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. Author manuscript; available in PMC: 2016 Sep 1.
Published in final edited form as: Gastroenterology. 2015 May 27;149(3):614–622. doi: 10.1053/j.gastro.2015.05.038

Table 2.

Colorectal cancer-specific mortality and overall mortality according to MIC1 levels.

Quartile of plasma MIC1a
Analysis 1 2 3 4 Ptrendb
All-cause mortality (n=618)
    No. of events/No. at risk 25/119 62/160 83/174 96/165
    Age-adjusted HR (95% CI) 1 (referent) 1.88 (1.17–3.03) 2.51 (1.57–3.99) 2.85 (1.78–4.58) <0.0001
    MV-adjusted HR (95% CI)c 1 (referent) 1.77 (1.07–2.91) 2.55 (1.55–4.19) 2.63 (1.60–4.32) 0.0002
    MV-adjusted HR (95% CI)d 1 (referent) 1.74 (1.06–2.88) 2.54 (1.54–4.19) 2.63 (1.60–4.32) 0.0002
CRC-specific mortality (n=618)
    No. of events/No. at risk 19/119 43/160 59/174 57/165
    Age-adjusted HR (95% CI) 1 (referent) 1.94 (1.12–3.37) 2.64 (1.54–4.51) 2.73 (1.57–4.75) 0.003
    MV-adjusted HR (95% CI)c 1 (referent) 1.65 (0.92–2.94) 2.60 (1.45–4.67) 2.34 (1.30–4.21) 0.01
    MV-adjusted HR (95% CI)d 1 (referent) 1.67 (0.93–3.00) 2.67 (1.49–4.80) 2.40 (1.33–4.34) 0.009
a

Quartiles of plasma MIC1 were defined by the distribution among control individuals without CRC in our previous study.9 We assigned participants to quartile categories based upon cohort-specific cutpoints (NHS: Q1 <565; Q2 565–747, Q3 748–953, Q4 >953 pg/mL) (HPFS: Q1 <610; Q2 610–825; Q3 826–1060; Q4 >1060 pg/mL).

b

Tests for linear trend were conducted using the median values for each quartile of MIC1.

c

Additionally adjusted for the following potential confounders: cohort (sex); date of blood draw; race; body mass index (BMI) at the time of blood draw; physical activity (in MET-hours/week) at the time of blood draw; family history of CRC at time of blood draw; regular use of aspirin or NSAIDs at the time of blood draw; stage at diagnosis; history of polyps at the time of blood draw; grade (poor/unknown vs. well vs. moderate) at diagnosis; and anatomic tumor location (colon vs. rectum) at diagnosis

d

Multivariate models additionally adjusted for the plasma inflammatory markers CRP and IL6 as continuous measures as well as the factors listed in c