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Comment
. 2024 Jul 11;73(8):1400-1402.
doi: 10.1136/gutjnl-2023-331115.

FGF-21 analogues for treatment of non-alcoholic steatohepatitis and fibrosis: a meta-analysis with fragility index of phase 2 randomised placebo-controlled trials

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Comment

FGF-21 analogues for treatment of non-alcoholic steatohepatitis and fibrosis: a meta-analysis with fragility index of phase 2 randomised placebo-controlled trials

Alessandro Mantovani et al. Gut. .
No abstract available

Keywords: LIVER BIOPSY; META-ANALYSIS; NONALCOHOLIC STEATOHEPATITIS.

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Conflict of interest statement

Competing interests: HT is an associate editor of the journal and GT is an editorial board member of the journal.

Figures

Figure 1
Figure 1
Forest plots and pooled estimates of the effects of long-acting FGF-21 analogues on the histological resolution of NASH with no worsening of fibrosis ((A), n=3 RCTs6–8) or the improvement in fibrosis of one stage or more without worsening of NASH ((B), n=5 RCTs4–8) compared with placebo. The pooled and individual effect sizes for all RCTs are expressed as OR and 95% CIs, as estimated by both common-effects and random-effects models. For the active-comparator group (ie, participants using FGF-21 analogues), we calculated the individual effect sizes of each RCT by combining the treatment effect data of variable dosages of FGF-21 analogues into a single group (to avoid including individuals in the placebo group several times in the analysis). With regard to this, it is important to note that before combining the data of the active-comparator group for each RCT, we have previously tested in a multivariate meta-regression analysis that neither the different type nor the different dosage of FGF-21 analogue used in each RCT were significant predictors of the observed effects of this drug class on the histological liver endpoints. FGF-21, fibroblast growth factor-21; NASH, non-alcoholic steatohepatitis; RCT, non-alcoholic steatohepatitis.

Comment on

References

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