An Evaluation of DNA Methyltransferase 1 (DNMT1) Single Nucleotide Polymorphisms and Chemotherapy-Associated Cognitive Impairment: A Prospective, Longitudinal Study

被引:12
作者
Chan, Alexandre [1 ,2 ,3 ]
Yeo, Angie [1 ]
Shwe, Maung [1 ]
Tan, Chia Jie [1 ]
Foo, Koon Mian [4 ]
Chu, Pat [5 ]
Khor, Chiea Chuen [6 ,7 ]
Ho, Han Kiat [1 ]
机构
[1] Natl Univ Singapore, Dept Pharm, Singapore, Singapore
[2] Natl Canc Ctr Singapore, Dept Pharm, Singapore, Singapore
[3] Duke NUS Grad Med Sch Singapore, Singapore, Singapore
[4] KK Womens & Childrens Hosp, Dept Pharm, Singapore, Singapore
[5] Singapore Cord Blood Bank, Singapore, Singapore
[6] Genome Inst Singapore, Human Genet, Singapore, Singapore
[7] Singapore Eye Res Inst, Singapore, Singapore
关键词
BREAST-CANCER; FUNCTIONAL ASSESSMENT; BRAIN; METHYLATION; DYSFUNCTION; CYTOKINES; SURVIVORS; VARIANTS;
D O I
10.1038/s41598-019-51203-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Strong evidence suggests that genetic variations in DNA methyltransferases (DNMTs) may alter the downstream expression and DNA methylation patterns of neuronal genes and influence cognition. This study investigates the association between a DNMT1 polymorphism, rs2162560, and chemotherapy-associated cognitive impairment (CACI) in a cohort of breast cancer patients. This is a prospective, longitudinal cohort study. From 2011 to 2017, 351 early-stage breast cancer patients receiving chemotherapy were assessed at baseline, the midpoint, and the end of chemotherapy. DNA was extracted from whole blood, and genotyping was performed using Sanger sequencing. Patients' self-perceived cognitive function and cognitive performance were assessed at three different time points using FACT-Cog (v.3) and a neuropsychologica I battery, respectively. The association between DNMT1 rs2162560 and cognitive function was evaluated using logistic regression analyses. Overall, 33.3% of the patients reported impairment relative to baseline in one or more cognitive domains. Cognitive impairment was observed in various objective cognitive domains, with incidences ranging from 7.2% to 36.9%. The DNMT1 rs2162560 A allele was observed in 21.8% of patients and this was associated with lower odds of self-reported cognitive decline in the concentration (OR = 0.45, 95% CI: 0.25-0.82, P= 0.01) and functional interference (OR = 0.48, 95% CI: 0.24-0.95, P = 0.03) domains. No significant association was observed between DNMT1 rs2162560 and objective cognitive impairment. This is the first study to show a significant association between the DNMT1 rs2162560 polymorphism and CACI. Our data suggest that epigenetic processes could contribute to CACI, and further studies are needed to validate these findings.
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页数:8
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