Literature DB >> 24906628

A complement factor B mutation in a large kindred with atypical hemolytic uremic syndrome.

Michinori Funato1, Osamu Uemura, Katsumi Ushijima, Hidenori Ohnishi, Kenji Orii, Zenichiro Kato, Satoshi Yamakawa, Takuhito Nagai, Osamu Ohara, Hideo Kaneko, Naomi Kondo.   

Abstract

PURPOSE: Gain-of-function mutations in complement factor B (CFB) were recently identified in patients with atypical hemolytic uremic syndrome (aHUS), but are extremely rare. Our purpose is to describe a large kindred with aHUS associated with a CFB mutation and to further understand CFB-mutated aHUS patients. METHODS AND
RESULTS: We report a large kindred in which 3 members had aHUS. This kindred revealed that 9 of 12 members, including 2 affected patients, had persistent activation of the alternative pathway with low complement component 3 and that those 9 members showed a CFB mutation (c.1050G > C, p.Lys350Asn) in exon 8. This missense mutation was heterozygous in 8 of them and homozygous in only one. From structural studies, this mutation is shown to be located in close proximity to the Mg2-binding site within a von Willebrand factor type A domain of CFB, resulting in a gain-of-function effect of CFB and predisposition to aHUS. At present, 2 of the 3 members with aHUS have maintained normal renal function for a long-term period.
CONCLUSIONS: This kindred illustrates that a CFB mutation (c.1050G > C, p.Lys350Asn) can result in aHUS. In the future, phenotype-genotype correlations and outcome in CFB-mutated aHUS patients need to be further investigated by accumulation of a number of cases.

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Year:  2014        PMID: 24906628     DOI: 10.1007/s10875-014-0058-8

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  18 in total

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4.  Complete primary structure for the zymogen of human complement factor B.

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5.  Mutations of the type A domain of complement factor B that promote high-affinity C3b-binding.

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Authors:  Tara K Maga; Carla J Nishimura; Amy E Weaver; Kathy L Frees; Richard J H Smith
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10.  Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics.

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Journal:  Pediatr Nephrol       Date:  2012-03-13       Impact factor: 3.714

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  7 in total

1.  Synergistic effects of ADAMTS13 deficiency and complement activation in pathogenesis of thrombotic microangiopathy.

Authors:  Liang Zheng; Di Zhang; Wenjing Cao; Wen-Chao Song; X Long Zheng
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Review 2.  Kidney Disease Caused by Dysregulation of the Complement Alternative Pathway: An Etiologic Approach.

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Journal:  J Am Soc Nephrol       Date:  2015-07-16       Impact factor: 10.121

3.  Factor D Inhibition Blocks Complement Activation Induced by Mutant Factor B Associated With Atypical Hemolytic Uremic Syndrome and Membranoproliferative Glomerulonephritis.

Authors:  Sigridur Sunna Aradottir; Ann-Charlotte Kristoffersson; Lubka T Roumenina; Anna Bjerre; Pavlos Kashioulis; Runolfur Palsson; Diana Karpman
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4.  Diabetic ketoacidosis presenting with atypical hemolytic uremic syndrome associated with a variant of complement factor B in an adult: a case report.

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Review 6.  Atypical Hemolytic Uremic Syndrome: A Brief Review.

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7.  Novel Variation in CFB Adult Onset Atypical Hemolytic Uremic Syndrome: A Case Report and Review.

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