Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome

Details

Serval ID
serval:BIB_FFAC6FA82A1D
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome
Journal
Blood
Author(s)
Fakhouri F., Jablonski M., Lepercq J., Blouin J., Benachi A., Hourmant M., Pirson Y., Durrbach A., Grunfeld J. P., Knebelmann B., Fremeaux-Bacchi V.
ISSN
1528-0020 (Electronic)
ISSN-L
0006-4971
Publication state
Published
Issued date
2008
Volume
112
Number
12
Pages
4542-5
Language
english
Notes
Fakhouri, Fadi
Jablonski, Mathieu
Lepercq, Jacques
Blouin, Jacques
Benachi, Alexandra
Hourmant, Maryvonne
Pirson, Yves
Durrbach, Antoine
Grunfeld, Jean-Pierre
Knebelmann, Bertrand
Fremeaux-Bacchi, Veronique
eng
Multicenter Study
Blood. 2008 Dec 1;112(12):4542-5. doi: 10.1182/blood-2008-03-144691. Epub 2008 Jul 24.
Abstract
The HELLP syndrome, defined by the existence of hemolysis, elevated liver enzymes, and low platelet count, is a serious complication of pregnancy-related hypertensive disorders and shares several clinical and biologic features with thrombotic microangiopathy (TMA). Several recent studies have clearly shown that an abnormal control of the complement alternative pathway is a major risk for the occurrence of a peculiar type of TMA involving mainly the kidney. The aim of this study was to screen for complement abnormalities in 11 patients with HELLP syndrome and renal involvement. We identified 4 patients with a mutation in one of the genes coding for proteins involved in the regulation of the alternative pathway of complement. Our results suggest that an abnormal control of the complement alternative pathway is a risk factor for the occurrence of HELLP syndrome.
Keywords
Adult, Complement Factor H/*genetics, Complement System Proteins/genetics, DNA Mutational Analysis, Female, Fibrinogen/*genetics, Genetic Predisposition to Disease, Gestational Age, HELLP Syndrome/*genetics, Humans, Membrane Cofactor Protein/*genetics, *Mutation, Missense, Pregnancy, Risk Factors, Young Adult
Pubmed
Create date
01/03/2022 11:18
Last modification date
02/03/2022 7:36
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