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DOI: 10.1055/a-2514-7520
Clinical and Genetic Characterization of 51 Patients with Congenital Fibrinogen Disorders from China
Funding This work was supported by the National Natural Science Foundation of China (no. 82170131 and no. 82470134), the Young Top-notch Talent Cultivation Program of Hubei Province (no. 202117), and the National Key R&D Program of China (no. 2022YFC2304600 and no. 2023YFC2509500).

Abstract
Objective To investigate the classification, clinical manifestations, laboratory findings, and genetic mutations associated with hereditary fibrinogen disorders in Chinese population.
Methods Between February 2015 and February 2022, 65 patients with congenital fibrinogen disorders (CFD) were identified at Wuhan Union Hospital. Comprehensive data were available for 51 patients, allowing for a retrospective analysis.
Results The cohort comprised 17 males (33.3%) and 34 females (66.7%), with a median diagnosis age of 35.0 years (interquartile range: 25.5–42.5). Of the patients, 35 (68.6%) were diagnosed with dysfibrinogenemia, 8 (15.7%) with hypofibrinogenemia, 7 (13.7%) with hypodysfibrinogenemia, and 1 (2.0%) with afibrinogenemia. The median diagnosis ages for the asymptomatic, Grade 1, Grade 2, and Grade 3 groups were 44.5 years (range: 37–58.5), 28 years (22.5–36.5), 35.5 years (21.75–41), and 28 years (22.75–30.75), respectively. The asymptomatic group had the latest diagnosis age, whereas Grade 3 had the earliest. A negative correlation was observed between Fg:C levels and bleeding severity (rs = − 0.2937, p = 0.0365). In total, 52 variants were found in 51 unrelated patients, with one patient carrying two mutations. The 37 distinct mutations included 11 in FGA, 3 in FGB, and 23 in FGG.
Conclusion This study investigates the clinical, laboratory, and genetic characteristics of patients with CFD in China, revealing a negative correlation between Fg:C levels and bleeding severity. Female patients are at higher risk for gynecological complications due to physiological traits. Additionally, R35 in FGA and R301 in FGG were identified as hotspot mutations.
Ethical Approval Statement
The study was approved by the Ethics Committee of the Union Hospital affiliated to Huazhong University of Science and Technology, Wuhan, China.
Authors' Contribution
Y.C. and H.L.: Drafted the manuscript, analyzed the data, participated in data curation, and contributed to writing. L.V.T. and Y.H.: Designed the study, obtained funding for the project, and contributed to conceptualization, methodology, project administration, and supervision. Y.X. and Z.C.: Responsible for data acquisition and contributed to investigation and resources. W.L.: Contributed to data analysis and interpretation. T.W.: Provided technical support and contributed to software and visualization. All authors reviewed the manuscript.
* These authors are co-first authors.
Publikationsverlauf
Eingereicht: 15. Oktober 2024
Angenommen: 16. Dezember 2024
Accepted Manuscript online:
13. Januar 2025
Artikel online veröffentlicht:
31. Januar 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
Georg Thieme Verlag KG
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