Literature DB >> 33563658

Euglycemic Ketoacidosis as a Complication of SGLT2 Inhibitor Therapy.

Biff F Palmer1, Deborah J Clegg2.   

Abstract

Sodium-glucose cotransporter-2 (SGLT2) inhibitors are drugs designed to lower plasma glucose concentration by inhibiting Na+-glucose-coupled transport in the proximal tubule. Clinical trials demonstrate these drugs have favorable effects on cardiovascular outcomes to include slowing the progression of CKD. Although most patients tolerate these drugs, a potential complication is development of ketoacidosis, often with a normal or only a minimally elevated plasma glucose concentration. Inhibition of sodium-glucose cotransporter-2 in the proximal tubule alters kidney ATP turnover so that filtered ketoacids are preferentially excreted as Na+ or K+ salts, leading to indirect loss of bicarbonate from the body and systemic acidosis under conditions of increased ketogenesis. Risk factors include reductions in insulin dose, increased insulin demand, metabolic stress, low carbohydrate intake, women, and latent autoimmune diabetes of adulthood. The lack of hyperglycemia and nonspecific symptoms of ketoacidosis can lead to delays in diagnosis. Treatment strategies and various precautions are discussed that can decrease the likelihood of this complication.
Copyright © 2021 by the American Society of Nephrology.

Entities:  

Keywords:  euglycemic ketoacidosis; sodium glucose co-transporter inhibitor

Mesh:

Substances:

Year:  2021        PMID: 33563658      PMCID: PMC8455044          DOI: 10.2215/CJN.17621120

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   10.614


  61 in total

1.  Euglycemic Diabetic Ketoacidosis: A Predictable, Detectable, and Preventable Safety Concern With SGLT2 Inhibitors.

Authors:  Julio Rosenstock; Ele Ferrannini
Journal:  Diabetes Care       Date:  2015-09       Impact factor: 19.112

2.  Effects of gender on neuroendocrine and metabolic counterregulatory responses to exercise in normal man.

Authors:  S N Davis; P Galassetti; D H Wasserman; D Tate
Journal:  J Clin Endocrinol Metab       Date:  2000-01       Impact factor: 5.958

3.  SGLT2 Protein Expression Is Increased in Human Diabetic Nephropathy: SGLT2 PROTEIN INHIBITION DECREASES RENAL LIPID ACCUMULATION, INFLAMMATION, AND THE DEVELOPMENT OF NEPHROPATHY IN DIABETIC MICE.

Authors:  Xiaoxin X Wang; Jonathan Levi; Yuhuan Luo; Komuraiah Myakala; Michal Herman-Edelstein; Liru Qiu; Dong Wang; Yingqiong Peng; Almut Grenz; Scott Lucia; Evgenia Dobrinskikh; Vivette D D'Agati; Hermann Koepsell; Jeffrey B Kopp; Avi Z Rosenberg; Moshe Levi
Journal:  J Biol Chem       Date:  2017-02-14       Impact factor: 5.157

4.  SGLT Inhibitors for Type 1 Diabetes: Proceed With Extreme Caution.

Authors:  Joseph I Wolfsdorf; Robert E Ratner
Journal:  Diabetes Care       Date:  2019-06       Impact factor: 19.112

5.  SGLT2 inhibitors and diabetic ketoacidosis: data from the FDA Adverse Event Reporting System.

Authors:  Gian Paolo Fadini; Benedetta Maria Bonora; Angelo Avogaro
Journal:  Diabetologia       Date:  2017-05-12       Impact factor: 10.122

6.  Efficacy and Safety of Dapagliflozin in Patients With Inadequately Controlled Type 1 Diabetes (the DEPICT-2 Study): 24-Week Results From a Randomized Controlled Trial.

Authors:  Chantal Mathieu; Paresh Dandona; Pieter Gillard; Peter Senior; Christoph Hasslacher; Eiichi Araki; Marcus Lind; Stephen C Bain; Serge Jabbour; Niki Arya; Lars Hansen; Fredrik Thorén; Anna Maria Langkilde
Journal:  Diabetes Care       Date:  2018-07-19       Impact factor: 19.112

7.  Altered Patterns of Early Metabolic Decompensation in Type 1 Diabetes During Treatment with a SGLT2 Inhibitor: An Insulin Pump Suspension Study.

Authors:  Neha S Patel; Michelle A Van Name; Eda Cengiz; Lori R Carria; Stuart A Weinzimer; William V Tamborlane; Jennifer L Sherr
Journal:  Diabetes Technol Ther       Date:  2017-10-25       Impact factor: 6.118

8.  Dapagliflozin in Patients with Chronic Kidney Disease.

Authors:  Hiddo J L Heerspink; Bergur V Stefánsson; Ricardo Correa-Rotter; Glenn M Chertow; Tom Greene; Fan-Fan Hou; Johannes F E Mann; John J V McMurray; Magnus Lindberg; Peter Rossing; C David Sjöström; Roberto D Toto; Anna-Maria Langkilde; David C Wheeler
Journal:  N Engl J Med       Date:  2020-09-24       Impact factor: 91.245

Review 9.  SGLT2 Inhibitors: A Systematic Review of Diabetic Ketoacidosis and Related Risk Factors in the Primary Literature.

Authors:  Kelly R Burke; Christine A Schumacher; Spencer E Harpe
Journal:  Pharmacotherapy       Date:  2017-01-16       Impact factor: 4.705

Review 10.  Euglycaemic diabetic ketoacidosis as a complication of SGLT-2 inhibitors: epidemiology, pathophysiology, and treatment.

Authors:  Erasmia Sampani; Pantelis Sarafidis; Aikaterini Papagianni
Journal:  Expert Opin Drug Saf       Date:  2020-06-10       Impact factor: 4.250

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  4 in total

Review 1.  Prescribing SGLT2 Inhibitors in Patients With CKD: Expanding Indications and Practical Considerations.

Authors:  Kevin Yau; Atit Dharia; Ibrahim Alrowiyti; David Z I Cherney
Journal:  Kidney Int Rep       Date:  2022-05-05

Review 2.  Considerations and possibilities for sodium-glucose cotransporter 2 inhibitors in pediatric CKD.

Authors:  Alexander J Kula
Journal:  Pediatr Nephrol       Date:  2022-01-27       Impact factor: 3.651

3.  Relationship of concomitant anti-diabetic drug administration with sodium-glucose co-transporter 2 inhibitor-related ketosis.

Authors:  Cheng-Wei Lin; Shih-Yuan Hung; I-Wen Chen
Journal:  J Int Med Res       Date:  2022-03       Impact factor: 1.671

Review 4.  Sodium-glucose cotransporter-2 inhibitors (SGLT2i) in kidney transplant recipients: what is the evidence?

Authors:  Aditi Ujjawal; Brittany Schreiber; Ashish Verma
Journal:  Ther Adv Endocrinol Metab       Date:  2022-04-13       Impact factor: 4.435

  4 in total

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