Effects of Ocufolin on retinal microvasculature in patients with mild non-proliferative diabetic retinopathy carrying polymorphisms of the MTHFR gene

被引:8
|
作者
Liu, Zhiping [1 ,2 ]
Jiang, Hong [2 ,3 ]
Townsend, Justin H. [2 ]
Wang, Jianhua [2 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 2, Ophthalm Ctr, Guangzhou, Guangdong, Peoples R China
[2] Univ Miami, Miller Sch Med, Dept Ophthalmol, Miami, FL 33136 USA
[3] Univ Miami, Miller Sch Med, Dept Neurol, Miami, FL 33136 USA
关键词
diabetes mellitus; type; 2; retina; A1298C POLYMORPHISM; TISSUE PERFUSION; BLOOD-FLOW; HOMOCYSTEINE; ASSOCIATION; SUPPLEMENTATION; PLASMA; RISK;
D O I
10.1136/bmjdrc-2021-002327
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction To evaluate effects of Ocufolin on retinal microvasculature in mild non-proliferative diabetic retinopathy patients who carried methylenetetrahydrofolate reductase (MTHFR) polymorphisms (DR+MTHFRP). Research design and methods This is a prospective cohort study. Eight DR+MTHFRP (administrated Ocufolin for 6 months) and 15 normal controls (NCs) were recruited. MTHFR polymorphisms were subtyped as normal, C677T, or A1298C. Best-corrected visual acuity (BCVA) was evaluated. Retinal vessel density (VD) and microstructure were evaluated by optical coherence tomography angiography. Results BCVA and vascular indices of DR+MTHFRP at baseline were worse than those of NC and improved. Compared with baseline, DR+MTHFRP had significantly improved BCVA during follow-up period (p<0.05). VD of superficial vascular plexus was increased at 4 months (p=0.012), while VD of retinal vascular network did not change (p>0.05). Carriers of A1298C and C677T showed statistically significant increase in VD at all layers by 6 months, while carriers of C677T alone showed no significant change and carriers of A1298C alone showed decreased density from 4 months to 6 months. Microstructure did not change during the follow-up period. Conclusion A 6-month intake of Ocufolin is capable of reversing structural changes of microangiopathy in mild non-proliferative DR+MTHFRP. This suggests a novel way to address these impairments prior to catastrophic vision loss.
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页数:9
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