Sharon Yael, Shochat Tzipora, Rudman Yaron, Kushnir Shiri, Zahavi Alon, Shimon Ilan, Fleseriu Maria, Akirov Amit
Ophthalmology Department, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Acta Ophthalmol. 2025 May;103(3):e176-e182. doi: 10.1111/aos.16787. Epub 2024 Nov 5.
Glaucoma incidence in patients with endogenous Cushing's syndrome (CS) has never been established. We aim to assess the risk for glaucoma among CS patients compared to controls and determine the age of disease onset.
A nationwide retrospective matched-cohort study of patients with endogenous CS diagnosed between 2000 and 2023. Patients with CS were matched in a 1:5 ratio, with a control group individually matched for age, sex, socioeconomic status and body mass index. Main outcomes were the incidence of glaucoma and disease onset.
A total of 609 patients [396 women (65%); mean age 48.1 ± 17 years] were included in the CS group and 3018 controls. Follow-up duration was 14.6 years (IQR 9.8-20.2) for the study group. The aetiology of hypercortisolism was divided into pituitary (259, 42.6%), adrenal (206, 33.8%) and unconfirmed aetiology (144, 23.6%) patients. At baseline, 44 (7.2%) CS patients had a diagnosis of glaucoma, compared with 151 (5%) controls. The overall risk for glaucoma was 74% higher in patients with CS compared with matched controls (hazard ratio = 1.74, p = 0.002). Patients with CS who developed glaucoma were younger (mean age of 62 ± 14.7 years) than controls (mean age of 66 ± 11.3 years), (p = 0.02) [Correction added on 1 February 2025, after first online publication: The mean age has been corrected in the preceding sentence]. The overall risk for glaucoma in CS was high for both patients in remission and patients with persistent hypercortisolism (p = 0.048). Patients with active hypercortisolism experienced an earlier glaucoma onset (82.1 ± 88.0 months).
Endogenous CS is associated with increased risk for glaucoma regardless of remission status and develops at a younger age compared with the general population.
内源性库欣综合征(CS)患者的青光眼发病率尚未确定。我们旨在评估CS患者与对照组相比患青光眼的风险,并确定疾病发病年龄。
一项针对2000年至2023年间诊断为内源性CS患者的全国性回顾性匹配队列研究。CS患者与对照组按1:5的比例匹配,对照组在年龄、性别、社会经济地位和体重指数方面进行个体匹配。主要结局是青光眼的发病率和疾病发病情况。
CS组共纳入609例患者[396例女性(65%);平均年龄48.1±17岁]和3018例对照组。研究组的随访时间为14.6年(四分位间距9.8 - 20.2年)。皮质醇增多症的病因分为垂体性(259例,42.6%)、肾上腺性(206例,33.8%)和病因未确诊(144例,23.6%)患者。基线时,44例(7.2%)CS患者被诊断为青光眼,而对照组为151例(5%)。与匹配的对照组相比,CS患者患青光眼的总体风险高74%(风险比 = 1.74,p = 0.002)。发生青光眼的CS患者比对照组年轻(平均年龄62±14.7岁)(平均年龄66±11.3岁),(p = 0.02)[2025年2月1日首次在线发表后添加的更正:上一句中的平均年龄已更正]。缓解期患者和持续性皮质醇增多症患者患青光眼的总体风险均较高(p = 0.048)。活动性皮质醇增多症患者青光眼发病较早(82.1±88.0个月)。
内源性CS与青光眼风险增加相关,无论缓解状态如何,且与普通人群相比发病年龄更小。