Orbital Clinicopathological Differences in Thyroid Eye Disease: An Analysis of Cytokines With Histopathological and Clinical Correlation
To explore the pathological differences in orbital adipose/connective tissue between active and inactive thyroid eye disease (TED) subjects and their correlations with clinical characteristics. Orbital adipose/connective tissue samples from 42 TED subjects (20 active, 22 inactive) were collected dur...
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Published in | Investigative ophthalmology & visual science Vol. 66; no. 3; p. 33 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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03.03.2025
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ISSN | 1552-5783 1552-5783 |
DOI | 10.1167/iovs.66.3.33 |
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Abstract | To explore the pathological differences in orbital adipose/connective tissue between active and inactive thyroid eye disease (TED) subjects and their correlations with clinical characteristics.
Orbital adipose/connective tissue samples from 42 TED subjects (20 active, 22 inactive) were collected during decompression surgery. We analyzed cytokine expression, inflammatory cell infiltration, inherent cell populations, and interstitial changes by Luminex and histopathology. Correlations were analyzed using Pearson and Spearman correlation analyses.
Among the 108 cytokines detected, active TED exhibited elevated platelet endothelial cell adhesion molecule 1 (PECAM-1), interleukin-23 (IL-23), a proliferation-inducing ligand (APRIL), IL-6, C-C motif chemokine ligand 2 (CCL2), β-nerve growth factor (NGF), and lower CCL21 and CCL5. The extent of infiltration by helper T (Th) cells and monocytes was significantly greater in the active group than in the inactive group. Adipocyte density was significantly elevated in active TED, whereas fibrosis was more prominent in inactive TED. Fifteen cytokines were significantly associated with inflammatory cell infiltration, with IL-16 showing the strongest correlations with T cells. Ten cytokines showed significant positive correlations with fibrosis. Four cytokines (IL-6, PECAM-1, IL-23 and transforming growth factor β1), Th cell infiltration and adipocyte density were significantly positively correlated with clinical activity score (CAS). Sixteen cytokines, along with adipocyte density, were significantly positively correlated with disease severity of TED.
The orbital adipose/connective tissues of active and inactive TED subjects showed significant differences in terms of cytokines, inflammatory cells infiltration, inherent cells and interstitium. These pathological changes were correlated with clinical characteristics of TED. |
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AbstractList | To explore the pathological differences in orbital adipose/connective tissue between active and inactive thyroid eye disease (TED) subjects and their correlations with clinical characteristics.
Orbital adipose/connective tissue samples from 42 TED subjects (20 active, 22 inactive) were collected during decompression surgery. We analyzed cytokine expression, inflammatory cell infiltration, inherent cell populations, and interstitial changes by Luminex and histopathology. Correlations were analyzed using Pearson and Spearman correlation analyses.
Among the 108 cytokines detected, active TED exhibited elevated platelet endothelial cell adhesion molecule 1 (PECAM-1), interleukin-23 (IL-23), a proliferation-inducing ligand (APRIL), IL-6, C-C motif chemokine ligand 2 (CCL2), β-nerve growth factor (NGF), and lower CCL21 and CCL5. The extent of infiltration by helper T (Th) cells and monocytes was significantly greater in the active group than in the inactive group. Adipocyte density was significantly elevated in active TED, whereas fibrosis was more prominent in inactive TED. Fifteen cytokines were significantly associated with inflammatory cell infiltration, with IL-16 showing the strongest correlations with T cells. Ten cytokines showed significant positive correlations with fibrosis. Four cytokines (IL-6, PECAM-1, IL-23 and transforming growth factor β1), Th cell infiltration and adipocyte density were significantly positively correlated with clinical activity score (CAS). Sixteen cytokines, along with adipocyte density, were significantly positively correlated with disease severity of TED.
The orbital adipose/connective tissues of active and inactive TED subjects showed significant differences in terms of cytokines, inflammatory cells infiltration, inherent cells and interstitium. These pathological changes were correlated with clinical characteristics of TED. To explore the pathological differences in orbital adipose/connective tissue between active and inactive thyroid eye disease (TED) subjects and their correlations with clinical characteristics.PurposeTo explore the pathological differences in orbital adipose/connective tissue between active and inactive thyroid eye disease (TED) subjects and their correlations with clinical characteristics.Orbital adipose/connective tissue samples from 42 TED subjects (20 active, 22 inactive) were collected during decompression surgery. We analyzed cytokine expression, inflammatory cell infiltration, inherent cell populations, and interstitial changes by Luminex and histopathology. Correlations were analyzed using Pearson and Spearman correlation analyses.MethodsOrbital adipose/connective tissue samples from 42 TED subjects (20 active, 22 inactive) were collected during decompression surgery. We analyzed cytokine expression, inflammatory cell infiltration, inherent cell populations, and interstitial changes by Luminex and histopathology. Correlations were analyzed using Pearson and Spearman correlation analyses.Among the 108 cytokines detected, active TED exhibited elevated platelet endothelial cell adhesion molecule 1 (PECAM-1), interleukin-23 (IL-23), a proliferation-inducing ligand (APRIL), IL-6, C-C motif chemokine ligand 2 (CCL2), β-nerve growth factor (NGF), and lower CCL21 and CCL5. The extent of infiltration by helper T (Th) cells and monocytes was significantly greater in the active group than in the inactive group. Adipocyte density was significantly elevated in active TED, whereas fibrosis was more prominent in inactive TED. Fifteen cytokines were significantly associated with inflammatory cell infiltration, with IL-16 showing the strongest correlations with T cells. Ten cytokines showed significant positive correlations with fibrosis. Four cytokines (IL-6, PECAM-1, IL-23 and transforming growth factor β1), Th cell infiltration and adipocyte density were significantly positively correlated with clinical activity score (CAS). Sixteen cytokines, along with adipocyte density, were significantly positively correlated with disease severity of TED.ResultsAmong the 108 cytokines detected, active TED exhibited elevated platelet endothelial cell adhesion molecule 1 (PECAM-1), interleukin-23 (IL-23), a proliferation-inducing ligand (APRIL), IL-6, C-C motif chemokine ligand 2 (CCL2), β-nerve growth factor (NGF), and lower CCL21 and CCL5. The extent of infiltration by helper T (Th) cells and monocytes was significantly greater in the active group than in the inactive group. Adipocyte density was significantly elevated in active TED, whereas fibrosis was more prominent in inactive TED. Fifteen cytokines were significantly associated with inflammatory cell infiltration, with IL-16 showing the strongest correlations with T cells. Ten cytokines showed significant positive correlations with fibrosis. Four cytokines (IL-6, PECAM-1, IL-23 and transforming growth factor β1), Th cell infiltration and adipocyte density were significantly positively correlated with clinical activity score (CAS). Sixteen cytokines, along with adipocyte density, were significantly positively correlated with disease severity of TED.The orbital adipose/connective tissues of active and inactive TED subjects showed significant differences in terms of cytokines, inflammatory cells infiltration, inherent cells and interstitium. These pathological changes were correlated with clinical characteristics of TED.ConclusionsThe orbital adipose/connective tissues of active and inactive TED subjects showed significant differences in terms of cytokines, inflammatory cells infiltration, inherent cells and interstitium. These pathological changes were correlated with clinical characteristics of TED. |
Author | Deng, Aijun Rong, Liyuan Jing, Gaojing Wu, Wei Yang, Xinji Li, Yueyue Tang, Jiaqi Kang, Xin Liu, Wenlu Yao, Lan Li, Yue Lv, Xiaohui Ma, Rui |
Author_xml | – sequence: 1 givenname: Yue surname: Li fullname: Li, Yue organization: School of Clinical Medicine, Shandong Second Medical University, Weifang, Shandong, China, Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China – sequence: 2 givenname: Jiaqi surname: Tang fullname: Tang, Jiaqi organization: School of Clinical Medicine, Shandong Second Medical University, Weifang, Shandong, China, Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China – sequence: 3 givenname: Gaojing surname: Jing fullname: Jing, Gaojing organization: Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China, Department of Endocrinology, The First Hospital of Lanzhou University, Lanzhou, Gansu, China – sequence: 4 givenname: Yueyue surname: Li fullname: Li, Yueyue organization: Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China – sequence: 5 givenname: Rui surname: Ma fullname: Ma, Rui organization: Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China – sequence: 6 givenname: Xin surname: Kang fullname: Kang, Xin organization: Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China – sequence: 7 givenname: Liyuan surname: Rong fullname: Rong, Liyuan organization: Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China, Stem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China – sequence: 8 givenname: Wenlu surname: Liu fullname: Liu, Wenlu organization: Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China – sequence: 9 givenname: Lan surname: Yao fullname: Yao, Lan organization: Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China – sequence: 10 givenname: Xiaohui surname: Lv fullname: Lv, Xiaohui organization: School of Clinical Medicine, Shandong Second Medical University, Weifang, Shandong, China – sequence: 11 givenname: Aijun surname: Deng fullname: Deng, Aijun organization: School of Clinical Medicine, Shandong Second Medical University, Weifang, Shandong, China – sequence: 12 givenname: Wei surname: Wu fullname: Wu, Wei organization: Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China – sequence: 13 givenname: Xinji surname: Yang fullname: Yang, Xinji organization: School of Clinical Medicine, Shandong Second Medical University, Weifang, Shandong, China, Senior Department of Ophthalmology, 3rd Medical Center of Chinese PLA General Hospital, Beijing, China |
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SubjectTerms | Adipose Tissue - metabolism Adipose Tissue - pathology Adult Aged Cytokines - metabolism Female Graves Ophthalmopathy - metabolism Graves Ophthalmopathy - pathology Graves Ophthalmopathy - surgery Humans Male Middle Aged Orbit - metabolism Orbit - pathology |
Title | Orbital Clinicopathological Differences in Thyroid Eye Disease: An Analysis of Cytokines With Histopathological and Clinical Correlation |
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