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Essential phospholipids reduced hepatic steatosis and improved HbA1c in patients with MASLD and type 2 diabetes over 6 months.

Essential phospholipids reduced hepatic steatosis and improved HbA1c in patients with MASLD and type…
Photo by Steve A Johnson / Unsplash
Key Takeaway
Consider essential phospholipids for reducing hepatic steatosis and improving HbA1c in patients with MASLD and type 2 diabetes.

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.

Study Details

Study typeRct
EvidenceLevel 2
PublishedMay 2026
View Original Abstract ↓
BACKGROUND AND AIMS: Metabolic dysfunction-associated steatotic liver disease (MASLD) poses a significant health burden and impacts quality of life (QoL). This study evaluates the effects of essential phospholipids (EPL) on liver steatosis, QoL, and other liver and metabolic parameters in patients with MASLD and associated comorbidities. METHODS: In this multicenter, double-blind, randomised, placebo-controlled phase 4 clinical trial, patients with MASLD and type 2 diabetes, hyperlipidemia, or obesity received either EPL or placebo, alongside standard of care. PRIMARY ENDPOINT: change in hepatic steatosis from baseline to 6 months (measured by Controlled Attenuation Parameter [CAP] score); secondary endpoints: changes in QoL (measured by the Chronic Liver Disease Questionnaire [CLDQ-MASLD]), symptom changes; other endpoints: other liver, metabolic, and lipid parameters, and safety. RESULTS: Of 193 randomised patients, 165 constituted the modified intention-to-treat population (median age: 56.5 years [EPL arm], 55.0 years [placebo arm]). More than ¾ of patients were obese and had CAP score ≥ 280 dB/m. At 6 months, EPL treatment significantly reduced CAP (p = 0.0269) versus placebo. This effect was evident at 3 months (p = 0.0049) and sustained until 3 months post treatment (p = 0.0234). QoL total score showed numerical improvement, with statistically significant improvement in fatigue subscore (p = 0.0229) with EPL versus placebo at 6 months. EPL significantly improved HbA1c levels (p = 0.0069) over 6 months. No safety concerns arose. CONCLUSIONS: The beneficial effects of EPL on hepatic steatosis, QoL and glycemic control, and its favourable safety profile make it a promising candidate for managing steatosis and enhancing overall liver health in MASLD patients with cardiometabolic risk. TRIAL REGISTRATION: The trial was registered in the EudraCT (2021-006069-39).
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