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特应性皮炎患者接受度普利尤单抗治疗后的眼表面疾病:一项前瞻性病例对照研究。

Ocular Surface Disease in Patients With Atopic Dermatitis Treated With Dupilumab: A Prospective Case-Control Study.

机构信息

Department of Ophthalmology, University of Turin, Turin, Italy.

Department of Medical Sciences, Section of Dermatology, University of Turin, Turin, Italy.

出版信息

Cornea. 2024 Feb 1;43(2):221-227. doi: 10.1097/ICO.0000000000003341. Epub 2023 Jul 4.

Abstract

PURPOSE

The aim of this study was to evaluate the variation of dry eye disease (DED) prevalence in patients with atopic dermatitis (AD) treated with dupilumab.

METHODS

This prospective case-control study included consecutive patients with moderate-to-severe AD scheduled for dupilumab between May and December 2021 and healthy subjects. DED prevalence, the Ocular Surface Disease Index, tear film breakup time test, osmolarity, Oxford staining score, and Schirmer test results were collected at baseline, 1 month, and 6 months after dupilumab therapy. The Eczema Area and Severity Index was assessed at baseline. Ocular side effects and discontinuation of dupilumab were also recorded.

RESULTS

Seventy-two eyes from 36 patients with AD treated with dupilumab and 36 healthy controls were included. Prevalence of DED increased from 16.7% at baseline to 33.3% at 6 months in the dupilumab group ( P = 0.001), whereas it remained unchanged in the control group ( P = 0.110). At 6 months, the Ocular Surface Disease Index and Oxford score increased (from 8.5 ± 9.8 to 11.0 ± 13.0, P = 0.068, and from 0.1 ± 0.5 to 0.3 ± 0.6, P = 0.050, respectively), the tear film breakup time test and Schirmer test results decreased (from 7.8 ± 2.6 s to 7.1 ± 2.7 s, P < 0.001, and from 15.4 ± 9.6 mm to 13.2 ± 7.9 mm, P = 0.036, respectively) in the dupilumab group, whereas they remained stable in the control group ( P > 0.05). Osmolarity was unchanged (dupilumab P = 0.987 and controls P = 0.073). At 6 months after dupilumab therapy, 42% of patients had conjunctivitis, 36% blepharitis, and 2.8% keratitis. No severe side effects were reported, and none of the patients discontinued dupilumab. No association between Eczema Area and Severity Index and DED prevalence was shown.

CONCLUSIONS

DED prevalence increased in patients with AD treated with dupilumab at 6 months. However, no severe ocular side effects were found and no patient discontinued therapy.

摘要

目的

本研究旨在评估接受度匹鲁单抗治疗的特应性皮炎(AD)患者干眼症(DED)患病率的变化。

方法

这是一项前瞻性病例对照研究,纳入了 2021 年 5 月至 12 月期间接受度匹鲁单抗治疗的中重度 AD 连续患者和健康受试者。在接受度匹鲁单抗治疗前、1 个月和 6 个月时,收集 DED 患病率、眼表疾病指数、泪膜破裂时间测试、渗透压、牛津染色评分和泪液分泌试验结果。在基线时评估特应性皮炎面积和严重程度指数。还记录了眼部副作用和度匹鲁单抗的停药情况。

结果

纳入了 36 例 AD 患者的 72 只眼接受度匹鲁单抗治疗和 36 例健康对照者。在接受度匹鲁单抗治疗的患者中,DED 的患病率从基线时的 16.7%增加到 6 个月时的 33.3%(P = 0.001),而对照组的患病率无变化(P = 0.110)。在 6 个月时,眼表疾病指数和牛津评分增加(分别从 8.5 ± 9.8 增至 11.0 ± 13.0,P = 0.068,和从 0.1 ± 0.5 增至 0.3 ± 0.6,P = 0.050),泪膜破裂时间测试和泪液分泌试验结果下降(分别从 7.8 ± 2.6 秒降至 7.1 ± 2.7 秒,P < 0.001,和从 15.4 ± 9.6 毫米降至 13.2 ± 7.9 毫米,P = 0.036),而对照组则保持稳定(P > 0.05)。渗透压无变化(度匹鲁单抗 P = 0.987,对照组 P = 0.073)。在接受度匹鲁单抗治疗 6 个月后,42%的患者出现结膜炎,36%出现睑缘炎,2.8%出现角膜炎。未报告严重眼部副作用,也没有患者停止使用度匹鲁单抗。特应性皮炎面积和严重程度指数与 DED 患病率之间无关联。

结论

接受度匹鲁单抗治疗的 AD 患者在 6 个月时 DED 患病率增加。然而,未发现严重眼部副作用,也没有患者停止治疗。

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