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新型血管易感性基因 Ninjurin2(NINJ2)的遗传多态性与阿尔茨海默病风险降低相关。

Genetic polymorphisms of a novel vascular susceptibility gene, Ninjurin2 (NINJ2), are associated with a decreased risk of Alzheimer's disease.

机构信息

Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.

出版信息

PLoS One. 2011;6(6):e20573. doi: 10.1371/journal.pone.0020573. Epub 2011 Jun 6.

Abstract

BACKGROUND

Accumulated evidences have shown that vascular risk factors, e.g., hypertension, diabetes mellitus and hyperlipidemia, may be related to the risk of dementia. This study investigated the association between genetic polymorphisms of a vascular susceptibility gene, Ninjurin2 (NINJ2), and the risk of dementia, which has not been explored previously.

METHODS

A total of 275 Alzheimer's disease (AD) patients and 119 vascular dementia (VaD) patients aged 50 or older were recruited from three teaching hospitals from 2007 to 2010. Healthy controls (n = 423) with the same age of cases were recruited from the health checkup and volunteers worked at the hospital during the same time period. Five common (frequency >5%) haplotype-tagging single nucleotide polymorphisms (htSNPs) in NINJ2 were genotyped to test for the association between sequence variants of NINJ2 and dementia risk, and how vascular risk factors modify this association.

RESULTS

Homozygosity of two NINJ2 SNPs was significantly associated with a decreased risk of AD [rs11833579: adjusted odds ratio (AOR) = 0.43; 95% confidence interval (CI)= 0.23-0.80; rs12425791: AOR= 0.33, 95% CI= 0.12-0.96]. Five common haplotypes (cumulative frequency= 97%) were identified. The global test for the association between NINJ2 haplotypes and AD was significant (p = 0.03). Haplotype CAGGA was significantly associated with a decreased risk of AD (AOR= 0.32, 95% CI= 0.11-0.94). No associations were observed for VaD.

CONCLUSION

Inherited polymorphisms of the vascular susceptibility gene NINJ2 were associated with AD risk.

摘要

背景

已有大量证据表明,血管危险因素,如高血压、糖尿病和高脂血症,可能与痴呆风险有关。本研究探讨了血管易感性基因 Ninjurin2(NINJ2)的遗传多态性与痴呆风险之间的关系,这在以前尚未得到探索。

方法

本研究共纳入了 2007 年至 2010 年期间来自三家教学医院的 275 名阿尔茨海默病(AD)患者和 119 名血管性痴呆(VaD)患者,以及年龄相同的 423 名健康对照者(来自同期医院体检和志愿者)。选择 NINJ2 中 5 个常见(频率>5%)单核苷酸多态性(htSNPs)作为标签单核苷酸多态性(tagSNPs)进行基因分型,以检验 NINJ2 序列变异与痴呆风险之间的关系,以及血管危险因素如何修饰这种关联。

结果

两个 NINJ2 SNPs 的纯合性与 AD 风险降低显著相关 [rs11833579:调整后的优势比(AOR)=0.43;95%置信区间(CI)=0.23-0.80;rs12425791:AOR=0.33,95%CI=0.12-0.96]。鉴定出 5 个常见单倍型(累积频率=97%)。NINJ2 单倍型与 AD 之间的关联的总体检验具有统计学意义(p=0.03)。CAGGA 单倍型与 AD 风险降低显著相关(AOR=0.32,95%CI=0.11-0.94)。但未观察到与 VaD 的关联。

结论

血管易感性基因 NINJ2 的遗传多态性与 AD 风险相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee7d/3108950/8da7cad7bf0c/pone.0020573.g001.jpg

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