甲状腺功能减退患者铁谱与甲状腺谱的关系

Santosh Kumar, J. Keshari, R. Kumari, P. Prakash, U. Kumar, Ved Prakash
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引用次数: 0

摘要

甲状腺激素的生物合成依赖于铁的代谢。铁代谢的变化及其缺乏可能导致甲状腺激素的变化。在贫血或其他情况下,这种干扰会导致甲状腺功能减退。目的:探讨甲状腺功能减退患者铁谱各参数与正常健康人甲状腺谱的关系。材料与方法:本病例对照研究于2017年4月至2018年6月在巴特那IGIMS内分泌科进行,选取50例甲状腺功能减退患者和50例同龄健康受试者。采用化学发光免疫分析法(CLIA)测定血清铁蛋白和血清T3、T4、促甲状腺激素(TSH)水平。血清铁含量测定采用TPTZ(2,4,6-三吡啶-s-三嗪)法,总铁结合能力(TIBC)测定采用亚硝基PSAP法。所有统计检验和分析均在社会科学统计软件包(SPSS) 16.0进行。各检验变量组间均值的差异在方差齐性检验和正态性检验(Kolmogorov-Smirnov检验)后,采用Student 's t检验。结果:甲状腺功能减退患者平均年龄30.28±10.5岁,对照组平均年龄31.14±10.4岁。研究发现,甲状腺功能减退患者的平均血清铁蛋白水平和铁水平显著低于对照组(p<0.001),而TIBC显著高于对照组(p<0.001)。血清铁蛋白和铁分别与TSH呈负相关(-0.695和-0.541),与T3和T4呈正相关。结论:评价甲状腺疾病患者的铁谱对治疗方式和预后有一定的指导意义
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relationship between Iron Profile and Thyroid Profile in Hypothyroid Patients
Introduction: Thyroid hormone biosynthesis is dependent on iron metabolism. Changes in iron metabolism and its deficiency may cause a change in the profile of thyroid hormone. Such interferences caused can lead to hypothyroidism in case of anaemia or the other way round. Aim: To find a relationship between various parameters of iron profile to that of thyroid profile in hypothyroid patients when compared to normal healthy subjects. Materials and Methods: Present case-control study was conducted on 50 hypothyroid patients and 50 healthy subjects of same age, in the Department of Endocrinology, IGIMS, Patna between April 2017 to June 2018. Serum ferritin and Serum T3, T4, and Thyroid Stimulating Hormone (TSH) were estimated by Chemiluminescence Immuno Assay (CLIA) method. Serum iron estimation was done using TPTZ (2,4,6-Tripyridyl-s-triazine) method and Total Iron Binding Capacity (TIBC) estimation was done by Nitroso PSAP method. All statistical test and analysis were performed in Statistical Package for the Social Science (SPSS) 16.0. The differences between mean values of groups for each test variable were tested by Student’s t-test after testing for homogeneity of variance and normality test (Kolmogorov-Smirnov test). Results: The mean age of the hypothyroid patients was 30.28±10.5 years while it was 31.14±10.4 years in control group. It was observed from the study that mean serum ferritin level and iron level were significantly lower in hypothyroid subjects compared to control groups (p<0.001) while TIBC was significantly higher (p<0.001). Serum ferritin and iron were found to be negatively correlated with TSH (-0.695 and -0.541) and positively correlated to T3 and T4, respectively. Conclusion: Evaluating iron profile in thyroid disorder may be an aid to the treatment modality and disease outcome
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