Barely Significant

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highly significantp<0.00010.0× alphaqualifiedgold
After accounting for differences due to strategy, mean age and mean PSA in the meta-regression analysis, the amount of residual heterogeneity between studies was calculated to be 76.0, which is highly significant at the 5% level (QE = 176.8, p<0.0001).
highly significantp < .00010.0× alphaqualifiedgold
Discrimination followed the order IL‐2 > IL‐13 > IFN‐γ with, however, only subtle differences in the respective highly significant AUC (0.9310, 0.8994, 0.8316) values (all p < .0001; Figure S7 A), which was similar to the results obtained with gradient‐purified PBMC with regard to IL‐13 and IFN‐γ while IL‐2 levels were clearly lower and less discriminatory after 6 days (Figure S4 A).
highly significantP < 0.00010.0× alphaqualifiedgold
This increase was especially pronounced for moribund individuals and during the “High & Prolonged 1” trial (Supporting Information Figure S2 ), and is supported by the highly significant differences in CIE b * values between trials ( F = 38.17, df = 6, P < 0.0001) and between monitoring periods ( F = 6.21, df = 4, P < 0.0001).
highly significantp < 0.00010.0× alphaqualifiedgold
There were consistent and highly significant (p < 0.0001) reductions of blood pressure, fasting plasma glucose, abdominal obesity, triglycerides and an increase in HDL cholesterol after 9 months of treatment with Irbesartan monotherapy as well as with the combination therapy (for individual figures see table 3 ).
nominally significantp < 0.00010.0× alphagold
Of note, each comparison of atropine sulfate 0.01% versus vehicle and atropine sulfate 0.03% versus vehicle was nominally significant ( p < 0.0001 and p = 0.0023, respectively) (Fig. 3 ). s In Fast Progressor Subgroup 2 (progression − 0.75 D/year or worse at baseline, n = 225), the mean (least squares means) APR from baseline to month 24 was − 0.53 D (95% CI − 0.63, − 0.43) in the vehicle group and − 0.38 D (95% CI − 0.47, − 0.30) in the combined atropine sulfate group.
highly significantP <0.00010.0× alphaqualifiedgold
Associations of biomarkers with all-cause mortality in X69 Highly significant associations for 10 of the evaluated biomarkers (all except bilirubin) with all-cause mortality were observed in X69 ( P <0.0001; Fig 3 and Table 2 ) when they were evaluated one by one adjusting for classical risk factors (age, sex, glucose, systolic blood pressure, BMI, total cholesterol and smoking).