Settin A, Abdel-Hady H, El-Baz R, Saber I
Pediatric Genetics Unit, Mansoura University Children Hospital, Mansoura, Egypt.
Pediatr Cardiol. 2007 Sep-Oct;28(5):363-71. doi: 10.1007/s00246-006-0002-7. Epub 2007 Jun 29.
Rheumatic heart disease (RHD) is an inflammatory disease of the heart tissues caused by interactive immune, genetic, and environmental factors. The objective of this study is to test for the association of polymorphisms related to cytokine genes with susceptibility and severity of RHD among affected children from the Nile Delta region of Egypt. The study included 50 children with chronic RHD (29 males and 21 females), with a mean age of 12.2 years, in addition to 98 healthy unrelated controls. Cases were further classified on the basis of echocardiographic findings into those with only mitral valve disease (MVD) or multivalvular lesions (MVLs) and also as mild, moderate, or severe valve lesions. For all cases and controls, DNA was extracted and amplified using polymerase chain reaction with sequence-specific primers for detection of single nucleotide polymorphisms (SNPs) in the promoter regions of cytokine genes tumor necrosis factor (TNF)-alpha(-308 )G/A, interleukin (IL)-10(-1082 )G/A, and IL-6(-174 )G/C as well as a variable number of tandem repeats (VNTRs) in intron 2 of the IL-1Ra gene. All cases showed a significantly higher frequency of homozygous genotypes of TNF-alpha(-308 )A/A [odds ratio (OR) = 5.7, p < 0.001], IL-10(-1082) A/A (OR = 3.1, p < 0.05), IL-10(-1082) G/G (OR = 5.2, p < 0.05), and IL-1Ra A1/A1 (OR = 2.2, p < 0.05). Cases with MVD showed higher frequencies of genotypes TNF-alpha(-308 )A/A, G/G; IL-10(-1082) G/G; and IL-1Ra(VNTR) A1/A1 (p < 0.05). Cases with MVL showed a significantly higher frequency of homozygous A/A genotype of both TNF-alpha(-308 )(OR = 10.6, p < 0.05) and IL-10(-1082) (OR = 5.2, p < 0.05). The same was observed for cases with severe valve lesions. On the other hand, all studied groups showed significantly lower frequency of heterozygous genotypes of TNF-alpha(-308 )G/A, IL-10(-1082) G/A, and IL-1Ra(VNTR) A1/A2. No significant difference was found regarding the frequency of IL-6(-174 )G/C polymorphisms in total cases or subgroups compared to controls (p > 0.05). Predisposition to RHD is influenced by genetic factors including cytokine gene polymorphisms, with possible susceptibility to severe disease with multivalvular affection among cases with composite polymorphism (TNF-alpha(-308 )A/A and IL-10(-1082) A/A) and (TNF-alpha(-308 )A/A and IL-10(-1082) G/G).
风湿性心脏病(RHD)是一种由免疫、遗传和环境因素相互作用引起的心脏组织炎症性疾病。本研究的目的是检测埃及尼罗河三角洲地区受影响儿童中细胞因子基因多态性与RHD易感性和严重程度之间的关联。该研究纳入了50例慢性RHD儿童(29例男性和21例女性),平均年龄为12.2岁,此外还有98名健康无关对照。病例根据超声心动图结果进一步分为仅患有二尖瓣疾病(MVD)或多瓣膜病变(MVL)的患者,以及轻度、中度或重度瓣膜病变患者。对于所有病例和对照,提取DNA并使用聚合酶链反应和序列特异性引物进行扩增,以检测细胞因子基因肿瘤坏死因子(TNF)-α(-308)G/A、白细胞介素(IL)-10(-1082)G/A和IL-6(-174)G/C启动子区域的单核苷酸多态性(SNP),以及IL-1Ra基因第2内含子中的可变数目串联重复序列(VNTR)。所有病例中,TNF-α(-308)A/A纯合基因型的频率显著更高[比值比(OR)=5.7,p<0.001],IL-10(-1082)A/A(OR=3.1,p<0.05),IL-10(-1082)G/G(OR=5.2,p<0.05),以及IL-1Ra A1/A1(OR=2.2,p<0.05)。患有MVD的病例中,TNF-α(-308)A/A、G/G基因型;IL-10(-1082)G/G基因型;以及IL-1Ra(VNTR)A1/A1基因型的频率更高(p<0.05)。患有MVL的病例中,TNF-α(-308)(OR=10.6,p<0.05)和IL-10(-