The relation of markers of inflammation and endothelial dysfunction to the prevalence and progression of diabetic retinopathy: Wisconsin epidemiologic study of diabetic retinopathy.
The relation of markers of inflammation and endothelial dysfunction to the prevalence and progression of diabetic retinopathy: Wisconsin epidemiologic study of diabetic retinopathy.
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DOI:
10.1001/archophthalmol.2009.172
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发表时间:
2009-09
影响因子:
--
通讯作者:
Klein, Ronald
中科院分区:
文献类型:
--
作者:
Klein, Barbara E. K.;Knudtson, Michael D.;Tsai, Michael Y.;Klein, Ronald
Levels of glycemia, blood pressure, and serum total cholesterol are associated with prevalence and incidence of diabetic retinopathy. It has been reported the markers of systemic inflammation and endothelial dysfunction may be important additional risk factors. To determine the association of several systemic markers of inflammation and endothelial dysfunction to prevalence and incidence of diabetic retinal outcomes in persons with long duration type 1 diabetes. Longitudinal population based study of persons with type 1 diabetes who were receiving care for their diabetes in south central Wisconsin in 1978-1979. Data for this investigation were from 1990-1992 through 2005-2007. Severity of diabetic retinopathy and macular edema. In prevalence data from 1990-1992, soluble vascular cell adhesion molecule (sVCAM-1), tumor necrosis factor alpha (TNF-α) and homocysteine (Hcy) were associated with increased odds of more severe retinopathy (Odds ratios [highest versus lowest quartile] 2.43, 95% Confidence Interval 1.56, 3.78; 3.14 [1.98, 4.99]; 3.79 [2.33, 6.15], respectively) in those with kidney disease while controlling for relevant confounders. Similar odds were found for proliferative diabetic retinopathy. Only homocysteine was associated with increased odds of macular edema (4.68; 1.25-17.57) irrespective of kidney disease. None of the markers were associated with incidence of proliferative retinopathy, macular edema, or progression of retinopathy 15 years later. A limited number of markers was associated with increased odds of prevalent retinal outcomes in persons with type 1 diabetes and kidney disease. Only Hcy was associated with macular edema in those with and without kidney disease. In the absence of kidney disease the markers do not add to the more conventional descriptors and predictors of diabetic retinopathy in persons with type 1 diabetes. This may reflect the close association of diabetic retinopathy and diabetic kidney disease.
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