This systematic review and meta-analysis pooled data from 11 observational studies involving 21,438 adults diagnosed with metabolic dysfunction-associated steatotic liver disease (MASLD). The analysis examined the prevalence and clinical characteristics of fatty pancreas disease (FPD) in this population, comparing those with FPD to those without FPD.
The pooled prevalence of FPD among patients with MASLD was 54.32% (95% CI 34.53 to 72.83). Significant regional variation was observed, with a prevalence of 35.59% in Asian studies and 75.05% in non-Asian studies (p=0.01). Patients with MASLD and concurrent FPD were characterized as older, having a higher body mass index, and having a greater likelihood of diabetes, hypertension, and metabolic syndrome compared to MASLD patients without FPD. Safety and tolerability data were not reported.
A key limitation is the exceptionally high statistical heterogeneity among the included studies (I²=99.6%), which significantly reduces confidence in the pooled estimate. The evidence is purely observational, establishing association only, not causation. The prognostic or therapeutic relevance of FPD in MASLD management is not established. For practice, clinicians should recognize that FPD is a common concurrent finding in MASLD, particularly in patients with more advanced metabolic comorbidities, but the clinical implications of this association remain unclear.
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BACKGROUND AND AIMS: Fatty pancreas disease (FPD), characterized by excessive intrapancreatic fat deposition (IPFD), is increasingly recognized as a manifestation of metabolic dysfunction. However, its epidemiology and clinical impact in patients with metabolic dysfunction-associated steatotic liver disease (MASLD) remain unclear. We conducted a systematic review and meta-analysis to quantify the prevalence of FPD in MASLD and to compare clinical characteristics between patients with and without FPD.
METHODS: A comprehensive search of the PubMed and Embase databases was conducted from inception to November 29, 2025, to identify observational studies reporting the prevalence and/or clinical impact of FPD in adults with MASLD. Pooled prevalence estimates were calculated using a generalized linear mixed model, and clinical features were compared using random-effects models.
RESULTS: We identified 11 studies (n = 21 438 patients). The pooled prevalence of FPD in MASLD was 54.32% (95% CI 34.53 to 72.83), with high heterogeneity (I = 99.6%). FPD prevalence was significantly lower in Asian studies (35.59%) than in non-Asian studies (75.05%) (p = 0.01). No differences in FPD prevalence were found when stratified by sample size, MASLD diagnosis, or IPFD assessment method. Patients with MASLD and FPD were found to be older, had a higher body mass index, and were more likely to have diabetes, hypertension, and metabolic syndrome.
CONCLUSIONS: Around half of patients with MASLD have concomitant FPD, which is associated with an adverse cardiometabolic phenotype. These findings support the need for integrated, longitudinal evidence to define the prognostic and therapeutic relevance of IPFD within a multiorgan ectopic fat framework of systemic metabolic dysfunction.