Barely Significant
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Influence of single-nucleotide polymorphisms in <i>TLR3</i> (rs3775291) and <i>TLR9</i> (rs352139) on the risk of CMV infection in kidney transplant recipients.

Front Immunol · 2022 · PMC9374175 · PMID 35967300

3
hedged sentences
0.2560
closest p · 5.1× alpha
0.2560
boldest claim

The sentences

did not reach statistical significanceP -value = 0.256not close (p > 0.1)
A numerical difference was also observed for TLR9 (rs5743836), where the alternative G allele both in heterozygous (AG) or homozygous states (GG) was apparently associated with CMV infection (cumulative incidence rates of 64.4% and 66.7%, respectively) compared to the AA genotype (51.7%), although the difference did not reach statistical significance (P -value = 0.256).

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showed a trendno p-value reported
Concordant with the results obtained for overall and high-level CMV infection, carriers of the G allele of TLR9 (rs5743836) in the homozygous or heterozygous state showed a trend toward a lower disease-free survival than homozygous carriers of the reference A allele (one-year survival rates: 83.2% versus 90.8%, respectively; log-rank test P -value = 0.149).

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borderline significanceno p-value reported
First, we have found that the presence in a homozygous state of the alternative allele of TLR3 (rs3775291) (TT genotype) exerts a protective role on the risk of CMV viremia at any level and, with borderline significance, at high-level (≥1,000 IU/ml) infection.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.