Disentangling the complexity of psoriasis in the post-genome-wide association era

被引:2
|
作者
Antonatos, Charalabos [1 ]
Grafanaki, Katerina [2 ]
Georgiou, Sophia [2 ]
Evangelou, Evangelos [3 ,4 ,5 ]
Vasilopoulos, Yiannis [1 ]
机构
[1] Univ Patras, Sect Genet Cell Biol & Dev, Dept Biol, Lab Genet, Patras 26504, Greece
[2] Univ Patras, Sch Med, Dept Dermatol Venereol, Patras 26504, Greece
[3] Univ Ioannina, Dept Hyg & Epidemiol, Sch Med, Ioannina 45110, Greece
[4] Fdn Res & Technol Hellas, Biomed Res Inst, Ioannina 45110, Greece
[5] Imperial Coll London, MRC Ctr Environm & Hlth, Dept Epidemiol & Biostat, London W2 1PG, England
关键词
GENE-GENE INTERACTIONS; HLA-C; SUSCEPTIBILITY LOCI; VARIANTS; DISEASE; RISK; IDENTIFICATION; POLYMORPHISMS; CALCIPOTRIOL; MULTICENTER;
D O I
10.1038/s41435-023-00222-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In recent years, genome-wide association studies (GWAS) have been instrumental in unraveling the genetic architecture of complex diseases, including psoriasis. The application of large-scale GWA studies in psoriasis has illustrated several associated loci that participate in the cutaneous inflammation, however explaining a fraction of the disease heritability. With the advent of high-throughput sequencing technologies and functional genomics approaches, the post-GWAS era aims to unravel the functional mechanisms underlying the inter-individual variability in psoriasis patients. In this review, we present the key advances of psoriasis GWAS in under-represented populations, rare, non-coding and structural variants and epistatic phenomena that orchestrate the interplay between different cell types. We further review the gene-gene and gene-environment interactions contributing to the disease predisposition and development of comorbidities through Mendelian randomization studies and pleiotropic effects of psoriasis-associated loci. We finally examine the holistic approaches conducted in psoriasis through system genetics and state-of-the-art transcriptomic analyses, discussing their potential implication in the expanding field of precision medicine and characterization of comorbidities.
引用
收藏
页码:236 / 247
页数:12
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