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. Author manuscript; available in PMC: 2014 Jun 1.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2013 Apr 29;22(6):1142–1152. doi: 10.1158/1055-9965.EPI-13-0108

Table 1.

Clinical, pathologic, and molecular characteristics of colorectal cancer cases according to post-diagnosis physical activity quartile

Clinical, pathologic or molecular feature Total N Post-diagnosis physical activity quartile
P value
Q1 (Lowest) Q2 (Second) Q3 (Third) Q4 (Highest)
All cases 605 152 146 158 149
Sex 0.99
 Male (HPFS) 305 (50%) 77 (51%) 75 (51%) 78 (49%) 75 (50%)
 Female (NHS) 300 (50%) 75 (49%) 71 (49%) 80 (51%) 74 (50%)
Mean age (SD) 67.3 (8.0) 68.2 (8.5) 67.8 (8.1) 66.7 (7.5) 66.4 (7.6) 0.025
Body mass index (kg/m2) 0.017
 <30 503 (83%) 116 (76%) 123 (84%) 130 (82%) 134 (90%)
 ≥30 102 (17%) 36 (24%) 23 (16%) 28 (18%) 15 (10%)
Family history of colorectal cancer in first degree relative(s) 0.93
 (−) 482 (80%) 122 (80%) 114 (78%) 128 (81%) 118 (79%)
 (+) 123 (20%) 30 (20%) 32 (22%) 30 (19%) 31 (21%)
Year of diagnosis 0.54
 Prior to 1995 243 (40%) 55 (36%) 65 (45%) 64 (41%) 59 (40%)
 1995 to 2006 362 (60%) 97 (64%) 81 (55%) 94 (59%) 90 (60%)
Post-diagnosis aspirin use 0.80
 Non-user 368 (61%) 93 (62%) 85 (58%) 95 (60%) 95 (64%)
 Aspirin user 236 (39%) 58 (38%) 61 (42%) 63 (40%) 54 (36%)
Post-diagnosis smoking status 0.10
 Never 238 (41%) 60 (42%) 58 (41%) 57 (38%) 63 (43%)
 Former 305 (53%) 72 (51%) 68 (49%) 84 (55%) 81 (55%)
 Current 37 (6.4%) 10 (7.0%) 14 (10%) 11 (7.2%) 2 (1.4%)
Post-diagnosis alcohol consumption 0.85
 None 229 (39%) 58 (41%) 56 (39%) 62 (40%) 53 (36%)
 Any 362 (61%) 85 (59%) 88 (61%) 94 (60%) 95 (64%)
Tumor location 0.92
 Cecum 108 (18%) 26 (17%) 23 (16%) 33 (21%) 26 (17%)
 Ascending to transverse colon 156 (26%) 36 (24%) 38 (26%) 43 (28%) 39 (26%)
 Splenic flexure to sigmoid 190 (32%) 47 (31%) 50 (34%) 44 (28%) 49 (33%)
 Rectosigmoid and rectum 149 (25%) 43 (28%) 35 (24%) 36 (23%) 35 (23%)
Disease stage 0.99
 I 161 (27%) 38 (25%) 38 (26%) 43 (27%) 42 (28%)
 II 212 (35%) 51 (34%) 54 (37%) 53 (34%) 54 (36%)
 III 165 (27%) 45 (30%) 38 (26%) 45 (28%) 37 (25%)
 Unknown 67 (11%) 18 (12%) 16 (11%) 17 (11%) 16 (11%)
Tumor differentiation 0.70
 Well to moderate 556 (93%) 142 (94%) 136 (94%) 140 (91%) 138 (93%)
 Poor 42 (7.0%) 9 (6.0%) 9 (6.2%) 14 (9.1%) 10 (6.8%)
CIMP status 0.21
 CIMP-low/0 483 (84%) 116 (82%) 119 (84%) 123 (81%) 125 (89%)
 CIMP-high 92 (16%) 26 (18%) 22 (16%) 29 (19%) 15 (11%)
MSI status 0.37
 MSS 482 (84%) 119 (83%) 118 (85%) 122 (81%) 123 (88%)
 MSI-high 90 (16%) 25 (17%) 21 (15%) 28 (19%) 16 (12%)
LINE-1 methylation level [Mean (SD)] 61.8 (9.5) 61.4 (9.9) 60.8 (10.0) 62.2 (9.3) 62.8 (8.9) 0.12
BRAF mutation 0.77
 (−) 510 (89%) 130 (90%) 124 (89%) 131 (87%) 125 (90%)
 (+) 64 (11%) 14 (9.7%) 16 (11%) 20 (13%) 14 (10%)
KRAS mutation 0.25
 (−) 364 (63%) 94 (65%) 87 (62%) 104 (68%) 79 (57%)
 (+) 213 (37%) 51 (35%) 53 (38%) 49 (32%) 60 (43%)
CDKN1B (p27) expression 0.36
 (−) 234 (39%) 52 (34%) 64 (44%) 63 (40%) 55 (37%)
 (+) 371 (61%) 100 (66%) 82 (56%) 95 (60%) 94 (63%)
Nuclear CTNNB1 (β-catenin) expression 0.53
 (−) 290 (53%) 76 (58%) 72 (54%) 75 (53%) 67 (49%)
 (+) 255 (47%) 56 (42%) 62 (46%) 66 (47%) 71 (51%)
PTGS2 (COX-2) expression 0.43
 (−) 223 (37%) 61 (40%) 58 (40%) 56 (35%) 48 (32%)
 (+) 382 (63%) 91 (60%) 88 (60%) 102 (65%) 101 (68%)

(%) indicates the proportion of cases with a specific clinical, pathologic, or molecular feature in a given physical activity quartile. A Chi squared P value is given for comparison across quartiles. ANOVA was used to compare the means of age and LINE-1 methylation. The Bonferroni-corrected P value for significance was P=0.0026 (0.05/19).

CIMP, CpG island methylator phenotype; HPFS, Health Professionals Follow-up Study; MSI, microsatellite instability; MSS, microsatellite stable; NHS, Nurses’ Health Study; SD, standard deviation.