Key result
Pemafibrate fails to improve blood rheology or leukocyte activity despite robust triglyceride lowering.
Why the study?
High serum triglyceride and free fatty acid levels exacerbate hemorheology and increase cardiovascular risk, but the effects of pemafibrate on hemorheology were unexplored.
Does pemafibrate improve whole blood transit time and leukocyte activity in patients with type 2 diabetes or metabolic syndrome complicated by hypertriglyceridemia?
Cohort (n=96)
No
Does pemafibrate improve whole blood transit time and leukocyte activity in patients with type 2 diabetes or metabolic syndrome complicated by hypertriglyceridemia?
Pemafibrate effectively lowers triglycerides and remnant lipoproteins but does not appear to improve ex vivo measures of blood rheology or microcirculation in patients with diabetes or metabolic syndrome.
No rheology benefit despite TG reduction in diabetes; leaves open microcirculatory effects and requires RCT confirmation.
Persistent high serum triglyceride (TG) and free fatty acid (FFA) levels, which are common in metabolic syndrome and type 2 diabetes, are risk factors for cardiovascular events because of exacerbated hemorheology. To explore the effects of pemafibrate, a selective peroxisome proliferator-activated receptor alpha modulator, on hemorheology, we performed a single-center, nonrandomized, controlled study in patients with type 2 diabetes (HbA1c 6–10%) or metabolic syndrome, with fasting TG levels of ≥ 150 mg/dL and a whole blood transit time of > 45 s on a microarray channel flow analyzer (MCFAN). Patients were divided into a study group, receiving 0.2 mg/day of pemafibrate (n = 50) for 16 weeks, and a non-pemafibrate control group (n = 46). Blood samples were drawn 8 and 16 weeks after entry to the study to evaluate whole blood transit time as a hemorheological parameter, leukocyte activity by MCFAN, and serum FFA levels. No serious adverse events were observed in either of the groups. After 16 weeks, the pemafibrate group showed a 38.6% reduction in triglycerides and a 50.7% reduction in remnant lipoproteins. Pemafibrate treatment did not significantly improve whole blood rheology or leukocyte activity in patients with type 2 diabetes mellitus or metabolic syndrome complicated by hypertriglyceridemia and exacerbated hemorheology.
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Iwakura et al. (2023) conducted a cohort in Type 2 diabetes or metabolic syndrome with hypertriglyceridemia (n=96). Pemafibrate vs. Non-pemafibrate control was evaluated on Whole blood transit time and leukocyte activity. Pemafibrate for 16 weeks did not significantly improve whole blood rheology or leukocyte activity despite a 38.6% reduction in triglycerides in patients with diabetes or metabolic syndrome.
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