| Literature DB >> 27974406 |
Rachel C Challis1, Troels Ring2, Yaobo Xu1, Edwin K S Wong1, Oliver Flossmann3, Ian S D Roberts4, Saeed Ahmed5, Michael Wetherall6, Giedrius Salkus7, Vicky Brocklebank1, Julian Fester8, Lisa Strain9, Valerie Wilson9, Katrina M Wood10, Kevin J Marchbank11, Mauro Santibanez-Koref1, Timothy H J Goodship1, David Kavanagh12.
Abstract
The demonstration of impaired C regulation in the thrombotic microangiopathy (TMA) atypical hemolytic uremic syndrome (aHUS) resulted in the successful introduction of the C inhibitor eculizumab into clinical practice. C abnormalities account for approximately 50% of aHUS cases; however, mutations in the non-C gene diacylglycerol kinase-ε have been described recently in individuals not responsive to eculizumab. We report here a family in which the proposita presented with aHUS but did not respond to eculizumab. Her mother had previously presented with a post-renal transplant TMA. Both the proposita and her mother also had Charcot-Marie-Tooth disease. Using whole-exome sequencing, we identified a mutation in the inverted formin 2 gene (INF2) in the mutational hotspot for FSGS. Subsequent analysis of the Newcastle aHUS cohort identified another family with a functionally-significant mutation in INF2 In this family, renal transplantation was associated with post-transplant TMA. All individuals with INF2 mutations presenting with a TMA also had aHUS risk haplotypes, potentially accounting for the genetic pleiotropy. Identifying individuals with TMAs who may not respond to eculizumab will avoid prolonged exposure of such individuals to the infectious complications of terminal pathway C blockade.Entities:
Keywords: complement; focal segmental glomerulosclerosis; hemolytic uremic syndrome
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Year: 2016 PMID: 27974406 PMCID: PMC5373440 DOI: 10.1681/ASN.2015101189
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121