The relationship between inflammatory cytokines and in‐hospital complications of acute pancreatitis

Objective Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute pancreatitis. This study aimed to investigate the relationship between 12 serum cytokines and the early complications and severity of acute p...

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Published inImmunity, Inflammation and Disease Vol. 12; no. 2; pp. e1203 - n/a
Main Authors Yao, Jiaxin, Zhang, Shuangshuang, Zhou, Fei, Zhuang, Mengting, Fei, Sujuan
Format Journal Article
LanguageEnglish
Published England John Wiley & Sons, Inc 01.02.2024
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Abstract Objective Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute pancreatitis. This study aimed to investigate the relationship between 12 serum cytokines and the early complications and severity of acute pancreatitis (AP). Methods We retrospectively analyzed the clinical data of 307 patients with AP, and divided them into severe group and mild‐to‐moderate group according to the revised Atlanta classification. Propensity score matching was used to control for confounding factors. Binary logistic regression analysis was used to explore the relationship between cytokine levels and early complications of AP. Results Serum levels of interleukin (IL)‐1β, IL‐5, IL‐6, IL‐8, IL‐10, IL‐17, and tumor necrosis factor‐α were significantly higher in the severe acute pancreatitis (SAP) group than in the non‐SAP group (p < .05). After adjusting for confounding factors, the upper quartiles of IL‐6, IL‐8, and IL‐10 were associated with an increased risk of ANC compared with those in the lowest quartile (IL‐6: quartile 3, odds ratio [OR] = 3.99, 95% confidence interval [CI] = 1.95–8.16; IL‐8: quartile 4, OR = 2.47, 95% CI = 1.27–4.84; IL‐10: quartile 2, OR = 2.22, 95% CI = 1.09–4.56). APFC was associated with high serum levels of IL‐6 (quartile 3, OR = 1.32, 95% CI = 1.02–1.72), pleural effusions were associated with high serum levels of IL‐1β, IL‐6, IL‐8, and IL‐10 (IL‐1β: quartile 4, OR = 2.36, 95% CI = 1.21–4.58; IL‐6: quartile 3, OR = 4.67, 95% CI = 2.27–9.61; IL‐8: quartile 3, OR = 2.95, 95% CI = 1.51–5.79; IL‐10: quartile 4, OR = 3.20, 95% CI = 1.61–6.36), and high serum levels of IL‐6 and IL‐10 were associated with an increased risk of ascites (IL‐6: quartile 3, OR = 3.01, 95% CI = 1.42–6.37; IL‐10: quartile 3, OR = 2.57, 95% CI = 1.23–5.37). Conclusion Serum cytokine levels, including IL‐1β, IL‐6, IL‐8, and IL‐10 may be associated with the occurrence of early complications of AP. In daily clinical practice, IL‐6 may be the most worthwhile cytokine to be detected. Acute necrotic collection, acute peripancreatic fluid collection, pleural effusion, and ascites are common early complications of acute pancreatitis (AP). This study aimed to investigate the relationship between 12 cytokines and the early complications and severity of AP.
AbstractList Acute necrotic collection, acute peripancreatic fluid collection, pleural effusion, and ascites are common early complications of acute pancreatitis (AP). This study aimed to investigate the relationship between 12 cytokines and the early complications and severity of AP.
Abstract Objective Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute pancreatitis. This study aimed to investigate the relationship between 12 serum cytokines and the early complications and severity of acute pancreatitis (AP). Methods We retrospectively analyzed the clinical data of 307 patients with AP, and divided them into severe group and mild‐to‐moderate group according to the revised Atlanta classification. Propensity score matching was used to control for confounding factors. Binary logistic regression analysis was used to explore the relationship between cytokine levels and early complications of AP. Results Serum levels of interleukin (IL)‐1β, IL‐5, IL‐6, IL‐8, IL‐10, IL‐17, and tumor necrosis factor‐α were significantly higher in the severe acute pancreatitis (SAP) group than in the non‐SAP group (p < .05). After adjusting for confounding factors, the upper quartiles of IL‐6, IL‐8, and IL‐10 were associated with an increased risk of ANC compared with those in the lowest quartile (IL‐6: quartile 3, odds ratio [OR] = 3.99, 95% confidence interval [CI] = 1.95–8.16; IL‐8: quartile 4, OR = 2.47, 95% CI = 1.27–4.84; IL‐10: quartile 2, OR = 2.22, 95% CI = 1.09–4.56). APFC was associated with high serum levels of IL‐6 (quartile 3, OR = 1.32, 95% CI = 1.02–1.72), pleural effusions were associated with high serum levels of IL‐1β, IL‐6, IL‐8, and IL‐10 (IL‐1β: quartile 4, OR = 2.36, 95% CI = 1.21–4.58; IL‐6: quartile 3, OR = 4.67, 95% CI = 2.27–9.61; IL‐8: quartile 3, OR = 2.95, 95% CI = 1.51–5.79; IL‐10: quartile 4, OR = 3.20, 95% CI = 1.61–6.36), and high serum levels of IL‐6 and IL‐10 were associated with an increased risk of ascites (IL‐6: quartile 3, OR = 3.01, 95% CI = 1.42–6.37; IL‐10: quartile 3, OR = 2.57, 95% CI = 1.23–5.37). Conclusion Serum cytokine levels, including IL‐1β, IL‐6, IL‐8, and IL‐10 may be associated with the occurrence of early complications of AP. In daily clinical practice, IL‐6 may be the most worthwhile cytokine to be detected.
Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute pancreatitis. This study aimed to investigate the relationship between 12 serum cytokines and the early complications and severity of acute pancreatitis (AP). We retrospectively analyzed the clinical data of 307 patients with AP, and divided them into severe group and mild-to-moderate group according to the revised Atlanta classification. Propensity score matching was used to control for confounding factors. Binary logistic regression analysis was used to explore the relationship between cytokine levels and early complications of AP. Serum levels of interleukin (IL)-1β, IL-5, IL-6, IL-8, IL-10, IL-17, and tumor necrosis factor-α were significantly higher in the severe acute pancreatitis (SAP) group than in the non-SAP group (p < .05). After adjusting for confounding factors, the upper quartiles of IL-6, IL-8, and IL-10 were associated with an increased risk of ANC compared with those in the lowest quartile (IL-6: quartile 3, odds ratio [OR] = 3.99, 95% confidence interval [CI] = 1.95-8.16; IL-8: quartile 4, OR = 2.47, 95% CI = 1.27-4.84; IL-10: quartile 2, OR = 2.22, 95% CI = 1.09-4.56). APFC was associated with high serum levels of IL-6 (quartile 3, OR = 1.32, 95% CI = 1.02-1.72), pleural effusions were associated with high serum levels of IL-1β, IL-6, IL-8, and IL-10 (IL-1β: quartile 4, OR = 2.36, 95% CI = 1.21-4.58; IL-6: quartile 3, OR = 4.67, 95% CI = 2.27-9.61; IL-8: quartile 3, OR = 2.95, 95% CI = 1.51-5.79; IL-10: quartile 4, OR = 3.20, 95% CI = 1.61-6.36), and high serum levels of IL-6 and IL-10 were associated with an increased risk of ascites (IL-6: quartile 3, OR = 3.01, 95% CI = 1.42-6.37; IL-10: quartile 3, OR = 2.57, 95% CI = 1.23-5.37). Serum cytokine levels, including IL-1β, IL-6, IL-8, and IL-10 may be associated with the occurrence of early complications of AP. In daily clinical practice, IL-6 may be the most worthwhile cytokine to be detected.
Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute pancreatitis. This study aimed to investigate the relationship between 12 serum cytokines and the early complications and severity of acute pancreatitis (AP).OBJECTIVEAcute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute pancreatitis. This study aimed to investigate the relationship between 12 serum cytokines and the early complications and severity of acute pancreatitis (AP).We retrospectively analyzed the clinical data of 307 patients with AP, and divided them into severe group and mild-to-moderate group according to the revised Atlanta classification. Propensity score matching was used to control for confounding factors. Binary logistic regression analysis was used to explore the relationship between cytokine levels and early complications of AP.METHODSWe retrospectively analyzed the clinical data of 307 patients with AP, and divided them into severe group and mild-to-moderate group according to the revised Atlanta classification. Propensity score matching was used to control for confounding factors. Binary logistic regression analysis was used to explore the relationship between cytokine levels and early complications of AP.Serum levels of interleukin (IL)-1β, IL-5, IL-6, IL-8, IL-10, IL-17, and tumor necrosis factor-α were significantly higher in the severe acute pancreatitis (SAP) group than in the non-SAP group (p < .05). After adjusting for confounding factors, the upper quartiles of IL-6, IL-8, and IL-10 were associated with an increased risk of ANC compared with those in the lowest quartile (IL-6: quartile 3, odds ratio [OR] = 3.99, 95% confidence interval [CI] = 1.95-8.16; IL-8: quartile 4, OR = 2.47, 95% CI = 1.27-4.84; IL-10: quartile 2, OR = 2.22, 95% CI = 1.09-4.56). APFC was associated with high serum levels of IL-6 (quartile 3, OR = 1.32, 95% CI = 1.02-1.72), pleural effusions were associated with high serum levels of IL-1β, IL-6, IL-8, and IL-10 (IL-1β: quartile 4, OR = 2.36, 95% CI = 1.21-4.58; IL-6: quartile 3, OR = 4.67, 95% CI = 2.27-9.61; IL-8: quartile 3, OR = 2.95, 95% CI = 1.51-5.79; IL-10: quartile 4, OR = 3.20, 95% CI = 1.61-6.36), and high serum levels of IL-6 and IL-10 were associated with an increased risk of ascites (IL-6: quartile 3, OR = 3.01, 95% CI = 1.42-6.37; IL-10: quartile 3, OR = 2.57, 95% CI = 1.23-5.37).RESULTSSerum levels of interleukin (IL)-1β, IL-5, IL-6, IL-8, IL-10, IL-17, and tumor necrosis factor-α were significantly higher in the severe acute pancreatitis (SAP) group than in the non-SAP group (p < .05). After adjusting for confounding factors, the upper quartiles of IL-6, IL-8, and IL-10 were associated with an increased risk of ANC compared with those in the lowest quartile (IL-6: quartile 3, odds ratio [OR] = 3.99, 95% confidence interval [CI] = 1.95-8.16; IL-8: quartile 4, OR = 2.47, 95% CI = 1.27-4.84; IL-10: quartile 2, OR = 2.22, 95% CI = 1.09-4.56). APFC was associated with high serum levels of IL-6 (quartile 3, OR = 1.32, 95% CI = 1.02-1.72), pleural effusions were associated with high serum levels of IL-1β, IL-6, IL-8, and IL-10 (IL-1β: quartile 4, OR = 2.36, 95% CI = 1.21-4.58; IL-6: quartile 3, OR = 4.67, 95% CI = 2.27-9.61; IL-8: quartile 3, OR = 2.95, 95% CI = 1.51-5.79; IL-10: quartile 4, OR = 3.20, 95% CI = 1.61-6.36), and high serum levels of IL-6 and IL-10 were associated with an increased risk of ascites (IL-6: quartile 3, OR = 3.01, 95% CI = 1.42-6.37; IL-10: quartile 3, OR = 2.57, 95% CI = 1.23-5.37).Serum cytokine levels, including IL-1β, IL-6, IL-8, and IL-10 may be associated with the occurrence of early complications of AP. In daily clinical practice, IL-6 may be the most worthwhile cytokine to be detected.CONCLUSIONSerum cytokine levels, including IL-1β, IL-6, IL-8, and IL-10 may be associated with the occurrence of early complications of AP. In daily clinical practice, IL-6 may be the most worthwhile cytokine to be detected.
ObjectiveAcute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute pancreatitis. This study aimed to investigate the relationship between 12 serum cytokines and the early complications and severity of acute pancreatitis (AP).MethodsWe retrospectively analyzed the clinical data of 307 patients with AP, and divided them into severe group and mild-to-moderate group according to the revised Atlanta classification. Propensity score matching was used to control for confounding factors. Binary logistic regression analysis was used to explore the relationship between cytokine levels and early complications of AP.ResultsSerum levels of interleukin (IL)-1β, IL-5, IL-6, IL-8, IL-10, IL-17, and tumor necrosis factor-α were significantly higher in the severe acute pancreatitis (SAP) group than in the non-SAP group (p < .05). After adjusting for confounding factors, the upper quartiles of IL-6, IL-8, and IL-10 were associated with an increased risk of ANC compared with those in the lowest quartile (IL-6: quartile 3, odds ratio [OR] = 3.99, 95% confidence interval [CI] = 1.95–8.16; IL-8: quartile 4, OR = 2.47, 95% CI = 1.27–4.84; IL-10: quartile 2, OR = 2.22, 95% CI = 1.09–4.56). APFC was associated with high serum levels of IL-6 (quartile 3, OR = 1.32, 95% CI = 1.02–1.72), pleural effusions were associated with high serum levels of IL-1β, IL-6, IL-8, and IL-10 (IL-1β: quartile 4, OR = 2.36, 95% CI = 1.21–4.58; IL-6: quartile 3, OR = 4.67, 95% CI = 2.27–9.61; IL-8: quartile 3, OR = 2.95, 95% CI = 1.51–5.79; IL-10: quartile 4, OR = 3.20, 95% CI = 1.61–6.36), and high serum levels of IL-6 and IL-10 were associated with an increased risk of ascites (IL-6: quartile 3, OR = 3.01, 95% CI = 1.42–6.37; IL-10: quartile 3, OR = 2.57, 95% CI = 1.23–5.37).ConclusionSerum cytokine levels, including IL-1β, IL-6, IL-8, and IL-10 may be associated with the occurrence of early complications of AP. In daily clinical practice, IL-6 may be the most worthwhile cytokine to be detected.
Objective Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute pancreatitis. This study aimed to investigate the relationship between 12 serum cytokines and the early complications and severity of acute pancreatitis (AP). Methods We retrospectively analyzed the clinical data of 307 patients with AP, and divided them into severe group and mild‐to‐moderate group according to the revised Atlanta classification. Propensity score matching was used to control for confounding factors. Binary logistic regression analysis was used to explore the relationship between cytokine levels and early complications of AP. Results Serum levels of interleukin (IL)‐1β, IL‐5, IL‐6, IL‐8, IL‐10, IL‐17, and tumor necrosis factor‐α were significantly higher in the severe acute pancreatitis (SAP) group than in the non‐SAP group (p < .05). After adjusting for confounding factors, the upper quartiles of IL‐6, IL‐8, and IL‐10 were associated with an increased risk of ANC compared with those in the lowest quartile (IL‐6: quartile 3, odds ratio [OR] = 3.99, 95% confidence interval [CI] = 1.95–8.16; IL‐8: quartile 4, OR = 2.47, 95% CI = 1.27–4.84; IL‐10: quartile 2, OR = 2.22, 95% CI = 1.09–4.56). APFC was associated with high serum levels of IL‐6 (quartile 3, OR = 1.32, 95% CI = 1.02–1.72), pleural effusions were associated with high serum levels of IL‐1β, IL‐6, IL‐8, and IL‐10 (IL‐1β: quartile 4, OR = 2.36, 95% CI = 1.21–4.58; IL‐6: quartile 3, OR = 4.67, 95% CI = 2.27–9.61; IL‐8: quartile 3, OR = 2.95, 95% CI = 1.51–5.79; IL‐10: quartile 4, OR = 3.20, 95% CI = 1.61–6.36), and high serum levels of IL‐6 and IL‐10 were associated with an increased risk of ascites (IL‐6: quartile 3, OR = 3.01, 95% CI = 1.42–6.37; IL‐10: quartile 3, OR = 2.57, 95% CI = 1.23–5.37). Conclusion Serum cytokine levels, including IL‐1β, IL‐6, IL‐8, and IL‐10 may be associated with the occurrence of early complications of AP. In daily clinical practice, IL‐6 may be the most worthwhile cytokine to be detected. Acute necrotic collection, acute peripancreatic fluid collection, pleural effusion, and ascites are common early complications of acute pancreatitis (AP). This study aimed to investigate the relationship between 12 cytokines and the early complications and severity of AP.
Author Zhang, Shuangshuang
Zhuang, Mengting
Fei, Sujuan
Zhou, Fei
Yao, Jiaxin
AuthorAffiliation 3 Key Laboratory of Gastrointestinal Endoscopy Xuzhou Medical University Xuzhou China
1 Department of Gastroenterology Xuzhou Medical University Xuzhou China
2 Department of Gastroenterology The Affiliated Hospital of Xuzhou Medical University Xuzhou China
AuthorAffiliation_xml – name: 1 Department of Gastroenterology Xuzhou Medical University Xuzhou China
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  givenname: Shuangshuang
  surname: Zhang
  fullname: Zhang, Shuangshuang
  organization: Xuzhou Medical University
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  givenname: Fei
  orcidid: 0009-0009-5457-1857
  surname: Zhou
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/38411379$$D View this record in MEDLINE/PubMed
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Issue 2
Keywords acute necrotic collection
cytokines
ascites
pleural effusion
acute peripancreatic fluid collection
acute pancreatitis
Language English
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2024 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd.
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Snippet Objective Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute...
Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute...
ObjectiveAcute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications of acute...
Acute necrotic collection, acute peripancreatic fluid collection, pleural effusion, and ascites are common early complications of acute pancreatitis (AP). This...
Abstract Objective Acute necrotic collection (ANC), acute peripancreatic fluid collection (APFC), pleural effusion, and ascites are common early complications...
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SubjectTerms Acute Disease
acute necrotic collection
acute pancreatitis
acute peripancreatic fluid collection
Ascites
Ascites - etiology
Autoimmune diseases
Blood
Body mass index
Cysts
Cytokines
Disease
Gender
Hospitals
Humans
Inflammation
Intensive care
Interleukin-10
Interleukin-1beta
Interleukin-6
Interleukin-8
Mortality
Neutrophils
Original
Pancreas
Pancreatitis
Pancreatitis - complications
Pleural effusion
Regression analysis
Retrospective Studies
Tomography
Trauma
Tumor necrosis factor-TNF
Variables
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Title The relationship between inflammatory cytokines and in‐hospital complications of acute pancreatitis
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fiid3.1203
https://www.ncbi.nlm.nih.gov/pubmed/38411379
https://www.proquest.com/docview/2932487728
https://www.proquest.com/docview/2932438449
https://pubmed.ncbi.nlm.nih.gov/PMC10898203
https://doaj.org/article/1f2e72a277e248daa792c93dbe2e44aa
Volume 12
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