individual had performed strenuous exercise the day before. After collection, the urine was centrifuged at 1500 rpm for 5 min, and the supernatant was frozen and stored at −20˚C. An 8-OHdG Check (Japan Institute for the Control of Aging (JaICA), Shizuoka, Japan) was used in the measurements, and the values obtained by dividing the calculated values by creatinine (ng/mg creatinine) were used. Triple checks were conducted, and measurement accuracy was R2 = 0.92 - 0.96 and cv = 0.021 - 0.023.

2.4. Statistical analysis

Spearman’s rank correlation coefficient was obtained for the relationship between the NEO-FFI and the SDS or STAI. The NEO-FFI N factor showed significant correlations with the SDS score and the STAI scores (trait anxiety and state anxiety) ((SDS r = 0.660, p = 0.003; STAI (trait anxiety) r = 0.671, p = 0.002; STAI (state anxiety) r = 0.575, p = 0.013). Therefore, subjects’ SDS score, STAI scores (trait anxiety and state anxiety), and U8-OHdG levels are expressed as means ± standard deviation adjusted for age, BMI, and NEO-FFI N factor. Repeated measures ANOVA was conducted with menstrual cycle (intra-individual levels in the follicular phase, ovulatory phase, and luteal phase) as a factor and SDS score, STAI scores, and U8-OHdG levels as dependent variables. Then, multiple comparisons were performed with Bonferroni’s method. Repeated measures ANOVA was also used with the time of classroom learning and before and after the national license examination (intra-individual levels at the time of classroom learning and one week before and the day after the national license examination) as individual factors and SDS score, STAI score, and U8-OHdG levels as dependent variables. Then, multiple comparisons were done with Bonferroni correction method. The normality of the SDS score, STAI scores, and U8-OHdG levels was confirmed with the Kolmogorov-Smirnov test (p = 0.065 - 0.200). Statistical analyses were performed using SPSS 21.0J (IBM Japan, Tokyo), and the level of significance was taken to be p < 0.05.

3. Results

3.1. During the Menstrual cycle

SDS score and STAI scores (trait anxiety and state anxiety) were measured in the follicular phase (43.7 ± 1.4, 50.9 ± 1.6, 46.8 ± 1.9), ovulatory phase (41.8 ± 1.3, 50.7 ± 1.7, 44.6 ± 2.1), and luteal phase (42.8 ± 1.1, 50.9 ± 1.8, 47.2 ± 2.1), respectively, and no significant differences were seen in the 3 items among the 3 phases during the menstrual cycle (Table 1: repeated measures 1-way ANOVA, p = 0.170 - 0.947). There was also no significant difference in U8-OHdG levels among the 3 phases during the menstrual cycle (Table 1).

3.2. Before and after the national license Examination

For the SDS score, no significant difference was seen 1 week before the national license examination (45.6 ± 2.0) compared with the time of classroom learning (42.7 ± 2.5) (Figure 1(A)). No significant difference was seen the day after the national license examination (39.3 ± 3.7) compared with 1 week before the examination (45.6 ± 2.0). On the STAI score (trait anxiety), no significant difference was seen 1 week before the national license examination (53.2 ± 3.4) compared with the time of classroom learning (50.9 ± 3.4). In contrast, it showed significantly lower scores on the day after the examination (46.7 ± 3.4) than during classroom learning and 1 week before the examination (Figure 1(B)). On the STAI score (state anxiety), the score was significantly higher 1 week before the national license examination (54.9 ± 40) compared with classroom learning (46.2 ± 3.1), showing that state anxiety was increased 1 week before the national license examination. In contrast, the score on the day after the national license examination (34.1 ± 4.0) was significantly lower compared with the time of classroom learning and 1 week before the examination, showing that state anxiety had decreased (Figure 1(C)). The U8-OHdG levels was significantly higher 1 week before the national license examination (11.4 ± 1.2 ng/mg creatinine) than at the time of classroom learning (7.5 ± 1.9 ng/mg creatinine) (p = 0.007). No difference was seen on the day after the national license examination (10.8 ± 1.5 ng/mg creatinine) compared with 1 week before the examination, and it was significantly higher than during classroom learning (Figure 1(D)).

Table 1. SDS score, STAI scores (trait anxiety and state anxiety) and U8-OHdG levels among the 3 phases during the menstrual cycle (n = 18).

P value: One-factor repeated measures analysis of variance; SD: standard deviation; 95% CI: 95% confidence interval; SDS: self-rating depression scale; STAI: State-Trait Anxiety Inventory; U8-OHdG: urine 8-hydroxy-2’-deoxyguanosine.

Figure 1. Comparisons of SDS score, STAI scores (trait anxiety and state anxiety) and U8-OHdG levels between before and after the national license examination. (A) SDS score in the upper left; (B) STAI score (trait anxiety) in the upper right; (C) STAI score (trait anxiety) in the lower left; (D) U8-OHdG levels in the lower right. Figures showed mean and SD error bar, and Numbers indicated mean (−1SD - +1SD). One-factor repeated measures analysis of variance: SDS score (p = 0.006), STAI score (trait anxiety) (p = 0.003), STAI score (state anxiety) (p < 0.001), U8-OHdG levels (p = 0.010). Bonferroni correction: †p < 0.05, ‡p < 0.01; a (vs a. Classroom lecture); b (vs b. One week before the national license examination); c (vs c. One day after the national license examination).

4. Discussion

It was demonstrated in this study that the oxidative stress biomarker U8-OHdG levels is not affected by changes in the menstrual cycle. U8-OHdG levels were shown to increase with the psychological stress from a national license examination. The results of this study suggest the possibility that U8-OHdG may be a biomarker of psychological stress in mental health care evaluations in women.

On the STAI score (state anxiety), a tool that has often been used as an indicator to evaluate psychological stress, the results showed that state anxiety increased significantly before the national license examination compared with the time of normal classroom learning, and that after the examination, it decreased significantly compared with the time of classroom learning and before the examination. This is similar to the results of a previous study [15] and suggests that national license examinations are valid as uniform psychological stressors.

There are many reports on the relationships between psychological stress and physical symptoms, including that psychological stress increases the risk of acute myocardial infarction [19] and diabetes [20] , and that psychological stress is related to dysmenorrhea [21] . At the same time, psychological stress is also reported to be difficult to assess objectively. Tools to test psychological stress are mainly questionnaires like the STAI and SDS, which rely on the subjective evaluations of subjects. In the search for objective assessment measures, the relationship between oxidative stress biomarkers and psychological stress has attracted attention in recent years [6] [7] .

Psychological stress is said to increase the production of ROS and increase oxidative stress in the body [1] [2] [3] [4] . Oxidative stress is defined as a state in which ROS production exceeds the body’s antioxidant capacity, and the balance between oxidation and antioxidation in the body is lost. Oxidative stress, by increasing the oxidative damage in the body, is said to facilitate the development of various diseases and aging. The body has a large antioxidant capacity, but excessive stress that exceeds the accommodation limit (threshold) weakens biological homeostasis. Disrupting the balance between ROS production and antioxidant defense leads to a state of oxidative stress, causing oxidative damage to biomolecules and then to cell and tissue damage. The psychological stress of national license examinations is thought to cause U8-OHdG levels to increase through these mechanisms.

Women have a menstrual cycle affected by sex hormones, in which various physiological reactions in the body [12] [22] and mental changes [23] [24] [25] occur. Sex hormones lead to the production of ROS via neutrophils, which have immune functions, and these ROS are reported to be involved in the occurrence of ovulation in the ovaries and subsequent follicle destruction [22] . After ovulation, the corpus luteum is formed and progesterone is secreted, but if pregnancy is not established, a process of functional corpus luteum regression begins. ROS are also said to play a role in promoting this functional corpus luteum regression [22] , and ROS production may be considered essential in maintaining homeostasis in ovarian function. The sex hormone estrogen is considered to have an antioxidant effect [26] , and the menstrual cycle is also thought to affect the antioxidant activity in the body. Consequently, since changes in the balance of ROS production and antioxidant activity occur through the secretion of menstrual cycle-dependent sex hormones, the menstrual cycle may be said to affect oxidative stress. Superoxide dismutase (SOD), glutathione reductase (GSHR), and glutathione peroxidase (GPx) are taken to be the main biomarkers of oxidative stress. However, tests using these biomarkers have confirmed that they increase in the ovulatory phase and decrease in the luteal phase, and the menstrual cycle has been reported to be involved in oxidative stress [27] . U8-OHdG is also commonly used as a biomarker of oxidative stress, and in a test of premenopausal women with uterine fibroids and healthy premenopausal women, the fluctuations in estrogen and progesterone levels accompanying the menstrual cycle in healthy women was not reported to interact with U8-OHdG levels [28] . The U8-OHdG used as a biomarker of oxidative stress in this study is a marker of DNA oxidative damage that is released extracellularly in the process of gene DNA repair and excreted in urine via the blood [29] . There are many types of oxidative damage to DNA, but U8-OHdG is excreted into urine without being subjected to secondary metabolism. This suggests the possibility that U8-OHdG reflects oxidative stress that is due to psychological stress by a mechanism that differs from the one for the production of oxidative stress accompanying the menstrual cycle.

Our study has some limitations. The subjects in this study were female students from a single university, and there may be a problem in generalizing the study results. However, their physical measurements were similar to the mean values for the representative national population [30] . Conversely, they were similar in terms of lifestyle and other factors, and so the results are thought to have a high level of internal validity. In this study, smoking history was self-reported. The confidentiality of the survey content was duly considered, but there is known to be a relationship between psychological stress and smoking [31] , and a study that measures urine cotinine levels may be needed in the future. Moreover, psychological stress was assessed only with the SDS and STAI. The subjects were not diagnosed by a psychiatrist. Since there was no psychiatric diagnosis, the possibility that the study included subjects with depression cannot be ruled out. A future investigation that determines depression together with a physician’s diagnosis may also be necessary.

5. Conclusion

In summary, U8-OHdG levels were shown to increase with the psychological stress from a national license examination, unaffected by the menstrual cycle. This result suggests the possibility that U8-OHdG may be a useful biomarker for the objective assessment of psychological stress. Many things are still not understood about the mechanism for the occurrence of oxidative stress from psychological stress. Thus, from the perspective of the prevention and treatment of oxidative stress as well, elucidation of the relationship between psychological stress and oxidative stress may be a topic for future study.


The authors would like to express their gratitude to all who so generously cooperated in this questionnaire survey. This work was supported by JSPS KAKENHI Grant-in-Aid for Scientific Research (C) Number 26350876.

Cite this paper
Iida, T. , Ito, Y. , Ishikawa, H. , Kanazashi, M. , Teradaira, R. , Tatsumi, A. and Ezoe, S. (2018) Effects of Psychological Stress from a National License Examination on the Urine 8-Hydroxy-Deoxyguanosine Levels in Young Female Students, Taking into Account the Menstrual Cycle. Open Journal of Preventive Medicine, 8, 21-31. doi: 10.4236/ojpm.2018.82003.
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