Ewha Med J.  2017 Jan;40(1):55-58. 10.12771/emj.2017.40.1.55.

Euglycemic Diabetic Ketoacidosis When Reducing Insulin Dosage in Patients Taking Sodium Glucose Cotransporter 2 Inhibitor

Affiliations
  • 1Department of Internal Medicine, Gwangmyeong Sungae Hospital, Gwangmyeong, Korea. dmbak@sungae.co.kr
  • 2Division of Endocrinology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Korea.
  • 3Department of Internal Medicine, Seoul Sungae Hospital, Seoul, Korea.

Abstract

Sodium glucose cotransporter 2 (SGLT2) inhibitor has been recently reported of diabetic ketoacidosis due to accumulation of ketone bodies in patients with severe dehydration caused from such like diarrhea even though the patient had normal glucose level. This is a case of ketoacidosis in normal glucose level as production of ketone bodies is stimulated in liver with increased secretion of glucagon by stimulation of α cells in pancreas due to increase of lipolysis caused from reducing insulin and by SGLT2 inhibitor among patients who are under concurrent insulin and SGLT2 inhibitor. Thus, insulin dosage reduction requires caution in order to control blood glucose level on combined treatment of SGLT2 inhibitor in a patient who is administering insulin because the patient may be caused ketoacidosis in normal blood glucose level.

Keyword

Diabetic ketoacidosis; Sodium glucose cotransporter 2

MeSH Terms

Blood Glucose
Dehydration
Diabetic Ketoacidosis*
Diarrhea
Glucagon
Glucose*
Humans
Insulin*
Ketone Bodies
Ketosis
Lipolysis
Liver
Pancreas
Sodium*
Blood Glucose
Glucagon
Glucose
Insulin
Ketone Bodies
Sodium

Reference

1. Jeon JY, Kim DJ, Ko SH, Kwon HS, Lim S, Choi SH, et al. Current status of glycemic control of patients with diabetes in Korea: the fifth Korea national health and nutrition examination survey. Diabetes Metab J. 2014; 38:197–203.
2. Nathan DM, Buse JB, Davidson MB, Ferrannini E, Holman RR, Sherwin R, et al. Medical management of hyperglycemia in type 2 diabetes: a consensus algorithm for the initiation and adjustment of therapy. A consensus statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2009; 32:193–203.
3. Nair S, Wilding JP. Sodium glucose cotransporter 2 inhibitors as a new treatment for diabetes mellitus. J Clin Endocrinol Metab. 2010; 95:34–42.
4. List JF, Woo V, Morales E, Tang W, Fiedorek FT. Sodium-glucose cotransport inhibition with dapagliflozin in type 2 diabetes. Diabetes Care. 2009; 32:650–657.
5. Peters AL, Buschur EO, Buse JB, Cohan P, Diner JC, Hirsch IB. Euglycemic diabetic ketoacidosis: a potential complication of treatment with sodium-glucose cotransporter 2 inhibition. Diabetes Care. 2015; 38:1687–1693.
6. Kim WJ, Kim SS. The side effects of sodium glucose cotransporter 2 (SGLT2) inhibitor. J Korean Diabetes. 2014; 15:158–162.
7. Wolfsdorf J, Glaser N, Sperling MA;. Diabetic ketoacidosis in infants, children, and adolescents: a consensus statement from the American Diabetes Association. Diabetes Care. 2006; 29:1150–1159.
8. Kitabchi AE, Umpierrez GE, Murphy MB, Barrett EJ, Kreisberg RA, Malone JI, et al. Management of hyperglycemic crises in patients with diabetes. Diabetes Care. 2001; 24:131–153.
9. Jun JH, Choe KJ, Woo YM, Park YR, Park YK, Kim WJ, et al. A case of diabetic ketoacidosis induced by sodium-glucose cotransporter 2 inhibitor. J Korean Diabetes. 2015; 16:310–314.
10. Taylor SI, Blau JE, Rother KI. SGLT2 inhibitors may predispose to ketoacidosis. J Clin Endocrinol Metab. 2015; 100:2849–2852.
Full Text Links
  • EMJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr