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Brain & Heart                                                       Pemafibrate in patients with dyslipidemia



            3.2. Pooled analysis of all studies                P < 0.00001; I² = 93%) (Figure  2). Within the group

            The primary outcome of interest was the percent reduction   receiving pemafibrate, there was an overall trend toward
            in total TG, which exhibited a significant improvement   an increased percent of HDL (MD: 13.84; 95% CI: 8.09
            in  the  pemafibrate  group  when  compared  with  placebo   – 19.59; P < 0.00001; I² = 95%) (Figure 3). Conversely, in
            across all doses (MD: −45.65; 95% CI: −57.31 – −33.98;   the placebo group, a significant decrease in LDL levels was
                                                               observed (MD: 11.82; 95% CI: 8.61 – 15.04; P < 0.00001;
                                                               I² = 57%) (Figure  4). However, there was no significant
                                                               difference in the percent of TC between patients who
                                                               received the placebo compared with those treated with all
                                                               doses of pemafibrate (MD: −1.74; 95% CI: −3.98 – 0.49;
                                                               P < 0.13; I² = 73%) (Figure 5).

                                                               3.3. Subanalysis of selected populations
                                                               In a subanalysis of patients treated with 0.4  mg/day of
                                                               pemafibrate versus placebo, the pemafibrate group exhibited
                                                               a higher percent of the decrease in serum TG (MD: −48.29;
                                                               95% CI: −61.45 – −35.13; P < 0.0001; I² = 93%) (Figure 6).
                                                               Furthermore, individuals receiving a daily dosage of 0.4 mg
                                                               of pemafibrate experienced a significant reduction in non-
                                                               HDL levels compared to the placebo group (MD: −6.35;
                                                               95% CI: −10.62 – −2.08; P = 0.004; I² = 82%) (Figure 7).
                                                               Placebo recipients had significantly lower LDL levels than
                                                               those treated with pemafibrate 0.4  mg/day (MD: 12.86;
                                                               95% CI: 9.43 – 16.29; P < 0.00001; I² = 40%) (Figure 8).
                                                               The pemafibrate group at the 0.4 mg/day dose exhibited a
                                                               significant increase in HDL levels (MD: 13.66; 95% CI: 8.06
                                                               – 19.27; P < 0.00001; I² = 92%) (Figure 9). No significant
                                                               differences were observed for adverse events (MD: 0.97;
                                                               95% CI: 0.73 – 1.29; P = 0.84; I² = 0%) (Figure 10) and TC
                                                               levels (MD: −1.73; 95% CI: −4.14 – 0.68; P = 0.16; I² = 65%)
            Figure 1. PRISMA flow diagram of study screening and selection.  (Figure 11).















            Figure 2. Significant reduction in total triglycerides within the pemafibrate group across all doses.













            Figure 3. Significant increase in high-density lipoprotein within the pemafibrate group across all doses.


            Volume 1 Issue 2 (2023)                         5                         https://doi.org/10.36922/bh.1629
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