Wu Tien-Yuan, Wang Chung-Hsing, Tien Ni, Lin Cheng-Li, Chu Fang-Yi, Chang Hsiao-Yun, Lim Yun-Ping
Department of Pharmacy, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Taichung City, Taiwan.
Department of Pharmacology, School of Medicine, Tzu Chi University, Hualien City, Taiwan.
Front Med (Lausanne). 2020 May 29;7:228. doi: 10.3389/fmed.2020.00228. eCollection 2020.
There have been no reports on the association of hyperthyroidism with hyperlipidemia in patients undergoing treatment especially in Asia. To determine the association between hyperthyroidism and the risk of hyperlipidemia in patients, we conducted a retrospective cohort study using Longitudinal Health Insurance Database (LHID) from Taiwan, R.O.C. We also evaluate the influence of 6--propyl-2-thiouracil (PTU) and methimazole (MMI) on hepatic genes to explain changes in blood lipid levels in a hepatic cell line model. The cohort study involved 13,667 patients with hyperthyroidism, and the corresponding comparison cohort had four times as many patients. Using Kaplan-Meier analysis method, the results showed that, compared to patients without hyperthyroidism, the overall incidence of hyperlipidemia was significantly higher in the hyperthyroidism patients (18.7 vs. 11.8 cases/1,000 persons-years; adjusted HR 1.5; 95% CI, 1.41-1.59). With only PTU or MMI/carbimazole (CBM) treatment, patients with hyperthyroidism showed a 1.78-fold (95% CI, 1.50-2.11) and 1.43-fold (95% CI, 1.27-1.60) higher risk of hyperlipidemia than those without hyperthyroidism, respectively. Additionally, hyperthyroidism patients that received surgery only or surgery with I therapy tended to have a higher risk of hyperlipidemia. Although PTU and MMI treatment decreased the expression levels of genes responsible for circulating remnant lipoproteins, they increased the levels of lipogenic gene expression in hepatic cells. Thus, treatment of hyperthyroid patients with anti-thyroid drugs (ATDs), I, or surgery is likely to induce hyperlipidemia. ATDs downregulate the expression of genes involved in lipoproteins clearance; increases lipogenic genes expression, which may partly contribute to abnormal blood lipid profiles.
尤其在亚洲,目前尚无关于接受治疗的甲状腺功能亢进症患者合并高脂血症的相关报道。为了确定甲状腺功能亢进症与患者高脂血症风险之间的关联,我们利用中国台湾地区的纵向健康保险数据库(LHID)进行了一项回顾性队列研究。我们还在肝细胞系模型中评估了6-丙基-2-硫氧嘧啶(PTU)和甲巯咪唑(MMI)对肝脏基因的影响,以解释血脂水平的变化。该队列研究纳入了13667例甲状腺功能亢进症患者,相应的对照队列患者数量是其四倍。采用Kaplan-Meier分析方法,结果显示,与未患甲状腺功能亢进症的患者相比,甲状腺功能亢进症患者高脂血症的总体发病率显著更高(18.7例/1000人年 vs. 11.8例/1000人年;校正风险比1.5;95%置信区间,1.41-1.59)。仅接受PTU或MMI/卡比马唑(CBM)治疗的甲状腺功能亢进症患者,发生高脂血症的风险分别比未患甲状腺功能亢进症的患者高1.78倍(95%置信区间,1.50-2.11)和1.43倍(95%置信区间,1.27-1.60)。此外,仅接受手术或接受手术加碘治疗的甲状腺功能亢进症患者发生高脂血症的风险往往更高。虽然PTU和MMI治疗降低了负责循环残余脂蛋白的基因表达水平,但它们增加了肝细胞中脂肪生成基因的表达水平。因此,用抗甲状腺药物(ATD)、碘或手术治疗甲状腺功能亢进症患者可能会诱发高脂血症。ATD下调参与脂蛋白清除的基因表达;增加脂肪生成基因的表达,这可能部分导致血脂异常。