Xu Zhen-e, Xie Yuan-yuan, Chen Jun-hua, Xing Lin-lin, Zhang Ai-hua, Li Ben-xiu, Zhu Chao-min
Department of Infectious Diseases and Gastroenterology, Children's Hospital of Chongqing Medical University, Chongqing 400014, China.
Zhonghua Er Ke Za Zhi. 2009 Mar;47(3):200-3.
The aims of this study were to evaluate whether the presence of -2518A/G polymorphism in the distal regulatory region of the monocyte chemotactic protein-1 (MCP-1) was associated with tuberculosis (TB) in Chongqing Han population and to find whether it has a significant impact on the pediatric patient.
One hundred children [ < or = 15 years old, mean age (7.3+/-4.6) years, 53 male, 47 female] and one hundred adults [51 male, 49 female, age (44.6+/-13.5) years with TB] and 200 healthy controls of comparable age were screened for genotype by PCR-sequence-specific primer (SSP) method. MCP-1 levels in the sera were detected by ELISA.
(1) TB patients and controls showed different single nucleotide polymorphism (SNP) distribution patterns (58%, 36%). MCP-1 alleles -2518G was associated with increased TB susceptibility (P<0.01). (2) The -2518 GG genotypes was associated with increased TB susceptibility (32% in TB patients and 13% in non-TB controls respectively, P<0.01). (3) The odds of developing TB in genotypes GG were higher than those in homozygous AA, and the risk was higher in children than in adult (7.0-fold in children and 5.1-fold in adults, respectively). (4) Cases of homozygous GG had the highest plasma levels of MCP-1, which increased the likelihood of developing TB. Furthermore, higher levels were observed in children than in adults.
These findings suggest that persons bearing the MCP-1 genotype GG produce high concentrations of MCP-1, which increases the risk of active TB infection in Chongqing Han people. These findings are more significant in child patients than in adult patients with TB.
本研究旨在评估单核细胞趋化蛋白-1(MCP-1)远端调控区-2518A/G多态性的存在是否与重庆汉族人群的结核病(TB)相关,并探究其对儿科患者是否有显著影响。
采用聚合酶链反应-序列特异性引物(PCR-SSP)方法,对100名儿童[年龄≤15岁,平均年龄(7.3±4.6)岁,男53例,女47例]、100名成人[男51例,女49例,年龄(44.6±13.5)岁,患有TB]以及200名年龄匹配的健康对照者进行基因型筛查。采用酶联免疫吸附测定(ELISA)法检测血清中MCP-1水平。
(1)TB患者和对照者呈现不同的单核苷酸多态性(SNP)分布模式(分别为58%、36%)。MCP-1等位基因-2518G与TB易感性增加相关(P<0.01)。(2)-2518 GG基因型与TB易感性增加相关(TB患者中为32%,非TB对照者中为13%,P<0.01)。(3)GG基因型发生TB的几率高于纯合子AA,且儿童的风险高于成人(儿童为7.0倍,成人分别为5.1倍)。(4)纯合子GG病例的血浆MCP-1水平最高,这增加了发生TB的可能性。此外,儿童中的水平高于成人。
这些发现表明,携带MCP-1基因型GG的个体产生高浓度的MCP-1,这增加了重庆汉族人群发生活动性TB感染的风险。这些发现在儿童患者中比在成人TB患者中更显著。