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Войти в исследования Case reports in neurology · 2023
Prodromal Dementia with Lewy Bodies: A Case Series of the 3 Prodromal Types from Clinical Practice.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Ge Chenyang, Wang Yizheng, Zhao Xuegang, Hao Jiawen, Zhang Jing, Lu Mengyuan, Li Congying, Feng Jianke, Zhang Qingfu
Аннотация
BACKGROUND: Research as shown that celiac disease (CD) is associated with skin diseases, but their causality remains unclear. Therefore, this Mendelian randomization (MR) study evaluated the causality between CD and skin diseases.
METHODS: Bidirectional MR analysis was performed on single nucleotide polymorphism (SNP) candidates identified from genome-wide association study (GWAS) datasets using inverse variance weighted (IVW), weighted median, MR-egger, weighted mode and simple mode. Multivariate MR (MVMR) analysis was subsequently conducted by adjusting for BMI, smoking, and alcohol use. Result reliability was assessed by horizontal pleiotropy and heterogeneity testing.
RESULTS: IVW analysis revealed that CD increased the risk of atopic dermatitis (OR = 1.042, 95% CI: 1.018-1.067, P = 5.75 × 10-4) and cellulitis (OR = 1.026, 95% CI: 1.006-1.046, P = 9.18×10-3). Additionally, psoriasis had a suggestive association with CD (OR=0.836, 95% CI: 0.710-0.983, P = 0.031). MVMR analysis demonstrated that CD had a direct effect on atopic dermatitis and cellulitis.
CONCLUSION: CD contributes to higher risks of atopic dermatitis and cellulitis. Additionally, psoriasis is suggestively associated with CD. Nonetheless, further research is warranted to confirm these findings and to elucidate the underlying mechanisms.
METHODS: Bidirectional MR analysis was performed on single nucleotide polymorphism (SNP) candidates identified from genome-wide association study (GWAS) datasets using inverse variance weighted (IVW), weighted median, MR-egger, weighted mode and simple mode. Multivariate MR (MVMR) analysis was subsequently conducted by adjusting for BMI, smoking, and alcohol use. Result reliability was assessed by horizontal pleiotropy and heterogeneity testing.
RESULTS: IVW analysis revealed that CD increased the risk of atopic dermatitis (OR = 1.042, 95% CI: 1.018-1.067, P = 5.75 × 10-4) and cellulitis (OR = 1.026, 95% CI: 1.006-1.046, P = 9.18×10-3). Additionally, psoriasis had a suggestive association with CD (OR=0.836, 95% CI: 0.710-0.983, P = 0.031). MVMR analysis demonstrated that CD had a direct effect on atopic dermatitis and cellulitis.
CONCLUSION: CD contributes to higher risks of atopic dermatitis and cellulitis. Additionally, psoriasis is suggestively associated with CD. Nonetheless, further research is warranted to confirm these findings and to elucidate the underlying mechanisms.