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Re: [GIWorld-Hepatitis] Ondansetron May Relieve Hepatitis C Fatigue

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  • avansi7465
    Well, Hallelujah!!!!!!!!! I speak to my doc about this next month. With that and Procrit, I might get through the next year without running (really crawling)
    Message 1 of 2 , Jul 26, 2005
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      Well, Hallelujah!!!!!!!!! I speak to my doc about this next month. With that and Procrit, I might get through the next year without running (really crawling) through the streets screaming (meowing, softly).....Thanks for the info Claudine. Anne

      -----Original Message-----
      From: claudine intexas <claudineintexas@...>
      Sent: Jul 26, 2005 7:33 PM
      To: giworld-hepatitis@yahoogroups.com,
      Web Warriors <HepCWebWarriors@yahoogroups.com>
      Subject: [GIWorld-Hepatitis] Ondansetron May Relieve Hepatitis C Fatigue


      Ondansetron May Relieve Hepatitis C Fatigue







      NEW YORK (Reuters Health) Jul 20 - The serotonin receptor antagonist ondansetron (Zofran) reduces depression and fatigue in patients with chronic hepatitis C, French researchers report in the August 5th issue of Gut.

      The fatigue associated with hepatitis C is believed to be associated with central dysfunction and altered opioid- and serotonin-mediated neuromodulation, Dr. T. Piche and colleagues observe. Because ondansetron has been shown to relieve fatigue in patients with chronic fatigue syndrome, the team theorized it would have similar clinical benefit in hepatitis C.

      Dr Piche of Hopital Archet, Nice and colleagues randomly assigned 18 patients to ondansetron 4 mg twice daily for 4 weeks and 18 to placebo. Fatigue was documented via the Fatigue Impact Scale questionnaire and depression with the Beck Depression Inventory (BDI).

      Ondansetron was associated with a 32.2% reduction in fatigue scores on day 15 and 37.8% on day 30. Corresponding reductions with placebo were 13.6% and 20.4%. Ondansetron continued to be associated with improvement on day 60 (31.5% reduction versus 5.8% reduction in the placebo group). Ondansetron was associated with significantly more relief of fatigue compared with placebo throughout the study period (p = 0.03).

      Findings were similar for depression, with 37.3%, 35.2% and 41.9% reductions in BDI scores in the ondansetron group and 17.3%, 20.4% and 5.8% in the placebo group on days 15, 30 and 60 (p > 0.05).

      Although puzzled by the prolonged effect of ondansetron beyond the treatment period, Dr. Piche and associates suggest that this effect could be related to sustained neuronal mechanisms, such as hippocampal neurogenesis.

      "Considering the negative impact of fatigue on quality of life and reduced adherence to antiviral therapy in infected patients," the authors conclude, "it is crucial to further confirm these data in large multicentre trials."

      In a related editorial, Dr. N. M Barnes, of the University of Birmingham comments that "Given the strong association of fatigue as a symptom of depressed patients, it would be pertinent to investigate whether the ondansetron-induced reduction in the two symptoms are interrelated."

      Gut 2005;54:1169-1173.





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