炎性蛋白和化脓性汗腺炎:来自遗传相关性和孟德尔随机化的见解。

IF 2.9 3区 医学 Q2 DERMATOLOGY Journal of Dermatology Pub Date : 2024-12-20 DOI:10.1111/1346-8138.17590
Hui Luo, Yang Chen, Jianrong Li, Yanmei Yang, Xiujun Wang, Ping Yang, Chuang Guo, Fei Liu
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引用次数: 0

摘要

先前的研究强调了炎症蛋白与化脓性汗腺炎(HS)的发生和进展之间的显著关联。然而,这些因素之间的潜在因果关系仍有待明确确定。为了研究炎症蛋白与HS的遗传相关性,采用连锁不平衡评分回归(LDSC)。采用孟德尔随机化(MR)分析,结合方差逆加权、MR- egger和加权中位数方法,评估循环炎症蛋白(cip)与HS之间可能的因果关系。此外,还进行了反向MR分析,以探索反向因果关系。91个cip的数据集来自全基因组蛋白质数量性状位点研究,而hs相关数据来自FinnGen研究。此外,通过敏感性分析评估因果关系的稳定性,包括多效性测试、异质性测试和遗漏分析。LDSC分析表明成纤维细胞生长因子21 (FGF-21)、干细胞因子和HS之间存在遗传相关性。MR分析发现t细胞表面糖蛋白CD5和C-X-C基序趋化因子11与HS风险升高有关。相反,C-C基序趋化因子4、蛋白S100-A12、白介素-10受体亚单位β和程序性细胞死亡1配体1与HS风险降低有关。此外,HS被证明可以增加四种cip的水平:白细胞介素-20、白血病抑制因子(LIF)、LIF受体和胸腺基质淋巴生成素。本研究结果为各种遗传预测的炎症蛋白与HS之间可能的遗传相关性和因果关系提供了提示性证据。迫切需要进一步的研究来阐明驱动这些关联的基本过程。
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Inflammatory proteins and hidradenitis suppurativa: Insights from genetic correlation and Mendelian randomization

Previous research has highlighted a significant association between inflammatory proteins and the development and progression of hidradenitis suppurativa (HS). Nevertheless, the potential causative link between these factors remains to be definitively established. To investigate the genetic correlation between inflammatory proteins and HS, linkage disequilibrium score regression (LDSC) was employed. Mendelian randomization (MR) analysis, incorporating inverse variance weighted, MR-Egger, and weighted median methodologies, was utilized to evaluate the possible causal relationship between circulating inflammatory proteins (CIPs) and HS. Additionally, reverse MR analysis was carried out to explore reverse causality. The data set for 91 CIPs was derived from a genome-wide protein quantitative trait loci study, while HS-related data were acquired from the FinnGen study. Moreover, the stability of the causal relationships was assessed via sensitivity analyses, encompassing tests for pleiotropy, heterogeneity, and leave-one-out analysis. The LDSC analysis suggested the existence of genetic correlations between the levels of Fibroblast growth factor 21 (FGF-21), stem cell factor, and HS. The MR analysis identified a suggestive association of T-cell surface glycoprotein CD5 and C-X-C motif chemokine 11 with an elevated risk of HS. Conversely, C-C motif chemokine 4, Protein S100-A12, Interleukin-10 receptor subunit beta, and Programmed cell death 1 ligand 1 were associated with a diminished risk of HS. Moreover, HS was demonstrated to increase the levels of four CIPs: Interleukin-20, Leukemia inhibitory factor (LIF), LIF receptor, and Thymic stromal lymphopoietin. The findings of this investigation offer suggestive evidence for possible genetic correlations and causal links between various genetically predicted inflammatory proteins and HS. There exists a pressing requirement for additional studies to elucidate the fundamental processes driving these associations.

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来源期刊
Journal of Dermatology
Journal of Dermatology 医学-皮肤病学
CiteScore
4.60
自引率
9.70%
发文量
368
审稿时长
4-8 weeks
期刊介绍: The Journal of Dermatology is the official peer-reviewed publication of the Japanese Dermatological Association and the Asian Dermatological Association. The journal aims to provide a forum for the exchange of information about new and significant research in dermatology and to promote the discipline of dermatology in Japan and throughout the world. Research articles are supplemented by reviews, theoretical articles, special features, commentaries, book reviews and proceedings of workshops and conferences. Preliminary or short reports and letters to the editor of two printed pages or less will be published as soon as possible. Papers in all fields of dermatology will be considered.
期刊最新文献
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