Suppression of insulin secretion in the treatment of obesity: a systematic review and meta-analysis
Open accessAbstract
Objective: This proof‐of‐concept study aimed to evaluate the efficacy and safety of suppression of insulin secretion in the treatment of obesity. Methods: A search of PubMed, Embase, and Cochrane databases was performed to identify randomized controlled trials (up to January 1, 2020) that used drugs that directly suppress insulin secretion (diazoxide or octreotide) in the treatment of obesity. The extracted data were analyzed using random‐effects meta‐analysis. Results: A total of seven randomized controlled trials were included, with four using diazoxide and three using octreotide to suppress insulin secretion. Suppression of insulin secretion significantly reduced fasting insulin level (mean difference: −3.94 mIU/L; 95% CI: −7.40 to −0.47) but slightly increased fasting blood glucose level (mean difference: 0.48 mmol/L; 95% CI: 0.24 to 0.72). Following the suppression of insulin secretion, significant reductions in body weight (mean difference: −3.19 kg; 95% CI: −5.71 to −0.66), BMI (mean difference: −1.65 kg/m 2; 95% CI: −2.41 to −0.90), and fat mass (mean difference: −5.92 kg; 95% CI: −8.28 to −3.56) were observed compared with placebo in the pooled data. No significant difference in fat‐free mass was observed (mean difference: 0.56 kg; 95% CI: −0.40 to 1.52). Conclusions: Results suggest that suppression of insulin secretion may lead to reduced body weight and fat mass with slightly increased blood glucose in individuals with obesity.
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In humans, insulin and drugs that increase insulin secretion or adipose insulin sensitivity cause weight gain, whereas those that decrease insulin secretion cause weight loss.
“In humans, insulin and drugs that increase insulin secretion or adipose insulin sensitivity cause weight gain, whereas those that decrease insulin secretion [including α-glucosidase inhibitors (68), which functionally lower the GI of starch] cause weight loss (69).”
From The carbohydrate-insulin model: A physiological perspective on the obesity pandemic (2021) · cites this paper as [69]
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References 46 · Cited by 13
- Authors
- Huang, Z., Wang, W., Huang, L., Guo, L., & Chen, C.
- Affiliations
- The University of Queensland (AU)
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Corresponding author
- Guo, Lixin
- Chen, Chen
- Venue
- Obesity
- Publisher
- Wiley
- Published
- 2020-11
- Volume
- 28
- Issue
- 11
- Pages
- 2098-2106
- ISSN
- 1930-7381 (ISSN-L)
- 1930-739X
- OpenAlex
- W3095540703
- Cited by
- 13
- References
- 46
- Citations by year
- 2026: 1 · 2024: 2 · 2023: 2 · 2022: 1 · 2021: 6 · 2020: 1
- FWCI
- 0.33
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- Locations
- Obesity (publishedVersion)
- PubMed (publishedVersion)
- Griffith Research Online (submittedVersion, other-oa)
- Funders
- National Natural Science Foundation of China (81471050, 81670763)
- National Health and Medical Research Council
- Topics
- Health Sciences › Medicine › Pharmacology › Pharmacology and Obesity Treatment
- Health Sciences › Medicine › Surgery › Bariatric Surgery and Outcomes
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Keywords
- obesity treatment, diazoxide, octreotide, fasting insulin, weight loss, body mass index, fat mass, fat-free mass, blood glucose, drug safety
- MeSH terms
- Proof of Concept Study, Insulin Secretion, Adult, Animals, Blood Glucose, Body Weight, Female, Humans, Insulin, Male, Obesity, Randomized Controlled Trials as Topic, Mice, Rats
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