Peripheral blood immune cell dynamics associate with growth of incidental indeterminate pulmonary nodules
Previous studies suggest peripheral blood immune cells associate with the progression and prognosis of lung cancer. The main purpose of this study was to explore the association of peripheral immune cell and its dynamics with the growth of pulmonary nodules. Of 9280 subjects whom had blood cell coun...
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Published in | Respiratory medicine Vol. 237; p. 107947 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.02.2025
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Online Access | Get full text |
ISSN | 0954-6111 1532-3064 1532-3064 |
DOI | 10.1016/j.rmed.2025.107947 |
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Abstract | Previous studies suggest peripheral blood immune cells associate with the progression and prognosis of lung cancer. The main purpose of this study was to explore the association of peripheral immune cell and its dynamics with the growth of pulmonary nodules.
Of 9280 subjects whom had blood cell counts and chest CT scan in health check-up, 1068 participants were enrolled with the incidental pulmonary nodules of above 5 mm in diameter and subsequently followed up for 2 years. The pulmonary nodules were identified as growth based on the increase of at least 2 mm in the diameters within the two years. The relationships of pulmonary nodules growth with peripheral immune cell dynamics and clinical variables were analyzed using univariable inter-group comparison and multivariable logistic regression analyses.
During the two years, 116 (10.9 %) of 1068 participants had the growth pulmonary nodules. Overall, emphysema, nodule diameter and non-solid characteristics associated with the growth of nodules. In the subgroup of pure solid nodules, high baseline eosinophil percentage (OR 1.220; 95 % CI 1.009–1.474; P = 0.040) and the increase of neutrophil count (OR 3.805; 95 % CI 1.027–14.093; P = 0.045) were significant risk factors for the nodule growth. In the subgroup of solid-predominant nodules, the increase of lymphocyte was associated with a lower risk of growth (OR 0.039; 95 % CI 0.002–0.839; P = 0.038).
High baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules. The decrease of lymphocyte related to the growth of solid-predominant nodules.
•Evaluated the associations between peripheral blood immune cell dynamics and the growth of incidental pulmonary nodules.•High baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules.3.The decrease of lymphocyte related to the growth of solid-predominant nodules.•The decrease of lymphocyte related to the growth of solid-predominant nodules.•Suggested the potential role of immune cells involved in the surveillance of early lung tumors. |
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AbstractList | Previous studies suggest peripheral blood immune cells associate with the progression and prognosis of lung cancer. The main purpose of this study was to explore the association of peripheral immune cell and its dynamics with the growth of pulmonary nodules.OBJECTIVESPrevious studies suggest peripheral blood immune cells associate with the progression and prognosis of lung cancer. The main purpose of this study was to explore the association of peripheral immune cell and its dynamics with the growth of pulmonary nodules.Of 9280 subjects whom had blood cell counts and chest CT scan in health check-up, 1068 participants were enrolled with the incidental pulmonary nodules of above 5 mm in diameter and subsequently followed up for 2 years. The pulmonary nodules were identified as growth based on the increase of at least 2 mm in the diameters within the two years. The relationships of pulmonary nodules growth with peripheral immune cell dynamics and clinical variables were analyzed using univariable inter-group comparison and multivariable logistic regression analyses.MATERIALS AND METHODOf 9280 subjects whom had blood cell counts and chest CT scan in health check-up, 1068 participants were enrolled with the incidental pulmonary nodules of above 5 mm in diameter and subsequently followed up for 2 years. The pulmonary nodules were identified as growth based on the increase of at least 2 mm in the diameters within the two years. The relationships of pulmonary nodules growth with peripheral immune cell dynamics and clinical variables were analyzed using univariable inter-group comparison and multivariable logistic regression analyses.During the two years, 116 (10.9 %) of 1068 participants had the growth pulmonary nodules. Overall, emphysema, nodule diameter and non-solid characteristics associated with the growth of nodules. In the subgroup of pure solid nodules, high baseline eosinophil percentage (OR 1.220; 95 % CI 1.009-1.474; P = 0.040) and the increase of neutrophil count (OR 3.805; 95 % CI 1.027-14.093; P = 0.045) were significant risk factors for the nodule growth. In the subgroup of solid-predominant nodules, the increase of lymphocyte was associated with a lower risk of growth (OR 0.039; 95 % CI 0.002-0.839; P = 0.038).RESULTSDuring the two years, 116 (10.9 %) of 1068 participants had the growth pulmonary nodules. Overall, emphysema, nodule diameter and non-solid characteristics associated with the growth of nodules. In the subgroup of pure solid nodules, high baseline eosinophil percentage (OR 1.220; 95 % CI 1.009-1.474; P = 0.040) and the increase of neutrophil count (OR 3.805; 95 % CI 1.027-14.093; P = 0.045) were significant risk factors for the nodule growth. In the subgroup of solid-predominant nodules, the increase of lymphocyte was associated with a lower risk of growth (OR 0.039; 95 % CI 0.002-0.839; P = 0.038).High baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules. The decrease of lymphocyte related to the growth of solid-predominant nodules.CONCLUSIONSHigh baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules. The decrease of lymphocyte related to the growth of solid-predominant nodules. Previous studies suggest peripheral blood immune cells associate with the progression and prognosis of lung cancer. The main purpose of this study was to explore the association of peripheral immune cell and its dynamics with the growth of pulmonary nodules. Of 9280 subjects whom had blood cell counts and chest CT scan in health check-up, 1068 participants were enrolled with the incidental pulmonary nodules of above 5 mm in diameter and subsequently followed up for 2 years. The pulmonary nodules were identified as growth based on the increase of at least 2 mm in the diameters within the two years. The relationships of pulmonary nodules growth with peripheral immune cell dynamics and clinical variables were analyzed using univariable inter-group comparison and multivariable logistic regression analyses. During the two years, 116 (10.9 %) of 1068 participants had the growth pulmonary nodules. Overall, emphysema, nodule diameter and non-solid characteristics associated with the growth of nodules. In the subgroup of pure solid nodules, high baseline eosinophil percentage (OR 1.220; 95 % CI 1.009–1.474; P = 0.040) and the increase of neutrophil count (OR 3.805; 95 % CI 1.027–14.093; P = 0.045) were significant risk factors for the nodule growth. In the subgroup of solid-predominant nodules, the increase of lymphocyte was associated with a lower risk of growth (OR 0.039; 95 % CI 0.002–0.839; P = 0.038). High baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules. The decrease of lymphocyte related to the growth of solid-predominant nodules. •Evaluated the associations between peripheral blood immune cell dynamics and the growth of incidental pulmonary nodules.•High baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules.3.The decrease of lymphocyte related to the growth of solid-predominant nodules.•The decrease of lymphocyte related to the growth of solid-predominant nodules.•Suggested the potential role of immune cells involved in the surveillance of early lung tumors. Previous studies suggest peripheral blood immune cells associate with the progression and prognosis of lung cancer. The main purpose of this study was to explore the association of peripheral immune cell and its dynamics with the growth of pulmonary nodules. Of 9280 subjects whom had blood cell counts and chest CT scan in health check-up, 1068 participants were enrolled with the incidental pulmonary nodules of above 5 mm in diameter and subsequently followed up for 2 years. The pulmonary nodules were identified as growth based on the increase of at least 2 mm in the diameters within the two years. The relationships of pulmonary nodules growth with peripheral immune cell dynamics and clinical variables were analyzed using univariable inter-group comparison and multivariable logistic regression analyses. During the two years, 116 (10.9 %) of 1068 participants had the growth pulmonary nodules. Overall, emphysema, nodule diameter and non-solid characteristics associated with the growth of nodules. In the subgroup of pure solid nodules, high baseline eosinophil percentage (OR 1.220; 95 % CI 1.009-1.474; P = 0.040) and the increase of neutrophil count (OR 3.805; 95 % CI 1.027-14.093; P = 0.045) were significant risk factors for the nodule growth. In the subgroup of solid-predominant nodules, the increase of lymphocyte was associated with a lower risk of growth (OR 0.039; 95 % CI 0.002-0.839; P = 0.038). High baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules. The decrease of lymphocyte related to the growth of solid-predominant nodules. |
ArticleNumber | 107947 |
Author | Xie, Min Zhang, Ni Guo, Mengyao Guan, Hanxiong Bai, Wenxue Hua, Lijuan Wang, Dongyuan Xu, Hui Sun, Wei Kuang, Dong Lv, Yongman Wang, Qi Li, Kaiyan Hao, Zhipeng Yu, Jun |
Author_xml | – sequence: 1 givenname: Dongyuan surname: Wang fullname: Wang, Dongyuan organization: Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 2 givenname: Lijuan surname: Hua fullname: Hua, Lijuan organization: Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 3 givenname: Wenxue surname: Bai fullname: Bai, Wenxue organization: Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 4 givenname: Mengyao surname: Guo fullname: Guo, Mengyao organization: Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 5 givenname: Yongman surname: Lv fullname: Lv, Yongman organization: Health Management Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 6 givenname: Dong surname: Kuang fullname: Kuang, Dong organization: Department of Pathology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 7 givenname: Hanxiong surname: Guan fullname: Guan, Hanxiong organization: Department of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 8 givenname: Jun surname: Yu fullname: Yu, Jun organization: Department of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 9 givenname: Qi surname: Wang fullname: Wang, Qi organization: Department of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 10 givenname: Zhipeng surname: Hao fullname: Hao, Zhipeng organization: Department of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 11 givenname: Wei surname: Sun fullname: Sun, Wei organization: Department of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 12 givenname: Ni surname: Zhang fullname: Zhang, Ni organization: Department of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 13 givenname: Kaiyan surname: Li fullname: Li, Kaiyan organization: Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 14 givenname: Hui surname: Xu fullname: Xu, Hui email: 1508030758@qq.com organization: Health Management Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China – sequence: 15 givenname: Min orcidid: 0000-0003-4052-1647 surname: Xie fullname: Xie, Min email: xie_m@126.com organization: Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China |
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Keywords | Neutrophil Indeterminate pulmonary nodule Lymphocyte Ground grass opacity Eosinophil |
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SubjectTerms | Aged Disease Progression Eosinophil Eosinophils - immunology Female Ground grass opacity Humans Incidental Findings Indeterminate pulmonary nodule Lung Neoplasms - blood Lung Neoplasms - diagnostic imaging Lung Neoplasms - immunology Lung Neoplasms - pathology Lymphocyte Male Middle Aged Multiple Pulmonary Nodules - blood Multiple Pulmonary Nodules - diagnostic imaging Multiple Pulmonary Nodules - immunology Multiple Pulmonary Nodules - pathology Neutrophil Neutrophils - immunology Prognosis Risk Factors Solitary Pulmonary Nodule - blood Solitary Pulmonary Nodule - diagnostic imaging Solitary Pulmonary Nodule - immunology Solitary Pulmonary Nodule - pathology Tomography, X-Ray Computed |
Title | Peripheral blood immune cell dynamics associate with growth of incidental indeterminate pulmonary nodules |
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