Clinical Study

Genetic Variations of α-Methylacyl-CoA Racemase Are Associated with Sporadic Prostate Cancer Risk in Ethnically Homogenous Koreans

Table 1

Demographic and clinical characteristics of the subjects.

VariablesCases Controls P valuea

Age, years (median) (68.0) (61.0)<0.001
Serum PSA, ng/mL (median) (9.8) (1.0)<0.001
 Serum PSA (ng/mL), no.<0.001
  <411 (5.7%)160 (94.7%)
  4–10 (≥4 to <10)87 (44.9%)8 (4.7%)
  10–20 (≥10 to <20)43 (22.2%)1 (0.6%)
  ≥2053 (27.3%)0 (0.0%)
BMI, kg/m2 (median) (24.1) (24.2)0.800
 BMI, no.0.388
  <25127 (65.5%)102 (61.1%)
  ≥2567 (34.5%)65 (38.9%)
Smoking, pack years (median) (18.3) (14.9)0.264
 Smoking status, no.0.672
  Never52 (26.8%)42 (24.9%)
  Ever142 (73.2%)127 (75.2%)
Drinking status, no.0.002
 Never68 (35.1%)34 (20.1%)
 Ever126 (65.0%)135 (79.9%)
Hypertension, no.0.502
 No120 (61.9%)109 (65.3%)
 Yes74 (38.1%)58 (34.7%)
Family history of prostate cancer0.132
 No186 (95.9%)146 (98.6%)
 Yes8 (4.1%)2 (1.4%)
Gleason score, no.
 2–699 (51.0%)
 762 (32.0%)
 8–1033 (17.0%)
pTstage, no.
 pT06 (3.1%)
 pT2a37 (19.1%)
 pT2b3 (1.6%)
 pT2c89 (45.9%)
 pT3a31 (16.0%)
 pT3b28 (14.4%)

Immunohistochemistry of AMACRSerum PSA, ng/mLP valuea
<44–10 (≥4 to <10)10–20 (≥10 to <20)≥20

0 (no staining)1 (2.6%)10 (25.6%)7 (18%)21 (53.9%)0.004
1+ (weakly positive)0 (0%)16 (47.1%)9 (26.5%)9 (26.5%)
2+ (positive)5 (9.1%)25 (45.5%)12 (21.8%)13 (23.6%)
3+ (strongly positive)5 (7.7%)36 (55.4%)15 (23.1%)9 (13.9%)

PSA: prostate specific antigen; BMI: body mass index; no.: number; AMACR: (R)-alpha-methyl-CoA racemase.
Pearson’s test for categorical variables and independent t-test for continuous variables; two-sided P-values.
“Family” represents relatives with the exception of first-degree relative, excluding 21 persons with missing values in the control group.