Clinical presentation and outcomes of childhood-onset membranous lupus nephritis
Background Best practices for managing childhood-onset membranous lupus nephritis (MLN) are not yet established. Most studies involve primarily or exclusively adult cohorts or pediatric cohorts with combinations of pure or mixed membranous and proliferative nephritis. Methods We performed a single-c...
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Veröffentlicht in: | Pediatric nephrology (Berlin, West) West), 2017-12, Vol.32 (12), p.2283-2291 |
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description | Background
Best practices for managing childhood-onset membranous lupus nephritis (MLN) are not yet established. Most studies involve primarily or exclusively adult cohorts or pediatric cohorts with combinations of pure or mixed membranous and proliferative nephritis.
Methods
We performed a single-center cohort study of consecutively diagnosed children with pure MLN from 1990 and 2016. Patients received care in Houston, Texas, one of the most diverse metropolitan areas in North America. Renal outcomes were obtained using consensus definitions from the Childhood Arthritis and Rheumatology Research Alliance (CARRA). Logistic regression was used to detect predictors of complete renal response.
Results
A total of 56 children with MLN were identified (82% females, 44% black, 35% Hispanic) with a median follow-up time of 4.1 years. The mean age of MLN onset was 13.7 ± 3.4 years. On initial presentation 69% had nephrotic syndrome and 11% had acute kidney injury. Glucocorticoids were prescribed in 96% of patients and anti-malarials in 88%. Mycophenolate mofetil was the most common non-steroid immunosuppressive agent (69%), followed by rituximab (25%), cyclophosphamide (18%), and azathioprine (9%). Renin–angiotensin aldosterone system blocking agents were prescribed in 78% of patients. Of 37 patients with ≥2 years of follow-up, 74% achieved complete renal response at 24 months. No predictor variable of complete renal response was identified in this small cohort. Renal flares occurred in 48% of patients (86% proteinuric, 14% nephritic). On subsequent renal biopsy, 13% patients had developed proliferative nephritis.
Conclusions
This single-center cohort of childhood-onset MLN showed favorable outcomes. Utilizing pediatric renal outcomes definitions, we found that response rates were high, as were rates of renal flare. |
doi_str_mv | 10.1007/s00467-017-3743-z |
format | Article |
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Best practices for managing childhood-onset membranous lupus nephritis (MLN) are not yet established. Most studies involve primarily or exclusively adult cohorts or pediatric cohorts with combinations of pure or mixed membranous and proliferative nephritis.
Methods
We performed a single-center cohort study of consecutively diagnosed children with pure MLN from 1990 and 2016. Patients received care in Houston, Texas, one of the most diverse metropolitan areas in North America. Renal outcomes were obtained using consensus definitions from the Childhood Arthritis and Rheumatology Research Alliance (CARRA). Logistic regression was used to detect predictors of complete renal response.
Results
A total of 56 children with MLN were identified (82% females, 44% black, 35% Hispanic) with a median follow-up time of 4.1 years. The mean age of MLN onset was 13.7 ± 3.4 years. On initial presentation 69% had nephrotic syndrome and 11% had acute kidney injury. Glucocorticoids were prescribed in 96% of patients and anti-malarials in 88%. Mycophenolate mofetil was the most common non-steroid immunosuppressive agent (69%), followed by rituximab (25%), cyclophosphamide (18%), and azathioprine (9%). Renin–angiotensin aldosterone system blocking agents were prescribed in 78% of patients. Of 37 patients with ≥2 years of follow-up, 74% achieved complete renal response at 24 months. No predictor variable of complete renal response was identified in this small cohort. Renal flares occurred in 48% of patients (86% proteinuric, 14% nephritic). On subsequent renal biopsy, 13% patients had developed proliferative nephritis.
Conclusions
This single-center cohort of childhood-onset MLN showed favorable outcomes. Utilizing pediatric renal outcomes definitions, we found that response rates were high, as were rates of renal flare.</description><identifier>ISSN: 0931-041X</identifier><identifier>EISSN: 1432-198X</identifier><identifier>DOI: 10.1007/s00467-017-3743-z</identifier><identifier>PMID: 28717937</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescent ; Aldosterone ; Angiotensin ; Arthritis ; Azathioprine ; Biopsy ; Care and treatment ; Child ; Childhood ; Children ; Cohort Studies ; Cyclophosphamide ; Diagnosis ; Female ; Follow-Up Studies ; Glomerulonephritis, Membranous - diagnosis ; Glomerulonephritis, Membranous - drug therapy ; Glucocorticoids ; Glucocorticoids - therapeutic use ; Health risk assessment ; Humans ; Immunosuppression ; Immunosuppressive Agents - therapeutic use ; Kidney - pathology ; Kidneys ; Logistic Models ; Lupus ; Lupus nephritis ; Lupus Nephritis - diagnosis ; Lupus Nephritis - drug therapy ; Male ; Medicine ; Medicine & Public Health ; Monoclonal antibodies ; Mycophenolate mofetil ; Mycophenolic acid ; Nephritis ; Nephrology ; Nephrotic syndrome ; Original Article ; Patient outcomes ; Pediatrics ; Renin ; Retrospective Studies ; Rituximab ; Texas ; Treatment Outcome ; Urology</subject><ispartof>Pediatric nephrology (Berlin, West), 2017-12, Vol.32 (12), p.2283-2291</ispartof><rights>IPNA 2017</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Pediatric Nephrology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-ee9296497a8546d6574ec8c4816ca464a8e4b23f038c83a0a2d1d594108705083</citedby><cites>FETCH-LOGICAL-c574t-ee9296497a8546d6574ec8c4816ca464a8e4b23f038c83a0a2d1d594108705083</cites><orcidid>0000-0002-8991-8277</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00467-017-3743-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00467-017-3743-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28717937$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pereira, Maria</creatorcontrib><creatorcontrib>Muscal, Eyal</creatorcontrib><creatorcontrib>Eldin, Karen</creatorcontrib><creatorcontrib>Hicks, M. John</creatorcontrib><creatorcontrib>Sagcal-Gironella, Anna Carmela P.</creatorcontrib><creatorcontrib>DeGuzman, Marietta</creatorcontrib><creatorcontrib>Wenderfer, Scott E.</creatorcontrib><title>Clinical presentation and outcomes of childhood-onset membranous lupus nephritis</title><title>Pediatric nephrology (Berlin, West)</title><addtitle>Pediatr Nephrol</addtitle><addtitle>Pediatr Nephrol</addtitle><description>Background
Best practices for managing childhood-onset membranous lupus nephritis (MLN) are not yet established. Most studies involve primarily or exclusively adult cohorts or pediatric cohorts with combinations of pure or mixed membranous and proliferative nephritis.
Methods
We performed a single-center cohort study of consecutively diagnosed children with pure MLN from 1990 and 2016. Patients received care in Houston, Texas, one of the most diverse metropolitan areas in North America. Renal outcomes were obtained using consensus definitions from the Childhood Arthritis and Rheumatology Research Alliance (CARRA). Logistic regression was used to detect predictors of complete renal response.
Results
A total of 56 children with MLN were identified (82% females, 44% black, 35% Hispanic) with a median follow-up time of 4.1 years. The mean age of MLN onset was 13.7 ± 3.4 years. On initial presentation 69% had nephrotic syndrome and 11% had acute kidney injury. Glucocorticoids were prescribed in 96% of patients and anti-malarials in 88%. Mycophenolate mofetil was the most common non-steroid immunosuppressive agent (69%), followed by rituximab (25%), cyclophosphamide (18%), and azathioprine (9%). Renin–angiotensin aldosterone system blocking agents were prescribed in 78% of patients. Of 37 patients with ≥2 years of follow-up, 74% achieved complete renal response at 24 months. No predictor variable of complete renal response was identified in this small cohort. Renal flares occurred in 48% of patients (86% proteinuric, 14% nephritic). On subsequent renal biopsy, 13% patients had developed proliferative nephritis.
Conclusions
This single-center cohort of childhood-onset MLN showed favorable outcomes. Utilizing pediatric renal outcomes definitions, we found that response rates were high, as were rates of renal flare.</description><subject>Adolescent</subject><subject>Aldosterone</subject><subject>Angiotensin</subject><subject>Arthritis</subject><subject>Azathioprine</subject><subject>Biopsy</subject><subject>Care and treatment</subject><subject>Child</subject><subject>Childhood</subject><subject>Children</subject><subject>Cohort Studies</subject><subject>Cyclophosphamide</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glomerulonephritis, Membranous - diagnosis</subject><subject>Glomerulonephritis, Membranous - drug therapy</subject><subject>Glucocorticoids</subject><subject>Glucocorticoids - therapeutic use</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Immunosuppression</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Kidney - pathology</subject><subject>Kidneys</subject><subject>Logistic Models</subject><subject>Lupus</subject><subject>Lupus nephritis</subject><subject>Lupus Nephritis - diagnosis</subject><subject>Lupus Nephritis - drug therapy</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Monoclonal antibodies</subject><subject>Mycophenolate mofetil</subject><subject>Mycophenolic acid</subject><subject>Nephritis</subject><subject>Nephrology</subject><subject>Nephrotic syndrome</subject><subject>Original Article</subject><subject>Patient outcomes</subject><subject>Pediatrics</subject><subject>Renin</subject><subject>Retrospective Studies</subject><subject>Rituximab</subject><subject>Texas</subject><subject>Treatment Outcome</subject><subject>Urology</subject><issn>0931-041X</issn><issn>1432-198X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kk-LFDEQxYMo7rj6AbxIgyBesiadpJMcl8F_sKAHhb2FTLp6Oks6aZPug_vpzTCr7spIIAWV33sUlYfQS0ouKCHyXSGEdxITKjGTnOHbR2hDOWsx1er6MdoQzSgmnF6foWel3BBClFDdU3TWKkmlZnKDvm6Dj97Z0MwZCsTFLj7Fxsa-Sevi0gSlSUPjRh_6MaUep1hgaSaYdtnGtJYmrHO9I8xj9osvz9GTwYYCL-7qOfr-4f237Sd89eXj5-3lFXZC8gUD6FZ3XEurBO_6rjbBKccV7ZzlHbcK-K5lA2HKKWaJbXvaC80pUZIIotg5env0nXP6sUJZzOSLgxBshDqWobqltNW1VPT1P-hNWnOs01VKcM0FE_QvtbcBjI9DWrJ1B1NzKShlXceVqBQ-Qe0hQrYhRRh8bT_gL07w9fQweXdS8OaeYAQblrGksB6-pTwE6RF0OZWSYTBz9pPNPw0l5hAPc4yHqfEwh3iY26p5dbeJdTdB_0fxOw8VaI9AqU9xD_neqv7r-gstlcJP</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Pereira, Maria</creator><creator>Muscal, Eyal</creator><creator>Eldin, Karen</creator><creator>Hicks, M. John</creator><creator>Sagcal-Gironella, Anna Carmela P.</creator><creator>DeGuzman, Marietta</creator><creator>Wenderfer, Scott E.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8991-8277</orcidid></search><sort><creationdate>20171201</creationdate><title>Clinical presentation and outcomes of childhood-onset membranous lupus nephritis</title><author>Pereira, Maria ; Muscal, Eyal ; Eldin, Karen ; Hicks, M. John ; Sagcal-Gironella, Anna Carmela P. ; DeGuzman, Marietta ; Wenderfer, Scott E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-ee9296497a8546d6574ec8c4816ca464a8e4b23f038c83a0a2d1d594108705083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>Aldosterone</topic><topic>Angiotensin</topic><topic>Arthritis</topic><topic>Azathioprine</topic><topic>Biopsy</topic><topic>Care and treatment</topic><topic>Child</topic><topic>Childhood</topic><topic>Children</topic><topic>Cohort Studies</topic><topic>Cyclophosphamide</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glomerulonephritis, Membranous - diagnosis</topic><topic>Glomerulonephritis, Membranous - drug therapy</topic><topic>Glucocorticoids</topic><topic>Glucocorticoids - therapeutic use</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Immunosuppression</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Kidney - pathology</topic><topic>Kidneys</topic><topic>Logistic Models</topic><topic>Lupus</topic><topic>Lupus nephritis</topic><topic>Lupus Nephritis - diagnosis</topic><topic>Lupus Nephritis - drug therapy</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Monoclonal antibodies</topic><topic>Mycophenolate mofetil</topic><topic>Mycophenolic acid</topic><topic>Nephritis</topic><topic>Nephrology</topic><topic>Nephrotic syndrome</topic><topic>Original Article</topic><topic>Patient outcomes</topic><topic>Pediatrics</topic><topic>Renin</topic><topic>Retrospective Studies</topic><topic>Rituximab</topic><topic>Texas</topic><topic>Treatment Outcome</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pereira, Maria</creatorcontrib><creatorcontrib>Muscal, Eyal</creatorcontrib><creatorcontrib>Eldin, Karen</creatorcontrib><creatorcontrib>Hicks, M. John</creatorcontrib><creatorcontrib>Sagcal-Gironella, Anna Carmela P.</creatorcontrib><creatorcontrib>DeGuzman, Marietta</creatorcontrib><creatorcontrib>Wenderfer, Scott E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric nephrology (Berlin, West)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pereira, Maria</au><au>Muscal, Eyal</au><au>Eldin, Karen</au><au>Hicks, M. John</au><au>Sagcal-Gironella, Anna Carmela P.</au><au>DeGuzman, Marietta</au><au>Wenderfer, Scott E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical presentation and outcomes of childhood-onset membranous lupus nephritis</atitle><jtitle>Pediatric nephrology (Berlin, West)</jtitle><stitle>Pediatr Nephrol</stitle><addtitle>Pediatr Nephrol</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>32</volume><issue>12</issue><spage>2283</spage><epage>2291</epage><pages>2283-2291</pages><issn>0931-041X</issn><eissn>1432-198X</eissn><abstract>Background
Best practices for managing childhood-onset membranous lupus nephritis (MLN) are not yet established. Most studies involve primarily or exclusively adult cohorts or pediatric cohorts with combinations of pure or mixed membranous and proliferative nephritis.
Methods
We performed a single-center cohort study of consecutively diagnosed children with pure MLN from 1990 and 2016. Patients received care in Houston, Texas, one of the most diverse metropolitan areas in North America. Renal outcomes were obtained using consensus definitions from the Childhood Arthritis and Rheumatology Research Alliance (CARRA). Logistic regression was used to detect predictors of complete renal response.
Results
A total of 56 children with MLN were identified (82% females, 44% black, 35% Hispanic) with a median follow-up time of 4.1 years. The mean age of MLN onset was 13.7 ± 3.4 years. On initial presentation 69% had nephrotic syndrome and 11% had acute kidney injury. Glucocorticoids were prescribed in 96% of patients and anti-malarials in 88%. Mycophenolate mofetil was the most common non-steroid immunosuppressive agent (69%), followed by rituximab (25%), cyclophosphamide (18%), and azathioprine (9%). Renin–angiotensin aldosterone system blocking agents were prescribed in 78% of patients. Of 37 patients with ≥2 years of follow-up, 74% achieved complete renal response at 24 months. No predictor variable of complete renal response was identified in this small cohort. Renal flares occurred in 48% of patients (86% proteinuric, 14% nephritic). On subsequent renal biopsy, 13% patients had developed proliferative nephritis.
Conclusions
This single-center cohort of childhood-onset MLN showed favorable outcomes. Utilizing pediatric renal outcomes definitions, we found that response rates were high, as were rates of renal flare.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28717937</pmid><doi>10.1007/s00467-017-3743-z</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-8991-8277</orcidid></addata></record> |
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subjects | Adolescent Aldosterone Angiotensin Arthritis Azathioprine Biopsy Care and treatment Child Childhood Children Cohort Studies Cyclophosphamide Diagnosis Female Follow-Up Studies Glomerulonephritis, Membranous - diagnosis Glomerulonephritis, Membranous - drug therapy Glucocorticoids Glucocorticoids - therapeutic use Health risk assessment Humans Immunosuppression Immunosuppressive Agents - therapeutic use Kidney - pathology Kidneys Logistic Models Lupus Lupus nephritis Lupus Nephritis - diagnosis Lupus Nephritis - drug therapy Male Medicine Medicine & Public Health Monoclonal antibodies Mycophenolate mofetil Mycophenolic acid Nephritis Nephrology Nephrotic syndrome Original Article Patient outcomes Pediatrics Renin Retrospective Studies Rituximab Texas Treatment Outcome Urology |
title | Clinical presentation and outcomes of childhood-onset membranous lupus nephritis |
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