Hou Fei, Wang Likui, Wang Hong, Gu Junchao, Li Meiling, Zhang Jingkai, Ling Xiao, Gao Xiaofang, Luo Cheng
Department of Infection, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, P.R. China.
CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Chaoyang, Beijing 100101, P.R. China.
Mol Med Rep. 2015 Jun;11(6):4345-52. doi: 10.3892/mmr.2015.3295. Epub 2015 Feb 4.
Inflammation is the predominant characteristic of pneumonia. The present study aimed to to identify a faster and more reliable novel inflammatory marker for the diagnosis of pneumonia. The expression of the S100A12 gene was analyzed by reverse transcription quantitative polymerase chain reaction in samples obtained from 46 patients with bacterial pneumonia and other infections, compared with samples from 20 healthy individuals, using the 2‑ΔΔCt method. The expression levels of S100A12 were increased in 12 patients with bacterial pneumonia. Compared with clinical inflammatory data, a positive correlation was observed between the expression of the S100A12 gene and levels of white blood cells, C‑reactive protein (CRP), thrombocytocrit, neutrophils, erythrocyte sedimentation and soterocytes, and an inverse correlation was observed with the width of red blood cell volume distribution and platelet distribution, monocytes and hemoglobin, using Pearson's product‑moment correlation method. The P‑value of CRP and erythrocyte sedimentation were revealed to be statistically significant (P<0.05). A sporadic distribution of S100A12 was observed in a heatmap among the patients with different infections and bacterial pneumonia. Furthermore, the expression of S100A12 occurred in parallel to the number of clumps of inflamed tissue observed in chest computed tomography and X‑ray. The value of gene expression of S100A12 (>1.0) determined using the 2‑ΔΔCt method was associated with more severe respiratory diseases in the patients compromised by bacterial pneumonia, sepsis and pancreatitis. These findings suggested that S100A12 is an effective marker for inflammatory diseases.
炎症是肺炎的主要特征。本研究旨在确定一种用于肺炎诊断的更快、更可靠的新型炎症标志物。采用2-ΔΔCt法,通过逆转录定量聚合酶链反应分析了46例细菌性肺炎和其他感染患者样本中S100A12基因的表达,并与20名健康个体的样本进行了比较。12例细菌性肺炎患者的S100A12表达水平升高。采用Pearson积矩相关法,将S100A12基因的表达与白细胞、C反应蛋白(CRP)、血小板压积、中性粒细胞、红细胞沉降率和嗜酸性粒细胞水平进行比较,发现呈正相关,与红细胞体积分布宽度、血小板分布、单核细胞和血红蛋白呈负相关。CRP和红细胞沉降率的P值具有统计学意义(P<0.05)。在不同感染患者和细菌性肺炎患者的热图中观察到S100A12呈散在分布。此外,S100A12的表达与胸部计算机断层扫描和X线检查中观察到的炎症组织团块数量平行。采用2-ΔΔCt法测定的S100A12基因表达值(>1.0)与细菌性肺炎、败血症和胰腺炎患者中更严重的呼吸系统疾病相关。这些发现表明S100A12是炎症性疾病的有效标志物。