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    Home > Active Ingredient News > Immunology News > CDSR: Research on the treatment of tophi in patients with gout

    CDSR: Research on the treatment of tophi in patients with gout

    • Last Update: 2021-11-12
    • Source: Internet
    • Author: User
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    Gout is the most common inflammatory arthritis in men.
    In Western countries, at least 1% of the population will be affected by gout
    .


    It is characterized by the formation of monosodium urate crystals in joints and other tissues


    It is characterized by the formation of monosodium urate crystals in joints and other tissues


    Main results:

    We included a trial in our initial evaluation
    .


    We have added four trials (1796 participants) in this update


    Due to the lack of blinding information from participants and experimenters, the performance and risk of detection bias in the two trials are unclear
    .


    The risk of bias in all other trials is low


    Moderately certain evidence (downgraded due to imprecision; one study; 79 participants) showed: 1.
    Pegloticase infusion every two weeks (biweekly) group Results: ①Compared with placebo group, 21/52 Two participants in the pegloticase treatment group could dissolve tophi, while the placebo group was 2/27, (risk ratio (RR) 5.
    45, 95% confidence interval (CI) 1.
    38-21.
    54; compared with placebo group (41/43) )Compared; ②The proportion of subjects in the biweekly pegloticase treatment group (80/85) had similar adverse events (RR 0.
    99, 95% CI 0.
    91-1.
    07).
    ③Compared
    with the placebo group (1/43) Participants in the biweekly pegloticase treatment group (15/85) had a higher percentage of withdrawal due to adverse events (RR 7.


    59, 95% CI 1.


    Moderately certain evidence (2 studies; 103 participants) showed that compared with placebo plus purinol group (16/50), Lesinurad 200 mg plus allopurinol group (11/53) had complete targeted tophi There is no clinically significant difference in regression (RR 0.
    40, 95% CI 0.
    04 to 4.
    57); compared with the placebo + allopurinol group (16/50), the Lesinurad 400mg + allopurinol group (12/48) is clinically There was no significant difference in complete remission (RR 0.
    79, 95% CI 0.
    42 to 1.
    49), while placebo group and placebo + allopurinol group (RR 0.
    79, 95% CI 0.
    42 to 1.
    49) compared with the difference Not significant (RR 0.
    40, 95% CI 0.
    04 to 4.
    57)
    .

    An extended experiment investigated the combination of lesinurad 200mg or 400mg with febuxostat or placebo (low certainty evidence, downgraded due to indirectness and imprecision)
    .


    In the initial study, subjects continued to use the same dose of Lesinurad


    Participants who did not take Lesinurad in the original study were randomized (CROSS) to take 200mg or 400mg, both of which were used in combination with febuxostat
    .


    Low-certainty evidence reduced due to indirectness and imprecision suggests that lesinurad 400 mg (CROSS) may cause tophus dissolution (17/34) compared to lesinurad 200 mg (CROSS) (14/33) (RR 1.


    Table 1 Comparison of tophi in the treatment of gout with Pegloticase every two weeks (biweekly) and placebo

    Table 1 Comparison of tophi in the treatment of gout with Pegloticase every two weeks (biweekly) and placebo

    Table 2 Comparison of the effects of Lesinurad 200 mg + allopurinol and placebo + allopurinol in the treatment of gout

    Table 2 Comparison of the effects of Lesinurad 200 mg + allopurinol and placebo + allopurinol in the treatment of gout

    Table 3 Comparison of the effects of Lesinurad 400mg + allopurinol and placebo + allopurinol in the treatment of gout

    Table 3 Comparison of the effects of Lesinurad 400mg + allopurinol and placebo + allopurinol in the treatment of gout

    Table 4 Comparison of the effects of Lesinurad 400mg+febuxostat and Lesinurad 200mg+febuxostat in the treatment of gout

    Table 4 Comparison of the effects of Lesinurad 400mg+febuxostat and Lesinurad 200mg+febuxostat in the treatment of gout

    Conclusion: Moderately certain evidence suggests that pegloticase may be beneficial to the dissolution of tophi in gout
    .


    Although there was little difference in adverse events in the pegloticase group compared with placebo, and due to adverse events, more patients in the pegloticase group discontinued the drug


    Pegloticase may help to dissolve tophi in gout


    Sriranganathan MK, Vinik O, Pardo Pardo J,et al.
    Interventions for tophi in gout.
    Cochrane Database Syst Rev 2021 Aug 11;8

    Interventions for tophi in gout.
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