Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/163806
Título: B Cells and Double-Negative B Cells (CD27−IgD−) Are Related to Acute Pancreatitis Severity
Autor: Malheiro, Filipa
Ângelo-Dias, Miguel
Lopes, Teresa
Azeredo-Lopes, Sofia
Martins, Catarina
BORREGO, LUIS MIGUEL
Palavras-chave: acute pancreatitis
B cell
biomarker
lymphocyte
prognosis
severity
T cell
Medicine(all)
Data: Jan-2024
Resumo: Acute pancreatitis (AP) is an increasingly frequent disease in which inflammation plays a crucial role. Fifty patients hospitalized with AP were included and peripheral blood samples were analyzed for B and T cell subpopulations at the time of hospitalization and 48 h after diagnosis. The Bedside Index of Severity in Acute Pancreatitis (BISAP) and length of hospital stay were also recorded. A healthy control (HC) group of 15 outpatients was included. AP patients showed higher neutrophil/lymphocyte (N/L) ratios and higher percentages of B cells than the HC group. The total B cell percentages were higher in patients with moderate/severe AP than in patients with mild AP. The percentages of B cells as well as the percentages of the CD27−IgD− B cell subset decreased from admission to 48 h after admission. The patients with higher BISAP scores showed lower percentages of peripheral lymphocytes but higher percentages of CD27−IgD− B cells. Higher BISAP scores, N/L ratios, and peripheral blood B cell levels emerged as predictors of hospital stay length in AP patients. Our findings underscore the importance of early markers for disease severity. Additionally, the N/L ratio along with the BISAP score and circulating B cell levels form a robust predictive model for hospital stay duration of AP patients.
Descrição: Funding Information: This research was funded by the Learning Health Hospital da Luz. LH.INV.F2019002. Publisher Copyright: © 2024 by the authors.
Peer review: yes
URI: http://hdl.handle.net/10362/163806
DOI: https://doi.org/10.3390/diseases12010018
ISSN: 2079-9721
Aparece nas colecções:NMS: CHRC - Artigos em revista internacional com arbitragem científica

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