Barely Significant
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“did not reach statistical significance”

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In the literature

Later age of symptom onset (70+ years) was associated with lower odds of genetic testing completion (OR 0.23; 95% CI 0.12–0.43; P < 0.001) compared to the reference group (10–19 years), while early symptom onset (0–9 years) showed a trend toward higher odds of genetic testing completion that approached but did not reach statistical significance (OR 1.53; 95% CI 1–2.37; P = 0.05).
After confirming a successful silencing of TGFBR2 by using two independent shRNAs (shTGFBR2_B: ~42% decrease, P <0.0001; shTGFBR2_D: ~57% decrease, P =0.001), we saw a trend in lower intracellular TREM2 levels, although it did not reach statistical significance (shTGFBR2_B: ~16% decrease, P =0.05; shTGFBR2_D: ~19% decrease, P =0.09; Fig. 4 E middle panel, Fig.
However, the adjusted hazard ratios (aHRs) for the comparison between the accelerated (Rabies+JE-Accelerated) and the conventional (Rabies+JE-Conventional) schedule did not reach statistical significance (p < 0.05), with aHRs of 1.34 (95% CI: 0.94–1.90, p = 0.1021) and 1.47 (95% CI: 0.98–2.22, p = 0.0620) in the FAS-2 and PPS-2, respectively ( Fig 4 and S2 Table ).
Intervention patients were 1.77 (CI 0.94, 3.34, p = 0.078) times more likely than controls to be abstinent (12 versus 8%), a difference that approached, but did not reach statistical significance, and surpassed controls on number of days quit (18.4 versus 12.2, p < .05) but not on number of quit attempts.
The risk of infection showed no significant associations with the TNF-α-238G>A and -863G>C SNP; carriers of the TNF-α-308A genetic variant were overrepresented among uninfected individuals, but the differences did not reach statistical significance (genotype comparisons, p = 0.05; allele comparisons, p = 0.07) (Table 2 ).
No differences in survival were observed for patients treated with chemotherapy when stratified by Treg infiltration ( P = 0.565) CXCL12 expression does not differ between the different intrinsic subtypes, and is associated with longer survival Although a smaller proportion of basal-like (16/27, 59%) and HER2 tumours (25/47, 53%) was positive for CXCL12 expression compared with luminal tumours (102/138, 74%), this did not reach statistical significance ( P = 0.050) (Table 2 ).