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ADAMTS-13 level in children with severe diarrhea-associated hemolytic uremic syndrome : unmasking new association
Severe deficiency of ADAMTS-13 leads to thrombotic thrombocytopenic purpura. Few studies have reported reduced activity of ADAMTS-13 in patients with atypical and typical hemolytic uremic syndrome (HUS). We hypothesized that ADAMTS-13 deficiency might play a role in the pathogenesis of severe HUS. T...
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Published in: | Saudi journal of kidney diseases and transplantation 2018-03, Vol.29 (2), p.303-309 |
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container_issue | 2 |
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container_title | Saudi journal of kidney diseases and transplantation |
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creator | Mursi, Said M. Tawfiq, Dua M. Khalifah, Nurah A. Khalifah, Najla A. Jawish, Hibah H. |
description | Severe deficiency of ADAMTS-13 leads to thrombotic thrombocytopenic purpura.
Few studies have reported reduced activity of ADAMTS-13 in patients with atypical and typical
hemolytic uremic syndrome (HUS). We hypothesized that ADAMTS-13 deficiency might play a
role in the pathogenesis of severe HUS. This study aimed to evaluate the ADAMTS-13 level in
severe typical HUS. This prospective case–control study was carried out in the Pediatric
Nephrology Unit and Clinical Pathology Department, Faculty of Medicine, Zagazig University
from February 2013 to February 2014. The study included 15 consecutive children with typical
HUS as well as 15 healthy children as a control group. Routine laboratory investigations were
performed. Assessment of serum ADAMTS-13 level was performed using the Quantikine human
ADAMTS-13 ELISA kit. Data were analyzed using Statistical Package for Social Sciences
version 16. Nonparametric values were expressed as median and range, and the median of two
groups was tested by Mann–Whitney test. The serum ADAMTS-13 level was significantly lower
in HUS patients when compared to the control group (P < 0.05). There were significant negative
correlations between ADAMTS-13 level and duration on dialysis, as well as serum urea and
creatinine. Furthermore, there were significant positive correlations between serum ADAMTS-13
level and both hemoglobin level and platelet count. Our study suggests that the ADAMTS-13
level was decreased in children with severe typical HUS and its deficiency correlated with disease
severity. |
doi_str_mv | 10.4103/1319-2442.229262 |
format | article |
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Few studies have reported reduced activity of ADAMTS-13 in patients with atypical and typical
hemolytic uremic syndrome (HUS). We hypothesized that ADAMTS-13 deficiency might play a
role in the pathogenesis of severe HUS. This study aimed to evaluate the ADAMTS-13 level in
severe typical HUS. This prospective case–control study was carried out in the Pediatric
Nephrology Unit and Clinical Pathology Department, Faculty of Medicine, Zagazig University
from February 2013 to February 2014. The study included 15 consecutive children with typical
HUS as well as 15 healthy children as a control group. Routine laboratory investigations were
performed. Assessment of serum ADAMTS-13 level was performed using the Quantikine human
ADAMTS-13 ELISA kit. Data were analyzed using Statistical Package for Social Sciences
version 16. Nonparametric values were expressed as median and range, and the median of two
groups was tested by Mann–Whitney test. The serum ADAMTS-13 level was significantly lower
in HUS patients when compared to the control group (P < 0.05). There were significant negative
correlations between ADAMTS-13 level and duration on dialysis, as well as serum urea and
creatinine. Furthermore, there were significant positive correlations between serum ADAMTS-13
level and both hemoglobin level and platelet count. Our study suggests that the ADAMTS-13
level was decreased in children with severe typical HUS and its deficiency correlated with disease
severity.</description><identifier>ISSN: 1319-2442</identifier><identifier>EISSN: 2320-3838</identifier><identifier>DOI: 10.4103/1319-2442.229262</identifier><identifier>PMID: 29657197</identifier><language>eng</language><publisher>Riyadh, Saudi Arabia: Saudi Center for Organ Transplantation</publisher><subject>Anemia ; Blood products ; Children ; Diarrhea ; Disease control ; E coli ; Enzymes ; Health aspects ; Health risk assessment ; Hemodialysis ; Hemolytic-uremic syndrome ; Hypertension ; Laboratories ; Medicine ; Mutation ; Nephrology ; Pathogenesis ; Pathology ; Pediatrics ; Risk factors ; Surveillance</subject><ispartof>Saudi journal of kidney diseases and transplantation, 2018-03, Vol.29 (2), p.303-309</ispartof><rights>COPYRIGHT 2018 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt. Ltd. Mar/Apr 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c633n-55e413176fef81d745da80ecf080b8f5559c83404d11bcd9cdc3c853d399b1303</citedby><cites>FETCH-LOGICAL-c633n-55e413176fef81d745da80ecf080b8f5559c83404d11bcd9cdc3c853d399b1303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2025622606?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29657197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mursi, Said M.</creatorcontrib><creatorcontrib>Tawfiq, Dua M.</creatorcontrib><creatorcontrib>Khalifah, Nurah A.</creatorcontrib><creatorcontrib>Khalifah, Najla A.</creatorcontrib><creatorcontrib>Jawish, Hibah H.</creatorcontrib><title>ADAMTS-13 level in children with severe diarrhea-associated hemolytic uremic syndrome : unmasking new association</title><title>Saudi journal of kidney diseases and transplantation</title><addtitle>Saudi J Kidney Dis Transpl</addtitle><description>Severe deficiency of ADAMTS-13 leads to thrombotic thrombocytopenic purpura.
Few studies have reported reduced activity of ADAMTS-13 in patients with atypical and typical
hemolytic uremic syndrome (HUS). We hypothesized that ADAMTS-13 deficiency might play a
role in the pathogenesis of severe HUS. This study aimed to evaluate the ADAMTS-13 level in
severe typical HUS. This prospective case–control study was carried out in the Pediatric
Nephrology Unit and Clinical Pathology Department, Faculty of Medicine, Zagazig University
from February 2013 to February 2014. The study included 15 consecutive children with typical
HUS as well as 15 healthy children as a control group. Routine laboratory investigations were
performed. Assessment of serum ADAMTS-13 level was performed using the Quantikine human
ADAMTS-13 ELISA kit. Data were analyzed using Statistical Package for Social Sciences
version 16. Nonparametric values were expressed as median and range, and the median of two
groups was tested by Mann–Whitney test. The serum ADAMTS-13 level was significantly lower
in HUS patients when compared to the control group (P < 0.05). There were significant negative
correlations between ADAMTS-13 level and duration on dialysis, as well as serum urea and
creatinine. Furthermore, there were significant positive correlations between serum ADAMTS-13
level and both hemoglobin level and platelet count. Our study suggests that the ADAMTS-13
level was decreased in children with severe typical HUS and its deficiency correlated with disease
severity.</description><subject>Anemia</subject><subject>Blood products</subject><subject>Children</subject><subject>Diarrhea</subject><subject>Disease control</subject><subject>E coli</subject><subject>Enzymes</subject><subject>Health aspects</subject><subject>Health risk assessment</subject><subject>Hemodialysis</subject><subject>Hemolytic-uremic syndrome</subject><subject>Hypertension</subject><subject>Laboratories</subject><subject>Medicine</subject><subject>Mutation</subject><subject>Nephrology</subject><subject>Pathogenesis</subject><subject>Pathology</subject><subject>Pediatrics</subject><subject>Risk factors</subject><subject>Surveillance</subject><issn>1319-2442</issn><issn>2320-3838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUstuEzEUHSEQLYU9G9BISIjNBL_m1V1UXpWKWFDWlmNfJ048dmvPEOXv8STN0CDkxZWuzzn3dbLsNUYzhhH9iCluC8IYmRHSkoo8yc4JJaigDW2eZufT91n2IsY1QmXZVtXz7Iy0VVnjtj7P7uef5t9vfxaY5hZ-g82Ny-XKWBXA5VvTr_KY0gFyZUQIKxCFiNFLI3pQ-Qo6b3e9kfkQoEsh7pwKvoP8Mh9cJ-LGuGXuYJsfSca7l9kzLWyEVw_xIvv15fPt1bfi5sfX66v5TSErSl1RlsBS_3WlQTdY1axUokEgNWrQotFlGkU2lCGmMF5I1UolqWxKqmjbLjBF9CK7PugqL9b8LphOhB33wvB9woclFyH1boEjihCA0FhTxQStmhqowJKB1mXNWJ20Phy07oK_HyD2vDNRgrXCgR8iJ4iUDaItwgn67h_o2g_BpUn3qIqQClV_UUuR6hunfR-EHEX5vKSsRTVqRtTsP6j01Lht70CblD8hvH9ESNey_Sp6O4x7j6dAdADK4GMMoKcFYcRHa_HRO3z0Dj9YK1HePgw2LDpQE-HoJTodcuttDyFu7LCFwBN24_z2RLh4JMzTrfjkQr53YZqVH12YdN8cdCHVAy2mysnkJWb0D0FO6vs</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Mursi, Said M.</creator><creator>Tawfiq, Dua M.</creator><creator>Khalifah, Nurah A.</creator><creator>Khalifah, Najla A.</creator><creator>Jawish, Hibah H.</creator><general>Saudi Center for Organ Transplantation</general><general>Wolters Kluwer India Pvt. 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Few studies have reported reduced activity of ADAMTS-13 in patients with atypical and typical
hemolytic uremic syndrome (HUS). We hypothesized that ADAMTS-13 deficiency might play a
role in the pathogenesis of severe HUS. This study aimed to evaluate the ADAMTS-13 level in
severe typical HUS. This prospective case–control study was carried out in the Pediatric
Nephrology Unit and Clinical Pathology Department, Faculty of Medicine, Zagazig University
from February 2013 to February 2014. The study included 15 consecutive children with typical
HUS as well as 15 healthy children as a control group. Routine laboratory investigations were
performed. Assessment of serum ADAMTS-13 level was performed using the Quantikine human
ADAMTS-13 ELISA kit. Data were analyzed using Statistical Package for Social Sciences
version 16. Nonparametric values were expressed as median and range, and the median of two
groups was tested by Mann–Whitney test. The serum ADAMTS-13 level was significantly lower
in HUS patients when compared to the control group (P < 0.05). There were significant negative
correlations between ADAMTS-13 level and duration on dialysis, as well as serum urea and
creatinine. Furthermore, there were significant positive correlations between serum ADAMTS-13
level and both hemoglobin level and platelet count. Our study suggests that the ADAMTS-13
level was decreased in children with severe typical HUS and its deficiency correlated with disease
severity.</abstract><cop>Riyadh, Saudi Arabia</cop><pub>Saudi Center for Organ Transplantation</pub><pmid>29657197</pmid><doi>10.4103/1319-2442.229262</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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subjects | Anemia Blood products Children Diarrhea Disease control E coli Enzymes Health aspects Health risk assessment Hemodialysis Hemolytic-uremic syndrome Hypertension Laboratories Medicine Mutation Nephrology Pathogenesis Pathology Pediatrics Risk factors Surveillance |
title | ADAMTS-13 level in children with severe diarrhea-associated hemolytic uremic syndrome : unmasking new association |
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