Ahmed Mostafa Saleh, Badr Eman Ae, Assar Mohamed Fa
Chemistry department, Biochemistry Division, Faculty of Science, Menoufia University, Shibin El Kom, Egypt.
Medical Biochemistry and Molecular Biology, Faculty of Medicine, Menoufia University, Shibin El Kom, Egypt.
Mol Biol Rep. 2025 Apr 9;52(1):376. doi: 10.1007/s11033-025-10437-y.
Hashimoto's thyroiditis (HT) is the most common cause of hypothyroidism and is also associated with an increased risk of thyroid malignancy. Identifying the exact initiators of the disease could aid in its accurate prevention and treatment. This study aims to clarify the role of Visfatin and Adiponutrin genes in the development of HT.
This case‒control study was carried out on patients from the Internal Medicine, Endocrinology Department, Menoufia University Hospital. Samples are collected from ninety-six patients with HT and ninety-six controls. The findings of this study indicate that the patient group has a significantly higher Body Mass Index (BMI), lipid dysregulation, and thyroid dysfunction compared to the control group. Additionally, the results suggest that the rs3801266 variant of Visfatin and the rs738409 variant of Adiponutrin are associated with the patient group. Specifically, the CC genotype (16.7% vs. 4.2%) and C allele (40.6% vs. 26.0%) of rs3801266, as well as the GG genotype (11.5% vs. 2.1%) and G allele (35.9% vs. 23.4%) of rs738409, are significantly more frequent in patients, indicating a potential genetic predisposition. Anti-Thyroglobulin (Anti-TG) and Anti-Thyroperoxidase (anti-TPO) levels varied significantly across genotypes. CC and TC carriers of rs3801266 had significantly higher anti-TG levels, while GG carriers of rs738409 showed a marked increase in both anti-TPO and anti-TG levels compared to other genotypes.
The involvement of both the Adiponutrin and Visfatin genes is believed to contribute to the pathogenesis of HT, either directly or as a consequence of obesity.
桥本甲状腺炎(HT)是甲状腺功能减退最常见的病因,还与甲状腺恶性肿瘤风险增加有关。确定该疾病的确切引发因素有助于其精准预防和治疗。本研究旨在阐明内脂素和脂肪营养蛋白基因在HT发病过程中的作用。
本病例对照研究针对米努夫大学医院内科内分泌科的患者开展。从96例HT患者和96例对照中采集样本。本研究结果表明,与对照组相比,患者组的体重指数(BMI)、脂质代谢紊乱和甲状腺功能障碍显著更高。此外,结果提示内脂素的rs3801266变异体和脂肪营养蛋白的rs738409变异体与患者组相关。具体而言,rs3801266的CC基因型(16.7%对4.2%)和C等位基因(40.6%对26.0%),以及rs738409的GG基因型(11.5%对2.1%)和G等位基因(35.9%对23.4%)在患者中显著更常见,表明存在潜在的遗传易感性。抗甲状腺球蛋白(Anti-TG)和抗甲状腺过氧化物酶(anti-TPO)水平在不同基因型间差异显著。rs3801266的CC和TC携带者的抗TG水平显著更高,而rs738409的GG携带者与其他基因型相比,抗TPO和抗TG水平均显著升高。
脂肪营养蛋白和内脂素基因的参与被认为直接或因肥胖导致HT的发病机制。