کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5509867 1538636 2016 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Reduced serum level of leukocyte cell-derived chemotaxin 2 is associated with the presence of diabetic retinopathy
ترجمه فارسی عنوان
کاهش سطح سرمی چموتاکسین 2 از سلول های لکوسیتی با وجود رتینوپاتی دیابتی
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
چکیده انگلیسی


- We attempt to investigate the relation between serum LECT2 and diabetic retinopathy.
- Serum LECT2 levels were lower in diabetic patients with retinopathy than without.
- Low circulating LECT2 level may be a risk factor for diabetic retinopathy.

BackgroundVascular endothelial growth factor (VEGF) signaling is an important pathway in the development of diabetic retinopathy (DR). A recent report showed that leukocyte cell-derived chemotaxin 2 (LECT2) suppresses the VEGF signaling in endothelial cells. However, the clinical relevance of LECT2 in DR is unknown. This study aimed to investigate serum LECT2 levels and the presence of DR.MethodsThe study included 230 people with type 2 diabetes mellitus (DM), 95 with DR and 135 without DR. Serum LECT2 levels were measured using an enzyme-linked immunosorbent assay. Data were evaluated using Spearman's rank correlation, univariate and multivariate logistic regression.ResultsSerum LECT2 levels were significantly lower in participants with DM having DR than in those not having DR (35.6 ± 14.9 ng/ml vs. 44.5 ± 17.6 ng/ml, P < 0.001). Spearman's rank correlation analysis revealed a significant association between serum LECT2 levels and the presence of DR (P < 0.001). Multiple regression analysis revealed that serum LECT2 levels were independently related to DR (P < 0.001).ConclusionsThese findings indicated that serum LECT2 level is negatively associated with the presence of DR and suggest that low circulating LECT2 level is a risk factor for DR.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Clinica Chimica Acta - Volume 463, 1 December 2016, Pages 145-149
نویسندگان
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