Hesampour Ardeshir, Jafarabadi Mina, Rajabi Shima, Rezayof Elahe, Nezamabadi Akram Ghahghaei
Department of Biology, Central Tehran Branch, Islamic Azad University, Tehran, Iran.
Vali-E-Asr Reproductive Health Research Center, Family Health Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
J Family Reprod Health. 2023 Dec;17(4):205-215. doi: 10.18502/jfrh.v17i4.14592.
Dual oxidases (DUOX1, DUOX2) belong to the NADPH oxidase (NOX) family, which produce H2O2 necessary for thyroid hormone biosynthesis. This study aims to evaluate gene expression for DUOX1, DUOX2 in PCOS patients and its relation with thyroid hormone and magnesium levels.
Totally 88 cases were studied including 24 people with PCOS and hypothyroidism, 44 people with PCOS and normal thyroid function, and 20 hypothyroid patients without PCOS. In comparison 40 healthy controls in the age group of 16-35 years matched for age group and BMI were evaluated. Using Vegaro syringe 5 cc of blood was sampled from all 128 people and after RNA extraction and cDNA synthesis using Real-Time PCR technique, the expression level of DUOX1 and DUOX2 genes was investigated.
The results of hormonal tests showed that there is a significant difference between the level of T4, T3, and TSH hormones in hypothyroid patients with or without PCOS in comparison to the control group. Regarding the level of Mg, the results showed that there is a significant difference between the levels of Mg in PCOS group with or without hypothyroidism in comparison to the control group. Gene expression results showed that the relative changes of DUOX1 gene expression in different groups compared to the control group were significantly reduced P<0.05. In the polycystic group with hypothyroidism, the gene expression level showed a decrease compared to the normo-thyroid polycystic group and the hypothyroid non-PCO group, which was statistically significant P<0.05.
According to the results of the present study and the previous studies that have been published in the field of Duox1, it can be assumed that the reduction of Duox1 expression can interfere with the oxidative stress system. Further studies with other molecular techniques may help to understand the exact action mechanism of these genes.
双氧化酶(DUOX1、DUOX2)属于NADPH氧化酶(NOX)家族,可产生甲状腺激素生物合成所需的过氧化氢。本研究旨在评估多囊卵巢综合征(PCOS)患者中DUOX1、DUOX2的基因表达及其与甲状腺激素和镁水平的关系。
共研究88例患者,包括24例患有PCOS和甲状腺功能减退的患者、44例患有PCOS且甲状腺功能正常的患者以及20例无PCOS的甲状腺功能减退患者。作为对照,评估了40名年龄在16 - 35岁、年龄组和体重指数相匹配的健康对照者。使用Vegaro注射器从所有128人采集5毫升血液,经RNA提取和cDNA合成后,采用实时PCR技术研究DUOX1和DUOX2基因的表达水平。
激素检测结果显示,与对照组相比,患有或未患有PCOS的甲状腺功能减退患者的T4、T3和TSH激素水平存在显著差异。关于镁水平,结果显示,与对照组相比,患有或未患有甲状腺功能减退的PCOS组的镁水平存在显著差异。基因表达结果显示,与对照组相比,不同组中DUOX1基因表达的相对变化显著降低(P<0.05)。在患有甲状腺功能减退的多囊卵巢组中,基因表达水平与甲状腺功能正常的多囊卵巢组和无PCOS的甲状腺功能减退组相比有所下降,具有统计学意义(P<0.05)。
根据本研究结果以及Duox1领域已发表的先前研究,可以推测Duox1表达的降低可能会干扰氧化应激系统。采用其他分子技术的进一步研究可能有助于了解这些基因的确切作用机制。