Influence of 4-week or 12-week glucocorticoid treatment on metabolic changes in patients with active moderate-to-severe thyroid-associated ophthalmopathy
- PMID: 33742766
- PMCID: PMC8504830
- DOI: 10.1111/cts.12999
Influence of 4-week or 12-week glucocorticoid treatment on metabolic changes in patients with active moderate-to-severe thyroid-associated ophthalmopathy
Abstract
Thyroid-associated ophthalmopathy (TAO) is a serious, progressive, vision-threatening and difficult-to-treat organ-specific autoimmune disease. The course, therapeutic effects and prognosis of moderate to severe TAO vary greatly. High-dose intravenous glucocorticoid (IVGC) therapy is considered a first-line treatment for active moderate-to-severe TAO, but there is still insufficient evidence regarding the treatment duration. Long-term IVGC therapy can influence the metabolism of glucose, lipids, and bone. This study was designed to compare changes in metabolic and immunological indexes as well as the magnetic resonance imaging apparent diffusion coefficient (ADC) of the extraocular muscles after 4 and 12 weeks of IVGC therapy. Forty-eight patients with active moderate-to-severe TAO were included in this retrospective cohort study. Metabolism and immunological indexes were measured before and after therapy. The ADC and clinical activity score (CAS) were used to evaluate the efficacy of treatment in these patients. We found that the patients in the 12-week group had increased fasting plasma glucose (p = 0.004), glycated hemoglobin (p = 0.028), total cholesterol (p < 0.001), and low-density lipoprotein (p < 0.001) after therapy. The patients in both groups had reduced bone metabolism markers after therapy. Thyroid peroxidase antibody and thyrotropin receptor antibody levels decreased after treatment in both groups (p < 0.001). A significant decrease in thyroglobulin antibody levels was found in the 4-week group (p = 0.006). The change in the ADC was higher in the 4-week group than in the 12-week group (p = 0.014). However, there were no significant differences in CAS values between the two groups. Therefore, 4-week IVGC therapy was recommended for patients with TAO with glucose and lipid disorders.
© 2021 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of the American Society for Clinical Pharmacology and Therapeutics.
Conflict of interest statement
The authors declared no competing interests for this work.
Figures


Similar articles
-
A single-center retrospective study of factors related to the effects of intravenous glucocorticoid therapy in moderate-to-severe and active thyroid-associated ophthalmopathy.BMC Endocr Disord. 2018 Feb 20;18(1):13. doi: 10.1186/s12902-018-0240-8. BMC Endocr Disord. 2018. PMID: 29463244 Free PMC article. Clinical Trial.
-
99Tcm-octreotide scintigraphy and serum eye muscle antibodies in evaluation of active thyroid-associated ophthalmopathy.Eye (Lond). 2017 May;31(5):668-676. doi: 10.1038/eye.2017.42. Epub 2017 Apr 7. Eye (Lond). 2017. PMID: 28387769 Free PMC article.
-
Fat-suppression T2 relaxation time and water fraction predict response to intravenous glucocorticoid therapy for thyroid-associated ophthalmopathy.Eur Radiol. 2025 Feb;35(2):957-967. doi: 10.1007/s00330-024-10868-4. Epub 2024 Aug 2. Eur Radiol. 2025. PMID: 39093414
-
Advances in treatment of active, moderate-to-severe Graves' ophthalmopathy.Lancet Diabetes Endocrinol. 2017 Feb;5(2):134-142. doi: 10.1016/S2213-8587(16)30046-8. Epub 2016 Jun 23. Lancet Diabetes Endocrinol. 2017. PMID: 27346786 Review.
-
Acute liver damage following intravenous glucocorticoid treatment for Graves' ophthalmopathy.Endocrine. 2016 Oct;54(1):259-268. doi: 10.1007/s12020-016-0928-3. Epub 2016 Mar 22. Endocrine. 2016. PMID: 27003434 Review.
Cited by
-
Decrease in Bone Formation and Bone Resorption during Intravenous Methylprednisolone Pulse Therapy in Patients with Graves' Orbitopathy.J Clin Med. 2022 Aug 26;11(17):5005. doi: 10.3390/jcm11175005. J Clin Med. 2022. PMID: 36078937 Free PMC article.
-
Application progress of magnetic resonance imaging in thyroid associated ophthalmopathy.Front Endocrinol (Lausanne). 2025 Jun 26;16:1537957. doi: 10.3389/fendo.2025.1537957. eCollection 2025. Front Endocrinol (Lausanne). 2025. PMID: 40642513 Free PMC article. Review.
-
Causality of blood metabolites and metabolic pathways on Graves' disease and Graves' ophthalmopathy: a two-sample Mendelian randomization study.Endocrine. 2024 Aug;85(2):786-793. doi: 10.1007/s12020-024-03761-z. Epub 2024 Mar 6. Endocrine. 2024. PMID: 38448677
-
Mechanisms of immune-related differentially expressed genes in thyroid-associated ophthalmopathy based on the GEO database.Ann Transl Med. 2022 Sep;10(17):926. doi: 10.21037/atm-22-3470. Ann Transl Med. 2022. PMID: 36172114 Free PMC article.
-
Association between initial lipid and lipoprotein levels, oxidative stress indicators and clinical efficacy of intravenous methylprednisolone in moderate-to-severe thyroid-associated ophthalmopathy: protocol for a real-world prospective cohort study.BMJ Open. 2025 Aug 5;15(8):e098243. doi: 10.1136/bmjopen-2024-098243. BMJ Open. 2025. PMID: 40764083 Free PMC article.
References
-
- Smith TJ, Hegedüs L. Graves’ disease. N Engl J Med. 2016;375(16):1552‐1565. - PubMed
-
- Taylor PN, Albrecht D, Scholz A, et al. Global epidemiology of hyperthyroidism and hypothyroidism. Nat Rev Endocrinol. 2018;14(5):301‐316. - PubMed
-
- Bartalena L, Baldeschi L, Dickinson A, et al. Consensus statement of the European Group on Graves’ orbitopathy (EUGOGO) on management of GO. Eur J Endocrinol. 2008;158(3):273‐285. - PubMed
-
- Shan SJ, Douglas RS. The pathophysiology of thyroid eye disease. J Neuroophthalmol. 2014;34:177‐185. - PubMed
-
- Bahn RS. Current insights into the pathogenesis of graves’ ophthalmopathy. Horm Metab Res. 2015;47:773‐778. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical