Morbidity in children with frequently relapsing nephrosis: 10-year follow-up of a randomized controlled trial

Background To investigate the long-term outcome in children with frequently relapsing nephrotic syndrome (FRNS) we conducted a follow-up of a previous randomized controlled trial (RCT) 10 years after the initiation of the treatment protocol. Methods We previously conducted an RCT on the efficacy of...

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Veröffentlicht in:Pediatric nephrology (Berlin, West) West), 2015-03, Vol.30 (3), p.459-468
Hauptverfasser: Ishikura, Kenji, Yoshikawa, Norishige, Nakazato, Hitoshi, Sasaki, Satoshi, Nakanishi, Koichi, Matsuyama, Takeshi, Ito, Shuichi, Hamasaki, Yuko, Yata, Nahoko, Ando, Takashi, Iijima, Kazumoto, Honda, Masataka
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container_issue 3
container_start_page 459
container_title Pediatric nephrology (Berlin, West)
container_volume 30
creator Ishikura, Kenji
Yoshikawa, Norishige
Nakazato, Hitoshi
Sasaki, Satoshi
Nakanishi, Koichi
Matsuyama, Takeshi
Ito, Shuichi
Hamasaki, Yuko
Yata, Nahoko
Ando, Takashi
Iijima, Kazumoto
Honda, Masataka
description Background To investigate the long-term outcome in children with frequently relapsing nephrotic syndrome (FRNS) we conducted a follow-up of a previous randomized controlled trial (RCT) 10 years after the initiation of the treatment protocol. Methods We previously conducted an RCT on the efficacy of cyclosporine for treating children with FRNS. After 2 years of treatment, a recommended a management protocol of steroids, and immunosuppressants was provided. Results Valid information was available for 46 of the 56 patients (82.1 %) enrolled in the original RCT. The median follow-up period was 10.3 years from the start of protocol treatment with cyclosporine. At last follow-up (mean age 18.7 years), only ten patients (21.7 %) showed disease-free remission (no relapse for at least 2 years). In contrast, 23 (50.0 %) continued to relapse frequently or were on immunosuppressants, eight patients (17.4 %) had infrequent relapses without immunosuppressants. Adverse effects attributable to treatment included short stature (6 patients), osteoporosis (six patients), obesity (4 patients), cataracts (3 patients) and hypertension (3 patients). No lethal event or renal dysfunction occurred during follow-up. Conclusions This 10-year follow-up study shows that most children with FRNS experience relapses after 2 years of cyclosporine treatment, in adolescence and into adulthood. Outcomes in terms of life expectancy and renal function are favorable.
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Methods We previously conducted an RCT on the efficacy of cyclosporine for treating children with FRNS. After 2 years of treatment, a recommended a management protocol of steroids, and immunosuppressants was provided. Results Valid information was available for 46 of the 56 patients (82.1 %) enrolled in the original RCT. The median follow-up period was 10.3 years from the start of protocol treatment with cyclosporine. At last follow-up (mean age 18.7 years), only ten patients (21.7 %) showed disease-free remission (no relapse for at least 2 years). In contrast, 23 (50.0 %) continued to relapse frequently or were on immunosuppressants, eight patients (17.4 %) had infrequent relapses without immunosuppressants. Adverse effects attributable to treatment included short stature (6 patients), osteoporosis (six patients), obesity (4 patients), cataracts (3 patients) and hypertension (3 patients). No lethal event or renal dysfunction occurred during follow-up. Conclusions This 10-year follow-up study shows that most children with FRNS experience relapses after 2 years of cyclosporine treatment, in adolescence and into adulthood. Outcomes in terms of life expectancy and renal function are favorable.</description><identifier>ISSN: 0931-041X</identifier><identifier>EISSN: 1432-198X</identifier><identifier>DOI: 10.1007/s00467-014-2955-8</identifier><identifier>PMID: 25277597</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Analysis ; Biopsy ; Care and treatment ; Child ; Child development ; Clinical trials ; Cyclosporine - therapeutic use ; Diagnosis ; Drug dosages ; Female ; Follow-Up Studies ; Humans ; Immunosuppressive agents ; Immunosuppressive Agents - therapeutic use ; Kidney diseases ; Life expectancy ; Male ; Medicine ; Medicine &amp; Public Health ; Morbidity ; Nephrology ; Nephrotic syndrome ; Nephrotic Syndrome - complications ; Nephrotic Syndrome - drug therapy ; Original Article ; Patients ; Pediatrics ; Prospective Studies ; Recurrence ; Remission (Medicine) ; Steroids ; Time Factors ; Toxicity ; Urology</subject><ispartof>Pediatric nephrology (Berlin, West), 2015-03, Vol.30 (3), p.459-468</ispartof><rights>IPNA 2014</rights><rights>COPYRIGHT 2015 Springer</rights><rights>IPNA 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c578t-de0d7ccd2e0406b2638dd18e133b53e29da262cdc72a52eef3d93b8f0d3b5e9f3</citedby><cites>FETCH-LOGICAL-c578t-de0d7ccd2e0406b2638dd18e133b53e29da262cdc72a52eef3d93b8f0d3b5e9f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00467-014-2955-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00467-014-2955-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25277597$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ishikura, Kenji</creatorcontrib><creatorcontrib>Yoshikawa, Norishige</creatorcontrib><creatorcontrib>Nakazato, Hitoshi</creatorcontrib><creatorcontrib>Sasaki, Satoshi</creatorcontrib><creatorcontrib>Nakanishi, Koichi</creatorcontrib><creatorcontrib>Matsuyama, Takeshi</creatorcontrib><creatorcontrib>Ito, Shuichi</creatorcontrib><creatorcontrib>Hamasaki, Yuko</creatorcontrib><creatorcontrib>Yata, Nahoko</creatorcontrib><creatorcontrib>Ando, Takashi</creatorcontrib><creatorcontrib>Iijima, Kazumoto</creatorcontrib><creatorcontrib>Honda, Masataka</creatorcontrib><creatorcontrib>Japanese Study Group of Renal Disease in Children</creatorcontrib><creatorcontrib>for Japanese Study Group of Renal Disease in Children</creatorcontrib><title>Morbidity in children with frequently relapsing nephrosis: 10-year follow-up of a randomized controlled trial</title><title>Pediatric nephrology (Berlin, West)</title><addtitle>Pediatr Nephrol</addtitle><addtitle>Pediatr Nephrol</addtitle><description>Background To investigate the long-term outcome in children with frequently relapsing nephrotic syndrome (FRNS) we conducted a follow-up of a previous randomized controlled trial (RCT) 10 years after the initiation of the treatment protocol. Methods We previously conducted an RCT on the efficacy of cyclosporine for treating children with FRNS. After 2 years of treatment, a recommended a management protocol of steroids, and immunosuppressants was provided. Results Valid information was available for 46 of the 56 patients (82.1 %) enrolled in the original RCT. The median follow-up period was 10.3 years from the start of protocol treatment with cyclosporine. At last follow-up (mean age 18.7 years), only ten patients (21.7 %) showed disease-free remission (no relapse for at least 2 years). In contrast, 23 (50.0 %) continued to relapse frequently or were on immunosuppressants, eight patients (17.4 %) had infrequent relapses without immunosuppressants. Adverse effects attributable to treatment included short stature (6 patients), osteoporosis (six patients), obesity (4 patients), cataracts (3 patients) and hypertension (3 patients). No lethal event or renal dysfunction occurred during follow-up. Conclusions This 10-year follow-up study shows that most children with FRNS experience relapses after 2 years of cyclosporine treatment, in adolescence and into adulthood. Outcomes in terms of life expectancy and renal function are favorable.</description><subject>Analysis</subject><subject>Biopsy</subject><subject>Care and treatment</subject><subject>Child</subject><subject>Child development</subject><subject>Clinical trials</subject><subject>Cyclosporine - therapeutic use</subject><subject>Diagnosis</subject><subject>Drug dosages</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunosuppressive agents</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Kidney diseases</subject><subject>Life expectancy</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Morbidity</subject><subject>Nephrology</subject><subject>Nephrotic syndrome</subject><subject>Nephrotic Syndrome - complications</subject><subject>Nephrotic Syndrome - drug therapy</subject><subject>Original Article</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Prospective Studies</subject><subject>Recurrence</subject><subject>Remission (Medicine)</subject><subject>Steroids</subject><subject>Time Factors</subject><subject>Toxicity</subject><subject>Urology</subject><issn>0931-041X</issn><issn>1432-198X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kltrFTEUhQdR7LH6A3yRgFB8Sc1lLhnfSvEGFV8U-hYyyZ4zKZlkTDKU4683h1O1lSN5SMj-1mJnZ1XVS0rOKSHd20RI3XaY0BqzvmmweFRtaM0Zpr24flxtSM8pJjW9PqmepXRDCBGNaJ9WJ6xhXdf03aaav4Q4WGPzDlmP9GSdieDRrc0TGiP8WMFnt0MRnFqS9VvkYZliSDa9Q5TgHaiIxuBcuMXrgsKIFIrKmzDbn2CQDj7HUi3HHK1yz6sno3IJXtztp9X3D--_XX7CV18_fr68uMK66UTGBojptDYMSE3agbVcGEMFUM6HhgPrjWIt00Z3TDUMYOSm54MYiSl16Ed-Wr05-C4xlCekLGebNDinPIQ1Sdo2rK5ZW9cFff0PehPW6Et3e4pwwRht_1Jb5UBaP4Ycld6byouadA0TvOsLhY9QW_AQlQseRluuH_DnR_iyDMxWHxWc3RNMoFyeUnBrtsGnhyA9gLr8VYowyiXaWcWdpETusyMP2ZElO3KfHSmK5tXdJNZhBvNH8TssBWAHIJWS30K8N6r_uv4C8l3NoQ</recordid><startdate>20150301</startdate><enddate>20150301</enddate><creator>Ishikura, Kenji</creator><creator>Yoshikawa, Norishige</creator><creator>Nakazato, Hitoshi</creator><creator>Sasaki, Satoshi</creator><creator>Nakanishi, Koichi</creator><creator>Matsuyama, Takeshi</creator><creator>Ito, Shuichi</creator><creator>Hamasaki, Yuko</creator><creator>Yata, Nahoko</creator><creator>Ando, Takashi</creator><creator>Iijima, Kazumoto</creator><creator>Honda, Masataka</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></search><sort><creationdate>20150301</creationdate><title>Morbidity in children with frequently relapsing nephrosis: 10-year follow-up of a randomized controlled trial</title><author>Ishikura, Kenji ; 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Methods We previously conducted an RCT on the efficacy of cyclosporine for treating children with FRNS. After 2 years of treatment, a recommended a management protocol of steroids, and immunosuppressants was provided. Results Valid information was available for 46 of the 56 patients (82.1 %) enrolled in the original RCT. The median follow-up period was 10.3 years from the start of protocol treatment with cyclosporine. At last follow-up (mean age 18.7 years), only ten patients (21.7 %) showed disease-free remission (no relapse for at least 2 years). In contrast, 23 (50.0 %) continued to relapse frequently or were on immunosuppressants, eight patients (17.4 %) had infrequent relapses without immunosuppressants. Adverse effects attributable to treatment included short stature (6 patients), osteoporosis (six patients), obesity (4 patients), cataracts (3 patients) and hypertension (3 patients). No lethal event or renal dysfunction occurred during follow-up. Conclusions This 10-year follow-up study shows that most children with FRNS experience relapses after 2 years of cyclosporine treatment, in adolescence and into adulthood. Outcomes in terms of life expectancy and renal function are favorable.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>25277597</pmid><doi>10.1007/s00467-014-2955-8</doi><tpages>10</tpages></addata></record>
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subjects Analysis
Biopsy
Care and treatment
Child
Child development
Clinical trials
Cyclosporine - therapeutic use
Diagnosis
Drug dosages
Female
Follow-Up Studies
Humans
Immunosuppressive agents
Immunosuppressive Agents - therapeutic use
Kidney diseases
Life expectancy
Male
Medicine
Medicine & Public Health
Morbidity
Nephrology
Nephrotic syndrome
Nephrotic Syndrome - complications
Nephrotic Syndrome - drug therapy
Original Article
Patients
Pediatrics
Prospective Studies
Recurrence
Remission (Medicine)
Steroids
Time Factors
Toxicity
Urology
title Morbidity in children with frequently relapsing nephrosis: 10-year follow-up of a randomized controlled trial
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