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and lymphocytic mtDNA deletions; however, this correlation did not reach statistical
          significance.
          Also, the median survival time for HCC patients with high mtDNA deletions (ΔCt ≥3.9)
          was significantly shorter (5.7+ 0.6 months) than those patients with low mtDNA deletions
          frequency (11.9+ 0.04 months) (fig.).

          Conclusions: This is the first study to our knowledge that explored mtDNA deletions
          and folate status in Egyptian patients with HCV related HCC and is the first to evaluate
          mtDNA deletions as a diagnostic marker for HCC at a cutoff value of 2.65 (ΔCt) with
          a sensitivity of 82% and a specificity of 60%. Our findings implied a causal relationship
          between folate deficiency and mtDNA deletions frequency among Egyptian patients with
          HCC. Moreover, mtDNA deletions correlated with the clinic-pathological features and
          poor survival in HCC patients.

          Figure:





        ePOSTER ABSTRACTS




























          Disclosure of Interest: None Declared



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