Trace Element Changes in Thoracic Aortic Dissection

被引:0
作者
Marie Edvinsson
Nils-Gunnar Ilbäck
Peter Frisk
Stefan Thelin
Christina Nyström-Rosander
机构
[1] Uppsala University,Department of Medical Sciences, Infectious Diseases
[2] University Hospital,Department of Surgical Sciences, Thoracic Surgery
[3] Uppsala University,Research in Metal Biology, Rudbeck Laboratory
[4] Uppsala University,Risk Benefit Assessment Department
[5] National Food Agency,undefined
来源
Biological Trace Element Research | 2016年 / 169卷
关键词
Aortic dissection; Inflammation; Copper; Zinc; Iron;
D O I
暂无
中图分类号
学科分类号
摘要
Thoracic aortic dissection is a life-threatening condition with an incompletely understood pathogenesis. Trace elements are essential for the functioning of different processes in the body, including the immune system and associated responses to infection/inflammation. Because inflammation may be part of the pathogenesis of thoracic aortic dissection, we investigated whether trace element changes associated with inflammation occur in serum and tissue samples during the disease. The study included 21 patients undergoing surgery for thoracic aortic dissection, 10 forensic autopsy specimens for tissue controls and 23 healthy blood donors for serum controls. Levels of magnesium (Mg), calcium (Ca), vanadium (V), manganese (Mn), iron (Fe), cobalt (Co), copper (Cu), zinc (Zn), arsenic (As), selenium (Se), cadmium (Cd) and mercury (Hg) were measured in the aortic tissue and serum by inductively coupled plasma-mass spectrometry (ICP-MS). In the serum, Ca, V, Cu and Zn decreased, whereas Fe increased. In the tissue, Cu and Zn decreased and Fe tended to increase. The Cu/Zn ratio in the serum, a marker of infection/inflammation, did not change in the patients. Concerning trace element changes in the serum and tissue, our data do not support the hypothesis that inflammation is involved in the pathogenesis of thoracic aortic dissection.
引用
收藏
页码:159 / 163
页数:4
相关论文
共 177 条
[1]  
Ramanath VS(2009)Acute aortic syndromes and thoracic aortic aneurysm Mayo Clin Proc 84 465-481
[2]  
Oh JK(2005)Aortic dissection—an update Curr Probl Cardiol 30 287-325
[3]  
Sundt TM(2006)Gene expression in acute Stanford type A dissection: a comparative microarray study J Transl Med 4 29-126
[4]  
Eagle KA(1999)Atherosclerosis—an inflammatory disease N Engl J Med 340 115-734
[5]  
Mukherjee D(1998)Role of infection as a risk factor for atherosclerosis, myocardial infarction, and stroke Clin Infect Dis 26 719-S410
[6]  
Eagle KA(2000)Background and current knowledge of Chlamydia pneumoniae and atherosclerosis J Infect Dis 181 S402-17
[7]  
Weis-Muller BT(2002)Evidence for infectious agents in cardiovascular disease and atherosclerosis Lancet Infect Dis 2 11-62
[8]  
Modlich O(2010)Presence of Chlamydophila pneumoniae DNA but not mRNA in stenotic aortic heart valves Int J Cardiol 143 57-110
[9]  
Drobinskaya I(2003)Interactions between Chlamydia pneumoniae and trace elements: a possible link to aortic valve sclerosis Biol Trace Elem Res 91 97-186
[10]  
Unay D(2010)Persistent Chlamydophila pneumoniae infection in thoracic aortic aneurysm and aortic dissection? Ups J Med Sci 115 181-335