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36                        Gonda et al. | Journal of Clinical and Translational Research 2024; 10(1): 33-51
        significantly decreased (P < 0.05). D-dimer decreased significantly   The  IgA  level  at  admission  in  the  uninfected  group  was
        on day 14 after admission (P < 0.05), and CRP was significantly   significantly  higher  than  the  IgA  level  on  day  5  in  both  the
        elevated (P < 0.05).                                    molnupiravir alone group and the molnupiravir plus CAM group
          In the molnupiravir plus CAM group, there were no significant   (P < 0.05).
        differences in any of the biomarkers between admission and day 5.   The  sIL2R  level  at  admission  in  the  uninfected  group  was
        In addition, the values of D-dimer decreased significantly on day   significantly  lower  than  the  sIL2R  level  on  day  5  in  both  the
        14 after admission (P < 0.05).                          molnupiravir alone group and the molnupiravir plus CAM group
          In the uninfected group, no significant differences in biomarkers   (P < 0.05).
        were  observed  before  infection,  on  day  5,  and  on  day  14. The   In the molnupiravir plus CAM group, the IgA level on day 14
        values of biomarkers, except for BNP, were within normal limits   was significantly higher than that on day 5, and the sIL2R level
        (Figure 2 and Supplementary Data 2).                    on day 14 was significantly lower than that on day 5 (P < 0.05).
                                                                   In the molnupiravir plus CAM group, the IgA level on day
        3.3. Dynamics of IgG, IgA, IgM, and sIl2R in advanced stages   14 was significantly higher (P < 0.05) and the sIL2R level was
        of disease in molnupiravir alone group, molnupiravir plus   significantly  lower  (P <  0.05) than  in  the  molnupiravir  alone
        clarithromycin group, and uninfected group
                                                                group. The values of IgG and IgM were within the normal limit.
          We measured baseline levels of immunological biomarkers on   3.4. Predictive factors as blood biomarker in molnupiravir alone
        days 5 and 14 from the start of oral administration at the time of   group and molnupiravir plus clarithromycin group
        infection in the molnupiravir alone group and the molnupiravir
        plus CAM group and on the day of admission in the uninfected   Multivariate  logistic  regression  analysis  based  on  the
        group (Figure 3 and Supplementary Data 3).              collection  and  analysis  of  clinical  and  laboratory  data  for  the







































        Figure 2. Time-series dynamics of blood biomarkers in the molnupiravir alone group, the molnupiravir plus clarithromycin (CAM) group, and the
        uninfected group. The molnupiravir plus CAM group had lower or higher values than the molnupiravir alone group and were close to the values of the
        uninfected group. The vertical axis indicates the value of each biomarker, while the horizontal axis indicates before infection, 5  days and 14  days
                                                                                                             th
                                                                                                   th
        after administration of molnupiravir. Red squares and dashed lines indicate molnupiravir; blue triangles and dotted lines indicate molnupiravir + CAM;
        black diamonds and bar-shaped line indicate no infection; double-headed arrow indicates within normal limits. *P < 0.05, **P < 0.05.
        Abbreviations: LDH: Lactate dehydrogenase, WBC: White blood cells, Hb: Hemoglobin, PLT: Platelet, CRP: C-reacted protein, NLR: Neutron–
        lymphocyte ratio, FDP: Fibrin degradation product, PT-INR: Prothrombin time–International Normalized Ratio, CPK: Creatinine phosphor kinase,
        BNP: Brain natriuretic peptide.
                                                  DOI: https://doi.org/10.36922/jctr.00075
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