Literature DB >> 35088160

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

Alexander J Kula1,2.   

Abstract

Sodium-glucose cotransporter 2 inhibitors (SGLT2is) were originally developed as glucose-lowering agents. These medications function by inhibiting glucose and sodium reabsorption in the S1 segment of the proximal tubule. Early clinical trials in adults with type 2 diabetes mellitus (T2DM) suggested a significant improvement in kidney and cardiovascular outcomes with SGLT2i therapy. Since then, SGLT2is have become a mainstay treatment for adult patients with CKD. A growing body of research has explored deploying these medications in new clinical contexts and investigated the mechanisms underlying their physiologic effects. However, patients under the age of 18 years have been largely excluded from all major trials of SGLT2i. This review aims to summarize the available clinical evidence, physiology, and mechanisms relating to SGLT2is to inform discussions about their implementation in pediatrics.
© 2022. The Author(s), under exclusive licence to International Pediatric Nephrology Association.

Entities:  

Keywords:  Mechanisms; Pediatric CKD; SGLT2 inhibitor

Mesh:

Substances:

Year:  2022        PMID: 35088160     DOI: 10.1007/s00467-022-05456-x

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.651


  62 in total

Review 1.  SGLT2 inhibition--a novel strategy for diabetes treatment.

Authors:  Edward C Chao; Robert R Henry
Journal:  Nat Rev Drug Discov       Date:  2010-05-28       Impact factor: 84.694

Review 2.  Development of SGLT1 and SGLT2 inhibitors.

Authors:  Timo Rieg; Volker Vallon
Journal:  Diabetologia       Date:  2018-08-22       Impact factor: 10.122

3.  SGLT2 Inhibitors-Sweet Success for Diabetic Kidney Disease?

Authors:  Ian H de Boer; Steven E Kahn
Journal:  J Am Soc Nephrol       Date:  2016-08-18       Impact factor: 10.121

Review 4.  Familial renal glucosuria and SGLT2: from a mendelian trait to a therapeutic target.

Authors:  René Santer; Joaquim Calado
Journal:  Clin J Am Soc Nephrol       Date:  2009-11-05       Impact factor: 8.237

Review 5.  Renal sodium-glucose transport: role in diabetes mellitus and potential clinical implications.

Authors:  George L Bakris; Vivian A Fonseca; Kumar Sharma; Ernest M Wright
Journal:  Kidney Int       Date:  2009-04-08       Impact factor: 10.612

6.  Discovery of dapagliflozin: a potent, selective renal sodium-dependent glucose cotransporter 2 (SGLT2) inhibitor for the treatment of type 2 diabetes.

Authors:  Wei Meng; Bruce A Ellsworth; Alexandra A Nirschl; Peggy J McCann; Manorama Patel; Ravindar N Girotra; Gang Wu; Philip M Sher; Eamonn P Morrison; Scott A Biller; Robert Zahler; Prashant P Deshpande; Annie Pullockaran; Deborah L Hagan; Nathan Morgan; Joseph R Taylor; Mary T Obermeier; William G Humphreys; Ashish Khanna; Lorell Discenza; James G Robertson; Aiying Wang; Songping Han; John R Wetterau; Evan B Janovitz; Oliver P Flint; Jean M Whaley; William N Washburn
Journal:  J Med Chem       Date:  2008-02-09       Impact factor: 7.446

7.  Advancing American Kidney Health and the Role of Sodium-Glucose Cotransporter-2 Inhibitors: A Missed Opportunity.

Authors:  Jiahua Li; Sri Lekha Tummalapalli; Mallika L Mendu
Journal:  Clin J Am Soc Nephrol       Date:  2021-06-16       Impact factor: 10.614

8.  Pharmacokinetic and pharmacodynamic profile of the sodium-glucose co-transporter-2 inhibitor empagliflozin in young people with Type 2 diabetes: a randomized trial.

Authors:  L M B Laffel; W V Tamborlane; A Yver; G Simons; J Wu; V Nock; D Hobson; K S Hughan; S Kaspers; J Marquard
Journal:  Diabet Med       Date:  2018-05-06       Impact factor: 4.359

9.  Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis.

Authors:  Jennifer R Donnan; Catherine A Grandy; Eugene Chibrikov; Carlo A Marra; Kris Aubrey-Bassler; Karissa Johnston; Michelle Swab; Jenna Hache; Daniel Curnew; Hai Nguyen; John-Michael Gamble
Journal:  BMJ Open       Date:  2019-02-01       Impact factor: 2.692

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