Genetic alterations and pathways in patients with Hereditary Angioedema of Unknown Cause (U-HAE)

Yıl 2021, , 274 - 278, 27.10.2021

Hande Kaymakcalan Hande Alp Ahmet Okay Caglayan Okan Gulbahar Emine Nihal Gokmen Emrah Nıkerel

https://doi.org/10.5472/marumj.1009115

Öz

Objective: Hereditary angioedema ( HAE) with normal C1 inhibitor (HAE-nC1-INH), is a genetically complex, rare disease and
mutations in F12, ANGPT1, PLG, MYOF genes are found in some families with HAE-nC1-INH. However, often a specific mutation
cannot be identified and this type is called as hereditary angioedema of unknown cause (U-HAE). Our aim was to identify putative
causative genetic alterations and/or pathways by whole exome sequencing in patients with U-HAE.
Patients and Methods: Nine patients from 8 families between the ages of 3 to 63 years with U-HAE and 6 controls were enrolled for
the study and whole exome sequencing were performed.
Results: No significant difference was found between the case and control group for the a priori suspected set of genes. Variants in the
genes; RAMP2, IL6, GP1BA, C1QBP were significantly different between U-HAE and control group. Downstream functional analysis
found that blood coagulation pathways were enriched in these genes.
Conclusion: Proteins that are not involved in contact pathways may also play a role in U-HAE. These variants need to be replicated in
larger cohorts and studied at the functional level to verify our findings.

Anahtar Kelimeler

Hereditary angioedema of unknown cause ( U-HAE), Whole exome sequencing (WES ), Genetic

Kaynakça

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