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Background: To evaluate the clinical value of fractional exhaled nitric oxide (FeNO) levels and peripheral blood eosinophil (EOS) counts and percentages in assessing airway eosinophilic inflammation in patients with acute exacerbations of chronic obstructive pulmonary disease (AECOPD).
Methods: In total, 119 AECOPD patients were included in the study. Patients were divided based on the percentage of EOS in their sputum into the airway EOS inflammation group (29 patients) and the non-airway EOS inflammation group (90 patients). The diagnostic values of FeNO and peripheral blood EOS for detecting airway EOS inflammation in AECOPD patients were assessed.
Results: The airway EOS inflammation group had higher peripheral blood EOS counts and percentages. FeNO, peripheral blood EOS counts and percentages were significantly correlated with sputum EOS percentages. ROC curve analysis showed that the optimal cut-off values for predicting airway EOS inflammation were 18.5 ppb for FeNO, with sensitivities and specificities of 76% and 61%, respectively; 0.335 × 10/L for peripheral blood EOS count, with sensitivities and specificities of 41% and 98%, respectively; and 3.56% for peripheral blood EOS percentage, with sensitivities and specificities of 59% and 86%, respectively.
Conclusions: FeNO, peripheral blood EOS counts and percentages have a strong correlation with airway EOS inflammation. The levels of FeNO and peripheral blood EOS counts and percentages can effectively predict airway EOS inflammation in AECOPD patients.
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http://dx.doi.org/10.1111/cyt.70009 | DOI Listing |
PLoS Pathog
September 2025
National Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.
Neuroinflammation within the central nervous system (CNS) is recognized as a critical pathological process in meningitic Escherichia coli (E. coli) infection, leading to severe neurodegenerative disorders and long-term sequelae. Astrocyte reactivity plays a pivotal role in driving the neuroinflammatory cascade in response to pathological stimuli from peripheral sources or other cellular components of the CNS.
View Article and Find Full Text PDFJ Laparoendosc Adv Surg Tech A
September 2025
Department of Anesthesiology, Shandong Provincial Third Hospital, Shandong University, Jinan, China.
This study aimed to identify the biomarkers that was associated with the postoperative incisional pain in patients with acute cholecystitis undergoing laparoscopic cholecystectomy surgery (ACC-LC). Sixty ACC-LC patients were enrolled and divided into mild pain (MP) and moderate-to-severe pain (MSP) groups based on their visual analog scale (VAS) scores 24 hours postoperatively. RNA sequencing was used to screen the potential pain associated markers, and ELISA were used to analyze the expression of one identified marker, CXCR5 in peripheral blood mononuclear cells (PBMCs).
View Article and Find Full Text PDFQJM
September 2025
Flat 6 Souchay Court, 1 Clothorn Road, Manchester, M20 6BR.
Int J Surg
September 2025
Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Background: Percutaneous transthoracic lung biopsy (PTNB) guided by Computed Tomography (CT) greatly depends on the operators' skill for accuracy. This study aimed to evaluate whether three-dimensionally(3D) printed navigational templates for percutaneous transthoracic lung biopsy achieve diagnostic yield comparable to conventional computed tomography guidance.
Materials And Methods: Conducted from 1 November 2020, to 27 July 2023, this noninferiority randomized clinical trial included 159 patients with peripheral lung masses (≥30 mm).
Cancer Epidemiol Biomarkers Prev
September 2025
Translational Medicine Research Unit, Medical Research Center Oulu, Oulu University Hospital, and University of Oulu, Oulu, Finland.
Background: T-cell densities are associated with colorectal cancer outcome, but the significance of specific Th cell subsets is incompletely understood. We aimed to investigate the role of Th1 and Th2 cells and associated cytokine profiles.
Methods: We used multiplex IHC to identify Th1 and Th2 cells on tumor samples of more than 2,000 patients with colorectal cancer (three independent cohorts).