研究目的
This study determined the relative importance of risk factors for Diabetic Retinopathy (DR) and Diabetic Macular Edema (DME) and assessed their independent and joint contributions.
研究成果
In conclusion, we demonstrated that the total variation; and independent and joint contributions of the key risk factors of DR and DME are markedly different in patients with type 2 diabetes. Our findings confirm that the ethology and pathogenesis of these two conditions are different and require prevention and intervention strategies.
研究不足
The targeted study sample, patients of specialised eye clinics, may mean that our results are not generalizable to a wider population of patients with diabetes and DR/DME. Finally, we lacked sufficient power to explore the relative importance of risk factors for the severity of DR/ DME and the relative importance of risk factors for DR in patients with Type 1 diabetes, and further work is required to investigate this.
1:Experimental Design and Method Selection:
A prospective study of patients with type 2 diabetes was conducted in a tertiary eye hospital in Melbourne, Australia. Patients underwent a comprehensive eye examination and completed standardized administered questionnaires. Blood samples were assessed for glycated haemoglobin (HbA1c); fasting blood glucose; and serum lipids. Dilated fundus photographs were obtained and graded for DR and DME. The relative importance of the risk factors was determined by the independent and common variance explained in DR and DME using Commonality analysis.
2:Sample Selection and Data Sources:
English-speaking adults aged 18 years or older with type 1 or type 2 diabetes, free of significant hearing and cognitive impairment, and living independently in the community were invited. Patients were primarily recruited from the Royal Victorian Eye and Ear Hospital (RVEEH).
3:List of Experimental Equipment and Materials:
Two-field 45° digital non-stereo colour fundus photographs of both eyes were taken from each individual using a non-mydriatic retinal camera (Canon CR6 – 45NM), Canon Inc, Japan, with all images being stored electronically using Digital Healthcare software. DR and DME were assessed using dilated fundus photography. Missing data (fundus images) were encountered in 13 cases (
4:5%).DR severity was classified according to the International Clinical Diabetic Retinopathy Severity Scale into:
1) non-proliferative DR (NPDR) and (2) proliferative DR (PDR). NPDR was further grouped into three progressive stages - mild, moderate and severe - with each stage having defined retinal pathologic signs.
5:Experimental Procedures and Operational Workflow:
All examinations were conducted at the Centre for Eye Research Australia (CERA) Melbourne Australia, located at the RVEEH.
6:Data Analysis Methods:
Continuous variables are presented as median (interquartile range [IQR]) for data with skewed distribution and mean (standard deviation [SD]) for normally distributed data, whereas categorical variables are presented as absolute (n) and relative frequencies (%) and 95% confidence interval (95% CI). Differences in continuous variables between participants with and without DR were evaluated by the Mann-Whitney-Wilcoxon test for skewed data, and the t-test for normally distributed data. The proportions between participants with and without DR were compared using the Chi-square test.
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