Acarbose Improves Hypoglycaemia Following Gastric Bypass Surgery Without Increasing Glucagon-Like Peptide 1 Levels
Abstract
Background Postprandial hypoglycaemia is a severe complication of Roux-en-Y gastric bypass (RYGBP). Acarbose, an α-glucosidase inhibitor (AGI), is employed in its treatment. Several studies have shown that AGIs increase the postprandial levels of glucagon-like peptide 1 (GLP-1). However, an excessive level of GLP-1 is one of the factors involved in the physiopathology of this condition. We analysed the effect of acarbose oral administration in eight RYBGP patients with clinically significant hypoglycaemia or dumping syndrome. Methods Glucose, insulin and GLP-1 plasma levels in fasting and after ingestion of a standard meal (Ensure Plus®; 13 g protein, 50 g carbohydrate, 11 g fat) were measured. The test was repeated the following week with the oral administration of 100 mg of acarbose 15 min prior to the meal. Results Five patients developed asymptomatic hypoglycaemia during the test (glucose level Conclusions Acarbose avoided postprandial hypoglycaemia following RYGBP by decreasing the hyperinsulinemic response. This was associated with a decrease in early GLP-1 secretion, in contrast to that observed in non-surgical subjects. This finding could be explained by the reduction of glucose load in the jejunum produced by the α-glucosidase inhibition, which is the main stimulus for GLP-1 secretion.
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Acarbose has been found to be an effective and affordable first option for PBH, although gastrointestinal side effects may limit patient tolerance.
“Acarbose, an oral α -glucosidase inhibitor, slows carbohydrate digestion and absorption and has been found to be an effective and affordable first option, although gastrointestinal side effects may limit patient tolerance [57].”
From Non-Diabetic Hypoglycemia: Evaluation and Management in Adults (2025) · cites this paper as [57]
Acarbose slows carbohydrate digestion and absorption.
“Acarbose, an oral α -glucosidase inhibitor, slows carbohydrate digestion and absorption and has been found to be an effective and affordable first option, although gastrointestinal side effects may limit patient tolerance [57].”
From Non-Diabetic Hypoglycemia: Evaluation and Management in Adults (2025) · cites this paper as [57]
Cites
Cryer, P. E., Axelrod, L., Grossman, A. B., Heller, S. R., Montori, V. M., Seaquist, E. R., & Service, F. J. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-1410 · Cited by 1,277 · cited 1× · see citing works
“Recently, the Endocrine Society Statement Clinical Practice Guideline defined a glycaemia value less than 55 mg/dl [21].”
Marsk, R., Jonas, E., Rasmussen, F., & Näslund, E. (2010) · Diabetologia · doi:10.1007/s00125-010-1798-5 · Cited by 273 · see citing works
Meier, J. J., Butler, A. E., Galasso, R., & Butler, P. C. (2006) · Diabetes Care · doi:10.2337/dc06-0392 · Cited by 249 · see citing works
Rumilla, K. M., Erickson, L. A., Service, F. J., Vella, A., Thompson, G. B., Grant, C. S., & Lloyd, R. V. (2009) · Modern Pathology · doi:10.1038/modpathol.2008.169 · Cited by 85 · cited 1× · see citing works
“However, the existence of nesidioblastosis following RYGBP in human subjects is a matter of controversy between researchers [16–18].”
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van Beek, A. P., Emous, M., Laville, M., & Tack, J. (2017) · Obesity Reviews · doi:10.1111/obr.12467 · Cited by 288 · see citing works
“(64) Case series N = 8 Acarbose 100 mg before a meal(1) • Avoided postprandial hypoglycemia”
BackgroundLee, C. J., Brown, T. T., Schweitzer, M., Magnuson, T., & Clark, J. M. (2018) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2018.01.028 · Cited by 49 · see citing works
Sheehan, A., & Patti, M. E. (2020) · Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy · doi:10.2147/dmso.s233078 · Cited by 39 · see citing works
Hypoglycemia after gastric bypass surgery
Singh, E., & Vella, A. (2012) · Diabetes Spectrum · doi:10.2337/diaspect.25.4.217 · Cited by 30 · see citing works
Non-Diabetic Hypoglycemia: Evaluation and Management in Adults
Looi, E., & Lawler, H. M. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14134393 · Cited by 10 · see citing works
“To date, there is no FDA-approved medication for use in treating PBH. Acarbose, an oral α -glucosidase inhibitor, slows carbohydrate digestion and absorption and has been found to be an effective and affordable first option, although gastrointestinal side effects may limit patient tolerance [57].”
- Authors
- Valderas, J. P., Ahuad, J., Rubio, L., Escalona, M., Pollak, F., & Maiz, A.
- Affiliations
- Pontificia Universidad Católica de Chile (CL)
- Corresponding author
- Valderas, Juan Patricio
- Venue
- Obesity Surgery
- Published
- 2011-12-13
- Volume
- 22
- Issue
- 4
- Pages
- 582-586
- ISSN
- 0960-8923 (ISSN-L)
- 1708-0428
- OpenAlex
- W2150155701
- Cited by
- 97
- References
- 4
- Citations by year
- 2026: 4 · 2025: 4 · 2024: 7 · 2023: 8 · 2022: 8 · 2021: 4 · 2020: 6 · 2019: 9 · 2018: 6 · 2017: 5 · 2016: 14 · 2015: 14 · 2014: 5 · 2013: 2 · 2012: 1
- FWCI
- 2.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Obesity Surgery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Bariatric Surgery and Outcomes
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Keywords
- acarbose, Roux-en-Y gastric bypass
- MeSH terms
- Administration, Oral, Adult, Blood Glucose, Diabetes Mellitus, Dumping Syndrome, Female, Humans, Hypoglycemia, Insulin, Male, Obesity, Morbid, Gastric Bypass, Treatment Outcome, Postprandial Period, Acarbose, Glucagon-Like Peptide 1
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