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本文引用的文献

1
Elevated hemostasis markers after pneumonia increases one-year risk of all-cause and cardiovascular deaths.肺炎后止血标志物升高增加了全因和心血管死亡的一年风险。
PLoS One. 2011;6(8):e22847. doi: 10.1371/journal.pone.0022847. Epub 2011 Aug 10.
2
The resolution of inflammation: the devil in the flask and in the details.炎症的消退:烧瓶中的魔鬼与细节之处
FASEB J. 2011 May;25(5):1441-8. doi: 10.1096/fj.11-0502ufm.
3
Understanding the potential role of statins in pneumonia and sepsis.了解他汀类药物在肺炎和脓毒症中的潜在作用。
Crit Care Med. 2011 Aug;39(8):1871-8. doi: 10.1097/CCM.0b013e31821b8290.
4
Molecular inflammation as an underlying mechanism of the aging process and age-related diseases.分子炎症作为衰老过程和与年龄相关疾病的潜在机制。
J Dent Res. 2011 Jul;90(7):830-40. doi: 10.1177/0022034510387794. Epub 2011 Mar 29.
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The effects of age on inflammatory and coagulation-fibrinolysis response in patients hospitalized for pneumonia.肺炎住院患者炎症和凝血-纤溶反应的年龄影响。
PLoS One. 2010 Nov 4;5(11):e13852. doi: 10.1371/journal.pone.0013852.
6
The lingering consequences of sepsis: a hidden public health disaster?脓毒症的长期后果:一场隐匿的公共卫生灾难?
JAMA. 2010 Oct 27;304(16):1833-4. doi: 10.1001/jama.2010.1546.
7
Long-term cognitive impairment and functional disability among survivors of severe sepsis.严重脓毒症幸存者的长期认知障碍和功能残疾。
JAMA. 2010 Oct 27;304(16):1787-94. doi: 10.1001/jama.2010.1553.
8
Macrophage migration inhibitory factor (MIF): a promising biomarker.巨噬细胞移动抑制因子(MIF):一种有前景的生物标志物。
Drug News Perspect. 2010 May;23(4):257-64. doi: 10.1358/dnp.2010.23.4.1453629.
9
Inflammatory networks during cellular senescence: causes and consequences.细胞衰老过程中的炎症网络:原因与后果。
Trends Mol Med. 2010 May;16(5):238-46. doi: 10.1016/j.molmed.2010.03.003. Epub 2010 May 3.
10
Pneumococcal pathogenesis: "innate invasion" yet organ-specific damage.肺炎球菌发病机制:“先天侵袭”与器官特异性损伤。
J Mol Med (Berl). 2010 Feb;88(2):103-7. doi: 10.1007/s00109-009-0578-5. Epub 2010 Feb 17.

衰老对危重病连续体中炎症和止血的影响。

Effects of Aging on Inflammation and Hemostasis through the Continuum of Critical Illness.

机构信息

The Clinical Research, Investigation, and Systems Modeling of Acute Illness (CRISMA) Laboratory, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Aging Dis. 2011 Dec;2(6):501-11. Epub 2011 Dec 2.

PMID:22396897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3295067/
Abstract

Older age has long been associated with altered inflammation and hemostasis regulation. Emerging evidence suggests that age-related differences in inflammation and hemostasis abnormalities may play a role in the development of and long-term outcomes after critical illness. A better understanding of underlying mechanisms may provide new possibilities for therapeutic interventions. In this review, we will examine how age-related differences in inflammatory and coagulation responses are affected through the continuum of healthy state, before infection occurs, to severe sepsis and recovery.

摘要

老年一直与炎症和止血调节的改变有关。新出现的证据表明,与年龄相关的炎症和止血异常差异可能在危重病的发生和长期结局中起作用。更好地了解潜在的机制可能为治疗干预提供新的可能性。在这篇综述中,我们将研究炎症和凝血反应的年龄相关差异如何通过健康状态的连续体受到影响,从感染前到严重败血症和恢复。