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. 2021 Aug 31;11:17463. doi: 10.1038/s41598-021-97069-x

Table 2.

Associations between genetically predicted SMOX activity from SSI-IHPS newborn cohort (SSI-IHPS instrument) and SMOX expression from the EGCUT adult cohort (EGCUT instrument), based on SNP rs1741315, and six site-specific cancers (prostate, breast, lung, colorectal and neuroblastoma).

Outcome Cases, No Controls, No EAF SSI-IHPS instrument EGCUT instrument
Odds ratio (95% CI) P Odds ratio (95% CI) P
Prostate cancer 79,194 61,112 0.430 0.98 (0.96–1.00) 0.046 0.96 (0.92–1.00) 0.046
Breast cancer 62,533 60,976 0.434 0.99 (0.96–1.02) 0.465 0.98 (0.93–1.03) 0.465
Lung cancer 29,266 56,450 0.442 0.97 (0.94–1.00) 0.084 0.95 (0.89–1.01) 0.084
Colorectal cancer 5,693 386,740 0.439 0.96 (0.91–1.01) 0.097 0.92 (0.83–1.02) 0.097
Gastric cancer 6,563 195,745 0.361 1.02 (0.97–1.07) 0.543 1.03 (0.93–1.14) 0.543
Neuroblastoma 2,101 4,202 0.412 1.07 (0.97–1.19) 0.182 1.16 (0.93–1.44) 0.182

All estimations were based on the Wald ratio method, with A being the effect allele. EAF, effect allele frequency in each cohort (cases and controls combined); P, p-value. An increased spermidine/spermine ratio represents increased SMOX activity.