Importance of gene variants and co-factors of folate metabolic pathway in the etiology of idiopathic intellectual disability

被引:10
作者
Dutta, Samikshan [1 ]
Shaw, Jyoti [1 ]
Chatterjee, Arpita [1 ]
Sarkar, Kanyakumarika [1 ]
Usha, Rajamma [1 ]
Chatterjee, Anindita [1 ]
Sinha, Swagata [1 ]
Mukhopadhyay, Kanchan [1 ]
机构
[1] Manovikas Biomed Res & Diagnost Ctr, Kolkata 700107, India
关键词
Folate; MN; MTR; MTRR; Vitamin B6; METHIONINE SYNTHASE REDUCTASE; MENTAL-RETARDATION; METHYLENETETRAHYDROFOLATE REDUCTASE; PLASMA HOMOCYSTEINE; CHROMOSOME BREAKAGE; SOUTH INDIANS; DOWN-SYNDROME; POLYMORPHISMS; DEFICIENCY; RISK;
D O I
10.1179/1476830511Y.0000000016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Different components of the folate metabolic cycle are crucial for maintaining integrity of DNA. The present study was aimed at exploring the role of some important constituents of the folate cycle in the etiology of idiopathic intellectual disability (IID). Nuclear families with IID probands (n = 226) and ethnically matched controls (n = 181) were recruited for micronucleus, karyotype, genetic polymorphism (MTR rs1805087, MTRR rs1801394, and DHFR rs70991108), folate, vitamin B6, vitamin B12, and cysteine analysis. Significant difference in genotype frequencies in IID probands and their parents were observed for rs1805087 (P = 0.03, 0.02), rs1801394 (P = 0.03, 0.001), and rs70991108 ((P = 0.03, 0.02) as compared to controls. IID probands showed significantly higher micronucleus frequency (P = 0.01) and decreased vitamin B6 level (P = 0.002). A strong correlation between rs1801394 'G' allele and micronucleus was also noticed. From the present investigation, a role of genetic polymorphisms and vitamin B6 levels could be hypothesized in the etiology of IID.
引用
收藏
页码:202 / 209
页数:8
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