{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T06:08:46Z","timestamp":1790662126690,"version":"4.1.0"},"reference-count":22,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"11","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":["JASN"],"published-print":{"date-parts":[[2021,11]]},"abstract":"<jats:sec>\n                    <jats:title>Significance Statement<\/jats:title>\n                    <jats:p>\n                      Long-term outcome of COVID-19\u2013associated collapsing glomerulopathy is unknown. In this study of 23 patients, most were Black, had mild to moderate COVID-19, and presented with nephrotic-range proteinuria and AKI, requiring dialysis in 14 (61%). Immunostaining and\n                      <jats:italic toggle=\"yes\">in situ<\/jats:italic>\n                      hybridization did not detect direct viral infection of the kidney. Of 17 genotyped patients, 16 (94%) had a high-risk\n                      <jats:italic toggle=\"yes\">APOL1<\/jats:italic>\n                      genotype. Among 22 patients (96%) with follow-up (median 155 days), 11 (50%) received therapy directed to COVID-19, and eight (36%) received glucocorticoid therapy for podocytopathy. At follow-up, 19 (86%) of the patients survived, 15 (68%) were dialysis free, and eight (36%) achieved partial remission of proteinuria with residual CKD. Seven of the 14 patients who initially required dialysis came off dialysis. Despite the frequent reversibility of initial AKI, prognosis remains guarded, and more effective therapy is needed.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>The long-term outcome of COVID-19\u2013associated collapsing glomerulopathy is unknown.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      We retrospectively identified 76 native kidney biopsies from patients with history of COVID-19 between March 2020 and April 2021. Presenting and outcome data were obtained for all 23 patients with collapsing glomerulopathy and for seven patients with noncollapsing podocytopathies. We performed\n                      <jats:italic toggle=\"yes\">APOL1<\/jats:italic>\n                      genotyping by Sanger sequencing, immunostaining for spike and nucleocapsid proteins, and\n                      <jats:italic toggle=\"yes\">in situ<\/jats:italic>\n                      hybridization for SARS-CoV-2.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The 23 patients with COVID-19\u2013associated collapsing glomerulopathy were median age 57 years (range, 35\u201372), included 16 men, and were predominantly (91%) Black. Severity of COVID-19 was mild or moderate in most (77%) patients. All but one patient presented with AKI, 17 had nephrotic-range proteinuria, and six had nephrotic syndrome. Fourteen (61%) patients required dialysis at presentation. Among 17 patients genotyped, 16 (94%) were high-risk\n                      <jats:italic toggle=\"yes\">APOL1<\/jats:italic>\n                      . Among 22 (96%) patients with median follow-up at 155 days (range, 30\u2013412), 11 (50%) received treatment for COVID-19, and eight (36%) received glucocorticoid therapy for podocytopathy. At follow-up, 19 (86%) patients were alive, and 15 (68%) were dialysis free, including seven of 14 who initially required dialysis. The dialysis-free patients included 64% (seven of 11) of those treated for COVID-19 and 75% (six of eight) of those treated with glucocorticoids for podocytopathy. Overall, 36% achieved partial remission of proteinuria, 32% had no remission, and 32% reached combined end points of ESKD or death. Viral infection of the kidney was not detected.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Half of 14 patients with COVID-19\u2013associated collapsing glomerulopathy requiring dialysis achieved dialysis independence, but the long-term prognosis of residual proteinuric CKD remains guarded, indicating a need for more effective therapy.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1681\/asn.2021070931","type":"journal-article","created":{"date-parts":[[2021,10,20]],"date-time":"2021-10-20T13:54:17Z","timestamp":1634738057000},"page":"2958-2969","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":49,"title":["Longitudinal Outcomes of COVID-19\u2013Associated Collapsing Glomerulopathy and Other Podocytopathies"],"prefix":"10.1681","volume":"32","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8396-9877","authenticated-orcid":false,"given":"Satoru","family":"Kudose","sequence":"first","affiliation":[{"name":"Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dominick","family":"Santoriello","sequence":"additional","affiliation":[{"name":"Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrew S.","family":"Bomback","sequence":"additional","affiliation":[{"name":"Department of Medicine, Division of Nephrology, Columbia University Irving Medical Center, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7938-1816","authenticated-orcid":false,"given":"Miroslav","family":"Sekulic","sequence":"additional","affiliation":[{"name":"Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ibrahim","family":"Batal","sequence":"additional","affiliation":[{"name":"Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M. 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