# Etiological shifts and clinical outcomes of acute pancreatitis between urban and rural areas: evidence from a 20-year retrospective database

**Authors:** Ximei Cao, Zide Liu, Jingwen Rao, Jie Wu, Xin Huang, Liang Xia, Lingyu Luo, Xu Shu, Yin Zhu, Nonghua Lu, Wenhua He

PMC · DOI: 10.3389/fmed.2025.1640267 · Frontiers in Medicine · 2025-07-17

## TL;DR

This study shows urban and rural areas have different causes and outcomes for acute pancreatitis, with urban areas seeing more hypertriglyceridemia cases and rural areas facing more severe outcomes.

## Contribution

The study provides new insights into urban–rural disparities in acute pancreatitis etiology and outcomes using a 20-year retrospective database.

## Key findings

- Urban areas showed a higher rise in hypertriglyceridemia-induced AP compared to rural areas.
- Rural patients had longer symptom-to-admission intervals and more severe AP outcomes.
- Both urban and rural groups experienced accelerated growth in hypertriglyceridemia-induced AP after 2020.

## Abstract

Acute pancreatitis (AP) is a well-recognized digestive emergency with established clinical significance. However, current evidence regarding urban–rural distribution patterns of AP patients remains relatively limited. Through large-scale data analysis, this study aims to provide preliminary epidemiological references for this understudied area.

This 20-year retrospective cohort study (2005–2024) analyzed 12,214 acute pancreatitis (AP) cases from a tertiary medical center to investigate urban–rural disparities in etiology and clinical outcomes. Patients were stratified into urban (n = 5,002) and rural (n = 7,212) groups based on residential location. We compared demographic characteristics, etiological distributions, disease severity, complications, and hospitalization outcomes between the groups. Risk factors for moderate-to-severe AP were assessed using multivariable logistic regression, with adjustment for demographic, clinical, and temporal covariates.

Urban patients exhibited a rising burden of hypertriglyceridemia-induced AP (HTG-AP; 30.6% vs. rural 26.3%, p < 0.001), surpassing biliary AP as the dominant etiology by 2023, while rural populations maintained higher biliary AP prevalence (56.4% vs. 51.7%, p < 0.001). Rural patients demonstrated prolonged symptom-to-admission intervals (median 3 vs. 2 days), elevated APACHE II scores (8 vs. 7), and increased severe AP incidence (20.7% vs. 18.3%, p < 0.01), with higher risks of infected pancreatic necrosis (5.3% vs. 4.3%) and abdominal compartment syndrome (1.7% vs. 1.1%). Multivariable analysis suggested that rural group may be associated with increased risk of moderate-to-severe AP (aOR = 1.13, p = 0.005), alongside hypertriglyceridemia (aOR = 2.06) and delayed admission (aOR = 1.01/day). Temporal trends revealed accelerated HTG-AP growth post-2020 in both groups, paralleling metabolic syndrome escalation.

These findings underscore the imperative for dual interventions: urban-focused metabolic risk mitigation and rural-targeted biliary disease management, informed by evolving etiological landscapes.

## Linked entities

- **Diseases:** acute pancreatitis (MONDO:0006515), metabolic syndrome (MONDO:0000816)

## Full-text entities

- **Diseases:** gallstone (MESH:D042882), COVID-19 (MESH:D000086382), autoimmune (MESH:D001327), HTG (MESH:D015228), alcoholic (MESH:D000437), acute respiratory failure (MESH:D012131), pancreatic cancer (MESH:D010190), periampullary diverticulum (MESH:D004240), biliary stones (MESH:D002137), hyperlipidemia (MESH:D006949), hypertension (MESH:D006973), circulatory failure (MESH:D012769), SAP (MESH:D045169), papillary sphincter dysfunction (MESH:D002291), biliary disease (MESH:D001660), Acute (MESH:D000208), Alcoholic AP (MESH:D010195), coronary heart disease (MESH:D003327), cerebral infarction (MESH:D002544), metabolic syndrome (MESH:D024821), compartment syndrome (MESH:D003161), abdominal compartment syndrome (MESH:D059325), fever (MESH:D005334), diabetes (MESH:D003920), septic shock (MESH:D012772), acute kidney injury (MESH:D058186), enteric fistula (MESH:D004751), gallstone disease (MESH:D002769), thrombotic (MESH:D013927), chronic renal failure (MESH:D007676), ampullary cancer (MESH:D009369), metabolic diseases (MESH:D008659), multiple organ failure (MESH:D009102), infected (MESH:D007239), heart failure (MESH:D006333), cirrhosis (MESH:D005355), parapapillary diverticulum of duodenum (MESH:D004379), COPD (MESH:D029424), infected pancreatic necrosis (MESH:D019283)
- **Chemicals:** carbohydrate (MESH:D002241), alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12310655/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12310655/full.md

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Source: https://tomesphere.com/paper/PMC12310655