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Correspondence| Volume 53, ISSUE 7, P800, July 2021

Reply to: “Liver fibrosis and adverse outcomes in COVID-19”

  • Astrid Ruiz-Margáin
    Affiliations
    Department of Gastroenterology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

    Liver Fibrosis and Nutrition lab (LFN-Lab), Mexico City, Mexico

    MICTLÁN Network: mechanisms of liver injury, cell death and translational nutrition in liver diseases-research network
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  • Alejandro Campos-Murguía
    Affiliations
    Department of Gastroenterology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico
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  • José Alberto González-Regueiro
    Affiliations
    Department of Gastroenterology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico
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  • Berenice Monserrat Román-Calleja
    Affiliations
    Department of Gastroenterology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico
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  • Deyanira Kúsulas Delint
    Affiliations
    Department of Gastroenterology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

    Liver Fibrosis and Nutrition lab (LFN-Lab), Mexico City, Mexico

    MICTLÁN Network: mechanisms of liver injury, cell death and translational nutrition in liver diseases-research network
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  • Ricardo Ulises Macías-Rodríguez
    Correspondence
    Corresponding author at: Department of Gastroenterology, Liver Fibrosis and Nutrition lab, MICTLÁN Network, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga 15, Belisario Domínguez Sección XVI, Tlalpan, Mexico City 14080, Mexico.
    Affiliations
    Department of Gastroenterology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

    Liver Fibrosis and Nutrition lab (LFN-Lab), Mexico City, Mexico

    MICTLÁN Network: mechanisms of liver injury, cell death and translational nutrition in liver diseases-research network
    Search for articles by this author
Published:April 17, 2021DOI:https://doi.org/10.1016/j.dld.2021.04.001
      Dear Editor,
      We appreciate Dr. Jianmin Huang letter [
      • Huang J.
      J. Liver fibrosis and adverse outcomes in COVID-19.
      ] and interest in our work, as well as the important comments provided for our retrospective cohort study entitled “Liver fibrosis in patients with metabolic associated fatty liver disease is a risk factor for adverse outcomes in COVID-19” published in Digestive and Liver Disease.
      We agree with the comments made regarding descriptive data; in Table 2 we presented the data as mean ± SD, however it would certainly be more appropriate to use median for their description. Here we provide the median values for D-Dimer, CPK and troponins in patients with fatty liver in the group of no fibrosis vs fibrosis:
      Tabled 1
      No fibrosisFibrosisp value
      D-dimer595 (416–1011)640 (425–955)p = 0.970
      CPK127 (65–229)313 (101–611)p < 0.001
      Troponins4.2 (3.15–6.3)6.7 (5–12.5)p = 0.001
      We did find a change in troponin description, that was significantly different according to the presence of fibrosis. We performed the same multivariate analysis including troponins, however, this did not affect the conclusions nor the main findings mentioned in the paper, as liver fibrosis remained associated with poor prognosis (AKI, mechanical ventilation and mortality), independently of several biochemical markers, including troponins. In this cohort, troponins were also significantly associated with mortality, but not orotracheal intubation or acute kidney injury.
      With regards to the second comment, the main aim of our study was to evaluate the association between the presence of liver fibrosis evaluated by non-invasive scores in patients with fatty liver diagnosed by CT scan and clinical outcomes in patients admitted for COVID-19. Our study did not intend to attain new prognostic markers nor evaluate the performance of the different markers in patients with COVID-19, as would be adding AST/ALT ratio, in which case we would have used a different design. The reason why transaminases were not added to the models, was the fact that both ALT and AST are already present in the two used fibrosis scores, thus creating collinearity in the model, which would be unfitting.
      Finally, as Huang J referred, the severity of COVID-19 is associated with poor prognosis. Although COVID-19 can be classified into 4 subtypes (mild, moderate, severe, and critical) according to the World Health Organization, our cohort only included hospitalized patients, consequently, only severe and critical subtypes were included. Therefore, in our cohort, it is not feasible to evaluate liver fibrosis in the full spectrum of COVID-19. However, our analysis shows that patients with severe fibrosis measured by NFS/APRI score have a significant risk [OR: 2.59 (1.18–5.66)] to have a critical presentation of the disease, and therefore worse prognosis, compared with patients without severe fibrosis. And the proportion of patients with liver fibrosis was 35.6% in patients that required mechanical ventilation compared with 16.2% in those without mechanical ventilation (p = 0.006).
      We hope this information is able to address the questions raised and preclude misinterpretation of the study results.
      Sincerely,
      Astrid Ruiz-Margáin, Alejandro Campos-Murguía, José Alberto González-Regueiro, Berenice Monserrat Román-Calleja, Deyanira Kúsulas Delint, Ricardo Ulises Macías-Rodríguez.

      Declaration of Competing Interest

      The authors declare no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

      Financial disclosure

      This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

      Reference

        • Huang J.
        J. Liver fibrosis and adverse outcomes in COVID-19.
        Dig Liver Dis. 2021; 53: 799

      Linked Article

      • Liver fibrosis and adverse outcomes in COVID-19
        Digestive and Liver DiseaseVol. 53Issue 7
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          Recently, an interesting study entitled “Liver fibrosis in patients with metabolic associated fatty liver disease is a risk factor for adverse outcomes in COVID-19” was published in Digestive and Liver Disease [1]. In this retrospective cohort study, the authors explored the relationship between liver fibrosis and poor prognosis in patients with coronavirus disease (COVID-19). After controlling for potential confounding factors, the authors found that the presence of liver fibrosis was associated with higher mechanical ventilation, acute kidney injury (AKI), and mortality.
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