Asymptomatic Abdominal Aortic Aneurysms Show Histological Signs of Progression: A Quantitative Histochemical Analysis

被引:21
作者
Eberlova, Lada [1 ,2 ]
Tonar, Zbynek [1 ,6 ]
Witter, Kirsti [7 ]
Krizkova, Vera [1 ]
Nedorost, Lukas [1 ]
Korabecna, Marie [3 ]
Tolinger, Pavel [1 ]
Kocova, Jitka [1 ]
Boudova, Ludmila [3 ]
Treska, Vladislav [4 ]
Houdek, Karel [4 ]
Molacek, Jiri [4 ]
Vrzalova, Jindra [5 ]
Pesta, Martin [5 ]
Topolcan, Ondrej [5 ]
Valenta, Jiri [2 ]
机构
[1] Charles Univ Prague, Fac Med Pilsen, Univ Hosp Pilsen, Dept Histol & Embryol, CZ-30166 Plzen, Czech Republic
[2] Charles Univ Prague, Fac Med Pilsen, Univ Hosp Pilsen, Dept Anat, CZ-30166 Plzen, Czech Republic
[3] Charles Univ Prague, Dept Pathol, Univ Hosp Pilsen, CZ-30166 Plzen, Czech Republic
[4] Charles Univ Prague, Dept Surg, Univ Hosp Pilsen, CZ-30166 Plzen, Czech Republic
[5] Charles Univ Prague, Dept Nucl Med, Univ Hosp Pilsen, CZ-30166 Plzen, Czech Republic
[6] Univ W Bohemia, Fac Appl Sci, European Ctr Excellence NTIS New Technol Informat, Plzen, Czech Republic
[7] Univ Vet Med Vienna, Dept Pathobiol, Inst Anat Histol & Embryol, Vienna, Austria
关键词
Abdominal aortic aneurysm; Histology; Immunohistochemistry; Stereology; Multiplex immunoanalysis; MATRIX METALLOPROTEINASES; INTRALUMINAL THROMBUS; MURAL THROMBUS; WALL; INFLAMMATION; DEGENERATION; EXPRESSION; MEDIATORS; MORTALITY; REVEALS;
D O I
10.1159/000339304
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: Abdominal aortic aneurysm (AAA) is a serious disease due to its covert nature, relatively high prevalence and fatal prognosis in the case of rupture. To obtain new insights into AAA pathogenesis, we examined the relationships between histopathology, multiplex in vitro immunoassay data, diameter and symptomatology. Methods: In a prospective, non-randomised study, we evaluated samples from 6 normal infrarenal aortae and 65 AAA patients (65 walls, 55 thrombi). The AAA patients were either asymptomatic (n = 44), symptomatic (n = 7) or with ruptured AAA (n = 14). The AAA diameter was classified as small (<5 cm, n = 18), medium (5-7 cm, n = 26) and large (>7 cm, n = 21). We quantified the histopathology of the AAA wall and the adjacent thrombus. We assessed the expression of proteins in the same samples. Results: Asymptomatic AAAs had walls with more abundant inflammatory infiltrates, lower amounts of PAI-1, a higher number of tPA-positive elements, a tendency towards decreased collagen content, whereas the adjacent thrombi had a greater concentration of VCAM-1 and MMP-2 when compared with symptomatic AAAs. Compared with the aneurysmatic aorta, the normal aorta contained less collagen and more elastin, actin, desmin and PAI-1-positive elements; in addition, it was more vascular. Medium-sized AAAs were the most actin and vimentin rich, and large AAAs were the most vascular. Conclusion: Our results show that asymptomatic AAA walls often have more potentially deleterious histopathological alterations than symptomatic AAA walls. This result indicates that a progression from an asymptomatic AAA to rupture can be expected and screening patients who are at risk of rupture could be beneficial. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:11 / 23
页数:13
相关论文
共 58 条
[1]  
Acoltzin Vidal Cuauhtémoc, 2004, Arch. Cardiol. Méx., V74, P176
[2]   Smooth muscle phenotypic modulation is an early event in aortic aneurysms [J].
Ailawadi, Gorav ;
Moehle, Christopher W. ;
Pei, Hong ;
Walton, Sandra P. ;
Yang, Zequan ;
Kron, Irving L. ;
Lau, Christine L. ;
Owens, Gary K. .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2009, 138 (06) :1392-1399
[3]   ABDOMINAL AORTIC-ANEURYSMS - THE CHANGING NATURAL-HISTORY [J].
BICKERSTAFF, LK ;
HOLLIER, LH ;
VANPEENEN, HJ ;
MELTON, LJ ;
PAIROLERO, PC ;
CHERRY, KJ .
JOURNAL OF VASCULAR SURGERY, 1984, 1 (01) :6-12
[4]   Urokinase-generated plasmin activates matrix metalloproteinases during aneurysm formation [J].
Carmeliet, P ;
Moons, L ;
Lijnen, HR ;
Baes, M ;
Lemaitre, V ;
Tipping, P ;
Drew, A ;
Eeckhout, Y ;
Shapiro, S ;
Lupu, F ;
Collen, D .
NATURE GENETICS, 1997, 17 (04) :439-444
[5]   A review of biological factors implicated in abdominal aortic aneurysm rupture [J].
Choke, E ;
Cockerill, G ;
Wilson, WRW ;
Sayed, S ;
Dawson, J ;
Loftus, I ;
Thompson, MM .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 2005, 30 (03) :227-244
[6]   Whole Genome-expression Profiling Reveals a Role for Immune and Inflammatory Response in Abdominal Aortic Aneurysm Rupture [J].
Choke, E. ;
Cockerill, G. W. ;
Laing, K. ;
Dawson, J. ;
Willson, W. R. W. ;
Loftus, I. M. ;
Thompson, M. M. .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 2009, 37 (03) :305-310
[7]   Role of medical intervention in slowing the growth of small abdominal aortic aneurysms [J].
Cooper, D. G. ;
King, J. A. ;
Earnshaw, J. J. .
POSTGRADUATE MEDICAL JOURNAL, 2009, 85 (1010) :688-692
[8]   Thrombus versus Wall Biological Activities in Experimental Aortic Aneurysms [J].
Coutard, Michele ;
Touat, Ziad ;
Houard, Xavier ;
Leclercq, Anne ;
Michel, Jean-Baptiste .
JOURNAL OF VASCULAR RESEARCH, 2010, 47 (04) :355-366
[9]  
DARLING RC, 1977, CIRCULATION, V56, P161
[10]   Genetically engineered resistance for MMP collagenases promotes abdominal aortic aneurysm formation in mice infused with angiotensin II [J].
Deguchi, Jun-o ;
Huang, Hayden ;
Libby, Peter ;
Aikawa, Elena ;
Whittaker, Peter ;
Sylvan, Jeremy ;
Lee, Richard T. ;
Aikawa, Masanori .
LABORATORY INVESTIGATION, 2009, 89 (03) :315-326