Literature DB >> 24867136

Risk factors of hyperthyroidism with hepatic function injury: a 4-year retrospective study.

C Li1, J Tan1, G Zhang1, Z Meng1, R Wang1, W Li1, W Zheng1.   

Abstract

Hepatic function injury is one of the common complications of hyperthyroidism (mainly Graves' disease), which affects the choice of treatment and the curative rate. Our goal was to describe clinical and biochemical patterns in patients suffering from Graves' disease (GD) and hepatic function injury and to determine the influential factors. A cohort of 1 070 patients who received (131)I treatment were studied. Many examinations were performed before (131)I therapy, such as: the 24-h radioactive iodine uptake of thyroid (RAIU(24 h)) and serum-free triiodothyronine (FT(3)), free thyroxine (FT(4)), sensitive thyroid-stimulating hormone (sTSH), antithyrotrophin receptor antibody (TRAb), thyroglobulin antibody (TgAb), and antithyroid peroxidase antibody (TPOAb), serum hepatic function tests, etc. Data were analyzed by the unpaired t-test, the independent samples t-test, the χ(2) test, logistic regression, and Pearson bivariate correlation. Age, course of GD, thyroid's weight, FT(4), TPOAb, and TRAb in GD patients with hepatic function injury were higher than those with normal hepatic function patients. The influential factors were age, hyperthyroidism duration, heart rate, thyroid's weight, FT(4), RAIU(24 h), TgAb, TPOAb, and TRAb. RAIU(24 h) was the protecting factor. Age, course of GD, heart rate, thyroid's weight, FT(4), TRAb, and TPOAb were the risk factors. Patients whose age was higher than 45 years old, heart rate above 90 bpm, thyroid weight more than 35 g, the hyperthyroidism duration more than 3 years, FT(4) higher than 70.5 pmol/l, the level of TPOAb above 360 IU/ml, and the level of TRAb above 15 IU/l have increased risk of hepatic function injury. As treatment (131)I therapy was found to be the best choice. © Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2014        PMID: 24867136     DOI: 10.1055/s-0034-1375690

Source DB:  PubMed          Journal:  Horm Metab Res        ISSN: 0018-5043            Impact factor:   2.936


  7 in total

1.  RNASET2, GPR174, and PTPN22 gene polymorphisms are related to the risk of liver damage associated with the hyperthyroidism in patients with Graves' disease.

Authors:  Qing Zhang; Shaozheng Liu; Yanxing Guan; Qingjie Chen; Qing Zhang; Xiang Min
Journal:  J Clin Lab Anal       Date:  2017-05-31       Impact factor: 2.352

2.  Graves' disease presenting as severe postpartum pruritus.

Authors:  Rachel Marinch Carpenter; Jessica Wongward
Journal:  BMJ Case Rep       Date:  2018-06-15

3.  Hyperthyroidism and hepatic dysfunction: Report of 17 cases.

Authors:  Benothman Wafa; Hadjkacem Faten; Elleuch Mouna; Mnif Fatma; Abid Mohamed
Journal:  JGH Open       Date:  2020-04-11

4.  Risk factors of hepatic dysfunction in patients with Graves' hyperthyroidism and the efficacy of 131iodine treatment.

Authors:  Renfei Wang; Jian Tan; Guizhi Zhang; Wei Zheng; Chengxia Li
Journal:  Medicine (Baltimore)       Date:  2017-02       Impact factor: 1.889

5.  Liver enzyme profile and progression in association with thyroid autoimmunity in Graves' disease.

Authors:  Albert Hsieh; Stephen Adelstein; Susan V McLennan; Paul F Williams; Elizabeth L Chua; Stephen M Twigg
Journal:  Endocrinol Diabetes Metab       Date:  2019-07-15

6.  Elevated Levels of Circulating Biomarkers Related to Leaky Gut Syndrome and Bacterial Translocation Are Associated With Graves' Disease.

Authors:  Dekai Zheng; Huimin Liao; Shuze Chen; Xiuying Liu; Chuyin Mao; Cangui Zhang; Min Meng; Zhi Wang; Ying Wang; Qinrui Jiang; Yaoming Xue; Lin Zhou; Ye Chen
Journal:  Front Endocrinol (Lausanne)       Date:  2021-12-16       Impact factor: 5.555

Review 7.  Hyperthyroidism and Liver Dysfunction: A Review of a Common Comorbidity.

Authors:  Ernest Yorke
Journal:  Clin Med Insights Endocrinol Diabetes       Date:  2022-02-07
  7 in total

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