Hedayat Mona, Mahmoudi Mohammad Jafar, Taghvaei Mohammad, Nematipour Ebrahim, Farhadi Elham, Esfahanian Nilufar, Mahmoudi Maryam, Sadr Maryam, Nourijelyani Keramat, Amirzargar Ali Akbar, Rezaei Nima
Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Boston, MA, USA.
Avicenna J Med Biotechnol. 2018 Apr-Jun;10(2):105-109.
Proinflammatory cytokines have been known to be elevated in patients with Chronic Heart Failure (CHF). Given the importance of proinflammatory cytokines in the context of the failing heart, the prevalence of Tumor Necrosis Factor-α (TNF-α), Interleukin (IL)-6 polymorphisms in patients with CHF was studied due to ischemic heart disease.
Forty three patients with ischemic heart failure were enrolled in this study and compared with 140 healthy individuals. The allele and genotype frequency of four Single Nucleotide Polymorphisms (SNPs) within the IL-6 (-174, nt565) and TNF-α (-308, -238) genes were determined, using Polymerase Chain Reaction with Sequence-Specific Primers (PCR-SSP) assay.
The frequency of the TNF-α (-238) A/A genotype was significantly higher in patients comparing to controls (p=0.043), while TNF-α G/A genotype at the same position decreased significantly, in comparison with controls (p=0.018). The most frequent haplotype for TNF-α was A/A in the patient group in comparison with controls (p=0.003). There was no significant difference in allele and genotype frequencies of IL-6 at positions -174 and nt565, and TNF-α at position -308.
Certain alleles, genotypes, and haplotypes in TNF-α, but not IL-6, gene were overrepresented in patients with ischemic heart failure, which may, in turn, predispose individuals to this disease.
已知慢性心力衰竭(CHF)患者体内促炎细胞因子水平升高。鉴于促炎细胞因子在心脏衰竭背景下的重要性,本研究针对因缺血性心脏病导致的CHF患者,对肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-6基因多态性的患病率进行了研究。
本研究纳入了43例缺血性心力衰竭患者,并与140名健康个体进行比较。采用序列特异性引物聚合酶链反应(PCR-SSP)分析法,测定IL-6(-174,nt565)和TNF-α(-308,-238)基因内四个单核苷酸多态性(SNP)的等位基因和基因型频率。
与对照组相比,患者中TNF-α(-238)A/A基因型的频率显著更高(p=0.043),而同一位置的TNF-α G/A基因型与对照组相比显著降低(p=0.018)。与对照组相比,患者组中TNF-α最常见的单倍型为A/A(p=0.003)。IL-6基因-174和nt565位置以及TNF-α基因-308位置的等位基因和基因型频率无显著差异。
在缺血性心力衰竭患者中,TNF-α基因而非IL-6基因的某些等位基因、基因型和单倍型的比例过高,这可能反过来使个体易患该病。