Brief Report - (2024) Volume 8, Issue 4
Genetic Variations in Thyroid Disorders: Insights into Autoimmune Thyroid Disease
Ines Vatavuk*
*Correspondence:
Ines Vatavuk, Department of Ophthalmology, Sestre Milosrdnice Zagreb UHC,
Croatia,
Email:
1Department of Ophthalmology, Sestre Milosrdnice Zagreb UHC, Croatia
, Manuscript No. rtr-25-160644;
, Pre QC No. P-160644;
, QC No. Q-160644;
, Manuscript No. R-160644;
, DOI: 10.37421/2684-4273.2024.8.92
Citation: Vatavuk, Ines. “ Genetic Variations in Thyroid Disorders: Insights into Autoimmune Thyroid Disease.” Rep Thyroid Res 8 (2024): 92.
Copyright: © 2024 Vatavuk I. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited
Introduction
Thyroid eye disease is a debilitating autoimmune condition that affects
the eyes and surrounding tissues. It is most commonly associated with
Graves' disease, an autoimmune disorder that affects the thyroid gland. TED
is characterized by inflammation, swelling, and tissue expansion in the orbit,
leading to symptoms such as proptosis (bulging eyes), double vision, and
eyelid retraction. The management of TED can be challenging, and treatment
options have traditionally focused on managing symptoms and preventing
complications. However, in recent years, there have been significant
advancements in the treatment of TED, offering new hope for patients with this
condition. Teprotumumab is a monoclonal antibody that targets the insulin-like
growth factor 1 receptor (IGF-1R), which plays a key role in the pathogenesis
of TED. IGF-1R is overexpressed in the orbital tissues of patients with TED and
is thought to contribute to the fibrosis and inflammation seen in the disease [1].
Description
Teprotumumab works by blocking the action of IGF-1R, thereby reducing
inflammation and tissue expansion in the orbit. The efficacy of teprotumumab
in the treatment of TED was demonstrated in the phase 2 and phases 3
clinical trials, which showed significant improvement in proptosis, diplopia, and
quality of life compared to placebo. Based on these results, teprotumumab
was approved by the FDA in 2020 for the treatment of TED, making it the
first targeted therapy approved for this condition. Alongside these significant
advancements, traditional treatments like doxycycline continue to play a
crucial role, providing an effective and accessible option for managing mild to
moderate cases. The combination of significant advancements and incremental
improvements underscores the importance of a multifaceted approach to TED
treatment, ensuring that patients receive the most appropriate care based on
their individual needs. As research continues to advance, the future of TED
treatment holds promise for even more effective and personalized therapies,
ultimately improving the quality of life for those affected by this challenging
condition [2]
Conclusion
The development of teprotumumab represents a significant advancement
in the treatment of TED, offering a targeted therapy that can improve symptoms
and quality of life for patients with this condition. However, teprotumumab is not
suitable for all patients with TED, and more research is needed to understand
its long-term safety and efficacy. On the other hand, doxycycline represents an
incremental step forward in TED management, offering a potentially effective
and affordable treatment option for patients with mild to moderate disease
References
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