Department of Biomedical Sciences, University of Cagliari, 09042, Monserrato, Italy.
Department of Medical Sciences and Public Health, University of Cagliari, 09042, Monserrato, Italy.
J Endocrinol Invest. 2021 Jun;44(6):1309-1319. doi: 10.1007/s40618-020-01434-y. Epub 2020 Oct 6.
The serum metabolic changes occurring during the transition from hypothyroidism to euthyroidism are not known. This study aimed to determine the metabolomic profile in hypothyroid patients before (HypoT) and after (HypoT) euthyroidism achieved through levothyroxine (L-T4) treatment.
Eighteen patients with overt primary hypothyroidism were recruited for the study. All patients were treated with L-T4 to achieve euthyroidism. Thyrotropin (TSH), free thyroxine (FT4), free triiodothyronine (FT3) and metabolomics profiles were measured before and after 3 months of treatment. The euthyroid control group consisted of 28 healthy volunteers. Metabolomics analysis was performed using Nuclear Magnetic Resonance (NMR) spectroscopy.
H NMR-based metabolomics profiling of patients with newly diagnosed hypothyroidism (HypoT) showed significantly higher levels of citrate, creatinine, glycerol, myo-inositol and serine, and lower levels of proline and taurine compared to controls. Interestingly, some metabolic changes were persistent three months after pharmacological treatments, despite normal serum TSH and thyroid hormone concentrations (HypoT). When an Orthogonal Partial Least Squares Discriminant Analysis (OPLS-DA) model was built to evaluate possible differences in the metabolic profile between HypoT and HypoT, the data obtained were not significantly different.
These results suggest that metabolic changes in the patients with hypothyroidism may persist after normalization of serum levels of FT3, FT4, and TSH, which currently represent the gold standard in laboratory testing for diagnosis and evaluation of thyroid pathology. So, the metabolomics approach may contribute to integrate classical hormone assays and to determine the euthyroid status achievement with greater efficacy.
甲状腺功能减退症向甲状腺功能正常过渡时发生的血清代谢变化尚不清楚。本研究旨在通过左甲状腺素(L-T4)治疗确定甲状腺功能减退症患者在达到甲状腺功能正常(HypoT)前后的代谢组学特征。
招募了 18 名患有显性原发性甲状腺功能减退症的患者进行研究。所有患者均接受 L-T4 治疗以达到甲状腺功能正常。在治疗前和治疗 3 个月后测量促甲状腺激素(TSH)、游离甲状腺素(FT4)、游离三碘甲状腺原氨酸(FT3)和代谢组学谱。健康对照组包括 28 名健康志愿者。采用核磁共振(NMR)光谱法进行代谢组学分析。
与对照组相比,新诊断为甲状腺功能减退症(HypoT)的患者的 H NMR 代谢组学分析显示柠檬酸、肌酸、甘油、肌醇和丝氨酸水平显著升高,脯氨酸和牛磺酸水平降低。有趣的是,尽管血清 TSH 和甲状腺激素浓度正常(HypoT),但一些代谢变化在药物治疗三个月后仍然存在。当建立正交偏最小二乘判别分析(OPLS-DA)模型来评估 HypoT 和 HypoT 之间代谢谱的可能差异时,获得的数据没有显著差异。
这些结果表明,甲状腺功能减退症患者的代谢变化可能在血清 FT3、FT4 和 TSH 水平正常化后仍然存在,目前这三项指标是实验室检测甲状腺病理的金标准。因此,代谢组学方法可能有助于整合经典激素检测,并更有效地确定甲状腺功能正常的状态。