Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study

dc.contributor.authorSelewski, David T.
dc.contributor.authorAmbruzs, Josephine M.
dc.contributor.authorAppel, Gerald B.
dc.contributor.authorBomback, Andrew S.
dc.contributor.authorMatar, Raed Bou
dc.contributor.authorCai, Yi
dc.contributor.authorCattran, Daniel C.
dc.contributor.authorChishti, Aftab S.
dc.contributor.authorD’Agati, Vivette D.
dc.contributor.authorD’Alessandri-Silva, Cynthia J.
dc.contributor.authorGbadegesin, Rasheed A.
dc.contributor.authorHogan, Jonathan J.
dc.contributor.authorIragorri, Sandra
dc.contributor.authorJennette, J. Charles
dc.contributor.authorJulian, Bruce A.
dc.contributor.authorKhalid, Myda
dc.contributor.authorLafayette, Richard A.
dc.contributor.authorLiapis, Helen
dc.contributor.authorLugani, Francesca
dc.contributor.authorMansfield, Sarah A.
dc.contributor.authorMason, Sherene
dc.contributor.authorNachman, Patrick H.
dc.contributor.authorNast, Cynthia C.
dc.contributor.authorNester, Carla M.
dc.contributor.authorNoone, Damien G.
dc.contributor.authorNovak, Jan
dc.contributor.authorO’Shaughnessy, Michelle M.
dc.contributor.authorReich, Heather N.
dc.contributor.authorRheault, Michelle N.
dc.contributor.authorRizk, Dana V.
dc.contributor.authorSaha, Manish K.
dc.contributor.authorSanghani, Neil S.
dc.contributor.authorSperati, C. John
dc.contributor.authorSreedharan, Rajasree
dc.contributor.authorSrivastava, Tarak
dc.contributor.authorSwiatecka-Urban, Agnieszka
dc.contributor.authorTwombley, Katherine
dc.contributor.authorVasylyeva, Tetyana L.
dc.contributor.authorWeaver, Donald J.
dc.contributor.authorYin, Hong
dc.contributor.authorZee, Jarcy
dc.contributor.authorFalk, Ronald J.
dc.contributor.authorGharavi, Ali G.
dc.contributor.authorGillespie, Brenda W.
dc.contributor.authorGipson, Debbie S.
dc.contributor.authorGreenbaum, Larry A.
dc.contributor.authorHolzman, Lawrence B.
dc.contributor.authorKretzler, Matthias
dc.contributor.authorRobinson, Bruce M.
dc.contributor.authorSmoyer, William E.
dc.contributor.authorFlessner, Michael
dc.contributor.authorGuay-Woodford, Lisa M.
dc.contributor.authorKiryluk, Krzysztof
dc.contributor.authorCureGN Consortium
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2019-06-11T14:08:27Z
dc.date.available2019-06-11T14:08:27Z
dc.date.issued2018-08-03
dc.description.abstractIntroduction: The Cure Glomerulonephropathy Network (CureGN) is a 66-center longitudinal observational study of patients with biopsy-confirmed minimal change disease, focal segmental glomerulosclerosis, membranous nephropathy, or IgA nephropathy (IgAN), including IgA vasculitis (IgAV). This study describes the clinical characteristics and treatment patterns in the IgA cohort, including comparisons between IgAN versus IgAV and adult versus pediatric patients. Methods: Patients with a diagnostic kidney biopsy within 5 years of screening were eligible to join CureGN. This is a descriptive analysis of clinical and treatment data collected at the time of enrollment. Results: A total of 667 patients (506 IgAN, 161 IgAV) constitute the IgAN/IgAV cohort (382 adults, 285 children). At biopsy, those with IgAV were younger (13.0 years vs. 29.6 years, P < 0.001), more frequently white (89.7% vs. 78.9%, P = 0.003), had a higher estimated glomerular filtration rate (103.5 vs. 70.6 ml/min per 1.73 m2, P < 0.001), and lower serum albumin (3.4 vs. 3.8 g/dl, P < 0.001) than those with IgAN. Adult and pediatric individuals with IgAV were more likely than those with IgAN to have been treated with immunosuppressive therapy at or prior to enrollment (79.5% vs. 54.0%, P < 0.001). Conclusion: This report highlights clinical differences between IgAV and IgAN and between children and adults with these diagnoses. We identified differences in treatment with immunosuppressive therapies by disease type. This description of baseline characteristics will serve as a foundation for future CureGN studies.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationSelewski, D. T., Ambruzs, J. M., Appel, G. B., Bomback, A. S., Matar, R. B., Cai, Y., … CureGN Consortium (2018). Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study. Kidney international reports, 3(6), 1373–1384. doi:10.1016/j.ekir.2018.07.021en_US
dc.identifier.urihttps://hdl.handle.net/1805/19582
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.ekir.2018.07.021en_US
dc.relation.journalKidney International Reportsen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourcePMCen_US
dc.subjectHenoch-Schönlein purpura (HSP)en_US
dc.subjectIgA nephropathy (IgAN)en_US
dc.subjectIgA vasculitis (IgAV)en_US
dc.subjectGlomerulonephritisen_US
dc.titleClinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Studyen_US
dc.typeArticleen_US
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