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editorial
. 2023 Mar 13;16(6):909–913. doi: 10.1093/ckj/sfad045

Table 1:

Main studies reporting outcomes of SGLT2is on KTRs

Study Design Population Intervention Results
Halden et al. 2019 [6] RCT, n = 49 (22 patients on empagliflozin) PTDM with KT >1 year, eGFR >30 ml/min/1.73 m2 Empagliflozin versus placebo Empagliflozin:
• Greater reduction of HbA1c: −0.2% (95% CI −0.6 to −0.1) versus 0.1% (95% CI −0.1–0.4)
• Greater reduction in body weight: −2.5 kg (95% CI −4.0 to −0.05) versus 1.0 kg (95% CI 0.0−2.0)
• No changes in BP or eGFR
• No relevant pharmacokinetic interactions with immunosuppressive drugs
• One case of urosepsis and one yeast infection
Rajasekeran et al. 2017 [10] Case series (4 SPKT, 6 KT) KT or SPKT on canagliflozin Canagliflozin • No UTI or mycotic infections
• No episodes of AKI
• Improvement in glycaemic control [HbA1c mean change −0.84% (SD 1.2)], weight [−2.14 kg (SD 2.8)] and BP [PAS −6.4 (SD 10.8)]
AlKindi et al. 2020 [9] Case series (8 KT) KT on SGLT2i (T2DM or PTDM) Empagliflozin (6 patients) and dapagliflozin (2 patients) At 12 months:
• Reduction in HbA1c from 9.34% (SD 1.36) to 7.41% (SD 1.44) at 12 months
• No significant changes in eGFR
• No significant change in BP
• Weight reduction from 84.8 kg (SD 12.8) to 82.8 kg (SD 11.4) at 6 months
• One episode of UTI, no fungal infections
Attallah and Yassine 2019 [13] Case series (8 KT) KT on empagliflozin (T2DM or PTDM) Empagliflozin At 12 months:
• HbA1c decrease of 0.85 g/dl
• Slight decrease in eGFR, then stabilized
• UPCR decrease of 0.6 g/day
• Weight decrease of 2.4 kg
• Two cases of UTI (one patient discontinued SGLT2i because of UTIs)
Schwaiger et al. 2019 [7] Prospective interventional study (14 KT) Stable KT with insulin Empagliflozin At 12 months:
• No decrease in HbA1c. Improvement in beta-cell glucose sensitivity
• Body weight decrease of 1.6 kg
• At 4 weeks, a decrease in eGFR from 55.6 ml/min/1.73 m2 (SD 20.3) to 47.5  ml/min/1.73 m2 (SD 15.1). No change in UACR
• During first 4 weeks: three UTI and one uncomplicated balanitis
Mahling et al. 2019 [14] Prospective case series (10 KT) Stable KT Empagliflozin At 12 months:
• Stable eGFR
• Median HbA1c 7.3–7.1%
• Decrease in body weight −1.9 kg
• Low rate of UTI and other side effects
Shah et al. 2019 [15] Prospective descriptive study (24 KT) Stable KT with T2DM or PTDM, minimum follow-up 6 months Canagliflozin At 6 months:
• Weight reduction 78.6 kg (SD 12.1) to 76.1 kg (SD 11.2)
• PAS from 142 (21) to 134 (SD 17) and PAD 81 (SD 9) to 79 (SD 8)
• No significant change in creatinine
• HbA1c 8.5% (SD 1.5) to 7.6% (SD 1)
• No increase in infections
Song et al. 2020 [16] Observational retrospective (50 KT) KT, eGFR >30 ml/min/1.73 m2 with T2DM or PTDM Empagliflozin (n = 43), canagliflozin (n =  6) or dapagliflozin (n = 1) At 6 months:
• Weight reduction of −2.95 kg (SD 3.54)
• 14% of patients had a UTI (similar to the rate reported in KTRs)
• No significant changes in renal function
• Therapy discontinued in nine patients
Lim et al. 2022 [8] Observational retrospective (226 KT) KT with T2DM on SGLT2i • Mean follow-up 69.2 months (SD 42.2)
SGLT2 group had:
• Lower risk of primary composite outcome (all-cause mortality, death-censored graft failure and serum creatinine doubling)
• Initial eGFR dip after initiation in 15.6% of KTRs, but eGFR recovered thereafter and remained stable
Lemke et al. 2022 [17] Observational retrospective (39 KT) KT on SGLT2i (T2DM or PTDM) Canagliflozin (n = 12), dapagliflozin (n = 3), empagliflozin (n =  24) At 12 months:
• No significant change in kidney function
• 25% of patients experienced an adverse event, with UTI the most common
• HbA1c decline from a median of 8.4% (IQR 7.8–9.2) to 7.5% (6.8–8.0)
• 17 patients (43%) discontinued the drug. The most common reasons were the cost of the drug and kidney function decline

IQR: interquartile range; PAD: diastolic blood pressure; PAS: systolic blood pressure; SPKT: simultaneous pancreas–kidney transplantation; UACR: urinary albumin:creatinine ratio.