Midani Fatma, Ben Amor Zohra, El Afrit Mohamed Ali, Kallel Amani, Feki Moncef, Soualmia Hayet
a Faculty of Sciences of Bizerte Zarzouna-Tunisia, University of Carthage , Tunis , Tunisia.
b Faculty of Medicine, Research Laboratory LR99ES11, CHU La Rabta, University of Tunis El Manar , Tunis , Tunisia.
Semin Ophthalmol. 2019;34(5):365-374. doi: 10.1080/08820538.2019.1632354. Epub 2019 Jun 29.
: In this study, we investigated the association of two polymorphisms (rs869109213 and rs2070744) in the gene and one polymorphism II in the αβ integrin gene () with the risk of diabetic retinopathy (DR) in a Tunisian population. : The study investigated of 110 type 2 diabetes mellitus (T2DM) and 127 DR patients. The genotypes of the 4b/4a (rs869109213) and -786T/C (rs2070744) polymorphisms and of the II polymorphism of were studied using the PCR or PCR-RFLP method. : The genotype distributions of the two polymorphisms in 4b4a and (-786T/C) were significantly different between T2DM and DR patients ( < .004 and = .033, respectively). These polymorphisms were associated with the risk of DR (OR = 2.65, 95%CI [1.45-4.84], = .002) for the 4b4a genotype and (OR = 2.43, 95%CI [1.06 - 5.56], = .036) for the CC genotype of the gene (-786T/C). Similarly, the genotype distribution of the II polymorphism was significantly different between the two groups studied ( = .037). This polymorphism was associated with an increased risk of DR (OR = 4.03, 95% CI [1.17 - 7.85], = .022) for II(+/+). : The present study suggests that the polymorphisms 4b4a and -786T/C in the gene might be associated with DR. In addition, the II polymorphism in the gene was a risk factor for DR.
在本研究中,我们调查了某基因中的两个多态性位点(rs869109213和rs2070744)以及αβ整合素基因中的一个多态性位点II与突尼斯人群糖尿病视网膜病变(DR)风险的关联。本研究纳入了110例2型糖尿病(T2DM)患者和127例DR患者。采用PCR或PCR-RFLP方法研究了4b/4a(rs869109213)和-786T/C(rs2070744)多态性位点以及αβ整合素基因II多态性位点的基因型。T2DM患者和DR患者之间,4b4a和αβ整合素基因(-786T/C)中两个多态性位点的基因型分布存在显著差异(分别为P<0.004和P=0.033)。对于4b4a基因型,这些多态性与DR风险相关(OR=2.65,95%CI[1.45-4.84],P=0.002);对于αβ整合素基因(-786T/C)的CC基因型,OR=2.43,95%CI[1.06-5.56],P=0.036。同样,II多态性的基因型分布在两组研究对象之间也存在显著差异(P=0.037)。对于II(+/+),这种多态性与DR风险增加相关(OR=4.03,95%CI[1.17-7.85],P=0.022)。本研究表明,某基因中的多态性位点4b4a和-786T/C可能与DR相关。此外,αβ整合素基因中的II多态性是DR的一个风险因素。