Tryptophan hydroxylase 2 gene is associated with cognition in late-onset depression in a Chinese Han population

2015 ◽  
Vol 600 ◽  
pp. 98-103 ◽  
Author(s):  
Xiaoquan Wang ◽  
Zusen Wang ◽  
Yanfeng Wu ◽  
Zhenghua Hou ◽  
Yonggui Yuan ◽  
...  
PLoS ONE ◽  
2013 ◽  
Vol 8 (5) ◽  
pp. e63621 ◽  
Author(s):  
Wei Xu ◽  
Jun Xu ◽  
Ying Wang ◽  
Huidong Tang ◽  
Yulei Deng ◽  
...  

2011 ◽  
Vol 26 (8) ◽  
pp. 627-630 ◽  
Author(s):  
Jian-Fang Ma ◽  
Li-hua Liu ◽  
Yu Zhang ◽  
Ying Wang ◽  
Yu-Lei Deng ◽  
...  

Objective: We conducted a case–control study to investigate whether clusterin polymorphism (rs11136000) was associated with late-onset Alzheimer’s disease in Chinese Han population. Methods: Polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) assay was performed on genotype rs11136000 and APOEε4 in 127 patients with late-onset Alzheimer’s disease and 143 control individuals. Previous published data from other Chinese samples was also included for further meta-analysis. Results: APOEε4 was demonstrated to increase the risk of Alzheimer’s disease in Chinese population (odds ratio = 2.35, 95% confidence interval: 1.40-3.96). There is no significant association between clusterin rs11136000 with late-onset sporadic AD in our small cohort. However, meta-analysis revealed significant allele and genotype differences between Alzheimer’s disease and controls following a recessive model. Conclusion: Clusterin (rs11136000) was associated with Alzheimer’s disease in Chinese Han population.


2021 ◽  
Author(s):  
Jingli Wang ◽  
Chengcheng Guan ◽  
Huabin Hou ◽  
Xinguo Peng ◽  
Yun Liu ◽  
...  

Abstract Backgroud: Inducible Nitric Oxide Synthase (iNOS) acts on the contraction and expansion of blood vessels by mediating the synthesis of Nitric Oxide (NO), which is implicated in the pathophysiology of preeclampsia (PE) associated with systemic vasoconstriction. The polymorphism of NOS2, the gene of coding iNOS, can affect the function of protein. Therefore, we aimed to explore whether the polymorphism site rs2297518 in NOS2 is associated with susceptibility of PE in a Chinese Han population. Methods and Results:Genotyping the NOS2 rs2297518 polymorphism through TaqMan real-time fluorescence quantitative polymerase chain reaction (PCR) after DNA extraction from blood samples in this case-control study including 979 PE patients and 1187 healthy pregnant women. Using independent sample t-test and chi-square test to analyse clinical data and experimental results. We performed the odds ratios (ORs) and 95% confidence intervals (CIs) to estimate the degree of the association.There was no statistical significance in the genetic distributions for the polymorphism of rs2297518 between the PE and control groups (c2=1.43, p=0.49 by genotype frequency, c2=0.85, p=0.36, odds ratio=1.07, 95% confidence interval 0.92-1.25 by allele frequency), and no differences among early/late-onset or mild/severe PE and controls was seen. Conclusion: Our results indicated that the NOS2 rs2297518 polymorphism may be not play a major role in the susceptibility to PE in the Chinese Han population. Therefore, it is essential to test other polymorphisms of this gene to validate a potential relationship for susceptibility to PE.


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