Association between polymorphisms and atopic dermatitis susceptibility: A systematic review and meta-analysis

被引:2
作者
Huang, Yunxia [1 ,2 ]
Zhou, Wei [2 ]
Liu, Shunan [1 ,2 ]
Zeng, Dan [2 ]
Zhou, Weikang [1 ,2 ]
机构
[1] Southwest Med Univ, Dept Dermatol, Affiliated Hosp, Luzhou 646000, Peoples R China
[2] Chongqing Gen Hosp, Dept Allergy, Chongqing 400014, Peoples R China
基金
中国国家自然科学基金;
关键词
Atopic dermatitis; Polymorphism; Meta; -analysis; FLG; Interleukin; SINGLE NUCLEOTIDE POLYMORPHISMS; CYTOKINE GENE POLYMORPHISMS; CHROMOSOME; 11Q13.5; VARIANT; FILAGGRIN MUTATIONS; SPINK5; GENE; INTERLEUKIN-4; RECEPTOR; EARLY-ONSET; PROINFLAMMATORY CYTOKINES; PROMOTER POLYMORPHISM; RISK-FACTOR;
D O I
10.1016/j.gene.2024.148397
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Aim: Atopic dermatitis (AD) is a chronic pruritic inflammatory skin disease that is closely linked to genetic factors. Previous studies have revealed numerous single nucleotide polymorphisms (SNPs) that been related to susceptibility to AD; however, the results are conflicting. Therefore, a meta-analysis was conducted to assess the associations of these polymorphisms and AD risk. Material and methods: PubMed, Web of Science, Embase, Cochrane Library, and China National Knowledge Infrastructure databases were retrieved to identify eligible studies, with selected polymorphisms being reported in a minimum of three separate studies. The Newcastle-Ottawa Scale (NOS) was used to evaluate study quality. Review Manager 5.3 and STATA 14.0 were used to perform the meta-analysis. Results: After screening, 64 studies involving 13 genes (24 SNPs) were selected for inclusion in the meta-analysis. Nine SNPs were positively correlated with AD susceptibility [filaggrin (FLG) R501X, FLG 2282del4, chromosome 11q13.5 rs7927894, interleukin (IL)-17A rs2275913, IL-18 -137 G/C, Toll-like receptor 2 (TLR2) rs5743708, TLR2 A-16934 T, serine protease inhibitor Kazal type-5 (SPINK5) Asn368Ser, interferon-gamma (IFN-gamma) T874A] and one was negatively associated with AD susceptibility (IL-4 -1098 T/G). The 14 remaining SNPs were not significantly associated with AD susceptibility. Conclusions: Nine SNPs that may be risk factors and one SNP that may be a protective factor for AD were identified, providing a reference for AD prediction, prevention, and therapy.
引用
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页数:15
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