Evidence map›Paper›PMID 42507042›Full record

ArticleEuropean journal of pediatrics2026

The spatial heterogeneity of intra-pancreatic fat deposition in children and adolescents with obesity.

Hanfang Xiao, Huanhuan Zhang, Hong Yang, Tingting Li, Xiao Chen

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Article in European journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Hanfang Xiao *Department of Radiology, Shanghai Children's Hospital, Shanghai, 200062, China.
Huanhuan Zhang *Department of Radiology, Shanghai Children's Hospital, Shanghai, 200062, China.
Hong YangDepartment of Radiology, Shanghai Children's Hospital, Shanghai, 200062, China. yanghongyh@sjtu.edu.cn.
Tingting LiDepartment of Radiology, Shanghai Children's Hospital, Shanghai, 200062, China. litt@shchildren.com.cn.
Xiao ChenDepartment of Radiology, the Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, China.

Funding

Peak Talent Program of Jiangsu Provincial Hospital of Chinese Medicine k2026yrc25
6 · The paper itself

Abstract

Childhood obesity is associated with an increased risk of metabolic associated fatty liver disease (MAFLD) and intra-pancreatic fat deposition (IPFD). Recent studies in adults suggest that pancreatic fat distribution is heterogeneous and that fat deposition in different regions may have distinct metabolic implications. However, data on regional IPFD patterns and their association with insulin resistance in children with obesity remain limited. This study aimed to investigate the regional distribution of pancreatic fat and its association with insulin resistance in children and adolescents with obesity. This retrospective study included 231 children and adolescents with obesity (156 boys, 75 girls; age range 8-18 years). All participants underwent magnetic resonance imaging (MRI) using the qDixon technique to quantify fat fractions in the pancreatic head, body, and tail, as well as in the liver. Insulin resistance was assessed using the homeostasis model assessment of insulin resistance (HOMA-IR). Statistical analyses included Spearman correlations, logistic regression, and receiver operating characteristic (ROC) curve analysis. The prevalence of high IPFD was higher in the pancreatic head than in the body and tail across all cutoff values (> 10%, > 15%, and > 20%) in both sexes (p < 0.01). Pancreatic head fat, but not body or tail fat, was significantly correlated with insulin levels and HOMA-IR (p < 0.01). In logistic regression models adjusted for confounders, pancreatic head fat (as a continuous variable and with a > 20% cutoff) was independently associated with high insulin (odds ratio (OR) = 1.02, 95% confidence interval (CI):1.002-1.043, and OR = 2.10, 95%CI: 1.00-4.47) and insulin resistance (OR = 1.02, 95% CI: 1.002-1.044; and OR = 2.31, 95% CI: 1.13-4.78, respectively). ROC analysis showed that pancreatic head fat had a significantly higher area under the curve (AUC = 0.65) for predicting insulin resistance than body, tail and liver fat (AUC = 0.60)(p = 0.02). In children and adolescents with obesity, the deposition of pancreatic fat is heterogeneous, with the greatest accumulation observed in the pancreatic head. Fat in the pancreatic head is independently associated with high insulin resistance, whereas fat in the body and tail is not. What is Known? • Obesity is associated with an increased risk of intra-pancreatic fat deposition (IPFD). • IPFD may be associated with metabolic risk. What is New? • This is the first study reporting the spatial heterogeneity of IPFD in children and adolescents with obesity. • Fat accumulation in the pancreatic head, but no in body and tail is associated with high level of insulin resistance.

Indexed as

Adipose TissueInsulin ResistancePancreasPediatric ObesityAdolescentChildFemaleHumansLogistic ModelsMagnetic Resonance ImagingMaleRetrospective StudiesROC CurveChildren and adolescentsIntra-Pancreatic fat depositionObesitySpatial heterogeneity

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.