Saravani Ramin, Hasanian-Langroudi Farzaneh, Validad Mohammad-Hosein, Yari Davood, Bahari Gholamreza, Faramarzi Mahmood, Khateri Mehdi, Bahadoram Somayeh
*Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan, Iran; †Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran; ‡Department of Ophthalmology, Alzahra Eye Hospital, Zahedan University of Medical Sciences, Zahedan, Iran; §Department of Immunology, Iran University of Medical Sciences (IUMS), Tehran, Iran; ¶Biotechnology Department, Pasteur Institute of Iran, Tehran, Iran; and #Department of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Cornea. 2015 Mar;34(3):318-22. doi: 10.1097/ICO.0000000000000356.
Keratoconus (KC) is a genetically heterogeneous corneal dystrophy with unknown etiology that causes loss of visual acuity. Evidence has shown that corneas from patients with KC contain reduced amounts of total collagen proteins, and collagen type IV has been suggested as a candidate gene in KC pathogenesis. This study aimed to evaluate the possible associations between collagen type IV alpha-4 chain (COL4A4) polymorphisms (rs2229813 G/A, M1327V and rs2228555 A/G, V1516V) and susceptibility to KC.
A total of 262 Iranian subjects including 112 patients with KC and 150 healthy individuals as controls were recruited in this case-control study. Diagnosis was based on clinical examination, electronic refractometry, and keratometry. Genotyping for the COL4A4 rs2229813 and rs2228555 variants was executed using allele-specific polymerase chain reaction and Tetra-ARMS polymerase chain reaction, respectively.
A significant difference was found between the 2 groups regarding allelic and genotyping distribution of COL4A4 polymorphism at position rs2229813 G>A. The COL4A4 rs2229813 AA and GA+AA genotypes were risk factors for developing KC (odds ratio [OR] = 2.1, P = 0.036 and OR = 1.7, P = 0.042, for the AA and GA+AA genotypes, respectively). The COL4A4 rs2229813 A allele was also associated with an increased risk for KC (OR = 1.5, 95% confidence intervals: 1.1-2.2, P = 0.018). However, in our study, we found no association between COL4A4 rs2228555 polymorphism and the risk of KC.
We suggest that the COL4A4 rs2229813 AA and GA+AA genotypes as well as the A allele play roles as risk factors for developing KC in our population.
圆锥角膜(KC)是一种病因不明的遗传性角膜营养不良,可导致视力丧失。有证据表明,KC患者的角膜中总胶原蛋白含量减少,IV型胶原蛋白被认为是KC发病机制中的候选基因。本研究旨在评估IV型胶原蛋白α-4链(COL4A4)多态性(rs2229813 G/A,M1327V和rs2228555 A/G,V1516V)与KC易感性之间的可能关联。
在这项病例对照研究中,共招募了262名伊朗受试者,其中包括112名KC患者和150名健康个体作为对照。诊断基于临床检查、电子验光和角膜曲率测量。分别使用等位基因特异性聚合酶链反应和四引物扩增受阻突变系统聚合酶链反应对COL4A4 rs2229813和rs2228555变体进行基因分型。
在rs2229813 G>A位点,两组之间COL4A4多态性的等位基因和基因分型分布存在显著差异。COL4A4 rs2229813 AA和GA+AA基因型是发生KC的危险因素(AA基因型的优势比[OR]=2.1,P=0.036;GA+AA基因型的OR=1.7,P=0.042)。COL4A4 rs2229813 A等位基因也与KC风险增加相关(OR=1.5,95%置信区间:1.1-2.2,P=0.018)。然而,在我们的研究中,未发现COL4A4 rs2228555多态性与KC风险之间存在关联。
我们认为,在我们的人群中,COL4A4 rs2229813 AA和GA+AA基因型以及A等位基因是发生KC的危险因素。