The long-term course of cyclosporine-associated chronic nephropathy
The long-term course of cyclosporine-associated chronic nephropathy. We evaluated a chronic renal injury in 37 cardiac transplant recipients treated for 12 to 24 months with cyclosporine (CsA). Twenty-four cardiac transplant recipients treated with azathioprine for more than 24 months served as cont...
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Veröffentlicht in: | Kidney international 1988-02, Vol.33 (2), p.590-600 |
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creator | Myers, Bryan D. Sibley, Richard Newton, Lynne Tomlanovich, Stephen J. Boshkos, Christopher Stinson, Edward Luetscher, John A. Whitney, Darlene J. Krasny, David Coplon, Norman S. Perlroth, Mark G. |
description | The long-term course of cyclosporine-associated chronic nephropathy. We evaluated a chronic renal injury in 37 cardiac transplant recipients treated for 12 to 24 months with cyclosporine (CsA). Twenty-four cardiac transplant recipients treated with azathioprine for more than 24 months served as controls. Despite equivalent cardiac performance, GFR in those treated with CsA was depressed, 47 ± 3 versus 94 ± 4 ml/min/1.73m2 (P < 0.001). CsA therapy was also associated with significant elevation of renal vascular resistance (RVR), proteinuria, arterial hypertension, and impaired intrarenal conversion of inactive prorenin to active renin. Histopathological changes associated with CsA included an obliterative arteriolopathy with deposition of protein-aceous material in necrotic arteriolar walls, and associated tubulointer-stitial damage. A minority of glomerbuli exhibited either ischemic collapse or sclerosis. Area perimeter analysis revealed enlargement of the remaining glomeruli with significant expansion of the mesangium. Longitudinal examination over a 48 month period (N = 15) during which CsA was reduced in dosage or withdrawn revealed persistent hypofiltration, increasingly elevated RVR and heavier proteinuria. Further histopathological deterioration was observed when renal tissue was sampled a second time in six patients, and three members of the experimental group developed end-stage renal disease. We conclude that continuous CsA therapy for more than 12 months causes a chronic injury to renal microvessels that is rarely reversible and potentially progressive. |
doi_str_mv | 10.1038/ki.1988.38 |
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We evaluated a chronic renal injury in 37 cardiac transplant recipients treated for 12 to 24 months with cyclosporine (CsA). Twenty-four cardiac transplant recipients treated with azathioprine for more than 24 months served as controls. Despite equivalent cardiac performance, GFR in those treated with CsA was depressed, 47 ± 3 versus 94 ± 4 ml/min/1.73m2 (P < 0.001). CsA therapy was also associated with significant elevation of renal vascular resistance (RVR), proteinuria, arterial hypertension, and impaired intrarenal conversion of inactive prorenin to active renin. Histopathological changes associated with CsA included an obliterative arteriolopathy with deposition of protein-aceous material in necrotic arteriolar walls, and associated tubulointer-stitial damage. A minority of glomerbuli exhibited either ischemic collapse or sclerosis. Area perimeter analysis revealed enlargement of the remaining glomeruli with significant expansion of the mesangium. Longitudinal examination over a 48 month period (N = 15) during which CsA was reduced in dosage or withdrawn revealed persistent hypofiltration, increasingly elevated RVR and heavier proteinuria. Further histopathological deterioration was observed when renal tissue was sampled a second time in six patients, and three members of the experimental group developed end-stage renal disease. We conclude that continuous CsA therapy for more than 12 months causes a chronic injury to renal microvessels that is rarely reversible and potentially progressive.</description><identifier>ISSN: 0085-2538</identifier><identifier>EISSN: 1523-1755</identifier><identifier>DOI: 10.1038/ki.1988.38</identifier><identifier>PMID: 3283402</identifier><identifier>CODEN: KDYIA5</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Biological and medical sciences ; Cyclosporins - adverse effects ; Drug toxicity and drugs side effects treatment ; Heart Transplantation ; Humans ; Kidney Diseases - chemically induced ; Kidney Diseases - pathology ; Kidney Diseases - physiopathology ; Kidney Failure, Chronic - chemically induced ; Kidney Glomerulus - pathology ; Kidney Glomerulus - ultrastructure ; Longitudinal Studies ; Medical sciences ; Microscopy, Electron ; Pharmacology. Drug treatments ; Postoperative Care ; Toxicity: urogenital system</subject><ispartof>Kidney international, 1988-02, Vol.33 (2), p.590-600</ispartof><rights>1988 International Society of Nephrology</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-b6ba7429cc8934681267b1093a7a030b872ac89bc57662c930c6a015c30b71613</citedby><cites>FETCH-LOGICAL-c481t-b6ba7429cc8934681267b1093a7a030b872ac89bc57662c930c6a015c30b71613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7126907$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3283402$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Myers, Bryan D.</creatorcontrib><creatorcontrib>Sibley, Richard</creatorcontrib><creatorcontrib>Newton, Lynne</creatorcontrib><creatorcontrib>Tomlanovich, Stephen J.</creatorcontrib><creatorcontrib>Boshkos, Christopher</creatorcontrib><creatorcontrib>Stinson, Edward</creatorcontrib><creatorcontrib>Luetscher, John A.</creatorcontrib><creatorcontrib>Whitney, Darlene J.</creatorcontrib><creatorcontrib>Krasny, David</creatorcontrib><creatorcontrib>Coplon, Norman S.</creatorcontrib><creatorcontrib>Perlroth, Mark G.</creatorcontrib><title>The long-term course of cyclosporine-associated chronic nephropathy</title><title>Kidney international</title><addtitle>Kidney Int</addtitle><description>The long-term course of cyclosporine-associated chronic nephropathy. We evaluated a chronic renal injury in 37 cardiac transplant recipients treated for 12 to 24 months with cyclosporine (CsA). Twenty-four cardiac transplant recipients treated with azathioprine for more than 24 months served as controls. Despite equivalent cardiac performance, GFR in those treated with CsA was depressed, 47 ± 3 versus 94 ± 4 ml/min/1.73m2 (P < 0.001). CsA therapy was also associated with significant elevation of renal vascular resistance (RVR), proteinuria, arterial hypertension, and impaired intrarenal conversion of inactive prorenin to active renin. Histopathological changes associated with CsA included an obliterative arteriolopathy with deposition of protein-aceous material in necrotic arteriolar walls, and associated tubulointer-stitial damage. A minority of glomerbuli exhibited either ischemic collapse or sclerosis. Area perimeter analysis revealed enlargement of the remaining glomeruli with significant expansion of the mesangium. Longitudinal examination over a 48 month period (N = 15) during which CsA was reduced in dosage or withdrawn revealed persistent hypofiltration, increasingly elevated RVR and heavier proteinuria. Further histopathological deterioration was observed when renal tissue was sampled a second time in six patients, and three members of the experimental group developed end-stage renal disease. We conclude that continuous CsA therapy for more than 12 months causes a chronic injury to renal microvessels that is rarely reversible and potentially progressive.</description><subject>Biological and medical sciences</subject><subject>Cyclosporins - adverse effects</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Heart Transplantation</subject><subject>Humans</subject><subject>Kidney Diseases - chemically induced</subject><subject>Kidney Diseases - pathology</subject><subject>Kidney Diseases - physiopathology</subject><subject>Kidney Failure, Chronic - chemically induced</subject><subject>Kidney Glomerulus - pathology</subject><subject>Kidney Glomerulus - ultrastructure</subject><subject>Longitudinal Studies</subject><subject>Medical sciences</subject><subject>Microscopy, Electron</subject><subject>Pharmacology. 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Drug treatments</topic><topic>Postoperative Care</topic><topic>Toxicity: urogenital system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Myers, Bryan D.</creatorcontrib><creatorcontrib>Sibley, Richard</creatorcontrib><creatorcontrib>Newton, Lynne</creatorcontrib><creatorcontrib>Tomlanovich, Stephen J.</creatorcontrib><creatorcontrib>Boshkos, Christopher</creatorcontrib><creatorcontrib>Stinson, Edward</creatorcontrib><creatorcontrib>Luetscher, John A.</creatorcontrib><creatorcontrib>Whitney, Darlene J.</creatorcontrib><creatorcontrib>Krasny, David</creatorcontrib><creatorcontrib>Coplon, Norman S.</creatorcontrib><creatorcontrib>Perlroth, Mark G.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Kidney international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Myers, Bryan D.</au><au>Sibley, Richard</au><au>Newton, Lynne</au><au>Tomlanovich, Stephen J.</au><au>Boshkos, Christopher</au><au>Stinson, Edward</au><au>Luetscher, John A.</au><au>Whitney, Darlene J.</au><au>Krasny, David</au><au>Coplon, Norman S.</au><au>Perlroth, Mark G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The long-term course of cyclosporine-associated chronic nephropathy</atitle><jtitle>Kidney international</jtitle><addtitle>Kidney Int</addtitle><date>1988-02-01</date><risdate>1988</risdate><volume>33</volume><issue>2</issue><spage>590</spage><epage>600</epage><pages>590-600</pages><issn>0085-2538</issn><eissn>1523-1755</eissn><coden>KDYIA5</coden><abstract>The long-term course of cyclosporine-associated chronic nephropathy. We evaluated a chronic renal injury in 37 cardiac transplant recipients treated for 12 to 24 months with cyclosporine (CsA). Twenty-four cardiac transplant recipients treated with azathioprine for more than 24 months served as controls. Despite equivalent cardiac performance, GFR in those treated with CsA was depressed, 47 ± 3 versus 94 ± 4 ml/min/1.73m2 (P < 0.001). CsA therapy was also associated with significant elevation of renal vascular resistance (RVR), proteinuria, arterial hypertension, and impaired intrarenal conversion of inactive prorenin to active renin. Histopathological changes associated with CsA included an obliterative arteriolopathy with deposition of protein-aceous material in necrotic arteriolar walls, and associated tubulointer-stitial damage. A minority of glomerbuli exhibited either ischemic collapse or sclerosis. Area perimeter analysis revealed enlargement of the remaining glomeruli with significant expansion of the mesangium. Longitudinal examination over a 48 month period (N = 15) during which CsA was reduced in dosage or withdrawn revealed persistent hypofiltration, increasingly elevated RVR and heavier proteinuria. Further histopathological deterioration was observed when renal tissue was sampled a second time in six patients, and three members of the experimental group developed end-stage renal disease. We conclude that continuous CsA therapy for more than 12 months causes a chronic injury to renal microvessels that is rarely reversible and potentially progressive.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>3283402</pmid><doi>10.1038/ki.1988.38</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Cyclosporins - adverse effects Drug toxicity and drugs side effects treatment Heart Transplantation Humans Kidney Diseases - chemically induced Kidney Diseases - pathology Kidney Diseases - physiopathology Kidney Failure, Chronic - chemically induced Kidney Glomerulus - pathology Kidney Glomerulus - ultrastructure Longitudinal Studies Medical sciences Microscopy, Electron Pharmacology. Drug treatments Postoperative Care Toxicity: urogenital system |
title | The long-term course of cyclosporine-associated chronic nephropathy |
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