Barely Significant
← all excerpts

Impact of the common MTHFR 677C→T polymorphism on blood pressure in adulthood and role of riboflavin in modifying the genetic risk of hypertension: evidence from the JINGO project.

BMC Med · 2020 · PMC7656675 · PMID 33172445

1
hedged sentence
closest p
boldest claim

The sentences

The OR for risk of hypertension associated with the TT genotype remained similar whether the logistic regression analysis was performed in all participants up to 70 years, or split into those treated or not treated with antihypertensive drugs, albeit the relationship failed to reach statistical significance within either treated or untreated categories (owing to the loss of statistical power as a result of a 50% reduction in the sample size when split and considering that the variant TT genotype is represented by just 12% of the overall cohort).

also in 6,035 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.