From: Clinical review: Adiponectin biology and its role in inflammation and critical illness
Year | Reference | Data |
---|---|---|
2000 | Yokota et al. [34] | In vitro studies of human myeloid cell lines show that adiponectin is a negative regulator of myelomonocytic progenitor growth and downregulates the inflammatory response |
2003 | Keller et al. [54] | Following induction of endotoxaemia in healthy humans, there was no significant alteration in adiponectin levels (healthy subjects n = 23: 4 females, 19 males) |
2006 | Tsuchihashi et al. [59] | In vitro studies of recombinant human adiponectin and reconstituted LPS show that adiponectin binds LPS and suppresses LAL |
2007 | Anderson et al. [55] | No significant alteration in adiponectin levels in endotoxaemia, but downregulation of adiponectin receptor mRNA in white cells (healthy subjects n = 20, 50% male) |
2009 | Jernås et al. [63] | Lower levels of adiponectin during intensive care stay compared with recovery (subarachnoid haemorrhage n = 8) |
2009 | Venkatesh et al. [64] | Lower levels of adiponectin in critically ill cohort, with a strong association between plasma cortisol and adiponectin and an inverse correlation between adiponectin and CRP (critically ill n = 20; historical controls n = 16) |
2009 | Langouche et al. [65] | Lower levels of circulating adiponectin in ICU patients on admission; these levels increased to normal reference values during the ICU stay. Intensive insulin therapy increased the rise of adiponectin over time in ICU. Critically ill n = 318, healthy subjects n = 22, acutely stressed subjects n = 22 |
2010 | Kaplan et al. [69] | Increased levels of HMW adiponectin on day 1 in paediatric septic shock cohort (SIRS/sepsis n = 22, septic shock n = 25, control n = 27) |
2010 | Hillenbrand et al. [58] | Lower levels of adiponectin in septic patients with negative correlation with SOFA scores (septic shock n = 33, control (blood donors) n = 60, morbidly obese n = 37) |
2010 | Walkey et al. [68] | Higher levels of adiponectin at baseline associated with increased 28-day mortality (acute respiratory failure n = 175) |