Self-esteem refers to the extent to which we feel positive or negative about ourselves, and reflects an individual’s subjective evaluation of personal worth and attitudes about the self. As one kind of positive psychosocial resources, high self-esteem has been found to buffer the effects of stress on physical health. However, little is known about the possible neural basis underlying the association between physical health and self-esteem. In the present study, we investigated whether the hippocampus served as a neuroanatomical basis for the association between self-esteem and physical health in a large population of healthy young adults. We examined self-esteem and self-reported physical health with the Rosenberg Self Esteem Scale (RSES) and the Chinese Constitution Questionnaire (CCQ) respectively, and gray matter volume of the hippocampus was measured using magnetic resonance imaging. As expected, we found that individuals with higher levels of self-esteem had better self-reported physical health. Importantly, the mediation analysis showed that the gray matter volume of the hippocampus mediated the link between self-esteem and physical health, suggesting its critical role in the neural circuitry through which self-esteem is related to physical health.
In our daily life, we all have a mental picture of who we are, how we look, what we’re good at, and what our weaknesses might be, which contributes to our self-esteem. Self-esteem is an overall reflection of an individual’s self-worth, and represents the capacity to feel worthy of happiness and be able to successfully address life challenges1,2. As a kind of important psychological resources, self-esteem is thought to be a protective factor for our physical health. Specifically, low self-esteem is accompanied by negative emotions such as anxiety and depression3,4, leads to unhealthy behaviors including smoking and alcohol abuse5,6, and then this combination increases the risk of heart diseases and other illness7. On the contrary, a high level of self-esteem is associated with positive feelings such as joy, pleasure, optimism, relaxation, and gratitude, which offer protection from stress and contribute to physical health3,8,9. In fact, many studies have demonstrated that higher self-esteem is related to better physical health and longer survival2,10,11,12,13. Several theories have been proposed to account for the cognitive mechanisms that link self-esteem to physical health13,14,15,16. However, little is known about the underlying neural basis through which self-esteem is related to physical health.
Abundant evidence suggests that the hippocampus is the core area of self-esteem17,18,19,20,21,22,23. For example, Pruessner et al.17 found that self-esteem was related to hippocampal volume in both young and old adults. A voxel-based morphometry (VBM) study18 showed that the gray matter (GM) volume of hippocampus was positively correlated with self-esteem. A recent study using a large sample also found that higher self-esteem was linked with greater GM volume of hippocampus, which was the region with the highest correlation to self-esteem within the whole brain19. On the other hand, the damage to the hippocampus has been demonstrated to be associated with not only a variety of neurological and psychiatric disorders, but also some physical diseases24,25. For example, studies of Type 2 diabetes have revealed reduced hippocampal volume26, hypertension was associated with hippocampal atrophy27. What’s more, the hippocampus shrinks in the pre-disease conditions, such as chronic jet-lag28 and elevated circulating inflammatory cytokines29. Meanwhile, greater hippocampal volume is associated with aerobic fitness which may improve our physical health30. In addition, in animal studies, hippocampal stimulation decreases heart rate, blood pressure and respiratory rate in awake rats31. Moreover, some recent studies have suggested the neural substrates that may underlie the interactions between psychological variables and physical health32,33,34. For example, Song et al. (2015) has shown that the amygdala underlies the association between emotion regulation and physical health. Similarly, recent work by Brody and colleagues has shown that enhancing supportive parenting can not only prevent the decline in volume of the hippocampus and amygdala but also reduce the incidence of prediabetes32,33. Therefore, we hypothesized that the hippocampus might serve as the neural substrate through which self-esteem is associated with physical health.
To test this hypothesis, we first examined the association between self-esteem and self-reported physical health in a large population of healthy young adults (N = 239) with two behavioral scales: the Rosenberg Self Esteem Scale (RSES)1 and the Chinese Constitution Questionnaire (CCQ)35 that is a national standard inventory on health in China. Then, we examined whether GM volume of the hippocampus mediated the relation between self-esteem and physical health, given that self-esteem is generally taken as a determinant of physical health not vice versa13,14,15,16.
Material and Methods
Two hundred and thirty nine college students (128 females; mean age = 22.8) from Beijing Normal University participated in this study. None of the participants reported history of neurological or psychiatric disorders. This study is part of an ongoing project (Gene Environment Brain and Behavior)20,34,36. Both the behavioral and fMRI protocol were approved by the Institutional Review Board (IRB) of Beijing Normal University and all experiments were performed in accordance with the relevant guidelines and regulations. All participants gave informed written consent prior to the experiments and then completed the paper-pencil questionnaires and structural MRI scanning. Because the acquisition of MRI data was time-consuming for the large sample of participants, the questionnaires were measured more than a month after MRI data acquisition.
Assessment of Self-Esteem
The self-esteem was assessed with RSES1, which contains ten items to assess one’s global self-worth incorporating both positive and negative feelings about the self (e.g., “On the whole, I am satisfied with myself”). Participants were instructed to report the extent to which they agreed or disagreed with each statement using a 6-point Likert-type scale (1 = strongly disagree, 6 = strongly agree). The total score of self-esteem was calculated by summing the score of each item, with higher scores indicating more positive evaluations of one’s worth and value.
Assessment of physical health
Physical health was assessed with the CCQ35, which was designed to measure the general physical health status of individuals in normal population. It contains 59 items on a variety of physical symptoms and health problems (e.g., “I catch cold more easily than others.”). Participants were instructed to answer each question based on their daily experiences on a 5-point Likert-scale (1 = Never, 5 = All the time). To get a pure measure of physical health, eight items that are related to psychological symptoms such as “I get anxious and worried easily” were excluded in future analyses. The total score of physical health was calculated by summing the score of remaining 51 items, with higher scores indicating better physical health. Previous studies have shown that the questionnaire has high reliability and validity35. A recent study34 showed that participants’ physical health assessed by the CCQ was positively correlated with their general evaluation about their physical health status (r = 0.34, p < 0.001), indicating that the CCQ had good validity.
MRI data acquisition and analysis
Structural MRI scanning was performed on a Siemens 3 T Trio scanner (MAGENTOM Trio with a Tim system) with a 12-channel phased-array head coil at BNU Imaging Center for Brain Research, Beijing, China. MPRAGE, an inversion prepared gradient echo sequence (bandwidth = 190 Hz/pixel, flip angle = 7 degree, TR/TE/TI = 2.53 s/3.39 ms/1.1 s), was used to acquire 3D T1-weighted whole brain structural images. One hundred and twenty-eight contiguous sagittal slices were imaged with 1 × 1 mm in-plane resolution and 1.33 mm slice thickness for whole brain coverage.
Voxel-based morphometry (VBM) which provides a quantitative measure of tissue volume per unit volume of spatially normalized image was used to explore the neural correlates of the behaviorally-observed association37. Specially, VBM was performed using SPM8 (Statistical Parametric Mapping, Wellcome Department of Imaging Neuroscience, London, UK). Preprocessing steps and an optimized VBM protocol were performed on T1-weighted structural images. First, image quality was assessed by manual visual examination. Five participants whose images had excessive scanner artifacts or showed gross anatomical abnormalities were excluded. Second, the origin of brain was manually set to the anterior commissure for each participant. Third, images were segmented into four distinct tissue classes: GM, white matter, cerebrospinal fluid and everything else (e.g., skull and scalp) using a unified segmentation approach38. Forth, the GM images for each participant were then normalized to a study-specific template in MNI152 space using the Diffeomorphic Anatomical Registration through Exponential Lie algebra (DARTEL) registration method39. The DARTEL registration involves iteratively computing the study-specific template, based on the average tissue probability maps from all participants, and then warping all participants’ tissue maps into the generated template to increasingly improve the alignment. Fifth, GM voxel values were modulated by multiplying the Jacobian determinants derived from the normalization to preserve the volume of tissue from each structure after warping. The modulated GM images were then smoothed with an 8 mm full width at half maximum (FWHM) isotropic Gaussian kernel. Finally, to exclude noisy voxels, the modulated images were masked using an absolute masking with a threshold of 0.2. The masked modulated GM images were used for further statistical analyses.
We used the Harvard-Oxford subcortical probabilistic structural atlas40 with a probability threshold of 50% to define the left and right hippocampus as regions of interest (ROI). We calculated averaged GM volume across all voxels in each ROI. To determine the neural correlates of behavioral measures, we performed Pearson correlation analyses between average GM volume of the left and right hippocampus and behavioral measures of self-reported physical health and self-esteem. Further, we performed stepwise regression analyses which took the total GM volume (TGMV) and gender as confounding covariates to confirm the results. Finally, we conducted a mediation analysis to examine whether the hippocampus served as a neuroanatomical basis for the association between self-esteem and physical health. Here bootstrap simulation was used to test the significance of the mediation effect. Because the sampling distribution of mediation effect is skewed, bootstrap approach has been proved to be more powerful than traditional methods (e.g., Sobel test) and has been widely used in mediation analysis in recent years41,42.
First, we used the RSES 1 and the CCQ35 to measure participants’ self-esteem and physical health respectively. The kurtosis (CCQ: −0.56, RSES: −0.42) and skewness (CCQ: −0.12, RSES: −0.28) of the two scales indicated the normality of the data, and both scales possessed excellent internal reliabilities (Cronbach’s αRSES = 0.897, Cronbach’s αCCQ = 0.92). The scores of both CCQ (mean = 187.41; SD = 44.78) and RSES (mean = 21.67; SD = 6.38) showed a significant amount of individual differences.
To investigate the relationship between self-esteem and physical health, we correlated self-esteem scores with self-reported physical health measured by the CCQ. The result showed that self-esteem was positively correlated with physical health (r = 0.271, p < 0.001; Fig. 1A), indicating that individuals with higher self-esteem possessed better physical health. The finding was further confirmed by a stepwise linear regression analysis which showed that self-esteem was significantly correlated with physical health with gender regressed out (β = 0.272, p < 0.001). Next, we investigated the neural basis through which self-esteem was associated with physical health.
Considering that self-esteem has been demonstrated to be related with the GM volume of hippocampus17,18,19,20,22 and the hippocampus is associated with some physical diseases such as hypertension and diabetes26,27, we hypothesized that the hippocampus might be the neural basis through which self-esteem is related to physical health. To examine this hypothesis, we first confirmed that the GM volume in both the left (r = 0.142, p = 0.028) and right hippocampus (r = 0.141, p = 0.029) was positively correlated with self-esteem, indicating that individuals with larger GM volume in the hippocampus possessed higher self-esteem. This association has been reported in our previous study using the same dataset19,20 as well as in several other studies17,18,22. Besides, the results also showed positive correlation between physical health and the GM volume in the left (r = 0.183, p = 0.005) and right hippocampus (r = 0.150, p = 0.021), suggesting that individuals with larger GM volume in the hippocampus had better physical health. The finding was further confirmed by stepwise linear regression analyses which showed that the GM volume in the left and right hippocampus was significantly related with individual’s self-esteem (βleft = 0.142, p = 0.028; βright = 0.141, p = 0.029) and physical health (βleft = 0.183, p = 0.005; βright = 0.150, p = 0.021) with TGMV and gender regressed out. Because similar results were observed in both hemispheres, the GM volume across the left and right hippocampus was collapsed (GM volume in the whole hippocampus and self-esteem: r = 0.144, p = 0.026, Fig. 1B; GM volume in the whole hippocampus and physical health: r = 0.170, p = 0.008, Fig. 1C).
Because individuals who had larger GM volume in the hippocampus possessed not only higher self-esteem but also better physical health, it is likely that the hippocampus serves as a possible neural substrate for the link between physical health and self-esteem. To test this hypothesis, a mediation analysis based on individual differences in self-esteem, physical health, and GM volume of the hippocampus was performed. The result showed that the correlation between self-esteem and physical health decreased (r = 0.252, p < 0.001) after their correlation (r = 0.271, p < 0.001) being adjusted by the mediator of the hippocampus (Fig. 1D). Bootstrap simulation (n = 5000) further confirmed that the indirect effect of self-esteem on physical health through the GM volume of the hippocampus was significant (p = 0.05) with 95% confidence interval (CI) of [0.007, 0.182]. The result suggests that self-esteem is related to physical health in part through the GM volume of hippocampus.
In the current study, we investigated the possible neural basis through which self-esteem was related to physical health. Our study not only reproduced the results that higher self-esteem was associated with better physical health, but also showed that the hippocampus mediated the link between self-esteem and physical health, suggesting its critical role in the neural circuit through which self-esteem is related to physical health.
Our study replicated previous findings that higher self-esteem is associated with better physical health2,10,11,12,13,43. Why is higher self-esteem link with better physical health? Several models used in health promotion or prevention offer insight into cognitive mechanisms that link self-esteem to health13,14,15,16. For example, the transactional model of stress and coping suggests that positive self-esteem can buffer stress by mitigating the perceived threat and by enhancing the selection and implementation of efficacious coping strategies, which in turn modulate physiological responses to stressors contributing to illness and physical health14. Generally, self-esteem can be seen as an internal moderator of stressors, and increasing the levels of self-esteem will reduce the incidence of illness15. Alternatively, the health behavior model has confirmed the role of self-esteem as a health behavioral determinant, that is, low self-esteem can trigger poor coping behavior or risk behavior that subsequently increases the likelihood of certain diseases, including mental disorders and physical diseases16,44. In fact, previous studies had verified that low levels of self-esteem was related to the incidence of health risk behaviors, such as smoking, alcohol consumption and drug use5,6,45, which may do harm to our health. Based on these models and evidences, self-esteem may be related to physical health by buffering the stress or increasing the health behaviors.
Our study showed that the GM volume of hippocampus was related to the individual difference in physical health in the healthy sample. The results extend the previous studies that have demonstrated the association between hippocampus volume and physical diseases such as hypertension and diabetes26,27. A large body of research has shown that the interaction of the hippocampus and the hypothalamic-pituitary-adrenal (HPA) axis might explain the onset of various illnesses25,46,47,48. The HPA axis has traditionally been regarded as the body’s stress tolerance and energy regulation system. Its hyperactivation is associated with excessive release of stress hormones (e.g. glucocorticoid, cortisol) and subsequently results in various health problems25,47. Meanwhile, the hippocampus activity has been suggested to exert a tonic inhibitory influence on the activation of HPA axis and subsequently decrease glucocorticoid secretion, and promote more efficient regulation of the HPA axis to ultimately promote physical health48.
Importantly, our study showed that self-esteem was associated with physical health through the hippocampus. This suggests that the hippocampus is a key node in the neural circuit underlying the link between self-esteem and physical health. In the face of stressful situations, the HPA axis, the autonomic nervous system, and the cardiovascular, metabolic, and immune systems interact with each other to achieve allostasis (adaptation) in the short term and lead to allostatic load (“the wear and tear on the body”) in the long term49. Allostatic load can result in altered brain architecture, especially in the hippocampus49. For example, there is evidence that prolonged stress which triggers the over release of glucocorticoids caused the atrophy of the hippocampus50,51,52,53,54,55,56,57. On the other hand, high self-esteem can help individuals to take effective coping strategies that buffers physiological responses to stressors17,20,22,23, and low self-esteem was related to higher cortisol response to stress task58 and lack of habituation to repeated stress exposure59. Consequently, high self-esteem can prevent the hippocampus from the harmful effects of allostatic load such as excessive glucocorticoids. Better preserved hippocampus in turn inhibits the prolonged excessive activity of the HPA, which can reduce allostatic load and guard against the disorders of neuroendocrine and immune systems, and ultimately promotes physical health46,60.
In sum, our study revealed the possible neural substrate underlying the association between physical health and self-esteem. Practically, given the protective role of self-esteem on physical health, it is recommended that its potential should be reconsidered in future health promotion programs. That is, a health promotion program should include a focus on fostering self-esteem, which can prevent an array of physical diseases. There are several issues unresolved in our study. First, the cross-sectional findings in the current study do not permit inference about the causal relationship among self-esteem, physical health, and the hippocampus, and future longitudinal studies are needed to provide better understanding for this topic. Secondly, we did not measure health behaviors in the current study and our results were inappropriate for providing neural constraints for the health behavior models. Therefore, future researches are needed to illuminate the neural mechanism through which physical health might be influenced by the interaction of self-esteem and health behaviors.
Rosenberg, M. The measurement of self-esteem. In: Rosenberg M, editor. Society and the adolescent self image. New York: Princeton University Press. pp. 297–307 (1965).
Antonucci, T. C. & Jackson, J. S. Physical health and self-esteem. Family & Community Health 6, 1–9 (1983).
Brown, J. D. & Marshall, M. A. Self-esteem and emotion: Some thoughts about feelings. Personality & Social Psychology Bulletin 27, 575–584 (2001).
Kamody, R. C. et al. Relating shape/weight based self-esteem, depression, and anxiety with weight and perceived physical health among young adults. Body Image 25, 168–176 (2018).
Dielman, T. E., Leech, S. L., Lorenger, A. T. & Horvath, W. J. Health locus of control and self-esteem as related to adolescent health behavior and intentions. Adolescence 19, 935 (1984).
Kavas, A. B. Self-esteem and health-risk behaviors among Turkish late adolescents. Adolescence 44, 187–198 (2009).
Trzesniewski, K. H. et al. Low self-esteem during adolescence predicts poor health, criminal behavior, and limited economic prospects during adulthood. Developmental psychology 42, 381–390 (2006).
Wenglert, L. & Rosén, A. S. Optimism, self-esteem, mood and subjective health. Personality & Individual Differences 18, 653–661 (1995).
Mäkikangas, A., Kinnunen, U. & Feldt, T. Self-esteem, dispositional optimism, and health: Evidence from cross-lagged data on employees. Journal of Research in Personality 38, 556–575 (2004).
O’Donnell, K., Brydon, L., Wright, C. E. & Steptoe, A. Self-esteem levels and cardiovascular and inflammatory responses to acute stress. Brain, behavior, and immunity 22, 1241–1247 (2008).
Christie-Mizell, C. A., Ida, A. K. & Keith, V. M. African Americans and Physical Health: The Consequences of Self-Esteem and Happiness. Journal of Black Studies 40, 1189–1211 (2010).
Marmot, M. Self esteem and health. Bmj 327, 574–575 (2003).
Mann, M., Hosman, C. M., Schaalma, H. P. & de Vries, N. K. Self-esteem in a broad-spectrum approach for mental health promotion. Health education research 19, 357–372 (2004).
Lazarus, R. S. & Folkman, S. Coping and adaptation. In Gentry, W.D. (ed.), The Handbook of Behavioral Medicine. Guilford, New York, pp. 282–325. (1984).
Albee, G. The argument for primary prevention. Journal of Primary Prevention 5, 213–219 (1985).
Godin, G. The theory of planned behavior: a review of its applications to health-related behaviors. American Journal of Health Promotion 11, 87 (1996).
Pruessner, J. C. et al. Self-esteem, locus of control, hippocampal volume, and cortisol regulation in young and old adulthood. NeuroImage 28, 815–826 (2005).
Agroskin, D., Klackl, J. & Jonas, E. The self-liking brain: a VBM study on the structural substrate of self-esteem. Plos One 9, e86430 (2014).
Wang, Y., Kong, F., Huang, L. & Liu, J. Neural Correlates of Biased Responses: The Negative Method Effect in the Rosenberg Self-Esteem Scale Is Associated with Right Amygdala Volume. Journal of Personality 84, 623–632 (2016).
Wang, Y. et al. Pathway to neural resilience: Self-esteem buffers against deleterious effects of poverty on the hippocampus. Human brain mapping 37, 3757–3766 (2016).
Yang, Z., Luo, Y., Ruolei, G. U., Liu, Y. & Cai, H. Self-esteem and brain: A social neuroscience approach. Advances in Psychological Science 25, 788 (2017).
Kubarych, T. S. et al. A multivariate twin study of hippocampal volume, self-esteem and well-being in middle-aged men. Genes, brain, and behavior 11, 539–544 (2012).
Pan, W. et al. The neural basis of trait self-esteem revealed by the amplitude of low-frequency fluctuations and resting state functional connectivity. Soc Cogn Affect Neurosci 11, 367–376 (2016).
Singh, A. K. & Vikas, D. Hippocampus in health and disease: An overview. Annals of Indian Academy of Neurology 15, 239–246 (2012).
Mcewen, B. S. The brain is the central organ of stress and adaptation. NeuroImage 47, 911–913 (2009).
Gold, S. M. et al. Hippocampal damage and memory impairments as possible early brain complications of type 2 diabetes. Diabetologia 50, 711–719 (2007).
Raz, N. et al. Regional Brain Changes in Aging Healthy Adults: General Trends, Individual Differences and Modifiers. Cerebral Cortex 15, 1676–1689 (2005).
Cho, K. Chronic ‘jet lag’ produces temporal lobe atrophy and spatial cognitive deficits. Nature Neuroscience 4, 567–568 (2001).
Reyes, E., Mohar, A., Mallory, M., Miller, A. & Masliah, E. Hippocampal involvement associated with human immunodeficiency virus encephalitis in Mexico. Archives of Pathology & Laboratory Medicine 118, 1130–1134 (1994).
Erickson, K. I. et al. Aerobic fitness is associated with hippocampal volume in elderly humans. Hippocampus 19, 1030–1039 (2009).
Ruit, K. G. & Neafsey, E. J. Cardiovascular and respiratory responses to electrical and chemical stimulation of the hippocampus in anesthetized and awake rats. Brain Research 457, 310–321 (1988).
Brody, G. H. et al. Protective Prevention Effects on the Association of Poverty With Brain Development. Jama Pediatrics 171 (2016).
Brody, G. H., Yu, T., Chen, E. & Miller, G. E. Family-centered prevention ameliorates the association between adverse childhood experiences and prediabetes status in young black adults. Preventive Medicine 100, 117 (2017).
Song, Y. et al. Regulating emotion to improve physical health through the amygdala. Social Cognitive & Affective Neuroscience 10, 523 (2015).
Zhu, Y., Origasa, H., Uebaba, K., Fenghao, X. U. & Wang, Q. Development and Validation of the Japanese Version of the Constitution in Chinese. Medicine Questionnaire (CCMQ). Kampo Medicine 320, 783–792 (2009).
Lu, H. et al. The brain structure correlates of individual differences in trait mindfulness: a voxel-based morphometry study. Neuroscience 272, 21–28 (2014).
Ashburner, J. & Friston, K. J. Voxel-based morphometry–the methods. NeuroImage 11, 805–821 (2000).
Ashburner, J. & Friston, K. J. Unified segmentation. NeuroImage 26, 839–851 (2005).
Ashburner, J. A fast diffeomorphic image registration algorithm. NeuroImage 38, 95–113 (2007).
Smith, S. M. et al. Advances in functional and structural MR image analysis and implementation as FSL. NeuroImage 23, S208–S219 (2004).
Bollen, K. A. & Stine, R. Direct and Indirect Effects: Classical and Bootstrap Estimates of Variability. Sociological Methodology 20, 115–140 (1990).
Shrout, P. E. & Bolger, N. Mediation in experimental and nonexperimental studies: new procedures and recommendations. Psychological Methods 7, 422 (2002).
Li, H. C., Chan, S. L., Chung, O. K. & Chui, M. L. Relationships among mental health, self-esteem and physical health in Chinese adolescents: an exploratory study. Journal of health psychology 15, 96–106 (2010).
Seigley, L. A. Self-esteem and health behavior: theoretic and empirical links. Nursing Outlook 47, 74 (1999).
McGee, R. & Williams, S. Does low self-esteem predict health compromising behaviours among adolescents? Journal of adolescence 23, 569–582 (2000).
McEwen, B. S. & Gianaros, P. J. Central role of the brain in stress and adaptation: links to socioeconomic status, health, and disease. Annals of the New York Academy of Sciences 1186, 190–222 (2010).
Phillips, L. J. et al. Stress, the hippocampus and the hypothalamic‐pituitary‐adrenal axis: implications for the development of psychotic disorders. Australian and New Zealand Journal of Psychiatry 40, 725–741 (2010).
Mcewen, B. S. & Seeman, T. Protective and damaging effects of mediators of stress. Elaborating and testing the concepts of allostasis and allostatic load. Annals of the New York Academy of Sciences 896, 30–47 (2010).
Mcewen, B. S. Protective and damaging effects of stress mediators. N Engl J Med 338, 171–179 (1998).
Mcewen, B. S., Gould, E. A. & Sakai, R. R. The vulnerability of the hippocampus to protective and destructive effects of glucocorticoids in relation to stress. British Journal of Psychiatry Supplement 160, 18–23 (1992).
Steinbehrens, B., Mattson, M. P., Chang, I., Yeh, M. & Sapolsky, R. Stress exacerbates neuron loss and cytoskeletal pathology in the hippocampus. Journal of Neuroscience 14, 5373–5380 (1994).
Fuchs, E. & Flügge, G. Stress, glucocorticoids and structural plasticity of the hippocampus. Neuroscience & Biobehavioral Reviews 23, 295–300 (1998).
Fuchs, E. et al. Psychosocial stress, glucocorticoids, and structural alterations in the tree shrew hippocampus. Physiology & Behavior 73, 285–291 (2001).
Joels, M. et al. Effects of chronic stress on structure and cell function in rat hippocampus and hypothalamus. Stress-the International Journal on the Biology of Stress 7, 221–231 (2004).
Mcewen, B. S. Plasticity of the Hippocampus: Adaptation to Chronic Stress and Allostatic Load. Annals of the New York Academy of Sciences 933, 265–277 (2010).
Mckittrick, C. R. et al. Chronic social stress reduces dendritic arbors in CA3 of hippocampus and decreases binding to serotonin transporter sites. Synapse 36, 85–94 (2015).
Mcewen, B. S. & Magarinos, A. M. Stress Effects on Morphology and Function of the Hippocampus. Annals of the New York Academy of Sciences 821, 271–284 (2010).
Pruessner, J. C., Hellhammer, D. H. & Kirschbaum, C. Low self-esteem, induced failure and the adrenocortical stress response. Personality & Individual Differences 27, 477–489 (1999).
Kirschbaum, C. et al. Persistent high cortisol responses to repeated psychological stress in a subpopulation of healthy men. Psychosomatic Medicine 57, 468–474 (1995).
McEwen, B. S. Central effects of stress hormones in health and disease: Understanding the protective and damaging effects of stress and stress mediators. European journal of pharmacology 583, 174–185 (2008).
This work was supported by project of China University of Geosciences (Beijing); Special Fund of Basic Research and Operating Expenses for Central Universities and Colleges in China (53200859213), the Social Science Foundation of Beijing (18JYC023), the National Natural Science Foundation of China (31221003, 31471067 and 31470055), the National Social Science Foundation of China (14ZDB160 and 15ZDB139), and Changjiang Scholars Programme of China.
The authors declare no competing interests.
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Lu, H., Li, X., Wang, Y. et al. The hippocampus underlies the association between self-esteem and physical health. Sci Rep 8, 17141 (2018). https://doi.org/10.1038/s41598-018-34793-x
- Rosenberg Self-Esteem Scale (RSES)
- Allostatic Load
- Future Health Promotion Programs
- General Physical Health Status
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