Barely Significant

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In addition, there was a decreasing trend of the risks of renal function decline in patients with better baseline eGFR (eGFR ≥ 90 mL/min/1.73 m 2 , HR = 0.31, 95% CI: 0.19–0.50; eGFR ≥ 60 to < 0 mL/min/1.73 m 2 , HR = 0.41, 95% CI: 0.27–0.62; eGFR ≥ 30 to < 60 mL/min/1.73 m 2 , HR = 0.66, CI: 0.44–1.00; eGFR ≥ 15 to < 30 mL/min/1.73 m 2 , HR = 0.50, CI: 0.19–1.34; p for interaction = 0.001).
A significant increase in AKT (Thr308) phosphorylation was also observed for circulating CD3 + CD8 + T cells, whereas the mTOR (Ser2448) phosphoresponse reached only borderline significance for this cell subset.
PMA combined with TCR activation (anti-CD3 + anti-CD28) also caused a highly significant increase in the phosphorylation of AKT (Thr308), mTOR (Ser2448) and STAT3 (Ser727) for both T cell subsets, but an additional increase in STAT3 (Tyr705) phosphorylation of borderline significance was observed only for CD3 + CD8 + cells after combined PMA+TCR stimulation ( Table 2 ).
The favorable outcomes group showed a slight trend towards increase in blood ammonia levels as prehospital time increased, while a stronger correlation was noted in the poor outcomes group; blood ammonia levels were markedly increased as a result of prolonged prehospital time.