PMID- 30431610 OWN - NLM STAT- MEDLINE DCOM- 20181126 LR - 20221005 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 97 IP - 46 DP - 2018 Nov TI - Serum levels of fetuin-A are negatively associated with log transformation levels of thyroid-stimulating hormone in patients with hyperthyroidism or euthyroidism: An observational study at a medical center in Taiwan. PG - e13254 LID - 10.1097/MD.0000000000013254 [doi] LID - e13254 AB - Fetuin-A is a protein with various biological functions. It plays a role in insulin resistance and arterial calcium deposition. Thyroid dysfunction may affect energy expenditure, glucose metabolism, and the risk of cardiovascular diseases. In the present study, we compared the serum fetuin-A concentrations in hyperthyroid patients with those in euthyroid patients.We recruited 30 newly-diagnosed hyperthyroid patients (the HY group) and treated them with anti-thyroid regimens as clinically indicated. We recruited 30 euthyroid individuals (the EU group) as controls. We compared laboratory parameters at the baseline and at 6 months. We then determined the associations between the levels of fetuin-A and free thyroxine (fT4), thyroid-stimulating hormone (TSH), or log transformation of TSH (logTSH).At the baseline, the HY patients had significantly higher serum fetuin-A levels than the EU patients (median [Q1, Q3]: 735.4 [537.9, 843.4] ng/mL vs 561.1[449.2, 670.5] ng/mL, P = .010). At 6 months, the serum fetuin-A levels of the HY patients decreased but were still higher than those of the EU patients (698.4 [627.6, 924.3] ng/mL vs 616.5 [498.2, 727.7] ng/mL, P = .002). At baseline, the serum levels of fetuin-A were negatively associated with logTSH (beta = -53.79, P = .010). At 6 months, the levels of fetuin-A were positively associated with fT4 (beta = 86.91, P = .039), and negatively associated with logTSH (beta = -104.28, P < .001). Changes to the levels of fetuin-A within 6 months were negatively associated with changes to logTSH (beta = -57.80, P = .019). The negative associations between fetuin-A levels and logTSH at baseline and at 6 months, and the changes during the 6 months remained significant after adjustment for sex and age (beta = -51.72, P = .016; beta = -103.11, P < .001; and beta = -59.36, P = .020, respectively).The patients with hyperthyroidism had higher serum fetuin-A levels than the patients with euthyroidism. In patients with hyperthyroidism, the serum fetuin-A concentrations decreased after the anti-thyroid treatment. In the present study, serum fetuin-A concentrations were negatively associated with logTSH. FAU - Tseng, Fen-Yu AU - Tseng FY AD - Department of Internal Medicine, National Taiwan University Hospital, and National Taiwan University College of Medicine. FAU - Chen, Yen-Ting AU - Chen YT AD - Graduate Institute of Clinical Medicine, College of Medicine. FAU - Chi, Yu-Chiao AU - Chi YC AD - Graduate Institute of Clinical Medicine, College of Medicine. FAU - Chen, Pei-Lung AU - Chen PL AD - Department of Internal Medicine, National Taiwan University Hospital, and National Taiwan University College of Medicine. AD - Department of Medical Genetics, National Taiwan University Hospital. AD - Graduate Institute of Medical Genomics and Proteomics, College of Medicine, National Taiwan University, Taipei, Taiwan. FAU - Yang, Wei-Shiung AU - Yang WS AD - Department of Internal Medicine, National Taiwan University Hospital, and National Taiwan University College of Medicine. AD - Graduate Institute of Clinical Medicine, College of Medicine. LA - eng PT - Journal Article PT - Observational Study PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - 0 (AHSG protein, human) RN - 0 (alpha-2-HS-Glycoprotein) RN - 9002-71-5 (Thyrotropin) RN - Q51BO43MG4 (Thyroxine) SB - IM EIN - Medicine (Baltimore). 2019 Apr;98(15):e15298. PMID: 30985733 MH - Adult MH - Euthyroid Sick Syndromes/*blood MH - Female MH - Humans MH - Hyperthyroidism/*blood MH - Male MH - Taiwan MH - Thyrotropin/*blood MH - Thyroxine/blood MH - alpha-2-HS-Glycoprotein/*analysis PMC - PMC6257609 COIS- The authors have no conflicts of interest to disclose. EDAT- 2018/11/16 06:00 MHDA- 2018/11/27 06:00 PMCR- 2018/11/16 CRDT- 2018/11/16 06:00 PHST- 2018/11/16 06:00 [entrez] PHST- 2018/11/16 06:00 [pubmed] PHST- 2018/11/27 06:00 [medline] PHST- 2018/11/16 00:00 [pmc-release] AID - 00005792-201811160-00052 [pii] AID - MD-D-18-05818 [pii] AID - 10.1097/MD.0000000000013254 [doi] PST - ppublish SO - Medicine (Baltimore). 2018 Nov;97(46):e13254. doi: 10.1097/MD.0000000000013254.