Barely Significant
← all excerpts

The MMP-9 -1562 C/T polymorphism in the presence of metabolic syndrome increases the risk of clinical events in patients with coronary artery disease.

PLoS One · 2014 · PMC4156385 · PMID 25191702

Europe PMCDOI
1
hedged sentence
0.0010
closest p · 0.0× alpha
0.0010
boldest claim

The sentences

highly significantp <0.001actually significant
The difference in number of endpoints between CC homozygous and T-allele carriers in the group with 4 or 5 MetS criteria was highly significant [OR = 13.3 (95% CI: 3.3, 53.5), p <0.001, adjusted].

also in 132,142 other papers

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.