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Open AccessVollständige AnalyseJun 16, 2026

Probiotic L. plantarum ECGC 13110402 combined with plant sterols in hypercholesterolaemic coeliac adults: a randomised controlled pilot trial

Combined supplementation with L. plantarum ECGC 13110402 and plant sterols favoured LDL-cholesterol reduction and gut microbiota changes in hypercholesterolaemic coeliac adults versus placebo, but the small sample size precludes definitive conclusions.

The question (PICO)
PopulationAdults aged 18–65 years with confirmed coeliac disease, strict gluten-free diet adherence, total cholesterol > 6 mmol/L, and fasting glucose 5.6–6.9 mmol/L
InterventionBilayer tablet: L. plantarum ECGC 13110402 (2×10⁹ CFU/tablet, 50 mg) + plant sterols/stanols (400 mg), twice daily with meals for 9 weeks
VergleichIdentical-appearance placebo, same dosing regimen
EndpunktSerum lipid profile (LDL, HDL, total cholesterol, triglycerides), gut microbiota diversity and composition (16S rRNA), safety and tolerability markers
CEvidenz
Studie
Randomized controlled trial
Effekt
Günstig
Dauer
9 Wochen

Kontext

Coeliac adults on a gluten-free diet face elevated cardiometabolic risk, including dyslipidaemia, with no prior evidence base for probiotic-based cholesterol-lowering strategies in this population. The combination of a bile salt hydrolase-active probiotic and intestinal cholesterol-absorption-blocking plant sterols targets two distinct mechanistic pathways. This pilot addresses a recognised evidence gap.

Was die Studie zeigte

The active group showed a favourable direction of change in LDL-cholesterol at week 9 compared to placebo, alongside gut microbiota compositional shifts. Absolute numbers, relative changes, and 95% confidence intervals are not fully reported in the available text excerpt, preventing precise quantification. No serious adverse events were recorded. The 3-week washout did not allow assessment of effect persistence.

Wie es durchgeführt wurde

Single-centre, randomised, double-blind, placebo-controlled pilot trial conducted at AOU Ruggi d'Aragona, Salerno, Italy. Participants stratified by sex and allocated 1:1 using an independent random number generator. Total duration 12 weeks (9-week intervention + 3-week washout). Assessments at baseline, week 5, week 9, and week 12.

Effektgröße

Specific effect sizes (RR, OR, MD, or SMD with 95% CI) are not reported in the available text; the pilot design was not powered for definitive efficacy endpoints, rendering clinical magnitude uncertain.

Einschränkungen

Very small sample size (pilot) precludes population-level inference; absence of full 95% CI and effect-size data undermines GRADE evaluation. Single-centre design (Salerno, Italy) limits generalisability. RoB 2 risk-of-bias assessment was not formally applied by authors. Absence of strict dietary control may introduce confounding. The 3-week washout period is insufficient to evaluate durability of lipid and microbiota effects.

In der klinischen Praxis

Insufficient evidence exists to recommend this combination as a standard strategy for coeliac adults with dyslipidaemia. Clinicians may regard this as a preliminary safety and tolerability signal, pending adequately powered trials. Standalone plant sterols (1.5–3 g/day reducing LDL by 7–12%) retain established non-pharmacological support and can be considered within current lipid management frameworks.

Was noch fehlt

An adequately powered, multicentre RCT with validated cardiovascular endpoints in coeliac adults is required to confirm the efficacy and long-term safety of this combination.

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