Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015:2015:317507.
doi: 10.1155/2015/317507. Epub 2015 Feb 15.

Sodium-glucose linked transporter-2 inhibitors in chronic kidney disease

Affiliations
Review

Sodium-glucose linked transporter-2 inhibitors in chronic kidney disease

L Zanoli et al. ScientificWorldJournal. 2015.

Abstract

SGLT2 inhibitors are new antihyperglycaemic agents whose ability to lower glucose is directly proportional to GFR. Therefore, in chronic kidney disease (CKD) the blood glucose lowering effect is reduced. Unlike many current therapies, the mechanism of action of SGLT2 inhibitors is independent of insulin action or beta-cell function. In addition, the mechanism of action of SGLT2 inhibitors is complementary and not alternative to other antidiabetic agents. SGLT2 inhibitors could be potentially effective in attenuating renal hyperfiltration and, consequently, the progression of CKD. Moreover, the reductions in intraglomerular pressure, systemic blood pressure, and uric acid levels induced by SGLT inhibition may potentially be of benefit in CKD subjects without diabetes. However, at present, only few clinical studies were designed to evaluate the effects of SGLT2 inhibitors in CKD. Consequently, safety and potential efficacy beyond blood glucose lowering should be better clarified in CKD. In this paper we provide an updated review of the use of SGLT2 inhibitors in clinical practice, with particular attention on subjects with CKD.

PubMed Disclaimer

References

    1. Whiting D. R., Guariguata L., Weil C., Shaw J. IDF Diabetes Atlas: global estimates of the prevalence of diabetes for 2011 and 2030. Diabetes Research and Clinical Practice. 2011;94(3):311–321. doi: 10.1016/j.diabres.2011.10.029. - DOI - PubMed
    1. Foley R. N., Collins A. J. End-stage renal disease in the United States: an update from the United States Renal Data System. Journal of the American Society of Nephrology. 2007;18(10):2644–2648. doi: 10.1681/asn.2007020220. - DOI - PubMed
    1. Coll-De-Tuero G., Mata-Cases M., Rodriguez-Poncelas A., et al. Chronic kidney disease in the type 2 diabetic patients: prevalence and associated variables in a random sample of 2642 patients of a Mediterranean area. BMC Nephrology. 2012;13(1, article 87) doi: 10.1186/1471-2369-13-87. - DOI - PMC - PubMed
    1. Koro C. E., Lee B. H., Bowlin S. J. Antidiabetic medication use and prevalence of chronic kidney disease among patients with type 2 diabetes mellitus in the United States. Clinical Therapeutics. 2009;31(11):2608–2617. doi: 10.1016/j.clinthera.2009.10.020. - DOI - PubMed
    1. UKPDS 34. Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). UK Prospective Diabetes Study (UKPDS) Group. The Lancet. 1998;352:854–865. - PubMed

MeSH terms

Substances