Molecular Genetic Mechanisms of Chronic Urticaria.
- Author:
Purevsuren LOSOL
1
;
Hye Soo YOO
;
Hae Sim PARK
Author Information
- Publication Type:Review
- Keywords: Chronic urticaria; genetic association; leukotriene; mast cell
- MeSH: Alleles; Classification; Cohort Studies; Dinoprostone; Ethnic Groups; Genome-Wide Association Study; Histamine; Humans; Leukotriene C4; Mast Cells; Metabolism; Molecular Biology*; Phenotype; Polymorphism, Genetic; Quality of Life; Skin Diseases; Urticaria*
- From:Allergy, Asthma & Immunology Research 2014;6(1):13-21
- CountryRepublic of Korea
- Language:English
- Abstract: Chronic urticaria (CU) is a common allergic skin disease that requires long-term pharmacological treatment. Some patients with severe CU suffer a poor quality of life. Although the pathogenic mechanisms of CU are not clearly understood, several groups have suggested that genetic mechanisms are involved in various CU cohorts. To further understand the molecular genetic mechanisms of CU, we summarize recent genetic data in this review. Although a few HLA alleles were suggested to be candidate markers in different ethnic groups, further replication studies that apply the recent classification are needed. Genetic polymorphisms in histamine-related genes, including FcepsilonRI and HNMT, were suggested to be involved in mast cell activation and histamine metabolism. Several genetic polymorphisms of leukotriene-related genes, such as ALOX5, LTC4S, and the PGE2 receptor gene PTGER4, were suggested to be involved in leukotriene overproduction, a pathogenic mechanism. Further investigations using candidate gene approaches and genome-wide association studies (GWAS) will provide new insights into the molecular genetic mechanisms of CU, which will provide new marker genes for differentiation of CU phenotypes and identification of potential therapeutic targets.
