Back to Search
Start Over
Fine mapping and subphenotyping implicates ADRA1B gene variants in psoriasis susceptibility in a Chinese population
- Source :
- Epigenomics. 11:455-467
- Publication Year :
- 2019
- Publisher :
- Future Medicine Ltd, 2019.
-
Abstract
- Aim: A genomic region on 5q33.3 lies between and encompasses the IL12B and PTTG1 genes, and contains many potential psoriasis causal variants. We aimed to further examine the influence of variants in and around this region. Materials & methods: We used least absolute shrinkage and selection operator (LASSO)-based regression analysis to assess independent contributions of 2171 variants to psoriasis susceptibility and tested them for association with different clinical psoriasis subtypes. Results: We found that ADRA1B gene variants contribute to psoriasis in Chinese population. ADRA1B gene variants have a stronger association with moderate-to-severe disease group and an earlier age at onset of psoriasis than IL-12B and PTTG1 variants. Conclusion: The association of variants in the ADRA1B gene with psoriasis could explain why variants in the IL-12B, ADRA1B and PTTG1 gene regions are associated with psoriasis.
- Subjects :
- Adult
Male
0301 basic medicine
China
Cancer Research
Quantitative Trait Loci
Inheritance Patterns
Disease
Alpha-1B adrenergic receptor
Biology
Polymorphism, Single Nucleotide
Linkage Disequilibrium
03 medical and health sciences
0302 clinical medicine
Asian People
Receptors, Adrenergic, alpha-1
Psoriasis
Genetics
medicine
Humans
SNP
Genetic Predisposition to Disease
Age of Onset
Gene
Alleles
Genetic Association Studies
Chinese population
Chromosome Mapping
Genetic Variation
Middle Aged
medicine.disease
Phenotype
030104 developmental biology
ROC Curve
Case-Control Studies
030220 oncology & carcinogenesis
PTTG1 Gene
Female
Selection operator
Research Article
Subjects
Details
- ISSN :
- 1750192X and 17501911
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Epigenomics
- Accession number :
- edsair.doi.dedup.....403ae3c9c217674db9da779c4bcedd02
- Full Text :
- https://doi.org/10.2217/epi-2018-0131