Barely Significant

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marginally non-significantp = 0.0591.2× alpha
When the RAR was analyzed by quartiles, compared to the lowest quartile (Q1, reference), Q2 showed significantly increased odds of PD in the crude model (OR = 1.65, 95% CI: 1.09–2.50, p = 0.018) and Model 1 (OR = 1.56, 95% CI: 1.02–2.36, p = 0.039), but this association became marginally non-significant in Model 2 (OR = 1.49, 95% CI: 0.99–2.27, p = 0.059) and Model 3 (OR = 1.48, 95% CI: 0.96–2.30, p = 0.076).
almost significantp = 0.05921.2× alphagold
Enhanced ADCC Activity in PBMCs from Oncohematological Individuals after ASCT Antibody-mediated cytotoxic activity against rituximab-coated Raji cells of peripheral blood lymphocytes (PBMCs) from oncohematological patients was increased 2.1-fold on average after ASCT, in comparison with healthy donors who recovered from mild COVID-19 ( Figure 3 ), but this difference was almost significant ( p = 0.0592). 3.5.
borderline significancep = 0.061.2× alpha
Interestingly, secondary analysis of data from a study of van Grootven and colleagues [ 47 ] revealed that among 86 patients aged 80 ± 7 years undergoing orthopedic surgery, the lowest intraoperative diastolic BP was the protective factor for POD (OR = 0.92; 95%CI 0.85–0.99, p = 0.03) and the protective impact of the highest systolic BP was of a borderline significance (OR = 0.97; 95%CI 0.94–1.0; p = 0.06).
a statistical trendp = 0.0601.2× alphagold
OASGs were not associated with the classification of IE (possible/definite) or type (native or prosthetic) of infected valve, but there was a statistical trend for a negative association between OASGs and the presence of mechanical prosthetic valves ( p = 0.060).
approaching significancep = 0.061.2× alphagold
The borderline protective signal observed with RAAS inhibitor use, approaching significance in subgroup analysis ( p = 0.06 for ΔFMD at 24 h) and showing consistent positive Spearman correlations at 24 h (ρ = +0.20) and one month (ρ = +0.30), is biologically plausible given the vasoprotective properties of this drug class through reduction in angiotensin II-mediated oxidative stress, preservation of bradykinin signaling, and upregulation of eNOS activity [ 34 ].