TY - JOUR
T1 - The role of complement in kidney disease
T2 - conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
AU - for Conference Participants
AU - Vivarelli, Marina
AU - Barratt, Jonathan
AU - Beck, Laurence H.
AU - Fakhouri, Fadi
AU - Gale, Daniel P.
AU - Goicoechea de Jorge, Elena
AU - Mosca, Marta
AU - Noris, Marina
AU - Pickering, Matthew C.
AU - Susztak, Katalin
AU - Thurman, Joshua M.
AU - Cheung, Michael
AU - King, Jennifer M.
AU - Jadoul, Michel
AU - Winkelmayer, Wolfgang C.
AU - Smith, Richard J.H.
AU - Alberici, Federico
AU - Antonucci, Luca
AU - Avcin, Tadej
AU - Bagga, Arvind
AU - Bajema, Ingeborg M.
AU - Blasco, Miquel
AU - Chauvet, Sophie
AU - Cook, H. Terence
AU - Cravedi, Paolo
AU - Dragon-Durey, Marie Agnès
AU - Fischer, Lauren
AU - Fogo, Agnes B.
AU - Frazer-Abel, Ashley
AU - Frémeaux-Bacchi, Véronique
AU - Görlich, Nina
AU - Haas, Mark
AU - Humphreys, Alister
AU - Jha, Vivekanand
AU - Jauhal, Arenn
AU - Kavanagh, David
AU - Kronbichler, Andreas
AU - Lafayette, Richard A.
AU - Lanning, Lynne D.
AU - Lemaire, Mathieu
AU - Le Quintrec, Moglie
AU - Licht, Christoph
AU - Liew, Adrian
AU - McAdoo, Steve
AU - Medjeral-Thomas, Nicholas R.
AU - Meroni, Pier Luigi
AU - Morelle, Johann
AU - Nester, Carla M.
AU - Praga, Manuel
AU - Ramachandran, Raja
N1 - Publisher Copyright:
© 2024 Kidney Disease: Improving Global Outcomes (KDIGO)
PY - 2024/9
Y1 - 2024/9
N2 - Uncontrolled complement activation can cause or contribute to glomerular injury in multiple kidney diseases. Although complement activation plays a causal role in atypical hemolytic uremic syndrome and C3 glomerulopathy, over the past decade, a rapidly accumulating body of evidence has shown a role for complement activation in multiple other kidney diseases, including diabetic nephropathy and several glomerulonephritides. The number of available complement inhibitor therapies has also increased during the same period. In 2022, Kidney Diseases: Improving Global Outcomes (KDIGO) convened a Controversies Conference, “The Role of Complement in Kidney Disease,” to address the expanding role of complement dysregulation in the pathophysiology, diagnosis, and management of various glomerular diseases, diabetic nephropathy, and other forms of hemolytic uremic syndrome. Conference participants reviewed the evidence for complement playing a primary causal or secondary role in progression for several disease states and considered how evidence of complement involvement might inform management. Participating patients with various complement-mediated diseases and caregivers described concerns related to life planning, implications surrounding genetic testing, and the need for inclusive implementation of effective novel therapies into clinical practice. The value of biomarkers in monitoring disease course and the role of the glomerular microenvironment in complement response were examined, and key gaps in knowledge and research priorities were identified.
AB - Uncontrolled complement activation can cause or contribute to glomerular injury in multiple kidney diseases. Although complement activation plays a causal role in atypical hemolytic uremic syndrome and C3 glomerulopathy, over the past decade, a rapidly accumulating body of evidence has shown a role for complement activation in multiple other kidney diseases, including diabetic nephropathy and several glomerulonephritides. The number of available complement inhibitor therapies has also increased during the same period. In 2022, Kidney Diseases: Improving Global Outcomes (KDIGO) convened a Controversies Conference, “The Role of Complement in Kidney Disease,” to address the expanding role of complement dysregulation in the pathophysiology, diagnosis, and management of various glomerular diseases, diabetic nephropathy, and other forms of hemolytic uremic syndrome. Conference participants reviewed the evidence for complement playing a primary causal or secondary role in progression for several disease states and considered how evidence of complement involvement might inform management. Participating patients with various complement-mediated diseases and caregivers described concerns related to life planning, implications surrounding genetic testing, and the need for inclusive implementation of effective novel therapies into clinical practice. The value of biomarkers in monitoring disease course and the role of the glomerular microenvironment in complement response were examined, and key gaps in knowledge and research priorities were identified.
KW - complement inhibitor
KW - complement-mediated injury
KW - glomerular injury
UR - https://www.scopus.com/pages/publications/85198089880
U2 - 10.1016/j.kint.2024.05.015
DO - 10.1016/j.kint.2024.05.015
M3 - Article
C2 - 38844295
AN - SCOPUS:85198089880
SN - 0085-2538
VL - 106
SP - 369
EP - 391
JO - Kidney International
JF - Kidney International
IS - 3
ER -