Ahirwar Ashok Kumar, Singh Archana, Jain Anju, Kaim Kirti, Bhardwaj Shilpa, Patra Surajeet Kumar, Goswami Binita, Bhatnagar M K, Bhattacharjee Jayashree
Department of Biochemistry, All India Institute of Medical Sciences (AIIMS), Room no. 3013, Third Floor, Teaching Block, AIIMS, Ansari Nagar, New Delhi-110029, India, Phone: +919654210832.
Department of Biochemistry, All India Institute of Medical Sciences (AIIMS), New Delhi-110029, India.
Horm Mol Biol Clin Investig. 2017 Dec 20;34(1):hmbci-2017-0046. doi: 10.1515/hmbci-2017-0046.
Background Metabolic syndrome (MetS) involves a cluster of cardiovascular risk factors, including abnormal lipids, insulin resistance and hypertension. The aim of the present study is to investigate associations between thyroid profile and the pro-thrombotic mediator, plasminogen activator inhibitor-1 (PAI-1), in MetS and identify associated biochemical markers. Materials and methods The present study was a case control study and consisted of 50 diagnosed cases of MetS and 50 healthy volunteers as controls. MetS cases were further divided into two groups based on the presence and absence of subclinical hypothyroidism (SCH). Data collected included demographic profile, clinical history and routine lab investigation. Special investigations included the thyroid function test and serum PAI-1 levels. Results The mean serum thyroid-stimulating hormone (TSH) levels were significantly higher in MetS cases as compared to controls (5.7 ± 1.2 mIU/L vs. 2.3 ± 1.6 mIU/L, p < 0.0001), although the mean triiodothyronine (T3) and thyroxine (T4) levels were comparable in two groups. The mean levels of serum PAI-1 were significantly higher in MetS cases as compared to controls(231 ± 87 ng/mL vs. 185 ± 96 ng/mL, p = 0.013). TSH and PAI-1 levels were positively correlated with various markers of MetS and negatively correlated with high-density lipoprotein (HDL). Conclusion The present study points towards the presence of thyroid dysfunction, in the form of subclinical hypothyroidism (SCH), in cases of MetS. In the presence of thyroid dysfunction, abnormal adipocytes may release adipokines, such as PAI-1, which lead to increased risk of thrombotic episodes in these patients. Hence, SCH should be appropriately managed.
背景 代谢综合征(MetS)涉及一系列心血管危险因素,包括血脂异常、胰岛素抵抗和高血压。本研究旨在探讨甲状腺指标与代谢综合征中促血栓形成介质纤溶酶原激活物抑制剂-1(PAI-1)之间的关联,并确定相关的生化标志物。
材料与方法 本研究为病例对照研究,包括50例确诊的代谢综合征患者和50名健康志愿者作为对照。代谢综合征患者根据是否存在亚临床甲状腺功能减退(SCH)进一步分为两组。收集的数据包括人口统计学资料、临床病史和常规实验室检查。特殊检查包括甲状腺功能测试和血清PAI-1水平。
结果 与对照组相比,代谢综合征患者的平均血清促甲状腺激素(TSH)水平显著升高(5.7±1.2 mIU/L对2.3±1.6 mIU/L,p<0.0001),尽管两组的平均三碘甲状腺原氨酸(T3)和甲状腺素(T4)水平相当。与对照组相比,代谢综合征患者的血清PAI-1平均水平显著升高(231±87 ng/mL对185±96 ng/mL,p=0.013)。TSH和PAI-1水平与代谢综合征的各种标志物呈正相关,与高密度脂蛋白(HDL)呈负相关。
结论 本研究表明,在代谢综合征患者中存在亚临床甲状腺功能减退(SCH)形式的甲状腺功能障碍。在存在甲状腺功能障碍的情况下,异常脂肪细胞可能释放脂肪因子,如PAI-1,这会导致这些患者血栓形成事件的风险增加。因此,应适当管理亚临床甲状腺功能减退。