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. Author manuscript; available in PMC: 2024 Aug 6.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2024 Feb 6;33(2):234–243. doi: 10.1158/1055-9965.EPI-23-0634

Table 2.

Top-ranking associations of the common variants analysis regarding the performance of the Trail making test.

Genotype Case*, N (%) Control*, N (%) Model Case*, N (%) Control*, N (%) P value** OR [95%-CI] P value adj***
AK8 rs17407084
All cohort, N=229
TT 11 (55.0) 188 (90.0) TT 11 (55.0) 188 (90.0) 2.16E-04d 7.3 [2.7–19.7] 4.52E-04
TC 7 (35.0) 21 (10.0) TC+CC 9 (45.0) 21 (10.0)
CC 2 (10.0) 0 (0.0)

ZNF382 rs61732180
Males, N=112
CC 3 (27.3) 65 (64.4) CC+CT 6 (54.5) 97 (96.0) 3.58E-04r 20.2 [4.3–95.4] 2.62E-04
CT 3 (27.3) 32 (31.6) TT 5 (45.5) 4 (4.0)
TT 5 (45.4) 4 (4.0)

AK8 rs17407084
Standard risk, N=105
TT 2 (28.6) 90 (91.8) TT 2 (28.6) 90 (91.8) 2.44E-04d 28.1 [4.7–168.8] 4.40E-04
TC 4 (57.1) 8 (8.2) TC+CC 5 (71.4) 8 (8.2)
CC 1 (14.3) 0 (0.0)

AK8: Adenylate Kinase 8; ZNF: Zinc Finger Protein 382; FDR: false discovery rate; OR: odds ratio. TT indicates homozygosity for the T allele; TC represents heterozygosity, with one copy of the T allele and one copy of the C allele; CC indicates homozygosity for the C allele.

*

Participants with and without indicated complications are defined as cases and controls, respectively.

**

P values are calculated by chi-square or Fisher exact test, as appropriate. The most representative genetic model used is indicated (a: Additive; d: Dominant, r: Recessive).

***

P value adj: p value from logistic regression adjusted for age at diagnosis, sex, time since the end of treatment, protocol, and treatment variable (chemotherapy only or chemotherapy and radiotherapy).