Homma Satoki, Troxclair Dana A, Zieske Arthur W, Malcom Gray T, Strong Jack P
Louisiana State University Health Sciences Center, Pathology, New Orleans, LA, USA.
Atherosclerosis. 2008 Apr;197(2):791-8. doi: 10.1016/j.atherosclerosis.2007.07.027. Epub 2007 Sep 14.
The histologically topographic comparisons on atherosclerosis progression among three anatomical sites, mid-thoracic and lower abdominal aorta and left anterior descending coronary artery (LAD) were performed using a young population (age 15-34 years) from the Pathobiological Determinants of Atherosclerosis in Youth (PDAY) study.
The histological classification based on the American Heart Association grading scheme showed that in the thoracic aorta type 2 lesions (numerous macrophage foam cells with fine particles but no pools of extracellular lipid) appeared in the first 10-year age group, with no significant change in prevalence in the next 10 years. Lesions greater than type 2 were rarely seen in the thoracic aorta. Although type 2 lesions appeared later in the LAD than in the aorta, the lesions within the LAD progressed rapidly to more advanced lesions (types 4 and 5) or atheroma. Lesion development in the abdominal aorta was intermediate to lesion development in the thoracic aorta and the LAD.
The most striking topographic difference on lesion progression among the three anatomical sites was the vulnerability of type 2 lesions to progress into advanced lesions. The histology study, including immunohistochemistry limited to the type 2 lesions suggested that lesion progression was related to the intimal thickness and the amount of collagen but not to the number of macrophage foam cells.
利用青少年动脉粥样硬化病理生物学决定因素(PDAY)研究中的年轻人群(年龄15 - 34岁),对胸主动脉中段、腹主动脉下段和左前降支冠状动脉(LAD)这三个解剖部位的动脉粥样硬化进展进行了组织学地形学比较。
基于美国心脏协会分级方案的组织学分类显示,在胸主动脉中,2型病变(有许多含细颗粒的巨噬细胞泡沫细胞但无细胞外脂质池)出现在第一个10岁年龄组,在接下来的10年中患病率无显著变化。胸主动脉中很少见到大于2型的病变。虽然2型病变在LAD中出现的时间比在主动脉中晚,但LAD内的病变迅速进展为更高级别的病变(4型和5型)或粥样瘤。腹主动脉中的病变发展介于胸主动脉和LAD中的病变发展之间。
三个解剖部位在病变进展方面最显著的地形学差异是2型病变发展为高级病变的易损性。包括限于2型病变的免疫组织化学在内的组织学研究表明,病变进展与内膜厚度和胶原量有关,而与巨噬细胞泡沫细胞数量无关。