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A Population-Based Cohort Study on the Association of Hyperthyroidism With the Risk of Hyperlipidemia and the Effects of Anti-thyroid Drugs on Hepatic Gene Expression

机译:一种基于人群的甲状腺功能亢进症与高脂血症风险的群体研究及抗甲状腺药物对肝基因表达的影响

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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-n-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 I131 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), I131, 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.
机译:甲状腺功能亢进与高脂血症的关联没有报告,尤其是在亚洲进行治疗的患者。为了确定甲状腺功能亢进的关联和患者高脂血症的风险,我们使用台湾的纵向健康保险数据库(LHID)进行了回顾性队列研究,R.O.C。我们还评估6-正丙基-2-硫嘧啶(PTU)和甲基唑(MMI)对肝基因的影响,以解释肝细胞系模型中血脂水平的变化。队列研究涉及13,667例甲状腺功能亢进患者,相应的比较队列有四倍的患者。使用Kaplan-Meier分析方法,结果表明,与没有甲状腺功能亢进症的患者相比,甲状腺功能亢进患者的总体血症的总发病率显着高(18.7例/ 1,000人 - 年;调整后的HR 1.5; 95%CI, 1.41-1.59)。只有PTU或MMI /甲氨唑(CBM)治疗,甲状腺功能亢进症患者显示1.78倍(95%CI,1.50-2.11)和1.43倍(95%CI,1.27-1.60)的高脂血症风险高于没有甲状腺功能亢进的人, 分别。此外,接受手术的甲状腺功能亢进患者,I131治疗的手术往往具有更高的高脂血症风险。虽然PTU和MMI处理降低了负责循环残余脂蛋白的基因的表达水平,但它们增加了肝细胞中脂肪生成基因表达的水平。因此,治疗甲状腺药物(ATDS),I131或手术的甲状腺功能亢进患者可能会诱导高脂血症。 ATD下调脂蛋白间隙所涉及的基因的表达;增加脂肪原基因表达,这可能部分有助于血脂异常。

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