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PTX3: A Potential Biomarker in Thyroid Associated Ophthalmopathy
Pei Mou1, Ziyu Chen1, Lihong Jiang2
1Department of Ophthalmology, Changzheng Hospital, Second Military Medical University, Shanghai 200003, China.
Biomed Research International
|April 21, 2018
Summary
Pentraxin-3 (PTX3) is elevated in thyroid-associated ophthalmopathy (TAO) patients, found in both orbital tissue and serum. This suggests PTX3 may play a role in the autoimmune inflammatory processes of TAO.
Area of Science:
- Immunology
- Endocrinology
- Ophthalmology
Background:
- Thyroid-associated ophthalmopathy (TAO) is an autoimmune condition characterized by inflammation and tissue remodeling.
- Pentraxin-3 (PTX3), an innate immune system component, has been linked to autoimmune diseases.
- PTX3's role in TAO pathogenesis warrants investigation.
Purpose of the Study:
- To investigate the expression and concentration of Pentraxin-3 (PTX3) in patients with thyroid-associated ophthalmopathy (TAO).
- To determine if PTX3 is present in orbital adipose-connective tissue and serum of TAO patients and correlate its levels with the disease.
Main Methods:
- Gene expression analysis using RNA-sequencing (RNA-seq) and quantitative PCR (qPCR) on orbital adipose-connective tissue from TAO patients and controls.
- Immunohistochemistry (IHC) to visualize PTX3 protein in orbital tissues.
- Enzyme-linked immunosorbent assay (ELISA) to quantify serum PTX3 levels.
Main Results:
- RNA-seq revealed significantly higher PTX3 gene expression in TAO orbital tissues compared to controls (FDR = 0.0059).
- qPCR confirmed a 5.59-fold increase in PTX3 expression in TAO tissues (p = 0.0012).
- Immunohistochemistry showed strong PTX3 protein staining in TAO tissues, with weak staining in controls. Serum PTX3 concentration was 1.9-fold higher in TAO patients (p < 0.0001).
Conclusions:
- Patients with TAO exhibit increased PTX3 presence in both orbital tissues and serum.
- These findings suggest a potential association between PTX3 and the inflammatory processes in thyroid-associated ophthalmopathy.
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