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1.
Intern Med ; 63(16): 2317-2320, 2024 Aug 15.
Article in English | MEDLINE | ID: mdl-38220196

ABSTRACT

Although endoscopic sinus surgery (ESS) is beneficial in improving asthma symptoms, its impact on the lung function in patients with asthma and chronic rhinosinusitis remains unclear. We herein report a case of severe asthma with eosinophilic chronic rhinosinusitis, in which ESS substantially improved airflow limitation and concomitantly reduced fractional exhaled nitric oxide and blood eosinophil counts. ESS likely relieved airflow limitation by suppressing type 2 inflammatory pathways. This case highlights ESS as a promising strategy for achieving clinical remission in patients with severe asthma and chronic rhinosinusitis.


Subject(s)
Asthma , Endoscopy , Rhinitis , Sinusitis , Humans , Sinusitis/surgery , Sinusitis/complications , Asthma/surgery , Asthma/complications , Asthma/physiopathology , Chronic Disease , Rhinitis/surgery , Rhinitis/complications , Endoscopy/methods , Eosinophilia/surgery , Eosinophilia/complications , Male , Severity of Illness Index , Middle Aged , Treatment Outcome , Female , Rhinosinusitis
2.
Respir Investig ; 61(2): 186-189, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36724582

ABSTRACT

BACKGROUND: Although pulmonary function tests (PFTs) are important in patients with interstitial lung disease (ILD), they cannot be easily performed in a primary healthcare setting. This study aimed to examine the usefulness of the difference between pulse oxygen saturation (SpO2) at rest and the lowest SpO2 during the 1-min sit-to-stand test (delta SpO2-1STST) for predicting pulmonary function impairment. METHODS: We retrospectively reviewed 116 patients with ILD who underwent 1STST and PFTs. RESULTS: The delta SpO2-1STST and diffusing capacity for carbon monoxide (DLco) strongly correlated (ρ = 0.70). The delta SpO2-1STST was effective in predicting impaired gas exchange (cut-off value, -4%; AUC, 0.86; sensitivity, 74%; specificity, 87%). CONCLUSIONS: The Delta SpO2-1STST may be a reasonable tool for predicting abnormalities in PFTs.


Subject(s)
Lung Diseases, Interstitial , Pulmonary Diffusing Capacity , Humans , Retrospective Studies , Lung Diseases, Interstitial/diagnosis , Lung , Respiratory Function Tests
3.
J Gastroenterol ; 53(4): 517-524, 2018 Apr.
Article in English | MEDLINE | ID: mdl-28823057

ABSTRACT

BACKGROUND: Accumulating evidence shows an overabundance of Fusobacterium nucleatum in colorectal tumor tissues. However, the correlation between the absolute copy number of F. nucleatum in colorectal cancer tissues and colorectal cancer progression is unclear from previous reports. Therefore, we performed a study to compare the abundance of F. nucleatum in colorectal tissues with clinicopathologic and molecular features of colorectal cancer. METHODS: We collected 100 colorectal cancer tissues and 72 matched normal-appearing mucosal tissues. Absolute copy numbers of F. nucleatum were measured by droplet digital PCR. RESULTS: The detection rates of F. nucleatum were 63.9% (46/72) in normal-appearing mucosal tissues and 75.0% (75/100) in CRC tissue samples. The median copy number of F. nucleatum was 0.4/ng DNA in the normal-appearing colorectal mucosa in patients with colorectal cancer and 1.9/ng DNA in the colorectal cancer tissues (P = 0.0031). F. nucleatum copy numbers in stage IV colorectal cancer tissues were significantly higher than those in the normal-appearing mucosa in patients with colorectal cancer (P = 0.0016). The abundance of F. nucleatum in colorectal cancer tissues correlated with tumor size and KRAS mutation and was significantly associated with shorter overall survival times; this trend was notable in the patients with stage IV colorectal cancer. Focusing on normal-appearing mucosa in the patients with colorectal cancer, the F. nucleatum copy number was significantly higher in the patients with stage IV rather than stages I-III. CONCLUSION: These results suggest that determining F. nucleatum levels may help predict clinical outcomes in colorectal cancer patients. Further confirmatory studies using independent datasets are required to confirm our findings.


Subject(s)
Colorectal Neoplasms/microbiology , Fusobacterium Infections/complications , Fusobacterium nucleatum/isolation & purification , Aged , Case-Control Studies , Colorectal Neoplasms/genetics , Colorectal Neoplasms/pathology , Colorectal Neoplasms/surgery , DNA, Bacterial/analysis , Disease Progression , Female , Fusobacterium Infections/genetics , Fusobacterium Infections/microbiology , Fusobacterium nucleatum/genetics , Gene Dosage , Humans , Intestinal Mucosa/microbiology , Kaplan-Meier Estimate , Male , Middle Aged , Mutation , Neoplasm Staging , Prognosis , Proto-Oncogene Proteins p21(ras)/genetics
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