Meta-analysis and meta-regression analysis of biomarkers for abdominal aortic aneurysm

被引:80
作者
Stather, P. W. [1 ]
Sidloff, D. A. [1 ]
Dattani, N. [1 ]
Gokani, V. J. [1 ]
Choke, E. [1 ]
Sayers, R. D. [1 ]
Bown, M. J. [1 ,2 ]
机构
[1] Univ Leicester, Dept Cardiovasc Sci, Leicester LE2 7LX, Leics, England
[2] Univ Leicester, Natl Inst Hlth Res, Leicester Biomed Res Unit, Leicester LE2 7LX, Leics, England
关键词
C-REACTIVE PROTEIN; NECROSIS-FACTOR-ALPHA; INTERCELLULAR-ADHESION MOLECULE-1; SMOOTH-MUSCLE-CELLS; RISK-FACTORS; MATRIX-METALLOPROTEINASE; PLASMA-LEVELS; ENHANCED EXPRESSION; RESPONSES PREVAIL; CONVERTING-ENZYME;
D O I
10.1002/bjs.9593
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Many studies have investigated the systemic and local expression of biomarkers in patients with abdominal aortic aneurysm (AAA). The natural history of AAA varies between patients, and predictors of the presence and diameter of AAA have not been determined consistently. The aim of this study was to perform a systematic review, meta-analysis and meta-regression of studies comparing biomarkers in patients with and without AAA, with the aim of summarizing the association of identified markers with both AAA presence and size. Methods and results: Literature review identified 106 studies suitable for inclusion. Meta-analysis demonstrated a significant difference between matrix metalloproteinase (MMP) 9, tissue inhibitor of matrix metalloproteinase 1, interleukin (IL) 6, C-reactive protein (CRP), alpha 1-antitrypsin, triglycerides, lipoprotein(a), apolipoprotein A and high-density lipoprotein in patients with and without AAA. Although meta-analysis was not possible for MMP-2 in aortic tissue, tumour necrosis factor alpha, osteoprotegerin, osteopontin, interferon gamma, intercellular cell adhesion molecule 1 and vascular cell adhesion molecule 1, systematic review suggested an increase in these biomarkers in patients with AAA. Meta-regression analysis identified a significant positive linear correlation between aortic diameter and CRP level. Conclusion: A wide variety of biomarkers are dysregulated in patients with AAA, but their clinical value is yet to be established. Future research should focus on the most relevant biomarkers of AAA, and how they could be used clinically.
引用
收藏
页码:1358 / 1372
页数:15
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