4.8 Article

Critical thresholds: key to unlocking the door to the prevention and specific treatments for acute pancreatitis

期刊

GUT
卷 70, 期 1, 页码 194-203

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/gutjnl-2020-322163

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资金

  1. DoD [PR182623, W81XWH-17-1-0339, U01DK108314, W81XWH1910888]
  2. National Research, Development and Innovation Office [FK123982, K131996]
  3. US NIH [R01 AA024464, P01 DK098108, P50 AA0119991, U01 DK108314]
  4. US DoD [W81XWH1910888]
  5. U.K. Medical Research Council
  6. National Institute for Health Research [EME 15/20/01]
  7. European Union Innovative Medicines Initiative
  8. GlaxoSmithKline PLC
  9. Hampson Trust
  10. NIHR
  11. NIH [U01 DK108300, DK092421]
  12. [UO1 DK108306]
  13. [GINOP 2.3.2-15-2016-00048]
  14. U.S. Department of Defense (DOD) [W81XWH1910888] Funding Source: U.S. Department of Defense (DOD)
  15. National Institutes of Health Research (NIHR) [EME/15/20/01] Funding Source: National Institutes of Health Research (NIHR)

向作者/读者索取更多资源

Acute pancreatitis (AP) is a common gastrointestinal disease with no specific treatments. Laboratory-based research is essential for understanding the pathophysiology of AP, but the reasons why only a minority of individuals develop AP and why some develop more severe manifestations remain unanswered questions.
Acute pancreatitis (AP), an acute inflammatory disorder of the exocrine pancreas, is one of the most common gastrointestinal diseases encountered in emergency departments with no specific treatments. Laboratory-based research has formed the cornerstone of endeavours to decipher the pathophysiology of AP, because of the limitations of such study in human beings. While this has provided us with substantial understanding, we cannot answer several pressing questions. These are: (a) Why is it that only a minority of individuals with gallstones, or who drink alcohol excessively, or are exposed to other causative factors develop AP? (b) Why do only some develop more severe manifestations of AP with necrosis and/or organ failure? (c) Why have we been unable to find an effective therapeutic for AP? This manuscript provides a state-of-the-art review of our current understanding of the pathophysiology of AP providing insights into the unanswered clinical questions. We describe multiple protective factors operating in most people, and multiple stressors that in a minority induce AP, independently or together, via amplification loops. We present testable hypotheses aimed at halting progression of severity for the development of effective treatments for this common unpredictable disease.

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