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DOI 10.2147/ndt.s322114

Медицинская библиотека · Neuropsychiatric disease and treatment · 2021

Association Between ZNF804A Gene rs1344706 Polymorphism and Brain Functions in Healthy Individuals: A Systematic Review and Voxel-Based Meta-Analysis.

Yang Liqiong, Xu Fan, He Yi, Li Yanzhang, Chen Zi, Wang Shuai

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Аннотация

OBJECTIVE

Zinc finger protein 804A (ZNF804A) protein participates in embryonic neural repair and development. The single nucleotide polymorphism rs1344706 in ZNF804A gene is closely related to functional abnormalities of the human brain. However, these results are inconsistent. This association was verified by meta-analysis in this study.

METHODS

Fifteen studies on functional magnetic resonance imaging involving 1710 healthy individuals were included in the systematic review and meta-analysis used by Anisotropic Effect-Size Signed Differential Mapping software.

RESULTS

Functional connectivity of the right dorsolateral prefrontal cortex (rDLPFC)-left hippocampus in the rs1344706 risk allele carrier was significantly increased (z = 2.066, p < 0.001), while those in the rDLPFC-left middle frontal gyrus (z = -1.420, p < 0.001) and rDLPFC-right middle frontal gyrus (z = -1.298, p < 0.001) were significantly decreased. Neural activity of the left anterior cingulate gyrus in the rs1344706 risk allele carrier was significantly decreased (z = -2.525, p < 0.001). Sensitivity analysis was almost stable, and no publication bias was found.

CONCLUSION

The changes in brain function have a clear correlation with ZNF804A gene in healthy individuals, which indicate the contribution of genetic variants on brain dysfunction.

REGISTRATION NUMBER: This meta-analysis is registered in PROSPERO (No. CRD42016051331).

Для цитирования: Yang Liqiong, Xu Fan, He Yi, Li Yanzhang, Chen Zi, Wang Shuai. Association Between ZNF804A Gene rs1344706 Polymorphism and Brain Functions in Healthy Individuals: A Systematic Review and Voxel-Based Meta-Analysis.. Neuropsychiatric disease and treatment. 2021. DOI: 10.2147/ndt.s322114.
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