The β‐chain mutation p.Trp433Stop impairs fibrinogen secretion: A novel nonsense mutation associated with hypofibrinogenemia. (29th June 2021)

• Record Type: Journal Article
• Authors: Yan, Jie; Wu, Yangyang; Liao, Lin; Xiang, Liqun; Qiu, Yuling; Lin, Faquan
• Is Part Of: International journal of laboratory hematology. Volume 43:Number 6(2021)
• Page Start: 1549
• Page End: 1556
• Publication Date: 2021-06-29
• Subjects: fibrinogen -- gene -- hypofibrinogenemia -- mutation; Hematology -- Periodicals; Blood -- Diseases -- Periodicals; Hematology -- Periodicals; 616.15005
• DOI: 10.1111/ijlh.13632
• Languages: English
• ISSNs: 1751-5521

Abstract

Abstract: Background: Congenital hypofibrinogenemia is characterized by proportional decreases in fibrinogen activity and immunoreactive fibrinogen levels. Here, we describe a new case with the bleeding risk identified in our hospital. Methods: The proband was cut and bled for 3 h. Coagulation testing, gene analysis, thrombelastogram, sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS‐PAGE), in vitro plasmid construction, and functional analyses were performed to explore the pathogenic mechanism. Results: Coagulation testing of the male proband revealed low levels of fibrinogen detected by two methods (the Clauss method and the PT‐derived method); his two sons had normal coagulation results. DNA sequencing of the proband revealed a heterozygous point mutation in exon 8 of the FGB gene causing Trp→Stop substitution and a polymorphic site (p.Leu92Phe). Human Trp433 was found to be highly conserved. SDS‐PAGE showed that the fibrinogen level of the proband was markedly lower than that of healthy controls. Using high‐performance liquid chromatography‐mass spectrometry, a mutated Bβ chain was not detected in circulation. In vitro expression analyses indicated that the mutation affected the secretion of fibrinogen. The TEG results indicated that the proband had a prolonged K time, a lower CI value, and a lower angle value. Conclusion: We report a new case with a novel nonsense mutation that resulted in hypofibrinogenemia. The results indicate that the nonsense mutation may cause misfolding of the D domain, which then affects the secretion of fibrinogen.