Nie Jin-shan, Chen Wei-chang
Department of Gastroenterology, the First Affiliated Hospital, Soochow University, Suzhou, Jiangsu, 215006 PR China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):598-600.
To study the relationship between monocyte chemoattractant protein-1 gene (MCP-1) -2518A/G polymorphism and acute pancreatitis (AP) in the Han population of Suzhou, China.
The polymorphisms were detected with polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The genotypes and allele frequencies of MCP-1 -2518A/G were calculated and analyzed in 101 AP patients including 78 mild AP (MAP) patients and 23 severe AP (SAP) patients, and 120 healthy individuals as control group.
The frequency of MCP-1 -2518 AA genotype in control group was significantly higher than that in SAP and MAP groups (P < 0.01). People with AG and GG genotypes had 5.896 times risk of developing MAP (P < 0.01, OR=5.896) compared with people with AA genotype. Subjects carrying G allele were at a 7-fold elevated risk for SAP (P < 0.05, OR=7.011) contrasted with subjects carrying AA genotype. However, no difference in AA genotypic distribution was noted between MAP and SAP groups (chi square=0.006, P=0.997). The frequency of G allele in healthy controls was obviously lower than that in MAP (P < 0.01, OR=0.318) and SAP groups (P < 0.01, OR=0.309). No difference of G allele frequency was found between SAP group and MAP group (P=0.623, OR=1.211).
The MCP-1 -2518 AA genotype of the population in Suzhou may be a protective genotype of AP. People with higher frequency of G allele is more likely to suffer from AP. Nonetheless, the genotype of AA and the frequency of G allele couldn't predict the risk of SAP.
研究中国苏州汉族人群中单核细胞趋化蛋白-1基因(MCP-1)-2518A/G多态性与急性胰腺炎(AP)的关系。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测多态性。计算并分析101例AP患者(包括78例轻症AP(MAP)患者和23例重症AP(SAP)患者)以及120例健康个体作为对照组中MCP-1 -2518A/G的基因型和等位基因频率。
对照组中MCP-1 -2518 AA基因型频率显著高于SAP组和MAP组(P < 0.01)。与AA基因型者相比,AG和GG基因型者发生MAP的风险高5.896倍(P < 0.01,OR = 5.896)。与携带AA基因型的受试者相比,携带G等位基因的受试者患SAP的风险升高7倍(P < 0.05,OR = 7.011)。然而,MAP组和SAP组之间AA基因型分布无差异(χ² = 0.006,P = 0.997)。健康对照组中G等位基因频率明显低于MAP组(P < 0.01,OR = 0.318)和SAP组(P < 0.01,OR = 0.309)。SAP组和MAP组之间G等位基因频率无差异(P = 0.623,OR = 1.211)。
苏州人群的MCP-1 -2518 AA基因型可能是AP的保护性基因型。G等位基因频率较高的人更易患AP。尽管如此,AA基因型和G等位基因频率无法预测SAP的风险。