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非变应性揉眼是圆锥角膜的主要行为危险因素。

Non-allergic eye rubbing is a major behavioral risk factor for keratoconus.

机构信息

Institute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.

Optegra Eye Health Care Clinic in Poznan, Poznan, Poland.

出版信息

PLoS One. 2023 Apr 13;18(4):e0284454. doi: 10.1371/journal.pone.0284454. eCollection 2023.

Abstract

Since the environmental, behavioral, and socioeconomic factors in the etiology of keratoconus (KTCN) remain poorly understood, we characterized them as features influencing KTCN phenotype, and especially affecting the corneal epithelium (CE). In this case-control study, 118 KTCN patients and 73 controls were clinically examined and the Questionnaire covering the aforementioned aspects was completed and then statistically elaborated. Selected KTCN-specific findings were correlated with the outcomes of the RNA-seq assessment of the CE samples. Male sex, eye rubbing, time of using a computer after work, and dust in the working environment, were the substantial KTCN risk factors identified in multivariate analysis, with ORs of 8.66, 7.36, 2.35, and 5.25, respectively. Analyses for genes whose expression in the CE was correlated with the eye rubbing manner showed the enrichment in apoptosis (TP53, BCL2L1), chaperon-related (TLN1, CTDSP2, SRPRA), unfolded protein response (NFYA, TLN1, CTDSP2, SRPRA), cell adhesion (TGFBI, PTPN1, PDPK1), and cellular stress (TFDP1, SRPRA, CAPZB) pathways. Genes whose expression was extrapolated to the allergy status didn't contribute to IgE-related or other inflammatory pathways. Presented findings support the hypothesis of chronic mechanical corneal trauma in KTCN. Eye-rubbing causes CE damage and triggers cellular stress which through its influence on cell apoptosis, migration, and adhesion affects the KTCN phenotype.

摘要

由于圆锥角膜(KTCN)病因中的环境、行为和社会经济因素仍知之甚少,我们将其特征化为影响 KTCN 表型的因素,尤其是影响角膜上皮(CE)的因素。在这项病例对照研究中,对 118 名 KTCN 患者和 73 名对照进行了临床检查,并完成了涵盖上述方面的问卷,然后进行了统计分析。选择的 KTCN 特异性发现与 CE 样本 RNA-seq 评估的结果相关。多变量分析确定男性、揉眼、工作后使用电脑时间、工作环境中的灰尘是 KTCN 的重要危险因素,其 OR 分别为 8.66、7.36、2.35 和 5.25。对与揉眼方式相关的 CE 中表达的基因进行分析表明,凋亡(TP53、BCL2L1)、伴侣蛋白相关(TLN1、CTDSP2、SRPRA)、未折叠蛋白反应(NFYA、TLN1、CTDSP2、SRPRA)、细胞黏附(TGFBI、PTPN1、PDPK1)和细胞应激(TFDP1、SRPRA、CAPZB)途径富集。与过敏状态相关的基因表达并不能促进 IgE 相关或其他炎症途径。目前的研究结果支持慢性机械性角膜创伤在 KTCN 中的假说。揉眼会导致 CE 损伤,并引发细胞应激,通过影响细胞凋亡、迁移和黏附,影响 KTCN 表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e948/10101517/a1433d5741b5/pone.0284454.g001.jpg

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