The odds ratios were conditioned on the matching variables and adjusted for exact
age, marital status, education, smoking, height and body mass index. Tests for
heterogeneity for the case-defined factors were obtained by fitting separate
models for each subgroup and assuming independence of the ORs using a method
analogous to a meta-analysis. Tests for heterogeneity for the other factors were
assessed with a χ2-test of interaction between the subgroup
and continuous trend test variable. Note that the number of cases for each
tumour subtype may be fewer than shown in the baseline tables since here the
analysis for each subgroup of a case-defined factor is restricted to complete
matched sets for each category of the factor in turn; some matched sets contain
a mixture of subtypes and while controls are allocated case-defined
characteristics in equal proportion to the cases, 25(OH)D may be unknown for
some participants, leading to incomplete matched sets.
Stage (early, T1 and/or stage I; other localized, T2/N0/M0 and/or stage II, and
advanced, T3-T4/N1/M1 and/or stage III-IV), grade (low-intermediate, Gleason sum
was < 8 or equivalent; high, Gleason sum was ≥ 8 or equivalent,
and aggressive (T4/N1/M1 and/or stage IV and/or prostate cancer death). White
ethnicity (89.4% yes, 10.6% no).