Plasma Ephrin-A1 level in a cohort of diabetic retinopathy patients

被引:4
作者
Mao, Danna [1 ]
Hu, Ying [1 ]
Bao, Qi [2 ]
Wu, Kewei [1 ]
Zheng, Yaoding [1 ]
Yang, Yukun [1 ]
Lei, Bo [3 ]
Jiang, Ying [1 ]
机构
[1] Med Community Fenghua Hosp Tradit Chinese Med, Dept Ophthalmol, 22 Zhong Shan Rd, Ningbo 315500, Zhejiang, Peoples R China
[2] Med Community Fenghua Hosp Tradit Chinese Med, Dept Clin Lab, Ningbo, Zhejiang, Peoples R China
[3] Zhengzhou Univ, Peoples Hosp, Henan Prov Peoples Hosp, Henan Eye Inst, 7 Weiwu Rd, Zhengzhou 450003, Henan, Peoples R China
关键词
Ephrin-A1; VEGF(165); Plasma; Diabetic retinopathy; ELISA; RECEPTOR; VEGF; ACTIVATION; THERAPY;
D O I
10.1186/s12886-020-01580-0
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
BackgroundTo determine plasma ephrin-A1 and VEGF(165) levels in a cohort of diabetic retinopathy patients.MethodsPlasma ephrin-A1 and VEGF(165) levels in fifty-five subjects including 19 individuals without diabetes (non-DM), 16 patients with diabetes (DM) but without diabetic retinopathy, and 20 patients with diabetic retinopathy (DR), were determined by ELISA. Serum creatinine, total cholesterol, fasting blood glucose and HbA1c were also measured. One-way ANOVA, Kruskal-Wallis Test, Mann-Whitney U Test corrected by Bonferroni, Pearson Correlation Analysis and Spearman Correlation Coefficient Analysis were used for data analysis.ResultsEphrin-A1 expression could be detected in human plasma with an average of 1.52 0.43 (mean +/- SEM) ng/ml. In DR subjects, the plasma ephrin-A1concentration was 3.63 +/- 4.63 ng/ml, which was significantly higher than that of the other two groups (non-DM: 0.27 +/- 0.13 ng/ml, DM: 0.35 +/- 0.34 ng/ml). The expression of VEGF(165) in human plasma was 34.00 +/- 42.55 pg/ml, with no statistical difference among the three groups. There was no correlation between ephrin-A1 and VEGF(165) in human plasma, but there was a correlation between plasma ephrin-A1 and duration of diabetes.Conclusions Plasma ephrin-A1 was highly expressed in patients with diabetic retinopathy, and there was no difference of plasma VEGF(165) expression in patients with diabetic retinopathy compared to the other two groups, suggesting that changes of plasma ephrin-A1 may be a more sensitive biomarker than plasma VEGF(165) in detecting diabetic retinopathy.
引用
收藏
页数:5
相关论文
共 20 条
[1]  
American Diabetes Association, 2018, Clin Diabetes, V36, P14, DOI 10.2337/cd17-0119
[2]   Angiogenic and cell survival functions of Vascular Endothelial Growth Factor (VEGF) [J].
Byrne, AM ;
Bouchier-Hayes, DJ ;
Harmey, JH .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2005, 9 (04) :777-794
[3]  
Cheng N, 2002, MOL CANCER RES, V1, P2
[4]   The definition and classification of glaucoma in prevalence surveys [J].
Foster, PJ ;
Buhrmann, R ;
Quigley, HA ;
Johnson, GJ .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2002, 86 (02) :238-242
[5]   Retinal angiogenesis in development and disease [J].
Gariano, RF ;
Gardner, TW .
NATURE, 2005, 438 (7070) :960-966
[6]   Early and Long-Term Responses to Anti Vascular Endothelial Growth Factor Therapy in Diabetic Macular Edema: Analysis of Protocol I Data [J].
Gonzalez, Victor H. ;
Campbell, Joanna ;
Holekamp, Nancy M. ;
Kiss, Szilard ;
Loewenstein, Anat ;
Augustin, Albert J. ;
Ma, Julia ;
Ho, Allen C. ;
Patel, Vaishali ;
Whitcup, Scott M. ;
Dugel, Pravin U. .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 2016, 172 :72-79
[7]   Advanced glycation end products increase retinal vascular endothelial growth factor expression [J].
Lu, M ;
Kuroki, M ;
Amano, S ;
Tolentino, M ;
Keough, K ;
Kim, I ;
Bucala, R ;
Adamis, AP .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (06) :1219-1224
[8]   Ephrin-A1 is expressed at sites of vascular development in the mouse [J].
McBride, JL ;
Ruiz, JC .
MECHANISMS OF DEVELOPMENT, 1998, 77 (02) :201-204
[9]   The ephrin-A1 ligand and its receptor, EphA2, are expressed during tumor neovascularization [J].
Ogawa, K ;
Pasqualini, R ;
Lindberg, RA ;
Kain, R ;
Freeman, AL ;
Pasquale, EB .
ONCOGENE, 2000, 19 (52) :6043-6052
[10]   EphrinA1 inhibits vascular endothelial growth factor-induced intracellular signaling and suppresses retinal neovascularization and blood-retinal barrier breakdown [J].
Ojima, T ;
Takagi, H ;
Suzuma, K ;
Oh, H ;
Suzuma, I ;
Ohashi, H ;
Watanabe, D ;
Suganami, E ;
Murakami, T ;
Kurimoto, M ;
Honda, Y ;
Yoshimura, N .
AMERICAN JOURNAL OF PATHOLOGY, 2006, 168 (01) :331-339