Table 3. Crude and adjusted OR and 95% CI for the associations between serum 25(OH) vitamin D concentration and risk of incident liver cancer in the case–control set nested in the Nutrition Intervention Trials cohort.
|
Continuousa |
Quartileb |
|||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
|
Q1 (n=266)c |
Q2 (n=265)c |
Q3 (n=266)c |
Q4 (n=265)c |
|
||||||||
OR | 95% CI | n | OR (Reference) | n | OR | 95% CI | n | OR | 95% CI | n | OR | 95% CI | Ptrend | Pinteraction | |
Crude | 1.00 | 0.94–1.06 | 63 | 1.00 | 55 | 0.88 | 0.59– 1.31 | 57 | 0.91 | 0.61–1.35 | 51 | 0.81 | 0.54–1.22 | 0.365 | — |
Age- and sex-adjusted | 0.98 | 0.92–1.04 | — | 1.00 | — | 0.88 | 0.59–1.31 | — | 0.90 | 0.61–1.35 | — | 0.81 | 0.54–1.21 | 0.352 | — |
Fully adjustedd | 0.95 | 0.88–1.03 | — | 1.00 | — | 0.91 | 0.60–1.37 | — | 0.87 | 0.57–1.31 | — | 0.74 | 0.47–1.18 | 0.208 | — |
Women | 0.95 | 0.81–1.11 | 28 | 1.00 | 19 | 0.75 | 0.39–1.42 | 26 | 0.94 | 0.51–1.73 | 18 | 0.69 | 0.34–1.39 | 0.421 | 0.617 |
Men |
0.95 |
0.87–1.05 |
35 |
1.00 |
36 |
1.02 |
0.59–1.77 |
31 |
0.81 |
0.46–1.44 |
33 |
0.79 |
0.42–1.48 |
0.338 |
|
Age at baseline | |||||||||||||||
<55 | 0.94 | 0.84–1.05 | 31 | 1.00 | 23 | 0.77 | 0.41–1.43 | 32 | 0.96 | 0.54–1.72 | 24 | 0.73 | 0.37–1.44 | 0.538 | 0.997 |
⩾55 |
0.97 |
0.88–1.08 |
32 |
1.00 |
32 |
1.11 |
0.63–1.93 |
25 |
0.79 |
0.44–1.44 |
27 |
0.80 |
0.42–1.53 |
0.349 |
|
Season of blood draw | |||||||||||||||
January–May | 0.97 | 0.89–1.06 | 62 | 1.00 | 53 | 0.90 | 0.60–1.37 | 50 | 0.85 | 0.56–1.30 | 32 | 0.81 | 0.50–1.31 | 0.345 | 0.703 |
August–September |
0.88 |
0.75–1.04 |
1 |
1.00 |
2 |
0.86 |
0.05–14.62 |
7 |
0.64 |
0.06–7.36 |
19 |
0.32 |
0.03–3.61 |
0.109 |
|
Follow-up years | |||||||||||||||
<7 | 0.95 | 0.84–1.08 | 14 | 1.00 | 16 | 1.27 | 0.59–2.74 | 14 | 0.88 | 0.40–1.96 | 18 | 0.86 | 0.36–2.05 | 0.576 | 0.989 |
⩾7 to <14 | 0.96 | 0.85–1.09 | 22 | 1.00 | 18 | 0.90 | 0.47–1.75 | 16 | 0.78 | 0.39–1.54 | 15 | 0.79 | 0.37–1.67 | 0.447 | |
⩾14 |
0.95 |
0.84–1.08 |
27 |
1.00 |
21 |
0.77 |
0.42–1.43 |
27 |
0.93 |
0.52–1.67 |
18 |
0.64 |
0.32–1.28 |
0.327 |
|
HBV/HCV seroposivity | |||||||||||||||
HBV+ | 0.97 | 0.89–1.05 | 43 | 1.00 | 37 | 0.85 | 0.53–1.36 | 40 | 0.90 | 0.56–1.44 | 37 | 0.79 | 0.47–1.32 | 0.425 | 0.442 |
HCV+ | 0.82 | 0.63–1.06 | 4 | 1.00 | 9 | 2.02 | 0.60–6.79 | 8 | 1.56 | 0.45–5.41 | 3 | 0.39 | 0.07–2.15 | 0.331 | 0.634 |
Neither |
0.98 |
0.86–1.12 |
18 |
1.00 |
17 |
0.97 |
0.49–1.93 |
15 |
0.86 |
0.42–1.76 |
14 |
0.80 |
0.36–1.76 |
0.538 |
— |
Calcium | |||||||||||||||
<1.485 mmol l−1 | 1.02 | 0.93–1.13 | 26 | 1.00 | 24 | 1.10 | 0.60–2.04 | 32 | 1.28 | 0.71–2.28 | 25 | 1.14 | 0.61–2.13 | 0.561 | 0.047 |
⩾1.485 mmol l−1 |
0.88 |
0.78–0.98 |
37 |
1.00 |
31 |
0.77 |
0.44–1.35 |
25 |
0.55 |
0.30–1.02 |
26 |
0.43 |
0.21–0.89 |
0.014 |
|
Trial | |||||||||||||||
Dysplasia Trial | 0.88 | 0.75–1.05 | 1 | 1.00 | 2 | 0.82 | 0.05–14.06 | 7 | 0.64 | 0.06–7.30 | 19 | 0.32 | 0.03–3.63 | 0.119 | 0.414 |
General Population Trial | 0.95 | 0.86–1.04 | 62 | 1.00 | 53 | 0.83 | 0.54–1.26 | 50 | 0.75 | 0.52–1.10 | 32 | 0.69 | 0.42–1.15 | 0.127 |
Abbreviations: BMI=body mass index; CI= confidence interval; HBcAg=hepatitis B core antigen; HBsAg=hepatitis B surface antigen; HBV=hepatitis B virus; HCsAg=hepatitis C surface antigen; HCV=hepatitis C virus; OR= odds ratio.
ORs for continuous vitamin D were scaled to one-half the interquartile range (7.9 nmol l–1).
We used sex-specific cutoff values to calculate relative risks. Quartile for women: <11.17, ⩾11.17 to <14.86, ⩾14.86 to <21.80, ⩾21.80 (nmol l–1); and quartile for men: <18.14, ⩾18.14 to <25.33, ⩾25.33 to <38.84, ⩾38.84 (nmol l–1).
Number of subjects in the control group.
Adjusted for age at baseline, sex, smoking, drinking, BMI, season of blood draw, HBsAg, HBcAg and HCsAg. The bold entries are considered statistically significant.