Risk factors and nomogram model construction for type 2 diabetes mellitus secondary to dry eye syndrome
10.3980/j.issn.1672-5123.2025.8.25
- VernacularTitle:2型糖尿病继发干眼的危险因素及列线图模型构建
- Author:
Wen ZHOU
1
;
Gongxun PING
1
Author Information
1. Department of Ophthalmology, Honghu People's Hospital, Honghu 433299, Hubei Province, China
- Publication Type:Journal Article
- Keywords:
type 2 diabetes mellitus;
dry eye syndrome;
risk factors;
nomogram
- From:
International Eye Science
2025;25(8):1352-1357
- CountryChina
- Language:Chinese
-
Abstract:
AIM: To investigate the risk factors for dry eye syndrome secondary to type 2 diabetes mellitus(T2DM), and to develop a nomogram model for early risk prediction.METHODS: A total of 347 T2DM patients treated in our hospital between March 2020 and April 2024 were enrolled and randomly divided into training(242 cases)and validation(105 cases)sets at a 7:3 ratio. Demographic data, glycemic parameters, and clinical treatments were compared between non-dry eye syndrome(control group, 86 cases)and dry eye syndrome to type 2 diabetes mellitus(dry eye group, 156 cases)in the training set. Statistically significant indicators were incorporated into multivariate Logistic regression to identify risk factors for secondary dry eye. These factors were then used to construct a nomogram model using R software, which was subsequently validated using the validation set.RESULTS:The percentage of patients with secondary dry eye syndrome in 242 cases of T2DM was 64.5%(156/242). Multifactorial Logistic regression revealed that blood glucose variability, glycosylated serum protein, retinopathy, meibomian gland functional status, duration of T2DM, and meibomian gland opening blockage were the risk factors for secondary dry eye(all OR>1, P<0.05). A nomogram prediction model was constructed based on the 6 indicators above, and the area under the receiver operating characteristics(ROC)curve of the training and validation sets was verified to be 0.994(95%CI: 0.989-0.999)and 0.990(95%CI: 0.977-0.999), respectively. The slopes of the calibration curves were similar, as tested by the Hosmer-Lemeshow test χ2=1.461, 1.566, P=0.993, 0.992. The nomogram model could provide good utility for clinical decision-making.CONCLUSION:Glycemic variability, glycated serum protein, retinopathy, meibomian gland dysfunction, T2DM duration, and meibomian gland orifice obstruction significantly increase the risk of dry eye secondary to T2DM. The constructed nomogram model serves as a valuable tool for early risk assessment and intervention, and it is helpful for early diagnosis and intervention, thus improving patients' quality of life.
