肝脏 ›› 2023, Vol. 28 ›› Issue (9): 1105-1109.

• 其他肝病 • 上一篇    下一篇

急性胰腺炎合并脂肪肝的CT特征及其对胰腺炎严重程度和持续性全身炎症反应综合征的影响

孙刚, 许磊磊, 谢慧   

  1. 215129 江苏 苏州高新区人民医院放射科(孙刚,谢慧);无锡市第五人民医院影像科(许磊磊)
  • 收稿日期:2023-05-07 出版日期:2023-09-30 发布日期:2023-10-24
  • 通讯作者: 谢慧,Email:sky_xiehui@163.com
  • 基金资助:
    苏州高新区人民医院科学创新基金面上项目(SGY2023B03)

Impact of fatty liver on acute pancreatitis severity and persistence of systemic inflammatory response syndrome: a CT imaging study

SUN Gang1, XU Lei-lei2, XIE Hui1   

  1. 1. Department of Radiological, Suzhou High-tech Zone People's Hospital, Jiangsu 215129, China;
    2. Department of Imaging, Wuxi No.5 People's Hospital, Jiangsu 214007, China
  • Received:2023-05-07 Online:2023-09-30 Published:2023-10-24
  • Contact: XIE Hui,Email:sky_xiehui@163.com

摘要: 目的 探讨急性胰腺炎(AP)合并脂肪肝的CT特征及脂肪肝对AP严重程度和持续性全身炎症反应综合征(SIRS)的影响。方法 选取2019年1月至2022年3月入院诊治AP患者102例,根据是否存在脂肪肝将患者分为脂肪肝组53例和非脂肪肝组49例,根据是否发生持续性SIRS将患者分为持续性SIRS组45例和非持续性SIRS组57例。比较患者临床特征、AP严重程度、持续性SIRS情况,进行持续性SIRS危险因素的多变量分析,并分析脂肪肝、APACHE Ⅱ评分和MCTSI评分对持续性SIRS的预测价值。结果 脂肪肝组酗酒、高脂血症、发生胰腺坏死及发生局部并发症的比例分别为9.4%、39.6%、24.5%和49.1%,高于非脂肪肝组的0、18.4%、8.2%和28.6%(P<0.05),而特发性胰腺炎的比例为20.8%,低于非脂肪肝组的46.9%(P<0.05)。脂肪肝组患者中度AP、重度AP、APACHE Ⅱ评分、MCTSI评分及持续性SIRS分别为34.0%、22.6%、6.2±3.8、4.9±1.9和58.5%,高于非脂肪肝组患者的26.5%、8.2%、5.0±3.0、4.0±2.2和26.5%(P<0.05),而轻度AP为43.4%,低于非脂肪肝组的65.3%(P<0.05)。持续性SIRS组高脂血症、C反应蛋白、TG、发生胰腺坏死及局部并发症分别为42.2%、91.2(1.8,357.0)mg/dL、(5.2±0.8)mg/dL、33.3%和64.4%,高于非持续性SIRS组的15.8%、26.9(0.2,308.2)mg/dL 、(2.2±0.7)mg/dL 、3.5%和17.5%(P<0.05),而胆石症为24.4%,低于非持续性SIRS组的49.1%(P<0.05)。持续性SIRS组患者中度AP、重度AP、APACHE Ⅱ评分及MCTSI评分分别为40.0%、33.3%、7.1±3.7和5.7±1.9,高于非持续性SIRS组的22.8%、1.8%、4.5±2.7和3.5±1.8(P<0.05),而轻度AP为26.7%,低于非持续性SIRS组的75.4%(P<0.05)。持续性SIRS危险因素分析可知,脂肪肝、APACHE Ⅱ评分≥6分、MCTSI评分≥4分是AP患者发生持续性SIRS的独立危险因素。脂肪肝预测持续性SIRS的AUC为0.663,灵敏度为0.673,特异度为0.644;APACHE Ⅱ≥6分预测持续性SIRS的AUC为0.701,灵敏度为0.503,特异度为0.781;MCTSI ≥4分预测持续性SIRS的AUC为0.782,灵敏度为0.676,特异度为0.792。结论 患有脂肪肝的AP患者在CT上更容易出现胰腺坏死和局部并发症,并容易发生更严重的AP和持续性SIRS,可作为预测AP患者是否发生持续性SIRS的独立危险因素。

关键词: 急性胰腺炎, 脂肪肝, 全身炎症反应综合征

Abstract: Objective To investigate the CT characteristics of acute pancreatitis (AP) in the context of preexisting fatty liver (FL) and to assess the influence of FL on AP severity and the persistence of systemic inflammatory response syndrome (SIRS).Methods Between January 2019 and March 2022, 102 patients diagnosed with AP were hospitalized and categorized into two distinct cohorts based on the presence or absence of fatty liver. Concurrently, these patients were stratified into groups experiencing either persistent SIRS or non-persistent SIRS. Comparative analyses were conducted to evaluate variations in clinical characteristics, AP severity, and the incidence of persistent SIRS between the cohorts. Employing multivariate analysis techniques, we identified salient risk factors associated with the onset persistent SIRS. Furthermore the predictive validity of fatty liver presence, APACHE II scores and MCTSI scores in forecasting persistent SIRS was rigorously examined. Results Our comparative analyses revealed significant differences in the clinical characteristics beween the fatty liver group and non-fatty liver cohorts. The fatty liver group exhibited higher incidences of alcoholism(9.4% vs. 0.04%), hyperlipidemia(39.6% vs. 18.4%), pancreatic necrosis(24.5% vs. 8.2%), and local complications(49.1% vs. 28.6%), all of which were statistically significant(P<0.05). Conversely, the incidence of idiopathic pancreatitis was considerably lower in the fatty liver group(20.8% vs. 46.9%, P<0.05). In terms of AP severity, the fatty liver group demonstrated significantly elevated rates of moderate and severe AP at 34.0% and 22.6%, respectively, compared to 26.5% and 8.2% in the non-fatty liver group(P<0.05). Similarly, the incidence of persistent SIRS was notably higher in the fatty liver group at 58.5%, as opposed to 26.5% in the non-fatty liver group(P<0.05). Additionally, mean APACHE II scores(6.26±3.84 vs. 5.0±3.0) and MCTSI scores(4.93±1.98 vs. 4.0±2.2) were significantly higher in the fatty liver cohort(P<0.05). Conversely, the proportion of mild AP cases was significantly 43.4% as opposed to 65.3% in the non-fatty liver group(P<0.05). Patients in the persistent SIRS cohort exhibited markedly elevated incidences of hyperlipidemia(42.2% vs. 15.8%), C-reactive protein level(91.2 [1.8, 357.0] mg/dL vs. 26.9 [0.2, 308.2]mg/dL), TG levels(5.2±0.8mg/dL vs. 2.2±0.7 mg/dL), pancreatic necrosis(33.3% vs. 3.5%), and local complications(64.4%, vs. 17.5%), all of which were statistically significant(P<0.05). The incidence of cholelithiasis was significantly lower in th persistent SIRS group, measured at 24.4% in contrast to 49.% in the non-persistent SIRS cohort(P<0.05). In comparing the severity of AP between the persistent SIRS group and non-persistent SIRS group, the persistent SIRS group exhibited a higher proportion of moderate(40.0% ) and severe AP(33.3%), along with elevated APACHE II scores(7.1±3.7) and MCTSI scores(5.7±1.9). These metrics were significantly higher than those in the non-persistent SIRS group, where the proportions of moderate and sever AP were 22.8% and 1.8%, and APACHE II and MCTSL scores were 4.5±2.7 and 3.5±1.8, respectively. Conversely, the proportion of mild AP cases in the persistent SIRS group was 26.7%, significantly lower than the 75.4% observed in the non-persistent SIRS group(P<0.05). Multivariate analysis identified fatty liver, an APACHE II score≥6 and an MCTSI score≥4 as independent risk factors for persistent SIRS in patients with AP. Upon evaluating the predictive value of theses factors for persistent SIRS, the flollowing results were obtained: For fatty liver, the AUC was 0.663, with a sensitivity of 0.673 and a specificity of 0.644. For an APACHE II score ≥6, the AUC was 0.701, with a sensitivity of 0.503 and a tspecificity of 0.781. For an MCTSI score ≥4,the AUC was 0.782, with a sensitivity of 0.676 and a specificity of 0.792. Conclusion Patients with preexisting FL are found to be more susceptible to developing necrosis and local complications, as evidence by CT scans. Additionally, these patients were more likely to exhibit severe AP and persistent SIRS. Importantly, preexisting FL is identified as an independent risk factor in predicting the presence of persistent SIRS in individuals with AP.

Key words: Acute pancreatitis, Fatty liver, Systemic inflammatory response syndrome