Three noninvasive methods in the evaluation of subclinical cardiovascular disease in patients with diabetic retinopathy: endothelial dysfunction, serum E-selectin level and monocyte to HDL ratio
Abstract
ABSTRACT
Aim: Cardiovascular risk has increased in diabetic retinopathy (DR). Brachial artery flow mediated dilation (FMD) is a non-invasive method used to evaluate endothelial dysfunction. Measurement of adhesion molecules such as E-selectin is the indirect method of predicting endothelial dysfunction. Monocyte/ HDL ratio (MHR) is a novel marker found to be related with cardiovascular diseases. In this study, in DR patients without an apparent cardiovascular disease, we aimed to investigate the relation between endothelial dysfunction indicators such as MHR, FMD, E-selectin and subclinical atherosclerosis.
Material and Method: In this study, 96 diabetic patients without apparent cardiac symptoms and 32 healthy control patients that matched for gender, age and body mass index (BMI) were included. The patients were separated into four groups as; nonproliferative diabetic retinopathy (NPDR, n=31), proliferative diabetic retinopathy (PDR, n=32), diabetic patients without a retinopathy (n=33) and control group (n=33). Anthropometric, biochemical values and FMD were measured. Correlation and regression analysis were done for the relation between MHR and FMD.
Results: MHR was significantly high in PDR group (p<.001). E-selectin and FMD which are indicators for endothelial dysfunction were significantly different between groups (p< .001). E-selectin measures were highest in PDR group, lower in NPDR group, however it was significantly higher than DM and control groups (p= .026). Inversely proportional to E-selectin, FMD was significantly higher in control and significantly lower in PDR group (p< .001). Univariate logistic regression method was used to determine factors that had an influence on FMD. Glucose, HbA1C, CRP and MHR had a negative effect.
Conclusion: In patients with DR, MHR levels might be used as a novel non-invasive marker to determine early atherosclerotic risk.
Keywords
References
- 1. Davignon J, Ganz P. Role of endothelial dysfunction in atherosclerosis. Circulation 2004; 109(23 Suppl 1): III27-32.
- 2. Korkmaz H, Onalan O. Evaluation of endothelial dysfunction: flow-mediated dilation. Endothelium 2008; 15(4): 157–63.
- 3. Libby P, Ridker PM, Hansson GK, Leducq Transatlantic Network on Atherothrombosis. Inflammation in atherosclerosis: from pathophysiology to practice. J Am Coll Cardiol 2009; 54(23): 2129–38.
- 4. Widlansky ME, Gokce N, Keaney JF, Vita JA. The clinical implications of endothelial dysfunction. J Am Coll Cardiol 2003; 42(7): 1149–60.
- 5. Mohamed Q, Gillies MC, Wong TY. Management of diabetic retinopathy: a systematic review. JAMA 2007; 298(8): 902–16.
- 6. Cheung N, Mitchell P, Wong TY. Diabetic retinopathy. Lancet (London, England) 2010; 376(9735): 124–36.
- 7. van Hecke M V, Dekker JM, Nijpels G, Moll AC, Heine RJ, Bouter LM, et al. Inflammation and endothelial dysfunction are associated with retinopathy: the Hoorn Study. Diabetologia 2005; 48(7): 1300–6.
- 8. Carbonell M, Castelblanco E, Valldeperas X, Betriu À, Traveset A, Granado-Casas M, et al. Diabetic retinopathy is associated with the presence and burden of subclinical carotid atherosclerosis in type 1 diabetes. Cardiovasc Diabetol 2018; 17(1): 66.
Details
Primary Language
English
Subjects
Health Care Administration
Journal Section
Research Article
Publication Date
January 15, 2020
Submission Date
October 31, 2019
Acceptance Date
November 16, 2019
Published in Issue
Year 2020 Volume: 3 Number: 1











