Essential phospholipids reduced hepatic steatosis and improved HbA1c in patients with MASLD and type 2 diabetes over 6 months.
This multicenter, randomised, placebo-controlled phase 4 clinical trial enrolled 193 randomised patients, with 165 included in the modified intention-to-treat population. Participants had metabolic dysfunction-associated steatotic liver disease, type 2 diabetes, hyperlipidemia, or obesity. The intervention group received essential phospholipids while the control group received placebo. Assessments occurred at baseline, 3 months, and 3 months post treatment, covering a total follow-up of 6 months.
The primary outcome measured the change in hepatic steatosis from baseline to 6 months using the Controlled Attenuation Parameter [CAP] score. EPL treatment significantly reduced CAP versus placebo at 3 months with a p value of 0.0049. At 3 months post treatment, CAP remained significantly reduced with a p value of 0.0234. At the 6-month endpoint, the reduction in CAP versus placebo was significant with a p value of 0.0269.
Secondary outcomes included quality of life, symptom changes, and metabolic parameters. EPL significantly improved HbA1c levels over 6 months with a p value of 0.0069. Fatigue subscores showed statistically significant improvement with EPL versus placebo, with a p value of 0.0229. Improvements in the QoL total score were noted, though specific p values were not reported for this metric.
Regarding safety, no safety concerns arose during the trial. Data on adverse events, serious adverse events, and discontinuations were not reported. The study was funded by an entity with conflicts of interest that were not reported. Given the observational nature of some secondary endpoints and the lack of reported absolute numbers, the clinical applicability remains to be fully established.