Association between gene polymorphisms of IL-12, IL-12 receptor and IL-27 and organ involvement in Iranian endometriosis patients

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY
Maryam Zare, Fatemeh Hesampour, Tahereh Poordast, Maryam Valibeigi, Maliheh Enayatmehri, Sahar Ahmadi, Fatemeh Nasri, Behrouz Gharesi-Fard
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引用次数: 0

Abstract

Endometriosis is an inflammatory disease characterized by the presence of ectopic endometrial tissue, immune cell dysfunction and abnormal cytokine secretion. In addition to immunological factors, genetic variations that influence endometriosis severity and cytokine expression levels play important roles in the pathogenesis of this disease. Interleukin-12 (IL-12), specifically its p40 subunit encoded by IL-12B gene and the interleukin-12 receptor β1 (IL-12Rβ2) chain of its receptor, as well as interleukin-27 (IL-27) are important in the establishment of endometriosis. So, in this study, we measured IL-12 and IL-27 serum levels and investigated the possible links between IL-12B rs3212227, IL-12Rβ2 rs3790565 and IL-27 rs153109 polymorphisms and the risk of developing endometriosis in a group of Iranian women. In this case-control study, 162 endometriosis patients and 151 healthy women were included and tested for the aforementioned polymorphisms using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. The enzyme-linked immunosorbent assay (ELISA) method was also used to measure IL-12 and IL-27 serum levels. Although there was no statistically significant association between the genotypes and alleles of the studied polymorphisms and the development of endometriosis in general, the AA genotype of IL-12B rs3212227 showed a significant association with uterine endometriosis when compared to AC+CC genotypes (p = .04, CI = 0.270–0.988, OR = 0.517). Indeed, the AA genotype of the IL-12B rs3212227 single nucleotide polymorphism (SNP) may be linked with a lower risk of developing uterine endometriosis. There was no significant difference in IL-27 levels between the two studied groups (p = .49), and IL-12 levels were undetectable in both groups. In conclusion, the AA genotype of IL-12B rs3212227 might be associated with a decreased risk of uterine involvement in endometriosis patients.

伊朗子宫内膜异位症患者IL-12、IL-12受体和IL-27基因多态性与器官受累的关系
子宫内膜异位症是一种以子宫内膜组织异位、免疫细胞功能障碍和细胞因子分泌异常为特征的炎症性疾病。除免疫因素外,影响子宫内膜异位症严重程度和细胞因子表达水平的遗传变异在该病的发病机制中也起着重要作用。白细胞介素-12 (IL-12),特别是其由IL-12B基因编码的p40亚基及其受体的il - 12r - β2链,以及白细胞介素-27 (IL-27)在子宫内膜异位症的建立中起重要作用。因此,在本研究中,我们测量了一组伊朗妇女的IL-12和IL-27血清水平,并研究了IL-12B rs3212227、IL-12Rβ2 rs3790565和IL-27 rs153109多态性与发生子宫内膜异位症风险之间的可能联系。在本病例对照研究中,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术对162名子宫内膜异位症患者和151名健康女性进行上述多态性检测。采用酶联免疫吸附试验(ELISA)测定血清IL-12和IL-27水平。虽然所研究多态性的基因型和等位基因与子宫内膜异位症的发生总体上无统计学意义,但与AC+CC基因型相比,IL-12B rs3212227 AA基因型与子宫内膜异位症的发生有显著相关性(p = 0.04, CI = 0.270 ~ 0.988, OR = 0.517)。事实上,IL-12B rs3212227单核苷酸多态性(SNP)的AA基因型可能与发生子宫内膜异位症的风险较低有关。两组患者IL-27水平差异无统计学意义(p = 0.49), IL-12水平均未检测到。综上所述,IL-12B rs3212227的AA基因型可能与子宫内膜异位症患者子宫受累性风险降低有关。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
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