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丁酰胆碱酯酶K变异体与阿尔茨海默病风险:一项荟萃分析。

Butyrylcholinesterase K variant and Alzheimer's disease risk: a meta-analysis.

作者信息

Wang Zongcheng, Jiang Yuren, Wang Xi, Du Yangsen, Xiao Dandan, Deng Youchao, Wang Jinlian

机构信息

College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan, China (mainland).

出版信息

Med Sci Monit. 2015 May 16;21:1408-13. doi: 10.12659/MSM.892982.

Abstract

BACKGROUND

Although many studies have estimated the association between the butyrylcholinesterase (BCHE) K variant and Alzheimer's disease (AD) risk, the results are still controversial. We thus conducted this meta-analysis.

MATERIAL/METHODS: We searched NCBI, Medline, Web of Science, and Embase databases to find all eligible studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of the association.

RESULTS

We found a significant association between BCHE K variant and AD risk (OR=1.20; 95% CI 1.03-1.39; P=0.02). In the stratified analysis by ethnicity, we observed a significant association between BCHE K variant and AD risk in Asians (OR=1.32; 95% CI 1.02-1.72; P=0.04). However, no significant association between BCHE K variant and AD risk in Caucasians was found (OR=1.14; 95% CI 0.95-1.37; P=0.16). When stratified by the age of AD onset, we found that late-onset AD (LOAD) was significantly associated with BCHE K variant (OR=1.44; 95% CI 1.05-1.97; P=0.02). No significant association between BCHE K variant and early-onset AD (EOAD) risk was observed (OR=1.16; 95% CI 0.89-1.51; P=0.27). Compared with non-APOE ε4 and non-BCHE K carriers, no significant association between BCHE K variant and AD risk was found (OR=1.11; 95% CI 0.91-1.35; P=0.30). However, APOE ε4 carriers showed increased AD risk in both non-BCHE K carriers (OR=2.81; 95% CI 1.75-4.51; P=0.0001) and BCHE K carriers (OR=3.31; 95% CI 1.82-6.02; P=0.0001).

CONCLUSIONS

The results of this meta-analysis indicate that BCHE K variant might be associated with AD risk.

摘要

背景

尽管许多研究已估算丁酰胆碱酯酶(BCHE)K变异体与阿尔茨海默病(AD)风险之间的关联,但结果仍存在争议。因此,我们进行了这项荟萃分析。

材料/方法:我们检索了NCBI、Medline、科学网和Embase数据库,以查找所有符合条件的研究。采用比值比(OR)及95%置信区间(CI)评估关联强度。

结果

我们发现BCHE K变异体与AD风险之间存在显著关联(OR = 1.20;95% CI 1.03 - 1.39;P = 0.02)。在按种族进行的分层分析中,我们观察到亚洲人中BCHE K变异体与AD风险之间存在显著关联(OR = 1.32;95% CI 1.02 - 1.72;P = 0.04)。然而,未发现高加索人中BCHE K变异体与AD风险之间存在显著关联(OR = 1.14;95% CI 0.95 - 1.37;P = 0.16)。按AD发病年龄分层时,我们发现晚发型AD(LOAD)与BCHE K变异体显著相关(OR = 1.44;95% CI 1.05 - 1.97;P = 0.02)。未观察到BCHE K变异体与早发型AD(EOAD)风险之间存在显著关联(OR = 1.16;95% CI 0.89 - 1.51;P = 0.27)。与非APOE ε4和非BCHE K携带者相比,未发现BCHE K变异体与AD风险之间存在显著关联(OR = 1.11;95% CI 0.91 - 1.35;P = 0.30)。然而,APOE ε4携带者在非BCHE K携带者(OR = 2.81;95% CI 1.75 - 4.51;P = 0.0001)和BCHE K携带者(OR = 3.31;95% CI 1.82 - 6.02;P = 0.0001)中均显示AD风险增加。

结论

这项荟萃分析的结果表明,BCHE K变异体可能与AD风险相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbda/4444173/3cf0e632d638/medscimonit-21-1408-g001.jpg

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