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. 2020 Nov 12;2020:5016916. doi: 10.1155/2020/5016916

Table 2.

Summary of studies evaluating the association of genetic variants and changes in gene expression with response to anti-VEGF therapies in diabetic macular edema.

Gene and variants Anti-VEGF drug DM type Response criteria Cohort size Follow-up (months) p value Country Reference
VEGFA
-634C>G (rs2010963)
Bevacizumab T2 Non-responder: increase in VA < 3 lines
AND <50% decrease in CMT
Responder: increase in VA ≥ 3 lines
AND ≥50% decrease in CMT
64 DME
Responder = 36eyes (24 patients)
Non − responder = 68eyes (40 patients)
9-12 p < 0.001 Egypt Shazly et al. [40]
VEGFA
rs2010963
rs2146323
rs10434
rs833069
rs6921438
Ranibizumab NA Non-responder: increase in VA < 2 lines
AND CMT > 300 microns
Responder: increase in VA ≥ 2 lines
AND CMT ≤ 300microns
95 DME
Responder = 53
Non − responder = 42
5 p > 0.05 for all variants Turkey Tetikoğlu et al. [85]
Transcriptome-wide gene expression analysis1 Bevacizumab T2 Non-responder: stable/worsening/<10% reduction in CMT
Responder: >10% reduction in CMT
Responder = 5
Non − responder = 5
NA 35 genes upregulated
26 genes downregulated
India Dabir et al. [86]
Expression of multiple lncRNA genes2 Aflibercept T2 Not defined 75 DME
Responder = 51
Non − responder = 9 (missingdata = 15)
1 p > 0.05 for all lncRNAs Egypt Toraih et al. [87]

Study evaluated mRNA expression in peripheral whole blood following bevacizumab treatment. Study evaluated serum levels of hyperglycaemia sensitive long non-coding RNA following aflibercept treatment. DM: diabetes mellitus; NA: not available; DME: diabetic macular edema; VA: visual acuity; CMT: central macular thickness; VEGFA: vascular endothelial growth factor A; lncRNA: long non-coding ribo-nucleic acid.