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在抗坏血酸缺乏情况下,钠依赖性维生素C转运蛋白基因多态性与血浆、房水及晶状体核中抗坏血酸浓度的关系

Polymorphisms in sodium-dependent vitamin C transporter genes and plasma, aqueous humor and lens nucleus ascorbate concentrations in an ascorbate depleted setting.

作者信息

Senthilkumari Srinivasan, Talwar Badri, Dharmalingam Kuppamuthu, Ravindran Ravilla D, Jayanthi Ramamurthy, Sundaresan Periasamy, Saravanan Charu, Young Ian S, Dangour Alan D, Fletcher Astrid E

机构信息

Department of Ocular Pharmacology, Aravind Medical Research Foundation, Madurai, Tamilnadu, India.

Aravind Eye Hospital Pondicherry, Aravind Eye Care, Pondicherry, India.

出版信息

Exp Eye Res. 2014 Jul;124:24-30. doi: 10.1016/j.exer.2014.04.022. Epub 2014 May 8.

Abstract

We have previously reported low concentrations of plasma ascorbate and low dietary vitamin C intake in the older Indian population and a strong inverse association of these with cataract. Little is known about ascorbate levels in aqueous humor and lens in populations habitually depleted of ascorbate and no studies in any setting have investigated whether genetic polymorphisms influence ascorbate levels in ocular tissues. Our objectives were to investigate relationships between ascorbate concentrations in plasma, aqueous humor and lens and whether these relationships are influenced by Single Nucleotide Polymorphisms (SNPs) in sodium-dependent vitamin C transporter genes (SLC23A1 and SLC23A2). We enrolled sixty patients (equal numbers of men and women, mean age 63 years) undergoing small incision cataract surgery in southern India. We measured ascorbate concentrations in plasma, aqueous humor and lens nucleus using high performance liquid chromatography. SLC23A1 SNPs (rs4257763, rs6596473) and SLC23A2 SNPs (rs1279683 and rs12479919) were genotyped using a TaqMan assay. Patients were interviewed for lifestyle factors which might influence ascorbate. Plasma vitamin C was normalized by a log10 transformation. Statistical analysis used linear regression with the slope of the within-subject associations estimated using beta (β) coefficients. The ascorbate concentrations (μmol/L) were: plasma ascorbate, median and inter-quartile range (IQR), 15.2 (7.8, 34.5), mean (SD) of aqueous humor ascorbate, 1074 (545) and lens nucleus ascorbate, 0.42 (0.16) (μmol/g lens nucleus wet weight). Minimum allele frequencies were: rs1279683 (0.28), rs12479919 (0.30), rs659647 (0.48). Decreasing concentrations of ocular ascorbate from the common to the rare genotype were observed for rs6596473 and rs12479919. The per allele difference in aqueous humor ascorbate for rs6596473 was -217 μmol/L, p < 0.04 and a per allele difference in lens nucleus ascorbate of -0.085 μmol/g, p < 0.02 for rs12479919. The β coefficients for the regression of log10 plasma ascorbate on aqueous humor ascorbate were higher for the GG genotype of rs6596473: GG, β = 1460 compared to carriage of the C allele, CG, β = 1059, CC, β = 1132, p interaction = 0.1. In conclusion we found that compared to studies in well-nourished populations, ascorbate concentrations in the plasma, aqueous humor and lens nucleus were low. We present novel findings that polymorphisms in SLC23A1/2 genes influenced ascorbate concentration in aqueous humor and lens nucleus.

摘要

我们之前报道过,印度老年人群血浆中抗坏血酸浓度较低,饮食中维生素C摄入量也较低,且这些因素与白内障呈强烈的负相关。对于习惯性抗坏血酸缺乏人群的房水和晶状体中的抗坏血酸水平,我们知之甚少,并且在任何环境下都没有研究调查过基因多态性是否会影响眼组织中的抗坏血酸水平。我们的目标是研究血浆、房水和晶状体中抗坏血酸浓度之间的关系,以及这些关系是否受钠依赖性维生素C转运蛋白基因(SLC23A1和SLC23A2)中的单核苷酸多态性(SNP)影响。我们招募了60名在印度南部接受小切口白内障手术的患者(男女数量相等,平均年龄63岁)。我们使用高效液相色谱法测量血浆、房水和晶状体核中的抗坏血酸浓度。使用TaqMan分析法对SLC23A1 SNP(rs4257763、rs6596473)和SLC23A2 SNP(rs1279683和rs12479919)进行基因分型。就可能影响抗坏血酸的生活方式因素对患者进行了访谈。血浆维生素C通过log10转换进行标准化。统计分析采用线性回归,使用β系数估计受试者内部关联的斜率。抗坏血酸浓度(μmol/L)分别为:血浆抗坏血酸,中位数和四分位间距(IQR),15.2(7.8,34.5);房水抗坏血酸的平均值(标准差),1074(545);晶状体核抗坏血酸,0.42(0.16)(μmol/g晶状体核湿重)。最小等位基因频率分别为:rs1279683(0.28),rs12479919(0.30),rs659647(0.48)。对于rs6596473和rs12479919,观察到从常见基因型到罕见基因型眼内抗坏血酸浓度逐渐降低。rs6596473的房水抗坏血酸每等位基因差异为 -217 μmol/L,p < 0.04;rs12479919的晶状体核抗坏血酸每等位基因差异为 -0.085 μmol/g,p < 0.02。rs6596473的GG基因型在log10血浆抗坏血酸与房水抗坏血酸回归中的β系数更高:GG,β = 1460;相比携带C等位基因的CG,β = 1059,CC,β = 1132,p相互作用 = 0.1。总之,我们发现与营养良好人群的研究相比,血浆、房水和晶状体核中的抗坏血酸浓度较低。我们提出了新的发现,即SLC23A1/2基因中的多态性会影响房水和晶状体核中的抗坏血酸浓度。

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