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. 2023 Dec 24;9(3):526-548.
doi: 10.1016/j.ekir.2023.12.019. eCollection 2024 Mar.

The Role of Sodium-Glucose Cotransporter-2 Inhibitors in the Treatment Paradigm of CKD in Africa: An African Association of Nephrology Panel Position Paper

Affiliations

The Role of Sodium-Glucose Cotransporter-2 Inhibitors in the Treatment Paradigm of CKD in Africa: An African Association of Nephrology Panel Position Paper

Faical Jarraya et al. Kidney Int Rep. .
No abstract available

Keywords: Africa; CKD management; SGLT2i; chronic kidney disease; diabetic kidney disease; sodium-glucose cotransporter-2 inhibitors.

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Figures

Figure 1
Figure 1
Overall prevalence of CKD in Africa. Adapted from Stanifer JW, Jing B, Tolan S, et al. The epidemiology of chronic kidney disease in sub-Saharan Africa: a systematic review and meta-analysis. Lancet Glob Health. 2014;2(3):e174-181. doi:10.1016/S2214-109X(14)70002-6; Kaze AD, Ilori T, Jaar BG, Echouffo-Tcheugui JB. Burden of chronic kidney disease on the African continent: a systematic review and meta-analysis. BMC Nephrol. 2018;19(1):125. doi:10.1186/s12882-018-0930-5. CKD, chronic kidney disease; SSA, sub-Saharan Africa.
Figure 2
Figure 2
Identification and referral pathway for the management of CKD. ACEi, angiotensin-converting enzyme inhibitors; AKI, acute kidney injury; ARB, angiotensin receptor blockers; CKD, chronic kidney disease; CV, cardiovascular; eGFR, estimated glomerular filtration rate; GLP-1 RA, glucagon-like peptide-1 receptor agonist; HbA1c, glycosylated hemoglobin; MBD, mineral bone diseases; RAASi, renin-angiotensin aldosterone system inhibitors; SBP, systolic blood pressure; SGLT2i, sodium-glucose cotransporter-2 inhibitors; UACR, urine albumin-to-creatinine ratio. aeGFR categories in CKD classification G1: ≥90 ml/min per 1.73 m2, G2: 60–89 ml/min per 1.73 m2, G3a: 45–59 ml/min per 1.73 m2, G3b: 30–44 ml/min per 1.73 m2, G4: 15–29 ml/min per 1.73 m2 and G5: <15 ml/min per 1.73 m2 (kidney failure) bUACR categories in CKD classification A1: <30 mg/g, A2: 30–300 mg/g, A3: >300 mg/g. Recreated with permission from Shlipak MG, Tummalapalli SL, Boulware LE, et al. The case for early identification and intervention of chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2021;99(1):34-47. doi:10.1016/j.kint.2020.10.012; permission conveyed through Copyright Clearance Center, Inc.
Figure 3
Figure 3
Mode of action of SGLT2is and beneficial effects. eGFR, estimated glomerular filtration rate.
Figure 4
Figure 4
Delayed risk of KF with the addition of SGLT2is to RAAS blockers. Reproduced from Meraz-Muñoz AY, Weinstein J, Wald R. eGFR Decline after SGLT2 Inhibitor Initiation: The Tortoise and the Hare Reimagined. Kidney360. 2021;2(6):1042-1047. doi:10.34067/KID.0001172021. eGFR, estimated glomerular filtration rate; RAASi, renin-angiotensin aldosterone system inhibitors.
Figure 5
Figure 5
Proposed treatment algorithm for SGLT2i therapy in patients with CKD. AKI, acute kidney injury; BP, blood pressure; CKD, chronic kidney disease; DKA, diabetic ketoacidosis; eGFR, estimated glomerular filtration rate; GLP1-RA, glucagon-like peptide 1 receptor agonist; HbA1c, glycosylated Hemoglobin; RAASi, renin-angiotensin aldosterone system inhibitors; SGLT2i, sodium-glucose cotransporter-2 inhibitor; SU, sulfonylureas; UACR, urine albumin-to-creatinine ratio. ∗Refer to Box C for more details. Recreated with permission from Yau K, Dharia A, Alrowiyti I, et al. Prescribing SGLT2 Inhibitors in Patients With CKD: Expanding Indications and Practical Considerations. Kidney Int Rep. 2022;7(7):1463-1476. doi:10.1016/j.ekir.2022.04.094; permission conveyed through Copyright Clearance Center, Inc.

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