2024/11/18 by Mia Jensen, Steffen Flindt Nielsen, Steffen Thiel +6 · 1 voice
Immunology and Microbiology · Medicine · #Complement system in diseases #Diabetes Treatment and Management #Erythropoietin and Anemia Treatment
paper · pdf · doi:10.1016/j.ekir.2024.11.014
openalex created_date 2024/11/18 · openalex publication_date 2024/11/18 · openalex updated_date 2026/07/23
Sodium-glucose cotransporter 2 inhibitors (SGLT-2i’s) improve kidney and cardiovascular outcomes in patients with diabetic nephropathy beyond antihypertensive and glucose-lowering effects.1 In patients with albuminuria, complement precursors are aberrantly filtered and subsequently activated in tubular fluid.2,3 Patients with diabetes and albuminuria are prone to complement binding to metabolically stressed and hyperactive SGLT-2–expressing tubular cells. Pattern-recognition molecules in the lectin pathway of complement, including MBL, collectin kidney 1 (CL-K1), and collectin liver 1 are associated with diabetic nephropathy.