Tiveron Marcos Gradim, Pomerantzeff Pablo Maria Alberto, de Lourdes Higuchi Maria, Reis Marcia Martins, de Jesus Pereira Jaqueline, Kawakami Joyce Tieko, Ikegami Renata Nishiyama, de Almeida Brandao Carlos Manuel, Jatene Fabio Biscegli
Program in Thoracic and Cardiovascular Surgery, Medical School, University of Sao Paulo, Av. Dr. Enéas de Carvalho Aguiar, 44, Sao Paulo, 05403-900, Sao Paulo, Brazil.
Heart Institute of the Clinical Hospital, Medical School, University of Sao Paulo, Sao Paulo, Brazil.
BMC Infect Dis. 2017 Apr 21;17(1):297. doi: 10.1186/s12879-017-2387-8.
The etiology of myxomatous mitral valve degeneration (MVD) is not fully understood and may depend on time or environmental factors for which the interaction of infectious agents has not been documented. The purpose of the study is to analyze the effect of Mycoplasma pneumoniae (Mp), Chlamydophila pneumoniae (Cp) and Borrelia burgdorferi (Bb) on myxomatous mitral valve degeneration pathogenesis and establish whether increased in inflammation and collagen degradation in myxomatous mitral valve degeneration etiopathogenesis.
An immunohistochemical test was performed to detect the inflammatory cells (CD20, CD45, CD68) and Mp, Bb and MMP9 antigens in two groups. The in situ hybridization was performed to detect Chlamydophila pneumoniae and the bacteria study was performed using transmission electron microscopy. Group 1 (n = 20), surgical specimen composed by myxomatous mitral valve degeneration, and group 2 (n = 20), autopsy specimen composed by normal mitral valve. The data were analyzed using SigmaStat version 20 (SPSS Inc., Chicago, IL, USA). The groups were compared using Student's t test, Mann-Whitney test. A correlation analysis was performed using Spearman's correlation test. P values lower than 0.05 were considered statistically significant.
By immunohistochemistry, there was a higher inflammatory cells/mm2 for CD20 and CD45 in group 1, and CD68 in group 2. Higher number of Mp and Cp antigens was observed in group 1 and more Bb antigens was detected in group 2. The group 1 exhibited a positive correlation between the Bb and MVD percentage, between CD45 and Mp, and between MMP9 with Mp. These correlations were not observed in the group 2. Electron microscopy revealed the presence of structures compatible with microorganisms that feature Borrelia and Mycoplasma characteristics.
The presence of infectious agents, inflammatory cells and collagenases in mitral valves appear to contribute to the pathogenesis of MVD. Mycoplasma pneumoniae was strongly related with myxomatous mitral valve degeneration. Despite of low percentage of Borrelia burgdorferi in MD group, this agent was correlated with myxomatous degeneration and this may occour due synergistic actions between these infectious agents likely contribute to collagen degradation.
黏液瘤样二尖瓣退化(MVD)的病因尚未完全明确,可能取决于时间或环境因素,而感染因子之间的相互作用尚无文献记载。本研究旨在分析肺炎支原体(Mp)、肺炎衣原体(Cp)和伯氏疏螺旋体(Bb)对黏液瘤样二尖瓣退化发病机制的影响,并确定炎症增加和胶原降解是否在黏液瘤样二尖瓣退化的病因发病机制中起作用。
对两组进行免疫组织化学检测,以检测炎性细胞(CD20、CD45、CD68)以及Mp、Bb和MMP9抗原。进行原位杂交以检测肺炎衣原体,并使用透射电子显微镜进行细菌研究。第1组(n = 20)为黏液瘤样二尖瓣退化的手术标本,第2组(n = 20)为正常二尖瓣的尸检标本。使用SigmaStat 20版软件(美国伊利诺伊州芝加哥市SPSS公司)对数据进行分析。采用学生t检验、曼-惠特尼检验对两组进行比较。使用斯皮尔曼相关检验进行相关性分析。P值低于0.05被认为具有统计学意义。
通过免疫组织化学,第1组中CD20和CD45的炎性细胞/mm²较高,第2组中CD68的炎性细胞/mm²较高。第1组中观察到较高数量的Mp和Cp抗原,第2组中检测到更多的Bb抗原。第1组中Bb与MVD百分比之间、CD45与Mp之间以及MMP9与Mp之间呈正相关。第2组未观察到这些相关性。电子显微镜显示存在与具有疏螺旋体和支原体特征的微生物相容的结构。
二尖瓣中感染因子、炎性细胞和胶原酶的存在似乎有助于MVD的发病机制。肺炎支原体与黏液瘤样二尖瓣退化密切相关。尽管MD组中伯氏疏螺旋体的比例较低,但该病原体与黏液瘤样退化相关,这可能是由于这些感染因子之间的协同作用可能导致胶原降解。