Pretreatment Nutrition-Inflammation Biomarkers Correlated with Differential Cytokine Profiles in Taiwanese Patients with Colorectal Cancer.

Systemic inflammation plays a pivotal role in colorectal cancer (CRC) development. Two hallmarks reflect the severity of inflammation—circulating cytokines and nutrition-inflammation biomarkers (NIBs); however, their interplay has not been fully investigated. In total, 128 CRC patients were included...

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Publicado en:Nutrition & Cancer Vol. 74; no. 5; pp. 1614 - 1625
Autores principales: Yu, Yen-Lin, Tseng, Wen-Ko, Fan, Chung-Wei, Chang, Pei-Hung, Kuo, Hsuan-Chih, Pan, Yi-Ping, Yeh, Kun-Yun
Formato: research tables/charts Journal Article
Publicado: Taylor & Francis Ltd 2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 2022
      vid: 74
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      pub: Taylor & Francis Ltd
      place: Philadelphia, Pennsylvania
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        10.1080/01635581.2021.1957130
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        atl: Pretreatment Nutrition-Inflammation Biomarkers Correlated with Differential Cytokine Profiles in Taiwanese Patients with Colorectal Cancer.
      aug:
        au:
          Yu, Yen-Lin
          Tseng, Wen-Ko
          Fan, Chung-Wei
          Chang, Pei-Hung
          Kuo, Hsuan-Chih
          Pan, Yi-Ping
          Yeh, Kun-Yun
        affil: Division of Colorectal Surgery, Department of Surgery, Chang Gung Memorial Hospital, Keelung, Taiwan
      sug:
        subj:
          Colorectal Neoplasms
          Cytokines Blood
          Inflammation
          Inflammation Mediators
          Biological Markers
          Human
          Taiwan
          Female
          Male
          Retrospective Design
          Cancer Patients
          Tumor Necrosis Factor Analysis
          Interleukins Analysis
          C-Reactive Protein
          Neutrophil Lymphocyte Ratio
          Transforming Growth Factor beta Analysis
          Medical Records
          Logistic Regression
          Body Mass Index
          Statistical Significance
          Cox Proportional Hazards Model
          Univariate Statistics
          Multivariate Analysis
          Correlation Coefficient
          Survival Analysis
          Descriptive Statistics
          Data Analysis Software
          Adolescence
          Young Adult
          Adult
          Middle Age
          Aged
          Aged, 80 and Over
          Funding Source
          Adolescent: 13-18 years
          Adult: 19-44 years
          Middle Aged: 45-64 years
          Aged: 65+ years
          Aged, 80 & over
          Female
          Male
      ab: Systemic inflammation plays a pivotal role in colorectal cancer (CRC) development. Two hallmarks reflect the severity of inflammation—circulating cytokines and nutrition-inflammation biomarkers (NIBs); however, their interplay has not been fully investigated. In total, 128 CRC patients were included. Ten circulating cytokines (TNF-α, TGF-β, IFN-γ, IL-1β, IL-4, IL-6, IL-10, IL-12, IL-13, and IL-23) and NIBs were analyzed. The relationship between cytokines, NIBs, clinicopathological variables, and overall survival (OS) was assessed using univariate and multivariate analyses. Three NIBs (CRP-to-albumin ratio [CAR]), neutrophil-to-lymphocyte ratio [NLR]), and prognostic nutritional index [PNI]) were associated with OS in univariate analysis; however, CAR was better for OS prediction in multivariate analysis (P = 0.015). None of the serum cytokines analyzed showed a significant association with OS. High CAR (≥0.25) and high IL-10 (≥76.6 pg/mL), high NLR (≥8.2) and high IL-23 (≥51.2 pg/mL), and high PNI (≥42.4) and high IL-1β (≥14.3 pg/mL) values were correlated. CAR, NLR, and PNI were not correlated with each other, whereas circulating cytokines were closely interrelated. High CAR was an independent predictor of poor OS in patients with CRC. Different NIBs have unique cytokine profiles, but show no correlation with each other. There is a close association among the circulating cytokines.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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