Zhang Pu, Jiang Bing, Xie Lili, Huang Wei
a Department of Ophthalmology , Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China.
Curr Eye Res. 2016 Dec;41(12):1561-1565. doi: 10.3109/02713683.2016.1143013. Epub 2016 Jun 23.
To determine the relationship between the polymorphisms of the prostaglandin F2α receptor (PTGFR) and solute carrier organic anion transporter family 2A1 (SLCO2A1) genes and response to latanoprost treatment in Han Chinese patients with glaucoma.
89 patients with POAG or OH received latanoprost treatment and intraocular pressure (IOP) data was collected on day 7 and day 30. The rs12093097, rs35586449, rs3753380, and rs3766355 single-nucleotide polymorphisms (SNPs) in the PTGFR gene and rs2370512, rs34550074, and rs4241366 SNPs in the SLCO2A1 gene were analyzed using direct DNA sequencing or polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).
The IOP in patients with GG allele of rs4241366 was lower than in patients with GC+CC on day 7 (p = 0.007). The IOP in patients with CC allele of rs3766355 was lower than in patients with CA+AA on day 30 (p = 0.024). Multiple regression analysis demonstrated that even after adjusting for baseline IOP, the rs4241366 in SLCO2A1 gene and the rs3766355 in PTGFR gene correlated with response to latanoprost on day 7 (rs4241366, p = 0.014) and day 30 (rs3766355, p = 0.035), respectively, in Han Chinese patients with glaucoma.
An association was found between single nucleotide polymorphisms of the PTGFR and SLCO2A1 genes and the response to latanoprost in Han Chinese patients with glaucoma. These SNPs may be important determinants of differential response to latanoprost.
确定前列腺素F2α受体(PTGFR)和溶质载体有机阴离子转运体家族2A1(SLCO2A1)基因多态性与汉族青光眼患者对拉坦前列素治疗反应之间的关系。
89例原发性开角型青光眼(POAG)或高眼压症(OH)患者接受拉坦前列素治疗,并在第7天和第30天收集眼压(IOP)数据。采用直接DNA测序或聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析PTGFR基因中的rs12093097、rs35586449、rs3753380和rs3766355单核苷酸多态性(SNP)以及SLCO2A1基因中的rs2370512、rs34550074和rs4241366 SNP。
rs4241366的GG等位基因患者在第7天的眼压低于GC+CC等位基因患者(p = 0.007)。rs3766355的CC等位基因患者在第30天的眼压低于CA+AA等位基因患者(p = 0.024)。多元回归分析表明,在汉族青光眼患者中,即使调整了基线眼压后,SLCO2A1基因中的rs4241366和PTGFR基因中的rs3766355分别与第7天(rs4241366,p = 0.014)和第30天(rs3766355,p = 0.035)对拉坦前列素的反应相关。
在汉族青光眼患者中,发现PTGFR和SLCO2A1基因的单核苷酸多态性与对拉坦前列素的反应之间存在关联。这些SNP可能是对拉坦前列素反应差异的重要决定因素。