Department of Ophthalmology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung 83301, Taiwan.
Department of Laboratory Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung 83301, Taiwan.
Int J Mol Sci. 2021 Jan 3;22(1):422. doi: 10.3390/ijms22010422.
Most studies about dry eye disease (DED) chose unilateral eye for investigation and drew conclusions based on monocular results, whereas most studies involving tear proteomics were based on the results of pooling tears from a group of DED patients. Patients with DED were consecutively enrolled for binocular clinical tests, tear biochemical markers of DED, and tear proteome. We found that bilateral eyes of DED patients may have similar but different ocular surface performance and tear proteome. Most ocular surface homeostatic markers and tear biomarkers were not significantly different in the bilateral eyes of DED subjects, and most clinical parameters and tear biomarkers were correlated significantly between bilateral eyes. However, discrepant binocular presentation in the markers of ocular surface homeostasis and the associations with tear proteins suggested that one eye's performance cannot represent that of the other eye or both eyes. Therefore, in studies for elucidating tear film homeostasis of DED, we may lose some important messages hidden in the fellow eye if we collected clinical and proteomic data only from a unilateral eye. For mechanistic studies, it is recommended that researchers collect tear samples from the eye with more severe DED under sensitive criteria for identifying the more severe eye and evaluating the tear biochemical and proteomic markers with binocular concordance drawn in prior binocular studies.
大多数关于干眼症(DED)的研究选择单侧眼睛进行调查,并根据单眼结果得出结论,而大多数涉及泪液蛋白质组学的研究则基于一组 DED 患者的泪液汇集结果。连续招募 DED 患者进行双眼临床检查、DED 的泪液生化标志物和泪液蛋白质组学检查。我们发现 DED 患者的双眼可能具有相似但不同的眼表功能和泪液蛋白质组。DED 受试者的双眼大多数眼表稳态标志物和泪液生物标志物无显著差异,大多数临床参数和泪液生物标志物在双眼之间呈显著相关。然而,眼部表面稳态标志物和与泪蛋白的关联存在不一致的双眼表现,表明一只眼睛的表现不能代表另一只眼睛或两只眼睛。因此,在研究 DED 的泪膜稳态时,如果我们仅从单侧眼睛收集临床和蛋白质组学数据,我们可能会错过隐藏在对侧眼睛中的一些重要信息。对于机制研究,建议研究人员根据识别更严重眼睛的敏感标准,从 DED 更严重的眼睛中收集泪液样本,并评估双眼研究中得出的双眼一致性的泪液生化和蛋白质组学标志物。