Tumor Etiology and Screening Department of Cancer Institute and General Surgery, the First Affiliated Hospital of China Medical University, and Key Laboratory of Cancer Etiology and Prevention (China Medical University), Liaoning Provincial Education Department, Shenyang, China.
Department of Cardiovascular Ultrasound, the First Affiliated Hospital of China Medical University, Shenyang, China.
Clin Genet. 2018 Jan;93(1):15-32. doi: 10.1111/cge.13050. Epub 2017 Jul 18.
It has been suggested that matrix metalloproteinase (MMP) polymorphisms are associated with the pathogenesis of aortic aneurysmal diseases. In this study, we conducted a systematic review with an update meta-analysis to investigate the relationship between MMP family polymorphisms and aortic aneurysmal diseases. We systematically reviewed 24 polymorphisms in 8 MMP genes related to the risk of abdominal aortic aneurysm (AAA), thoracic AA or thoracic aortic dissection (TAD). A total of 19 case-control studies with 15 highly studied MMP polymorphisms were included in our meta-analysis. Our results suggested that MMP2rs243865, MMP3rs3025058, MMP13rs2252070 polymorphisms were significantly associated with AAA risk, MMP2rs11643630, MMP8rs11225395 polymorphisms were correlated with TAD risk, and MMP9rs3918242 under the dominant model could increase AAA risk in hospital-based subgroup. No associations with aortic aneurysmal diseases were identified for other polymorphisms assessed in our meta-analysis. In summary, some studied MMP polymorphisms associated with the risk of aortic aneurysmal diseases are potential predictive biomarkers for the clinical application. Moreover, other MMP polymorphisms with limited studies but relevant to aortic aneurysmal formation and progression need further prospective and large investigations to confirm results.
有人提出基质金属蛋白酶 (MMP) 多态性与主动脉瘤疾病的发病机制有关。本研究通过系统综述和更新的荟萃分析,研究 MMP 家族多态性与主动脉瘤疾病的关系。我们系统地综述了与腹主动脉瘤(AAA)、胸主动脉瘤(TAA)或胸主动脉夹层(TAD)风险相关的 8 个 MMP 基因中的 24 个多态性。我们的荟萃分析共纳入了 19 项病例对照研究,其中包含 15 个高度研究的 MMP 多态性。结果表明,MMP2rs243865、MMP3rs3025058、MMP13rs2252070 多态性与 AAA 风险显著相关,MMP2rs11643630、MMP8rs11225395 多态性与 TAD 风险相关,在基于医院的亚组中,MMP9rs3918242 显性模型可增加 AAA 风险。本荟萃分析中评估的其他多态性与主动脉瘤疾病无相关性。总之,一些研究的 MMP 多态性与主动脉瘤疾病的风险相关,可能是临床应用的潜在预测生物标志物。此外,其他 MMP 多态性与主动脉瘤形成和进展相关,但研究有限,需要进一步进行前瞻性和大规模的研究来验证结果。