Alternative Pathway of Complement in Children with Diarrhea-Associated Hemolytic Uremic Syndrome
Author(s) -
Joshua M. Thurman,
Russell Marians,
Woodruff Emlen,
Susan Wood,
Christopher Smith,
Hillary Akana,
V. Michael Holers,
Martin Lesser,
Myriam Kline,
Cathy Hoffman,
Erica Christen,
Howard Trachtman
Publication year - 2009
Publication title -
clinical journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.755
H-Index - 151
eISSN - 1555-905X
pISSN - 1555-9041
DOI - 10.2215/cjn.02730409
Subject(s) - medicine , atypical hemolytic uremic syndrome , diarrhea , alternative complement pathway , complement system , complement (music) , immunology , gastroenterology , antibody , biochemistry , chemistry , complementation , gene , phenotype
Diarrhea-associated hemolytic uremic syndrome (D+HUS) is a common cause of acute kidney injury in children. Mutations in alternative pathway (AP) complement regulatory proteins have been identified in severe cases of thrombotic microangiopathy, but the role of the AP in D+HUS has not been studied. Therefore, we determined whether plasma levels of markers of activation of the AP are increased in D+HUS and are biomarkers of the severity of renal injury that predict the need for dialysis.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom