TY - JOUR
T1 - Persistent Disease Activity in Patients With Long-Standing Glomerular Disease
AU - CureGN Consortium
AU - Delbarba, Elisa
AU - Marasa, Maddalena
AU - Canetta, Pietro A.
AU - Piva, Stacy E.
AU - Chatterjee, Debanjana
AU - Kil, Byum Hee
AU - Mu, Xueru
AU - Gibson, Keisha L.
AU - Hladunewich, Michelle A.
AU - Hogan, Jonathan J.
AU - Julian, Bruce A.
AU - Kidd, Jason M.
AU - Laurin, Louis Philippe
AU - Nachman, Patrick H.
AU - Rheault, Michelle N.
AU - Rizk, Dana V.
AU - Sanghani, Neil S.
AU - Trachtman, Howard
AU - Wenderfer, Scott E.
AU - Gharavi, Ali G.
AU - Bomback, Andrew S.
AU - Ahn, Wooin
AU - Appel, Gerald B.
AU - Babayev, Revekka
AU - Batal, Ibrahim
AU - Brown, Eric
AU - Campenot, Eric S.
AU - Canetta, Pietro
AU - Chan, Brenda
AU - D'Agati, Vivette D.
AU - Fernandez, Hilda
AU - Foroncewicz, Bartosz
AU - Ghiggeri, Gian Marco
AU - Hines, William H.
AU - Jain, Namrata G.
AU - Kiryluk, Krzysztof
AU - Lau, Wai L.
AU - Lin, Fangming
AU - Lugani, Francesca
AU - Markowitz, Glen
AU - Mohan, Sumit
AU - Mucha, Krzysztof
AU - Nickolas, Thomas L.
AU - Piva, Stacy
AU - Radhakrishnan, Jai
AU - Rao, Maya K.
AU - Sanna-Cherchi, Simone
AU - Santoriello, Dominick
AU - Stokes, Michael B.
AU - Yu, Natalie
AU - Valeri, Anthony M.
AU - Zviti, Ronald
AU - Greenbaum, Larry A.
AU - Smoyer, William E.
AU - Al-Uzri, Amira
AU - Ashoor, Isa
AU - Aviles, Diego
AU - Baracco, Rossana
AU - Barcia, John
AU - Bartosh, Sharon
AU - Belsha, Craig
AU - Bowers, Corinna
AU - Braun, Michael C.
AU - Chishti, Aftab
AU - Claes, Donna
AU - Cramer, Carl
AU - Davis, Keefe
AU - Erkan, Elif
AU - Feig, Daniel
AU - Freundlich, Michael
AU - Gbadegesin, Rasheed
AU - Hanna, Melisha
AU - Hidalgo, Guillermo
AU - Hunley, Tracy E.
AU - Jain, Amrish
AU - Kallash, Mahmoud
AU - Khalid, Myda
AU - Klein, Jon B.
AU - Lane, Jerome C.
AU - Mahan, John
AU - Mathews, Nisha
AU - Nester, Carla
AU - Pan, Cynthia
AU - Patterson, Larry
AU - Patel, Hiren
AU - Revell, Adelaide
AU - Silva, Cynthia
AU - Sreedharan, Rajasree
AU - Srivastava, Tarak
AU - Steinke, Julia
AU - Twombley, Katherine
AU - Vasylyeva, Tetyana L.
AU - Weaver, Donald J.
AU - Wong, Craig S.
AU - Almaani, Salem
AU - Ayoub, Isabelle
AU - Budisavljevic, Milos
AU - Derebail, Vimal
AU - Fatima, Huma
AU - O'Shaughnessy, Michelle Marie
N1 - Publisher Copyright:
© 2020 International Society of Nephrology
PY - 2020/6
Y1 - 2020/6
N2 - Introduction: Glomerular diseases are characterized by variable disease activity over many years. We aimed to analyze the relationship between clinical disease activity and duration of glomerular disease. Methods: Disease activity in adults with chronic minimal change disease, focal segmental glomerulosclerosis, membranous nephropathy, and IgA nephropathy (IgAN; first diagnostic biopsy >5 years before enrollment; Of Longstanding Disease [OLD] cohort, n = 256) followed at Columbia University Medical Center (CUMC), was compared with disease activity of an internal and external cohort of patients with first diagnostic biopsy <5 years before enrollment drawn from the Cure Glomerulonephropathy Network (CureGN cohort, n = 1182; CUMC-CureGN cohort, n = 362). Disease activity was defined by (i) Kidney Disease: Improving Global Outcomes–recommended threshold criteria for initiation of immunosuppression in primary glomerulonephropathy (GN) and (ii) CureGN's Disease Activity Working Group definitions for activity. Results: No significant differences were detected among the 3 cohorts in terms of age, sex, serum creatinine, and urinary protein-to-creatinine ratio. For each GN subtype, disease activity in the OLD cohort was comparable with disease activity in the entire CureGN and the CUMC-CureGN cohort. When limiting our comparisons to disease activity in incident CUMC-CureGN patients (first diagnostic biopsy within 6 months of enrollment), OLD patients demonstrated similar activity rates as incident patients. Conclusion: Disease activity did not differ among patients with shorter versus longer duration of disease. Such survivor patients, with long-term but persistent disease, are potentially highly informative for understanding the clinical course and pathogenesis of GN and may help identify factors mediating more chronic subtypes of disease.
AB - Introduction: Glomerular diseases are characterized by variable disease activity over many years. We aimed to analyze the relationship between clinical disease activity and duration of glomerular disease. Methods: Disease activity in adults with chronic minimal change disease, focal segmental glomerulosclerosis, membranous nephropathy, and IgA nephropathy (IgAN; first diagnostic biopsy >5 years before enrollment; Of Longstanding Disease [OLD] cohort, n = 256) followed at Columbia University Medical Center (CUMC), was compared with disease activity of an internal and external cohort of patients with first diagnostic biopsy <5 years before enrollment drawn from the Cure Glomerulonephropathy Network (CureGN cohort, n = 1182; CUMC-CureGN cohort, n = 362). Disease activity was defined by (i) Kidney Disease: Improving Global Outcomes–recommended threshold criteria for initiation of immunosuppression in primary glomerulonephropathy (GN) and (ii) CureGN's Disease Activity Working Group definitions for activity. Results: No significant differences were detected among the 3 cohorts in terms of age, sex, serum creatinine, and urinary protein-to-creatinine ratio. For each GN subtype, disease activity in the OLD cohort was comparable with disease activity in the entire CureGN and the CUMC-CureGN cohort. When limiting our comparisons to disease activity in incident CUMC-CureGN patients (first diagnostic biopsy within 6 months of enrollment), OLD patients demonstrated similar activity rates as incident patients. Conclusion: Disease activity did not differ among patients with shorter versus longer duration of disease. Such survivor patients, with long-term but persistent disease, are potentially highly informative for understanding the clinical course and pathogenesis of GN and may help identify factors mediating more chronic subtypes of disease.
KW - focal segmental glomerulosclerosis
KW - glomerular disease
KW - glomerulonephropathy
KW - IgA nephropathy
KW - membranous nephropathy
KW - minimal change disease
UR - https://www.scopus.com/pages/publications/85084503957
U2 - 10.1016/j.ekir.2020.03.017
DO - 10.1016/j.ekir.2020.03.017
M3 - Article
AN - SCOPUS:85084503957
SN - 2468-0249
VL - 5
SP - 860
EP - 871
JO - Kidney International Reports
JF - Kidney International Reports
IS - 6
ER -