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基因变异与心房颤动复发之间的关联:一项更新的荟萃分析。

Association between gene variants and the recurrence of atrial fibrillation: An updated meta-analysis.

作者信息

Jiang Tao, Wang Ya-Nan, Qu Qiang, Qi Ting-Ting, Chen Yun-Dai, Qu Jian

机构信息

Department of Cardiovascular Medicine.

Department of Respiratory, Hospital of Laiwu Iron and Steel Co. Ltd, Laiwu.

出版信息

Medicine (Baltimore). 2019 Jun;98(23):e15953. doi: 10.1097/MD.0000000000015953.

DOI:10.1097/MD.0000000000015953
PMID:31169720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6571381/
Abstract

BACKGROUND

Studies showed the controversial results about the effect of common genetic polymorphisms on the atrial fibrillation (AF) recurrence. We performed the systematic review and meta-analysis to qualify the association between common genetic polymorphisms and AF recurrence.

METHODS

Articles were systematically retrieved PubMed, Web of Science, EMBASE, Wanfang, and CNKI database and 9 studies including 3204 patients were enrolled in our meta-analysis.

RESULTS

Results showed that the associations were significant under rs2200733 3 genetic models (TT vs CC: odds ratio [OR] [confidence interval [CI]] = 1.336 [1.061-1.683], P = .014; CT vs CC: OR [CI] = 0.759 [0.614-0.937], P = .01; TT vs CT + CC: OR [CI] = 2.308 [1.440-3.700], P = .001). The association was significant under rs10033464 genetic model (TT vs GG: OR [CI] = 1.517 [1.165-1.976], P = .002).

CONCLUSIONS

Rs13376333 on chromosome 1q21 (in KCNN3), rs7193343 and rs2106261 on chromosome 16q22 (in ZFHX3) were not associated with AF recurrence in our meta-analysis. In total, our meta-analysis found that rs2200733 and rs10033464 on chromosome 4q25 (near PITX2) were associated with the risk of AF recurrence.

摘要

背景

研究显示,常见基因多态性对房颤(AF)复发的影响存在争议性结果。我们进行了系统评价和荟萃分析,以确定常见基因多态性与AF复发之间的关联。

方法

通过系统检索PubMed、Web of Science、EMBASE、万方和知网数据库,纳入9项研究共3204例患者进行荟萃分析。

结果

结果显示,在rs2200733的3种遗传模型下关联具有显著性(TT与CC比较:比值比[OR][置信区间[CI]] = 1.336[1.061 - 1.683],P = 0.014;CT与CC比较:OR[CI] = 0.759[0.614 - 0.937],P = 0.01;TT与CT + CC比较:OR[CI] = 2.308[1.440 - 3.700],P = 0.001)。在rs10033464遗传模型下关联具有显著性(TT与GG比较:OR[CI] = 1.517[1.165 - 1.976],P = 0.002)。

结论

在我们的荟萃分析中,1号染色体q21(位于KCNN3基因)上的rs13376333、16号染色体q22(位于ZFHX3基因)上的rs7193343和rs2106261与AF复发无关。总体而言,我们的荟萃分析发现,4号染色体q25(靠近PITX2基因)上的rs2200733和rs10033464与AF复发风险相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/d8d84f47387d/medi-98-e15953-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/07947821c7ba/medi-98-e15953-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/981ea909ab6e/medi-98-e15953-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/b656b8c0b8b2/medi-98-e15953-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/d8d84f47387d/medi-98-e15953-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/07947821c7ba/medi-98-e15953-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/981ea909ab6e/medi-98-e15953-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/b656b8c0b8b2/medi-98-e15953-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6571381/d8d84f47387d/medi-98-e15953-g007.jpg

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