Article and Find Full Text PDFCureus
August 2025
Bioresource Engineering, Sejong University, Seoul, KOR.
Background Type 2 diabetes (T2D) is a complex metabolic disorder characterized by impaired glucose regulation and insulin resistance and frequently accompanied by obesity and dyslipidemia. The search for novel therapeutic agents to manage these metabolic parameters remains ongoing. Pepper fruit (cv.
View Article and Find Full Text PDFJ Enzyme Inhib Med Chem
December 2025
Department of Pharmacy, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, China.
The quest for effective and safe treatments for diabetes mellitus has led to the exploration of natural metabolites as potential α-glucosidase inhibitors. This study delves into the inhibition mechanism of wedelolactone against α-glucosidase and its hypoglycaemic activity. Activity assay results discovered that wedelolactone functioned as a mixed-type inhibitor, with an IC of 39.
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