Literature DB >> 30286829

Diagnostic Utility of Complement Serology for Atypical Hemolytic Uremic Syndrome.

Meera Sridharan1, Ronald S Go1, Roshini S Abraham2, Fernando C Fervenza3, Sanjeev Sethi2, Sandra C Bryant4, Grant M Spears4, David L Murray2, Maria A V Willrich5.   

Abstract

OBJECTIVE: To investigate the clinical utility of a 9-analyte complement serology panel (COMS) covering complement function (CH50 and AH50), components (C3, C4), factor B (CFB), factor H, and activation markers (C4d, Bb, and soluble membrane attack complex) for the diagnosis of atypical hemolytic uremic syndrome (aHUS).
METHODS: Physician orders for COMS from January 19, 2015, through November 4, 2016, were reviewed. Demographic characteristics, patient diagnosis, and laboratory parameters were recorded.
RESULTS: There were 177 COMS orders for 147 patients. The median patient age was 44.9 years (range, 0.9-88.0 years). Common reasons for ordering COMS included monitoring and diagnosis of C3 glomerulopathy and renal dysfunction and differentiation of aHUS from other thrombotic microangiopathies (TMAs). Forty-four patients had COMS ordered for TMAs: 8 had aHUS and all had 1 or more abnormalities within the alternative pathway of complement. Although the sensitivity of this finding for the diagnosis of aHUS is 100%, the specificity is only 28%, with a positive likelihood ratio of 1.39. Patients with aHUS had lower CH50, C3, and CFB than did those with secondary non-aHUS TMA (all P<.01). A combined CFB of 20.9 mg/dL or less and CH50 of 56% or less led to sensitivity of 75% with increased specificity of 88.9% and a diagnostic odds ratio of 24.
CONCLUSION: A COMS abnormality should not be interpreted in isolation. In conjunction with clinical presentation, a decrease in both CFB and CH50 may be an important clue to support the diagnosis of aHUS.
Copyright © 2018 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 30286829     DOI: 10.1016/j.mayocp.2018.07.008

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  6 in total

1.  Quantitative Alterations in Complement Alternative Pathway and Related Genetic Analysis in Severe Phenotype Preeclampsia.

Authors:  Layan Alrahmani; Maria L Gonzalez Suarez; Margot A Cousin; Ann M Moyer; Maria Alice V Willrich; Wendy M White; Myra J Wick; Linda J Tostrud; Kavita Narang; Vesna D Garovic
Journal:  Kidney360       Date:  2021-06-30

2.  Thrombotic microangiopathies: First report of 294 cases from a single institution experience in Argentina.

Authors:  Célia Dos Santos; Juvenal Paiva; María Lucila Romero; Mara Agazzoni; Ana Catalina Kempfer; Sabrina Rotondo; María Marta Casinelli; María Fabiana Alberto; Analía Sánchez-Luceros
Journal:  EJHaem       Date:  2021-01-19

3.  Atypical hemolytic uremic syndrome due to DGKE mutation and response to eculizumab: lessons for the clinical nephrologist.

Authors:  Danya Husain; Brian Barron; Anya Golkowski Barron; Ibrahim Sandokji; Olivera Marsenic; Jillian K Warejko
Journal:  J Nephrol       Date:  2021-03-22       Impact factor: 4.393

Review 4.  Systematic review of atypical hemolytic uremic syndrome biomarkers.

Authors:  Rupesh Raina; Sidharth K Sethi; Marie-Agnès Dragon-Durey; Amrit Khooblall; Divya Sharma; Priyanka Khandelwal; Ron Shapiro; Olivia Boyer; Hui Kim Yap; Arvind Bagga; Christoph Licht
Journal:  Pediatr Nephrol       Date:  2022-02-03       Impact factor: 3.651

Review 5.  Complement in Secondary Thrombotic Microangiopathy.

Authors:  Lilian Monteiro Pereira Palma; Meera Sridharan; Sanjeev Sethi
Journal:  Kidney Int Rep       Date:  2020-10-21

Review 6.  Pediatric Atypical Hemolytic Uremic Syndrome Advances.

Authors:  Rupesh Raina; Nina Vijayvargiya; Amrit Khooblall; Manasa Melachuri; Shweta Deshpande; Divya Sharma; Kashin Mathur; Manav Arora; Sidharth Kumar Sethi; Sonia Sandhu
Journal:  Cells       Date:  2021-12-18       Impact factor: 7.666

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.