Rajat Hegde, P. Gai, Smita Hegde, S. Kulkarni, Kusal K. Das
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Statistical analysis was performed using SPSS 15.0.\n\n\n\nPresent study included 85 males and 23 females with a mean age of 11.7±3.5 and 75 males and 33 females with a mean age of 11±2.0 in the control group. 32 (29.6%) autistic cases showed null genotypes for GSTT1 and 21(19.4%) autistic children showed null genotypes for GSTM1. 3 (2.85%) control children showed a null genotype for GSTT1 and 5 (4.6%) control children showed a null genotype for GSTM1. The GSTT1 and GSTM1 null genotypes were observed to be significantly associated with the risk of autism (p value-0.0001, OR-14.73, 95% CI 4.35-49.90) and (p value-0.003, OR-4.731, 95% CI 1.71-13.08) respectively.\n\n\n\nThe findings of our study suggested that GSTT1 and GSTM1 null genotype is one of the potential risk factors for autism through oxidative stress mechanism in our population.\n\n\n\nNone\n","PeriodicalId":36711,"journal":{"name":"Current Psychiatry Research and Reviews","volume":" ","pages":""},"PeriodicalIF":0.3000,"publicationDate":"2023-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Glutathione S Transferase Theta1 and Mu1 (GSTT1 and GSTM1 ) deletion among autistic population of India\",\"authors\":\"Rajat Hegde, P. Gai, Smita Hegde, S. Kulkarni, Kusal K. Das\",\"doi\":\"10.2174/2666082219666230302142608\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nOxidative stress is an imbalance between an organism's reactive oxygen species [ROS] production and antioxidant defence capacity. Long-term oxidative stress contributes to cellular ageing and plays a role in the pathogenesis of several diseases. Several investigations indicated that oxidative stress has a role in the pathogenesis of ASD.\\n\\n\\n\\nPresent study was undertaken to record the association of GSTTT1 and GSTM1 null genotype among the autistic population of India.\\n\\n\\n\\nGenomic DNA was isolated from 108 autistic children along with healthy age-matched control. The quality and quantity of the isolated genomic DNA were analysed. GSTT1 and GSTM1 null genotype was analysed using polymerase chain reaction with internal positive control. Statistical analysis was performed using SPSS 15.0.\\n\\n\\n\\nPresent study included 85 males and 23 females with a mean age of 11.7±3.5 and 75 males and 33 females with a mean age of 11±2.0 in the control group. 32 (29.6%) autistic cases showed null genotypes for GSTT1 and 21(19.4%) autistic children showed null genotypes for GSTM1. 3 (2.85%) control children showed a null genotype for GSTT1 and 5 (4.6%) control children showed a null genotype for GSTM1. The GSTT1 and GSTM1 null genotypes were observed to be significantly associated with the risk of autism (p value-0.0001, OR-14.73, 95% CI 4.35-49.90) and (p value-0.003, OR-4.731, 95% CI 1.71-13.08) respectively.\\n\\n\\n\\nThe findings of our study suggested that GSTT1 and GSTM1 null genotype is one of the potential risk factors for autism through oxidative stress mechanism in our population.\\n\\n\\n\\nNone\\n\",\"PeriodicalId\":36711,\"journal\":{\"name\":\"Current Psychiatry Research and Reviews\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2023-03-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Psychiatry Research and Reviews\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2666082219666230302142608\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PSYCHIATRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Psychiatry Research and Reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2666082219666230302142608","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0
摘要
氧化应激是机体活性氧(ROS)产生与抗氧化防御能力之间的失衡。长期氧化应激有助于细胞衰老,并在多种疾病的发病机制中发挥作用。一些研究表明,氧化应激在ASD的发病机制中起作用。本研究旨在记录GSTTT1和GSTM1零基因型在印度自闭症人群中的关联。研究人员从108名自闭症儿童和年龄匹配的健康对照组中分离出基因组DNA。分析分离基因组DNA的质量和数量。采用聚合酶链反应分析GSTT1和GSTM1零基因型,内阳性对照。采用SPSS 15.0进行统计学分析。本研究纳入男性85例,女性23例,平均年龄11.7±3.5岁;对照组男性75例,女性33例,平均年龄11±2.0岁。32例(29.6%)自闭症患儿GSTT1基因型为零,21例(19.4%)自闭症患儿GSTM1基因型为零。3例(2.85%)对照儿童GSTT1基因型为零,5例(4.6%)对照儿童GSTM1基因型为零。GSTT1和GSTM1零基因型分别与自闭症风险显著相关(p值0.0001,OR-14.73, 95% CI 4.35 ~ 49.90)和(p值0.003,OR-4.731, 95% CI 1.71 ~ 13.08)。本研究结果提示GSTT1和GSTM1零基因型通过氧化应激机制是我国人群自闭症的潜在危险因素之一。没有一个
Glutathione S Transferase Theta1 and Mu1 (GSTT1 and GSTM1 ) deletion among autistic population of India
Oxidative stress is an imbalance between an organism's reactive oxygen species [ROS] production and antioxidant defence capacity. Long-term oxidative stress contributes to cellular ageing and plays a role in the pathogenesis of several diseases. Several investigations indicated that oxidative stress has a role in the pathogenesis of ASD.
Present study was undertaken to record the association of GSTTT1 and GSTM1 null genotype among the autistic population of India.
Genomic DNA was isolated from 108 autistic children along with healthy age-matched control. The quality and quantity of the isolated genomic DNA were analysed. GSTT1 and GSTM1 null genotype was analysed using polymerase chain reaction with internal positive control. Statistical analysis was performed using SPSS 15.0.
Present study included 85 males and 23 females with a mean age of 11.7±3.5 and 75 males and 33 females with a mean age of 11±2.0 in the control group. 32 (29.6%) autistic cases showed null genotypes for GSTT1 and 21(19.4%) autistic children showed null genotypes for GSTM1. 3 (2.85%) control children showed a null genotype for GSTT1 and 5 (4.6%) control children showed a null genotype for GSTM1. The GSTT1 and GSTM1 null genotypes were observed to be significantly associated with the risk of autism (p value-0.0001, OR-14.73, 95% CI 4.35-49.90) and (p value-0.003, OR-4.731, 95% CI 1.71-13.08) respectively.
The findings of our study suggested that GSTT1 and GSTM1 null genotype is one of the potential risk factors for autism through oxidative stress mechanism in our population.
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