Murugesan Anandan, Kumar Lakshman, Janarthanan P
Department of Urology, PSG Institute of Medical Sciences and Research, Coimbatore, India.
Department of Biotechnology, Kongunadu Arts and Science College, Coimbatore, India.
Int J Appl Basic Med Res. 2018 Jan-Mar;8(1):38-41. doi: 10.4103/ijabmr.IJABMR_420_16.
Urine is a supersaturated solution with solutes in very high concentration. Matrix gla protein (MGP) is one of the proteins involved in inhibition of extracellular calcification. Among the various polymorphisms studied, polymorphism of SNP rs4236 in the MGP gene is found to have association with nephrolithiasis. We evaluated the significance of SNP rs4236 polymorphism in nephrolithiasis among the Indian population.
The study was conducted in 2013 and 2014 among fifty participants. Twenty-five of them were patients with documented symptomatic stone disease and the 25 controls had no history of stone disease and ultrasonogram was normal. Serum creatinine was estimated in all patients. DNA was isolated from the blood sample and amplified by polymerase chain reaction using defined primers. Single strand conformational polymorphism was done to identify abnormal bands and the same was sequenced.
The patients and controls were matched in age and sex. The serum creatinine levels were similar in both groups. The predominant change in SNP rs4236 in patients was a G to A nucleotide change, resulting in AA homozygous genotype. This was found in 60% of patients. The rest (40%) of patients and all (100%) controls had heterozygous AG genotype. This corresponds to a stone disease with an odds ratio (OR) of 75 ( < 0.003).
This first study in Indian population shows that genotype AA polymorphism of SNP rs4236 of MGP gene was found to be significant risk factor for renal stone disease. Studies with larger sample size may be needed to confirm this finding and elucidate the exact OR.
尿液是一种溶质浓度极高的过饱和溶液。基质γ-羧基谷氨酸蛋白(MGP)是参与抑制细胞外钙化的蛋白质之一。在已研究的各种多态性中,发现MGP基因中SNP rs4236的多态性与肾结石有关。我们评估了SNP rs4236多态性在印度人群肾结石中的意义。
该研究于2013年和2014年对50名参与者进行。其中25名是有症状性结石病记录的患者,25名对照者无结石病史且超声检查正常。对所有患者进行血清肌酐评估。从血样中提取DNA,并使用特定引物通过聚合酶链反应进行扩增。进行单链构象多态性分析以鉴定异常条带,并对其进行测序。
患者和对照者在年龄和性别上相匹配。两组的血清肌酐水平相似。患者中SNP rs4236的主要变化是核苷酸从G变为A,导致AA纯合基因型。这在60%的患者中被发现。其余40%的患者和所有(100%)对照者具有杂合AG基因型。这对应于结石病的优势比(OR)为75(<0.003)。
这项在印度人群中的首次研究表明,MGP基因SNP rs4236的AA基因型多态性被发现是肾结石病的重要危险因素。可能需要更大样本量的研究来证实这一发现并阐明确切的OR。