Journal of Hebei Medical University ›› 2024, Vol. 45 ›› Issue (2): 147-152.doi: 10.3969/j.issn.1007-3205.2024.02.005

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The relationship between FGF21, PERK and APACHE Ⅱ score in patients with mild acute pancreatitis and the risk assessment of disease progression

  

  1. Department of Gastroenterology, the Affiliated Hospital of Non-Commissioned Officer School, Army Medical University, Hebei Province, Shijiazhuang 050000, China

  • Online:2024-02-25 Published:2024-02-06

Abstract: Objective To investigate the relationship between fibroblast growth factor-21 (FGF-21), protein kinase R-like endoplasmic reticulum kinase (PERK) and acute physiology and chronic health system Ⅱ (APACHE Ⅱ) score in patients with mild acute pancreatitis (MAP), and to analyze the value of the two in evaluating the risk of disease progression after conservative treatment. 
Methods A total of 169 patients with MAP were selected and divided into a progression group (n=32) and a non-progression group (n=137) according to whether they progressed to moderately severe AP (MSAP) or severe AP (SAP) within 24 h after admission.The serum FGF-21 and PERK levels were detected at admission and 24 h after admission, and the APACHE II score was evaluated. The relationship between serum FGF-21 and PERK levels and APACHE Ⅱ score and their effects on disease progression were analyzed. Receiver operating characteristic curve (ROC) and decision curve analysis (DCA) were used to evaluate the value of serum FGF-21 and PERK in the progression of MAP patients. 
Results The levels of serum FGF-21 [(2.37±0.33) vs. (2.05±0.31),(2.57±0.36) vs. (1.89±0.32)ng/L], PERK[(24.68±4.35) vs. (20.43±4.08), (27.19±4.54) vs. (17.81±4.03)μg/L] and APACHE Ⅱ score [(12.54±2.62) vs. (9.87±2.58), (13.94±2.54) vs. (8.45±2.29)] in the progression group at admission and 24 h after admission were higher than those in the non-progression group (t=5.194, 10.566, 5.239, 11.569, 5.256,  11.958, P<0.001). The levels of serum FGF-21, PERK and APACHE Ⅱ score in the progression group at 24 h after admission were higher than those at admission, while these indicators in the non-progression group were lower than those at admission (P<0.05). The serum FGF-21 (r=0.872, 0.445, P<0.001) and PERK (r=0.852,0.372, P<0.001) levels were positively correlated with the APACHE Ⅱ score at admission and 24 h after admission (P<0.05). Logistic regression analysis model showed that FGF-21 and PERK were independent risk factors for disease progression (P<0.05). The area under the ROC curve (AUC) value of the combined assessment of FGF-21 and PERK for disease progression was 0.872, which was greater than that of FGF-21 (χ2=2.746, P=0.006) and PERK alone (χ2=2.784, P=0.005). Within the threshold range of 0.10 to 0.88, the net benefit rate of FGF-21 and PERK in combination to assess disease progression was superior to that of single detection. 
Conclusion The changes of serum FGF-21 and PERK levels in MAP patients are closely related to the APACHE Ⅱ score, and they are independent risk factors for the progression of MAP. They can provide a reference for clinical assessment of the risk of MAP progression.


Key words: pancreatitis, fibroblast growth factors 21, protein kinases