Ozek Dilay, Kemer Ozlem Evren, Omma Ahmet
Department of Ophthalmology, Ankara Numune Education and Research Hospital, Turkey.
Department of Rheumatology, Ankara Numune Education and Research Hospital, Turkey.
Arq Bras Oftalmol. 2019 Jan-Feb;82(1):45-50. doi: 10.5935/0004-2749.20190005. Epub 2018 Nov 1.
The aim of the present study was to compare the severity of ocular and systemic findings among patients with primary Sjögren syndrome.
The study followed a prospective controlled design and comprised two groups; the test group included 58 eyes of 58 patients newly diagnosed with primary Sjögren syndrome with poor dry eye test findings and the control group included 45 right eyes of 45 healthy age- and sex-matched individuals. The ocular surface disease index score, tear osmolarity, Schirmer I test without anesthesia, fluorescein tear breakup time, and cornea-conjunctiva staining with lissamine green (van Bijsterveld scoring) were used to examine tear function in the patients via a complete ophthalmological examination. The results were graded and classified on the basis of a Dry Eye WorkShop report and results of the corneal and conjunctival staining test, Schirmer's test, and fluorescein tear breakup time test. Discomfort, severity and frequency of symptoms, visual symptoms, conjunctival injection, eyelid-meibomian gland findings, and corneal-tear signs were interpreted. Disease activity was scored per the EULAR Sjögren's syndrome disease activity index (ESSDAI) via systemic examination and laboratory evaluations, and the EULAR Sjögren's syndrome patient-reported index (ESSPRI) assessed via a survey of patient responses.
Mean patient age was 48.15 ± 16.34 years in the primary Sjögren syndrome group and 44.06 ± 9.15 years in the control group. Mean fluorescein tear breakup time was 4.51 ± 2.89s in the primary Sjögren syndrome group and 10.20 ± 2.39 s in the control group. Mean Schirmer I test result was 3.51 ± 3.18 mm/5 min in the primary Sjögren syndrome group and 9.77±2.30 mm/5 min in the control group. Mean ocular surface disease index score was 18.56 ± 16.09 in the primary Sjögren syndrome group, and 19.92 ± 7.16 in the control group. Mean osmolarity was 306.48 ± 19.35 in the primary Sjögren syndrome group, and 292.54 ± 10.67 in the control group. Mean lissamine green staining score was 2.17 ± 2.76 in the primary Sjögren syndrome group, and 0.00 in the control group. Statistically significant differences were found berween the primary Sjögren syndrome group and control group in terms of fluorescein tear breakup time, Schirmer's test, lissamine green staining, and osmolarity tests (p=0.036, p=0.041, p=0.001, and p=0.001 respectively). The Dry Eye WorkShop score was 2.15 ± 0.98, the EULAR Sjögren's syndrome disease activity index score was 11.18 ± 4.05, and the EULAR Sjögren's syndrome patient-reported index score was 5.20±2.63. When potential associations of the Dry Eye Workshop Study scores and osmolarity scores with the Eular Sjögren's syndrome disease activity index scores were evaluated, the results were found to be statistically significant (p=0.001, p=0.001 respectively).
The results showed an association between dry eye severity and systemic activity index in primary Sjögren syndrome patients.
本研究旨在比较原发性干燥综合征患者眼部和全身表现的严重程度。
本研究采用前瞻性对照设计,分为两组;试验组包括58例新诊断为原发性干燥综合征且干眼试验结果不佳的患者的58只眼,对照组包括45例年龄和性别匹配的健康个体的45只右眼。通过全面的眼科检查,使用眼表疾病指数评分、泪液渗透压、无麻醉下的Schirmer I试验、荧光素泪膜破裂时间以及用丽丝胺绿进行角膜-结膜染色(范比斯特维尔德评分)来检查患者的泪液功能。根据干眼研讨会报告以及角膜和结膜染色试验、Schirmer试验和荧光素泪膜破裂时间试验的结果对结果进行分级和分类。对不适、症状的严重程度和频率、视觉症状、结膜充血、眼睑-睑板腺表现以及角膜-泪液体征进行解读。通过全身检查和实验室评估,根据欧洲抗风湿病联盟干燥综合征疾病活动指数(ESSDAI)对疾病活动进行评分,并通过对患者反应的调查评估欧洲抗风湿病联盟干燥综合征患者报告指数(ESSPRI)。
原发性干燥综合征组患者的平均年龄为48.15±16.34岁,对照组为44.06±9.15岁。原发性干燥综合征组的平均荧光素泪膜破裂时间为4.51±2.89秒,对照组为10.20±2.39秒。原发性干燥综合征组的平均Schirmer I试验结果为3.51±3.18毫米/5分钟,对照组为9.77±2.30毫米/5分钟。原发性干燥综合征组的平均眼表疾病指数评分为18.56±16.09,对照组为19.92±7.16。原发性干燥综合征组的平均渗透压为306.48±19.35,对照组为292.54±10.67。原发性干燥综合征组的平均丽丝胺绿染色评分为2.17±2.76,对照组为0.00。原发性干燥综合征组和对照组在荧光素泪膜破裂时间、Schirmer试验、丽丝胺绿染色和渗透压试验方面存在统计学显著差异(分别为p = 0.036、p = 0.041、p = 0.001和p = 0.001)。干眼研讨会评分为2.15±0.98,欧洲抗风湿病联盟干燥综合征疾病活动指数评分为11.18±4.05,欧洲抗风湿病联盟干燥综合征患者报告指数评分为5.20±2.63。当评估干眼研讨会研究评分和渗透压评分与欧洲抗风湿病联盟干燥综合征疾病活动指数评分的潜在关联时,发现结果具有统计学显著性(分别为p = 0.001、p = 0.001)。
结果表明原发性干燥综合征患者的干眼严重程度与全身活动指数之间存在关联。