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The Decrease of Peripheral Blood CD4+ T Cells Indicates Abdominal Compartment Syndrome in Severe Acute Pancreatitis.
Yao Liu1, Ling Wang2, Zhifang Cai2
1Department of Hepatobiliary Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, People's Republic of China; Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Zunyi Medical College, Zunyi, Guizhou Province, People's Republic of China.
Reduced CD4+ T lymphocytes in severe acute pancreatitis (SAP) correlate with abdominal compartment syndrome (ACS). This finding suggests CD4+ T cell counts may predict ACS development in SAP patients.
Area of Science:
- Immunology
- Gastroenterology
- Critical Care Medicine
Background:
- Abdominal compartment syndrome (ACS) is a severe complication of severe acute pancreatitis (SAP).
- The role of T lymphocytes and inflammatory cytokines in ACS development within SAP remains under-investigated.
Purpose of the Study:
- To investigate the association between T lymphocyte subsets and inflammatory markers with ACS in patients with SAP.
- To identify potential risk factors and predictors for ACS in SAP.
Main Methods:
- Retrospective analysis of 76 SAP patients, comparing 36 with ACS and 40 with intra-abdominal hypertension (IAH).
- Assessment of C-reactive protein (CRP), CD4+ and CD8+ T lymphocyte proportions, APACHE II score, and CTSI score at various time points post-admission.
Main Results:
- ACS patients exhibited higher CRP on day 7 and lower proportions of CD4+ T cells on days 1, 3, and 7 compared to IAH patients.
- A CD4+ T cell proportion of 30.3% on day 1 showed high predictive value for ACS (AUC 0.774, sensitivity 82.5%, specificity 72.0%).
- CD4+/CD8+ ratio and APACHE II score also demonstrated predictive capabilities for ACS.
Conclusions:
- A decrease in peripheral blood CD4+ T lymphocytes is significantly associated with the presence of ACS in SAP.
- Peripheral blood CD4+ T lymphocyte counts may serve as a valuable and early predictor for ACS in patients with SAP.
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