Plasma glycosylphosphatidylinositol phospholipase D (GPI-PLD) and abdominal aortic aneurysm

被引:0
|
作者
Lindqvist, Markus [1 ]
Wallinder, Jonas [2 ]
Bergstrom, Jorgen [3 ]
Henriksson, Anders E. [1 ,4 ]
机构
[1] Sundsvall Cty Hosp, Dept Clin Chem, SE-85186 Sundsvall, Sweden
[2] Sundsvall Cty Hosp, Dept Surg, SE-85186 Sundsvall, Sweden
[3] Univ Gothenburg, Prote Core Facil, Gothenburg, Sweden
[4] Mid Sweden Univ, Dept Nat Sci, Sundsvall, Sweden
关键词
Glycosylphosphatidylinositol phospholipase D; biomarker; aortic aneurysm; UROKINASE RECEPTOR; RUPTURE;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recent reviews state that a circulating biomarker predicting aortic rupture risk would be a powerful tool to stratify patients with small screen-detected abdominal aortic aneurysm (AAA). In a current proteomic pilot-study elevated levels of the enzyme Glycosylphosphatidylinositol-specific phospholipase D (GPI-PLD) was shown in patients with small AAA compared with controls without aneurysm. In the present study we investigated the impact of plasma GPI-PLD as a biomarker in patients with AAA in relation to aneurysm size, and rupture. Plasma GPI-PLD was measured in patients with AAA (nonruptured, n=78 and ruptured, n=55) and controls without aneurysm (n=41) matched by age, sex and smoking habit. The plasma GPI-PLD levels were significantly lower in patients with ruptured compared nonruptured AAA which we interpreted as a result of hemodilution due to hemorrhage in patients with ruptured AAA. The plasma GPI-PLD levels were similar in patients with nonruptured AAA compared to the controls without aneurysm. Furthermore, there was no correlation between plasma GPI-PLD and aneurysm size in the group of patients with nonruptured AAA. In conclusion, the present study fails to show a connection between GPI-PLD and AAA. However, the definite role of GPI-PLD as a predictive marker needs to be further clarified in a follow-up cohort study.
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页码:306 / 309
页数:4
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