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. 2011 Dec 28;6(12):e28520. doi: 10.1371/journal.pone.0028520

Table 2. Multivariable adjusted odds ratios (OR) of colorectal and colon cancer by median of plasma analyte level, HPFS and NHS combined.

Colorectal Cancer Colon Cancer
Plasma Marker Low* High* Low High
IGF-1
Cases/controls 220/497 279/495 156/360 210/367
OR (95% CI)$ 1.00 1.37 (1.05 to 1.78) 1.00 1.52 (1.11 to 2.07)
IGFBP3
Cases/controls 230/496 269/496 171/362 195/365
OR (95% CI) 1.00 0.96 (0.74 to 1.26) 1.00 0.91 (0.68 to 1.25)
Molar IGF-1/IGFBP3 Ratio
Cases/controls 219/497 280/495 159/353 207/374
OR (95% CI) 1.00 1.36 (1.08 to 1.73) 1.00 1.35 (1.02 to 1.79)
C-Peptide
Cases/controls 197/455 277/460 140/337 211/339
OR (95% CI) 1.00 1.37 (1.05 to 1.78) 1.00 1.58 (1.16 to 2.16)
Vitamin D
Cases/controls 302/498 197/494 224/354 142/373
OR (95% CI) 1.00 0.67 (0.53 to 0.86) 1.00 0.62(0.47 to 0.83)

*Low: below median level; high: equal or above median level.

Median vitamin D levels (controls): HPFS: 29.6 ng/mL; NHS: laboratory batch 1: 23.8 ng/mL; laboratory batch 2: 29.7 ng/mL, laboratory batch 3: 25.5 ng/mL.

$Multivariable adjusted for matching factors (age, year and month of blood donation), body mass index (kg/m2, continuous), packyears of smoking (continuous), physical activity (MET-hr week, continuous), intake of alcohol, methionine, folate, retinol, red and processed meat, calcium (all intake covariates as continuous variables), family historyof colorectal cancer (yes vs. no), sex, fasting status (0–2, 3–4, 5–8, ≥9 hours since last meal), aspirin use (<2 tablets/week, past, ≥2 tablets/week); models for IGF-1 were adjusted for IGF-BP3 (in tertiles) and vice versa.

Models for C-Peptide only included participants without self-reported diabetes mellitus.