Literature DB >> 27894216

Bone effects of canagliflozin, a sodium glucose co-transporter 2 inhibitor, in patients with type 2 diabetes mellitus.

Thomas C Blevins1, Azeez Farooki2.   

Abstract

Canagliflozin, a sodium glucose co-transporter 2 (SGLT2) inhibitor approved for the treatment of type 2 diabetes mellitus (T2DM), lowers blood glucose by inhibiting renal glucose reabsorption and increasing urinary glucose excretion. It has been reported that SGLT2 inhibitors may have potential adverse effects on bone, including increased fracture risk and decreased bone mineral density (BMD). Across clinical studies, canagliflozin was not associated with meaningful changes in serum or urine calcium, vitamin D, or parathyroid hormone. Minimal increases in serum phosphate and magnesium that were within normal limits were seen with canagliflozin versus placebo. Canagliflozin was associated with increases in serum collagen type 1 beta-carboxy telopeptide (beta-CTX), a bone resorption marker, and osteocalcin, a bone formation marker. Decreases in total hip BMD were seen with canagliflozin 100 and 300 mg versus placebo after 2 years (-1.7%, -2.1%, -0.8%; differences of -0.9% and -1.2%), but not at other skeletal sites (normal age-related bone loss, ~0.5-1.0%/year). Changes in beta-CTX and total hip BMD were significantly associated with weight loss, which is known to increase bone resorption markers and decrease BMD. Canagliflozin was associated with a higher fracture incidence in an interim analysis of the CANagliflozin cardioVascular Assessment Study (CANVAS) in patients with a history or high risk of cardiovascular disease (incidence per 100 patient-years of 1.6, 1.6, and 1.1 with canagliflozin 100 and 300 mg and placebo), but not in other clinical studies of patients with T2DM. Fractures tended to occur as early as 12 weeks after initiating treatment and were primarily located in the distal parts of the upper and lower extremities. The reason for increased fracture risk with canagliflozin treatment is unknown, but is likely not related to a direct effect of canagliflozin on bone-related biomarkers. Data from ongoing canagliflozin studies, including CANVAS, will provide additional information on fracture risk in patients with T2DM.

Entities:  

Keywords:  Bone mineral density; bone mineral metabolism; bone turnover markers; canagliflozin; fractures; type 2 diabetes mellitus

Mesh:

Substances:

Year:  2016        PMID: 27894216     DOI: 10.1080/00325481.2017.1256747

Source DB:  PubMed          Journal:  Postgrad Med        ISSN: 0032-5481            Impact factor:   3.840


  10 in total

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Authors:  Evangelia Kalaitzoglou; John L Fowlkes; Iuliana Popescu; Kathryn M Thrailkill
Journal:  Diabetes Metab Res Rev       Date:  2018-12-20       Impact factor: 4.876

Review 2.  Sodium-glucose cotransporter type 2 inhibitors for the treatment of type 2 diabetes mellitus.

Authors:  André J Scheen
Journal:  Nat Rev Endocrinol       Date:  2020-08-27       Impact factor: 43.330

Review 3.  Adverse drug events observed in patients with type 2 diabetes mellitus treated with 100 mg versus 300 mg canagliflozin: a systematic review and meta-analysis of published randomized controlled trials.

Authors:  Pravesh Kumar Bundhun; Girish Janoo; Feng Huang
Journal:  BMC Pharmacol Toxicol       Date:  2017-04-16       Impact factor: 2.483

4.  Effıcacy and safety of dapagliflozin on diabetic patients receiving high-doses of insulin.

Authors:  Meltem Sertbas; Yasar Sertbas; Nalan Okuroglu; Ali Burkan Akyildiz; Seda Sancak; Ali Ozdemir
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5.  Effects of sodium glucose cotransporter 2 inhibitors on mineral metabolism in type 2 diabetes mellitus.

Authors:  Joanna Sophia J Vinke; Hiddo J L Heerspink; Martin H de Borst
Journal:  Curr Opin Nephrol Hypertens       Date:  2019-07       Impact factor: 2.894

Review 6.  SGLT2 Inhibitors: A Review of Their Antidiabetic and Cardioprotective Effects.

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Journal:  Int J Environ Res Public Health       Date:  2019-08-17       Impact factor: 3.390

Review 7.  The Extraglycemic Effect of SGLT-2is on Mineral and Bone Metabolism and Bone Fracture.

Authors:  Bingzi Dong; Ruolin Lv; Jun Wang; Lin Che; Zhongchao Wang; Zhouyang Huai; Yangang Wang; Lili Xu
Journal:  Front Endocrinol (Lausanne)       Date:  2022-07-07       Impact factor: 6.055

Review 8.  Cardiovascular Effects of New Oral Glucose-Lowering Agents: DPP-4 and SGLT-2 Inhibitors.

Authors:  André J Scheen
Journal:  Circ Res       Date:  2018-05-11       Impact factor: 17.367

9.  Effects of the sodium-glucose co-transporter 2 inhibitor dapagliflozin in patients with type 2 diabetes and Stages 3b-4 chronic kidney disease.

Authors:  Claire C J Dekkers; David C Wheeler; C David Sjöström; Bergur V Stefansson; Valerie Cain; Hiddo J L Heerspink
Journal:  Nephrol Dial Transplant       Date:  2018-11-01       Impact factor: 5.992

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

Authors:  Anna Masajtis-Zagajewska; Tomasz Hołub; Katarzyna Pęczek; Agnieszka Makówka; Michał Nowicki
Journal:  Medicina (Kaunas)       Date:  2021-12-11       Impact factor: 2.430

  10 in total

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