Gene polymorphisms in the Hodgkin's lymphoma patients and in control subjects
Gene . | Genotype/phenotype . | Hodgkin patients . | Controls . | P† . | ||
---|---|---|---|---|---|---|
N . | % . | N . | % . | |||
UGT1A1 | Missing or rare* | 4 | 6 | .18 | ||
66 | 148 | 48 | 71 | 39 | ||
67 | 130 | 42 | 89 | 49 | ||
77 | 31 | 10 | 21 | 12 | ||
CYP3A4 | Missing | 3 | 3 | 1.00 | ||
AA | 278 | 90 | 166 | 90 | ||
AG | 29 | 9 | 17 | 9 | ||
GG | 3 | 1 | 1 | 1 | ||
GTPIE5 | Missing | 2 | 0 | .99 | ||
AA | 130 | 42 | 79 | 42 | ||
AG | 141 | 45 | 85 | 45 | ||
GG | 40 | 13 | 23 | 12 | ||
GTT1 | Missing | 1 | 3 | .67 | ||
0 | 48 | 15 | 31 | 17 | ||
1 | 264 | 85 | 153 | 83 | ||
GSTM1 | Missing | 1 | 3 | .35 | ||
0 | 164 | 53 | 105 | 57 | ||
1 | 148 | 47 | 79 | 43 |
Gene . | Genotype/phenotype . | Hodgkin patients . | Controls . | P† . | ||
---|---|---|---|---|---|---|
N . | % . | N . | % . | |||
UGT1A1 | Missing or rare* | 4 | 6 | .18 | ||
66 | 148 | 48 | 71 | 39 | ||
67 | 130 | 42 | 89 | 49 | ||
77 | 31 | 10 | 21 | 12 | ||
CYP3A4 | Missing | 3 | 3 | 1.00 | ||
AA | 278 | 90 | 166 | 90 | ||
AG | 29 | 9 | 17 | 9 | ||
GG | 3 | 1 | 1 | 1 | ||
GTPIE5 | Missing | 2 | 0 | .99 | ||
AA | 130 | 42 | 79 | 42 | ||
AG | 141 | 45 | 85 | 45 | ||
GG | 40 | 13 | 23 | 12 | ||
GTT1 | Missing | 1 | 3 | .67 | ||
0 | 48 | 15 | 31 | 17 | ||
1 | 264 | 85 | 153 | 83 | ||
GSTM1 | Missing | 1 | 3 | .35 | ||
0 | 164 | 53 | 105 | 57 | ||
1 | 148 | 47 | 79 | 43 |
Patients with rare or missing phenotypes were not included in the prognostic analyses. For GSTT1 and GSTM1, genotype is not available; the information 0 or 1 refers to the presence or the absence of gene expression.
Two missing and 2 rare phenotypes for UGT1A1 (1 phenotype 65, and 1 phenotype 75) in HD patients, 3 missing and 2 rare phenotypes (2 phenotypes 65, and 1 phenotype 86) in controls.
Comparison of the proportions of between Hodgkin patients and controls, Fisher exact test, patients with missing or rare genotypes/phenotypes excluded.