| Title | Association between CFH single nucleotide polymorphisms and response to photodynamic therapy in patients with central serous chorioretinopathy |
| Authors | Linghu, Dandan Xu, Hui Liang, Zhiqiao Gao, Tingting Lin, Zhaojun Li, Xiaoxin Huang, Lvzhen Zhao, Mingwei |
| Affiliation | Peking Univ, Dept Ophthalmol, Peoples Hosp, Xizhimen South St 11, Beijing 100044, Peoples R China Eye Dis & Optometry Inst, Beijing, Peoples R China Beijing Key Lab Diag & Therapy Retina & Choroid D, Beijing, Peoples R China Peking Univ, Coll Optometry, Hlth Sci Ctr, Beijing, Peoples R China |
| Keywords | COMPLEMENT FACTOR-H VARIANTS UPDATE |
| Issue Date | Apr-2020 |
| Publisher | INTERNATIONAL OPHTHALMOLOGY |
| Abstract | Purpose To evaluate the association between single nucleotide polymorphisms (SNPs) in the complement factor H (CFH) gene and response to PDT in patients with CSC. Methods 103 eyes from 93 patients with CSC were enrolled from Department of Ophthalmology of the People's Hospital Peking University. Genotyping for selected SNPs in the CFH gene was performed, and multivariate linear analysis was used to identify factors influencing PDT treatment outcomes. Genetics associations between SNPs in the CFH gene and response to PDT in patients with CSC were analyzed. Results None of the seven SNPs examined in this study (rs800292, rs1061170, rs3753394, rs3753396, rs2284664, rs1329428, and rs1065489) showed significant associations with 1-month outcomes after PDT in patients with CSC (P > 0.05). Baseline BCVA changed at 1 month after PDT (P < 0.001), and baseline retinal thickness was associated with changes in retinal thickness at 1 month after PDT (P < 0.001). Age was significantly associated with resolution of SRF at 1 month after PDT (P = 0.004). Conclusions There were no significant associations between SNPs in the CFH gene and 1-month outcomes after PDT in patients with CSC. However, baseline BCVA, baseline retinal thickness, and age were significantly associated with response to PDT in patients with CSC. Larger studies with more power are necessary to further determine whether an association exists between SNPs in the CFH gene and PDT in patients with CSC. |
| URI | http://hdl.handle.net/20.500.11897/588100 |
| ISSN | 0165-5701 |
| DOI | 10.1007/s10792-019-01261-y |
| Indexed | SCI(E) |
| Appears in Collections: | 人民医院 |
