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
. 2021 Dec 11;57(12):1352.
doi: 10.3390/medicina57121352.

Different Effects of Empagliflozin on Markers of Mineral-Bone Metabolism in Diabetic and Non-Diabetic Patients with Stage 3 Chronic Kidney Disease

Affiliations

Different Effects of Empagliflozin on Markers of Mineral-Bone Metabolism in Diabetic and Non-Diabetic Patients with Stage 3 Chronic Kidney Disease

Anna Masajtis-Zagajewska et al. Medicina (Kaunas). .

Abstract

Background and objectives: Treatment with sodium-glucose co-transporter 2 (SGLT2) inhibitors decrease tubular reabsorption of phosphate, which may explain the reduction of bone mineral density and an excess of bone fractures observed in some studies with this class of drugs. Since an increased risk of bone fractures may also be a result of diabetes itself, our study aimed to compare the effect of empagliflozin on the markers of mineral-bone metabolism between diabetic (DKD) and non-diabetic (ND-CKD) patients with stage 3 chronic kidney disease (CKD). Materials and Methods: Forty-two patients with stage 3 CKD and A2 albuminuria, including 18 with DKD and 24 ND-CKD, were investigated. All subjects received 10 mg empagliflozin for 7 days. Serum calcium, phosphate, parathormone (PTH), calcitriol, bone alkaline phosphatase (BAP), FGF-23 and urine calcium, phosphate, albumin and the renal tubular maximum reabsorption rate of phosphate to the glomerular filtration rate (TmP-GFR) were measured before and after empagliflozin administration. Differences in biomarkers response to empagliflozin between DKD and ND-CKD were the main measures of outcome. Results: There was a significant increase of PTH, FGF-23 and phosphate in DKD but not in ND-CKD whereas BAP and TmP/GFR did not change in either group. The reduction of albuminuria was only significant in ND-CKD. Conclusions: The effect of SGLT2 inhibitor on serum mineral and bone markers and on albuminuria in patients with CKD may be differently modified by the presence of diabetes mellitus.

Keywords: SGLT-2 inhibitors; albuminuria; calcium; diabetic kidney disease; phosphate; phosphatonins.

PubMed Disclaimer

Conflict of interest statement

The authors declare no potential conflicts of interest with respect to the research, authorship and/or publication of this article.

Figures

Figure 1
Figure 1
Flowchart of patients.
Figure 2
Figure 2
Urine albumin-to-creatinine ratio before and after the 7-day treatment with empagliflozin in diabetic and non-diabetic patients with chronic kidney disease. Abbreviations: UACR—urine albumin-to-creatinine ratio, DKD—diabetes kidney disease, non-DKD—non diabetes kidney disease.

References

    1. Juppner H. Phosphate and FGF-23. Kidney Int. Suppl. 2011;79:S24–S27. doi: 10.1038/ki.2011.27. - DOI - PMC - PubMed
    1. Tentori F., Blayney M.J., Albert J.M., Gillespie B.W., Kerr P.G., Bommer J., Young E.W., Akizawa T., Akiba T., Pisoni R.L., et al. Mortality risk for dialysis patients with different levels of serum calcium, phosphate, and PTH: The Dialysis Outcomes and Practice Patterns Study (DOPPS) Am. J. Kidney Dis. 2008;52:519–530. doi: 10.1053/j.ajkd.2008.03.020. - DOI - PubMed
    1. Tonelli M., Sacks F., Pfeffer M., Gao Z., Curhan G. Relation between serum phosphate level and cardiovascular event rate in people with coronary disease. Circulation. 2005;25:2627–2633. doi: 10.1161/CIRCULATIONAHA.105.553198. - DOI - PubMed
    1. Dhingra R., Sullivan L.M., Fox C.S., Wang T.J., D’Agostino R.B., Gaziano J.M., Ramachandran S.V. Relations of serum phosphate and calcium levels to the incidence of cardiovascular disease in the community. Arch. Intern. Med. 2007;14:879–885. doi: 10.1001/archinte.167.9.879. - DOI - PubMed
    1. Kandula P., Dobre M., Schold J.D., Schreiber M.J., Mehrotra R., Navaneethan S.D. Vitamin D supplementation in chronic kidney disease: A systematic review and meta-analysis of observational studies and randomized controlled trials. Clin. J. Am. Soc. Nephrol. 2011;6:50–62. doi: 10.2215/CJN.03940510. - DOI - PMC - PubMed