Skip to main content

ORIGINAL RESEARCH article

Front. Hum. Neurosci., 26 March 2019
Sec. Cognitive Neuroscience
This article is part of the Research Topic Positive Neuroscience: the Neuroscience of Human Flourishing View all 19 articles

The Immediate and Sustained Positive Effects of Meditation on Resilience Are Mediated by Changes in the Resting Brain

\r\nSeoyeon KwakSeoyeon Kwak1Tae Young LeeTae Young Lee2Wi Hoon JungWi Hoon Jung3Ji-Won HurJi-Won Hur4Dahye BaeDahye Bae1Wu Jeong HwangWu Jeong Hwang1Kang Ik K. Cho,Kang Ik K. Cho1,2Kyung-Ok LimKyung-Ok Lim5So-Yeon KimSo-Yeon Kim6Hye Yoon ParkHye Yoon Park7Jun Soo Kwon,,*Jun Soo Kwon1,2,7*
  • 1Department of Brain and Cognitive Sciences, Seoul National University College of Natural Sciences, Seoul, South Korea
  • 2Institute of Human Behavioral Medicine, Seoul National University College of Medicine (SNU-MRC), Seoul, South Korea
  • 3Department of Psychology, Daegu University, Gyeongsan, South Korea
  • 4Department of Psychology, Chung-Ang University, Seoul, South Korea
  • 5Department of Psychiatry, National Institute of Forensic Psychiatry, Ministry of Justice, Gongjusi, South Korea
  • 6Department of Psychology, Duksung Women’s University, Seoul, South Korea
  • 7Department of Psychiatry, Seoul National University College of Medicine, Seoul, South Korea

While recent studies have explored the maintenance of the effect of meditation on stress resilience, the underlying neural mechanisms have not yet been investigated. The present study conducted a highly controlled residential study of a 4-day meditation intervention to investigate the brain functional changes and long-term effects of meditation on mindfulness and resilience. Thirty participants in meditation practice and 17 participants in a relaxation retreat (control group) underwent magnetic resonance imaging scans at baseline and post-intervention and completed the Cognitive and Affective Mindfulness Scale (CAMS) and Resilience Quotient Test (RQT) at baseline, post-intervention, and the 3-month follow-up. All participants showed increased CAMS and RQT scores post-intervention, but only the meditation group sustained the enhancement after 3 months. Resting-state functional connectivity (rsFC) between the left rostral anterior cingulate cortex (rACC) and the dorsomedial prefrontal cortex (dmPFC), precuneus, and angular gyrus was significantly increased post-intervention in the meditation group compared with the relaxation group. The changes in rACC-dmPFC rsFC mediated the relationship between the changes in the CAMS and RQT scores and correlated with the changes in the RQT score both immediately and at 3 months post-intervention. Our findings suggest that increased rACC-dmPFC rsFC via meditation causes an immediate enhancement in resilience that is sustained. Since resilience is known to be associated with the preventative effect of various psychiatric disorders, the improvement in stress-related neural mechanisms may be beneficial to individuals at high clinical risk.

Introduction

Resilience is defined as an individual’s capacity for recovery after significant adversity. Recent studies have suggested the importance of strengthening individuals’ resilience through appropriate interventions (Padesky and Mooney, 2012; van der Werff et al., 2013; Vanhove et al., 2015). For individuals, especially those at risk of mental disorder, enhanced resilience helps protect against their clinical conversion due to various stressful events (Ludwig and Kabat-Zinn, 2008; Creswell and Lindsay, 2014; Goyal et al., 2014). Moreover, resilience serves as a framework to promote stable remission in individuals with psychiatric disorders and to attenuate symptom severity in patients with inadequate responses to medication (Segal et al., 2010; Hoge et al., 2013; Waugh and Koster, 2015; Sharma et al., 2016). In this context, meditation has been shown to exert psychological and physiological effects on stress resilience and self-awareness and has been acknowledged as a promising adjunctive treatment in a broad range of psychiatric patients (Rubia, 2009; van der Velden and Roepstorff, 2015). However, most previous studies, which adopted meditation intervention for a few weeks, included possible limitations, such as isolation of the effects of meditation from other confounding factors or difficulty for subjects to regularly participate in the intervention. Therefore, recent studies have adopted several-day intensive residential meditation retreats designed to maximize training compliance and minimize the effects of non-meditative factors (Tang et al., 2007, 2015; Xue et al., 2011; Hwang et al., 2017).

Despite the growing interest in meditation and the significant progress achieved in understanding the associated dynamic neural changes via meditation (Lazar et al., 2005; Tang et al., 2015, 2007; Jang et al., 2011; Kang et al., 2012), only a few studies have focused on the maintenance of the effect. According to studies involving several months of follow-up after the intervention, both the meditation and active control groups exhibit improvements in stress-related psychological or physiological characteristics immediately after the intervention, but the effect is maintained only in the meditation group (Epel et al., 2016; Hwang et al., 2017). These findings suggest that meditation practices may induce changes in neural mechanisms to maintain the improvement, but the putative neural correlates underlying the maintenance of the effect have not yet been explored in neuroimaging studies.

According to recent meta-analyses, changes in anterior cingulate cortex (ACC) activation is consistently reported under various types of meditation and in short-term meditation studies (Bush et al., 2000; Fox et al., 2016). The ACC functions as a nexus of information processing, and 1 month of 30-min meditation interventions were shown to significantly increase the network efficiency and connectivity of the ACC in terms of resting-state functional connectivity (rsFC; Bush et al., 2000; Xue et al., 2011). However, the ACC can be differentiated into the rostral ACC (rACC) and the caudal ACC (cACC) based on its cytoarchitecture and functional connectivity. In general, the rACC appears to mainly be involved in the default mode network (DMN) and affective system, while the cACC is related to the sensorimotor and attention network (Milham and Banich, 2005; Margulies et al., 2007; Mohanty et al., 2007; Habas, 2009). Despite its distinguishing features, the majority of studies on the effects of meditation on the brain have not addressed its subregions. Moreover, only a few studies have explored the neural mechanism underlying the improvement of resilience through meditation. Although a recent study identified a decrease in subgenual ACC-amygdala rsFC, the region was associated with the perceived stress level based on region of interest (ROI)-wise rsFC analysis, and such an ROI-based approach limits the understanding of changes in resilience in the whole brain (Taren et al., 2015). Therefore, the neural correlates of resilience that are altered by short-term meditation remain unknown.

Motivated by previous findings, we sought to investigate whether changes in the rsFC contribute to improved resilience and its maintenance after 4 days of intensive residential meditation. Hence, we estimated whole-brain seed-to-voxel rsFC with ACC subregions and explored group-by-time interactions in rsFC maps for each ACC subregion. We hypothesized that: (1) the meditation group would present significant changes in rACC functional connectivity after the intervention; and that (2) these neural changes would be associated with improved resilience both immediately and at the 3-month follow-up.

Materials and Methods

4-Day Intensive Meditation (Templestay) Project

This project is aimed to investigate the behavioral and neural effects of three nights and 4 days of intensive meditation (Templestay program) using multidimensional approaches, including self-reported questionnaires, behavioral tasks, and multiple brain imaging modalities. The data used in the current study are part of the Templestay project. This study was carried out in accordance with the recommendations of Institutional Review Board of Seoul National University Hospital Committee with written informed consent from all subjects. All subjects gave written informed consent in accordance with the Declaration of Helsinki. The protocol was approved by the Institutional Review Board of Seoul National University Hospital Committee. To minimize the placebo effect, all participants were informed about two types of Templestay programs—a Buddhism meditation type and a relaxation type—prior to participation. Those who were willing to be assigned to either type were enrolled and randomly allocated to either an intensive meditation group (MED) or the control group using a computerized algorithm based on 2:1 mixed block randomization (44 participants in the MED group, 23 participants in the control group). The brain imaging data were collected at two time points, baseline and immediately after the intervention, while self-report questionnaires were measured at three time points: baseline, immediate follow-up, and at a 3-month follow-up (Figure 1). The recruitment strategy, intervention program, and results from the self-report questionnaires were described thoroughly in a previous report (Hwang et al., 2017). A brief introduction to the materials is included in the Supplementary data and Supplementary Figure S1.

FIGURE 1
www.frontiersin.org

Figure 1. Flowchart of the intervention study, including enrollment, allocation, baseline, follow-up, and analysis.

Image Data Acquisition

Image data were acquired from all participants 2 to 3 days before and after the intervention using a 3T Trio scanner (Siemens Medical Systems, Erlangen, Germany) with a 32-channel head coil. All participants were asked to relax with their eyes open during the resting functional magnetic resonance imaging (fMRI) scan [repetition time (TR) = 2000 ms, echo time (TE) = 30 ms, 64 × 64 matrix, total of 150 volumes, one run, field of view (FOV) = 220 mm, flip angle (FA) = 80°, voxel size = 3.4 × 3.4 × 3.4 mm3, 34 slices, and no gap]. To ensure that the participants stayed awake, they were reminded to stay awake immediately before resting fMRI acquisition and were observed during acquisition through an eye-tracker in the MRI scanner. Additionally, high-resolution T1-weighted anatomical images were acquired with three-dimensional magnetization-prepared rapid gradient echo [TR = 1,670 ms, TE = 1.89 ms, FOV = 250 mm, flip angle (FA) = 9°, number of slices = 208, voxel size = 1.0 × 1.0 × 1.0 mm3].

Analyses of Psychological Measures

To assess individuals’ resilience and mindfulness, all participants completed the modified Korean version of the Resilience Quotient Test (RQT) and the Cognitive and Affective Mindfulness Scale (CAMS)-Revised at three time points: baseline (T0), immediately after (T1), and 3 months after the intervention (T2). The RQT, developed by Reivich and Shatté (2002), is an inventory consisting of 27 items rated on a 5-point Likert scale, ranging from 1 (not at all) to 5 (very much so). CAMS measures everyday mindfulness, focusing mainly on the degree of participants’ thoughts and feelings on their experiences (Feldman et al., 2007). It consists of 12 items and assesses the core characteristics of mindfulness: the ability to regulate attention and orientation, to be aware, and to be nonjudgmental towards experience. Each item is rated on a 4-point scale, ranging from 1 (rarely/not at all) to 4 (almost always).

Independent samples t-tests were conducted for each scale to compare the differences between the groups at each time point. The group-by-time interaction of each scale was analyzed with a 3 [time (baseline/immediate follow-up/3-month follow-up), within-subject factor]-by-2 (group, between-subject factor) mixed analysis of variance (ANOVA) in SPSS, version 23.0 (IBM). To examine the directions of changes, post hoc t-tests were also conducted. The short-term effects on psychological measures were estimated with the scores from T0 and T1, while the long-term effects were estimated with the scores from T0 and T2.

Functional Image Analysis

After discarding the first two scans, FMRIB Software Library (FSL1) was used to preprocess the image data. fMRI data analyses were performed with the following preprocessing steps: removal of nonbrain structures, slice-timing and motion correction, registration to T1-weighted images and spatial normalization to 2 mm the Montreal Neurological Institute (MNI) template using FMRIB’s Linear Image Registration Tool (FLIRT). In terms of mean head motion parameters, neither significant group differences nor time differences were observed (group comparison: t = −0.270, p = 0.788; time comparison in the MED group: t = −0.049, p = 0.961; time comparison in the control group: t = −1.704, p = 0.101; Van Dijk et al., 2012; Zeng et al., 2014b). Using a general linear model (GLM), we removed the effects of nuisance covariates, including six head motion parameters, and signals from cerebrospinal fluid and white matter segmented T1-weighted images. Residual images were spatially smoothed using a Gaussian kernel of full width at half maximum (4 mm) and were temporally smoothed using a high-pass filter of a Gaussian-weighted least-squares line fitted with sigma = 100.

According to previous neuroimaging studies on the effects of aging, we only included brain data from young adults (age 40 or younger) in the current study (Ferreira and Busatto, 2013); in this study, 34 participants were included in the MED group and 19 in the control group. Among the remaining 52 participants, data from five participants were excluded due to excessive head motion (>3 mm for x, y, z planes, n = 4) and image distortion during acquisition (n = 1). As a result, we included data from 30 participants in the MED group and 17 participants in the control group in the final analysis.

We then defined four seed regions, the rostral and cACC in each hemisphere, based on the Destrieux atlas (Destrieux et al., 2010). Next, we calculated the mean time series of each seed region and produced individual subject-level maps of all positively correlated voxels for each seed. Due to the debate about negative rsFC, we specifically focused on the positive connectivity maps (Fox et al., 2009; Murphy et al., 2009). To examine the group-by-time effect of the intervention, second-level analyses were carried out using GLM analysis. A one-sample t-test and a paired t-test for each group were also conducted to clarify our assumption regarding the distinctive rsFC of rACC and cACC and to investigate the effect of each intervention. Multiple comparisons for all the above mentioned statistical analyses were carried out at the cluster level using Gaussian random field theory (Z > 2.3; cluster significance; p < 0.010, corrected).

Correlation and Mediation Analyses

To evaluate the hypothesis regarding the relationship between changes in functional connectivity and mindfulness and resilience, Pearson’s r correlation analysis was performed using SPSS v23.0. In the MED group, one participant at baseline and three participants at the 3-month follow-up were not available and were therefore excluded from the subsequent analyses. Normality and outliers in the raw data were checked prior to the analyses. In the correlation analysis, the strength of individual connectivity based on the significant clusters identified via the above rsFC analysis was extracted, and its variation was compared with the results of the self-reported questionnaires, RQT and CAMS. Both short (T0 to T1) and long-term (T0 to T2) improvements were analyzed based on the rsFC results. A p-value < 0.05 was considered statistically significant.

The mediation analysis test evaluated whether the association between X (predictor) and Y (outcome variable) was significantly reduced by including M (mediator) in the model when compared with the total relationship between X and Y. Thus, we further examined whether the association between the changes in mindfulness (X) and those in resilience (Y) could be explained via the indirect pathway based on the neural changes observed according to rsFC (M) using Mediation Toolbox2. Three variable-path models with bootstrap tests (10,000 iterations) were assessed.

Analyses of the Effect of Religion

Since the meditation used in the study is based on Buddhism, the religious preferences of participants were collected to examine the potential effect of religion on the study result. Participants reported their religion among the following choices: Buddhist, Catholic, Presbyterian, none, or other.

Results

Demographic Characteristics

The demographic data for each group are summarized in Table 1. There were no significant differences detected in terms of demographic characteristics, including the age, sex, handedness, years of education, marital status, religion, or socioeconomic status of the participants or their parents.

TABLE 1
www.frontiersin.org

Table 1. Demographic and clinical characteristics.

Psychological Measures

The RQT and CAMS scores of both groups at three time points are provided in Table 1. The baseline RQT and CAMS scores of the MED group were lower than those of the control group, but not significantly lower (t = 3.19, p = 0.08, and t = 3.35, p = 0.07, respectively).

To test the short and long-term effects of the intervention on each psychological measure more objectively, group-by-time mixed ANOVAs were conducted. A significant group-by-time interaction (F(1,47) = 5.021, p = 0.031, and F(1,47) = 5.913, p = 0.020, respectively) and an effect of time (F(1,47) = 8.070, p = 0.007, and F(1,47) = 2.903, p = 0.096, respectively) were observed, but no effect of the group (F(1,47) = 0.615, p = 0.328, and F(1,47) = 0.129, p = 0.722, respectively) was observed. In the post hoc t-test, both groups demonstrated significant increases of RQT and CAMS scores in the T0 to T1 (MED group: t = 4.734, p < 0.001, and t = 3.532, p < 0.005, respectively/control group: t = −3.676, p < 0.005, and t = −2.826, p < 0.005, respectively). In the T0 to T2 comparison, only the MED group presented significant increases in both questionnaires (MED group: t = −3.567, p < 0.005, and t = −2.910, p < 0.001, respectively/control group: t = −0.955, p = 0.354, and t = −1.000, p = 0.332, respectively). In the T1 to T2 comparison, only the control group showed significant decreases in both questionnaires (MED group: t = 1.329, p = 0.189, and t = 0.203, p = 0.841, respectively/control group: t = 2.217, p < 0.05, and t = 2.309, p < 0.05, respectively).

Functional Connectivity Maps to Each Seed

As shown in Figure 2, the cACC and rACC seed regions exhibited distinct rsFC patterns based on network cortical maps (Yeo et al., 2011). Bilateral rACC seeds were largely connected with regions (medial prefrontal cortex, precuneus, angular gyrus, amygdala, and hippocampus) belonging to the limbic network and DMN, whereas bilateral cACC seeds were linked with regions (dorsolateral prefrontal cortex, inferior frontal gyrus, inferior parietal lobule, and supplementary motor area) belonging to the fronto-parietal network and the sensorimotor network.

FIGURE 2
www.frontiersin.org

Figure 2. Functional connectivity of anterior cingulate cortex (ACC) subregions: (A) rostral (green, red) and caudal (yellow, blue) ACC in each hemisphere. Distinct functional connectivity was observed in the bilateral (B) caudal ACC (cACC) and (C) rostral ACC (rACC).

Results of Group Analysis of Functional Connectivity Maps

Among the four seed regions, only the left rACC showed significant group-by-time interactions, in several regions. Compared with the control group, the MED group presented increased rsFC between the left rACC and the dorsomedial prefrontal cortex (dmPFC), precuneus and angular gyrus in the MED group at the immediate post-intervention follow-up, whereas there was no significant group difference in rsFC for this seed region at baseline (Figure 3).

FIGURE 3
www.frontiersin.org

Figure 3. Significant differences in the group-by-time interaction effect (meditation group > control group, minimum Z score >2.3, cluster significance: p < 0.05, corrected). Significant differences were observed in connectivity involved in the default mode network (DMN), including the left rACC, dorsomedial prefrontal cortex (dmPFC), precuneus and temporoparietal junction (TPJ).

To further investigate the effect of each intervention on the brain functional network for an exploratory purpose, paired t-tests were performed for each group. In the MED group, the rsFC between the left rACC and the regions involved in the DMN, including the dmPFC, precuneus, and angular gyrus, was significantly increased after the intervention. The rsFC of the right cACC with the posterior cingulate cortex (PCC) was also significantly increased after the intervention. No additional significant changes in rsFC with the right rACC and left cACC were observed. In the control group, bilateral rACC rsFC with the temporal gyrus was increased, while the rsFC of the right rACC with the thalamus was decreased after the intervention. No significant changes were observed in rsFC with the bilateral cACC (Supplementary Figure S2).

Correlation and Mediation Analyses

In the correlation analysis, the changes in the left rACC-left dmPFC connectivity in the MED group were significantly correlated with the changes in RQT and CAMS (r = 0.54, p = 0.002 and r = 0.41, p = 0.024, respectively) in terms of the short-term effect. However, this correlation was not observed in the control group. No other type of rsFC from the GLM analysis was significantly associated with psychological measures. Concerning the long-term effect, the change in the rsFC was still significantly correlated with improved RQT (r = 0.42, p = 0.034) but not for CAMS (r = 0.309, p = 0.124; Figure 4).

FIGURE 4
www.frontiersin.org

Figure 4. Scatterplots of the relationship between the changes in left rACC—dmPFC resting-state functional connectivity (rsFC) and the changes in the following psychological measures in the meditation group: (A) changes in the Resilience Quotient Test (RQT) between baseline and immediate follow-up (r = 0.54, p = 0.002), (B) changes in the Cognitive and Affective Mindfulness scale (CAMS) between baseline and immediate follow-up (r = 0.41, p = 0.024), (C) changes in RQT between baseline and 3-month follow-up (r = 0.42, p = 0.034), (D) the positive association between the changes in CAMS (X) and RQT (Y), mediated by the changes in left rACC-dmPFC rsFC (M), showing that changes in rsFC partially contribute to the prediction of resilience enhancement. a, b, and c are path coefficients. **p < 0.01, ***p < 0.001.

As shown in Figure 4, the mediation analysis revealed a significant partially mediating effect on the rACC-dmPFC rsFC through the relationship between CAMS and RQT. In other words, the coefficient between X and Y was decreased when the change in the rACC-dmPFC rsFC was included (c = 1.55, p < 0.001; c′ = 1.32, p < 0.001). Significant relationships were also observed for the path coefficients between X and M (a = 0.03, p = 0.006) and between M and Y (b = 7.61, p = 0.003).

Effect of Religion

To investigate the effect of the participants’ religious beliefs on our results, ANOVAs and independent sample t-tests were conducted for the MED group. There were no significant differences in the baseline of rACC-dmPFC rsFC (F(1,25) = 0.81, p = 0.498), CAMS (F(1,25) = 1.67, p = 0.199), or RQT (F(1,25) = 2.59, p = 0.075) depending on the participants’ religions. In addition, there were no significant differences detected between participants with religion and those without religion in terms of baseline of rACC-dmPFC rsFC (t = −0.41, p = 0.68), CAMS (t = 0.12, p = 0.90), or RQT (t = −1.25, p = 0.808). In terms of the changes at the immediate follow-up, there were no significant differences in the changes in rACC-dmPFC rsFC (F(1,25) = 1.203, p = 0.328), CAMS (F(1,25) = 0.925, p = 0.443), or RQT (F(1,25) = 0.121, p = 0.947) depending on the participants’ religion. In addition, there were no significant differences detected between participants with religion and those without religion in terms of changes in rACC-dmPFC rsFC (t = −0.93, p = 0.36), CAMS (t = 0.57, p = 0.57), or RQT (t = 1.70, p = 0.10).

Discussion

To our knowledge, this is the first highly controlled residential study to investigate the neural changes via short-term intensive meditation, which is associated with the enhancement and maintenance of resilience. Our results revealed that the DMN was significantly enhanced in the MED group after the intervention compared with that in the control group. In particular, the changes in the functional connectivity of the left rACC with the dmPFC were correlated with the change in resilience at both the immediate and 3-month follow-ups in the MED group. In addition, mediation analysis revealed that the change in the left rACC-dmPFC functional connectivity was a partial mediating factor in the association between the enhancement in mindfulness and resilience immediately after the intervention. Our results suggest that the increase in the rACC-dmPFC rsFC was not only related to the immediately enhanced level of resilience but also predicted the long-term maintenance of the improvement.

Consistent with previous studies, compared with the control group, the MED group showed significantly increased rsFC between the left rACC and dmPFC, precuneus and angular gyrus (Brewer et al., 2011; Jang et al., 2011; Hasenkamp et al., 2012; Prakash et al., 2012; Taylor et al., 2012; Garrison et al., 2013). Since the precuneus, angular gyrus, and dmPFC are the functional hubs of DMN, we suggest that there was an increase of DMN in the MED group after meditation (Andrews-Hanna et al., 2014). Among the regions, the rACC-dmPFC rsFC was specifically associated with the resilience improvement via meditation. Such changes in rACC and dmPFC activation have been observed consistently in previous meditation studies (Farb et al., 2007; Hölzel et al., 2007). Regarding the roles of the rACC and dmPFC in the monitoring of an individual’s affective state and in mentalizing, rACC-dmPFC connectivity may reflect individuals’ abilities to understand the mental state of self (Milham and Banich, 2005; Lombardo et al., 2010). As a central feature of Buddhist meditation, mentalization enhances self-awareness with mindfulness practices (Koriat, 2000). Moreover, it is considered a key component in strengthening individuals’ resilience and shares some of the underlying neural mechanisms (Stein, 2006). Taken together, our results suggested that changes in rsFC in the regions related to mentalizing and resilience caused by mindfulness practice facilitated the short and long-term improvements of resilience in the MED group.

At the 3-month follow-up, the improvement in the resilience scores was significantly maintained in the MED group compared with that in the control group. Resilience is known to be relevant to the onset, recurrence, and symptom severity of various psychiatric disorders, including depression and anxiety disorders (Ludwig and Kabat-Zinn, 2008; Segal et al., 2010; Goyal et al., 2014). For this reason, many adjunctive therapies have been constantly developed to improve resilience and have proven to be effective (Fava and Tomba, 2009; Padesky and Mooney, 2012). However, only the meditation intervention, along with a few other interventions, has been shown to be effective within the short term and is self-trainable without an instructor after appropriate professional training. Furthermore, our results suggest that improved resilience via short-term meditation is maintained for up to 3 months. This evidence supports the hypothesis that short-term meditation might be a useful adjunctive intervention for individuals at high risk of psychiatric disorders. Moreover, the changes in the rACC-dmPFC rsFC may predict the maintenance effects of adjunctive therapy.

Interestingly, both groups demonstrated significant enhancements in psychological variables at the immediate follow-up, but the changes in rACC-dmPFC rsFC show different patterns between the groups. These results suggest that each group adopted different underlying mechanisms beyond the increased resilience and mindfulness scores. In the MED group, intensive meditation training seems to facilitate the resilience-related network, which eventually led to the psychological enhancement and its maintenance. In contrast, the changes in psychological measures in the control group were not able to show either significant correlation with rsFC or the maintenance of the scores. We suspect that their temporarily increased scores are due to the escape from everyday stress and relaxation rather than to the improvement in resilience.

In the present study, the control group was also exposed to interventions, such as escape from everyday stress, changes in environment and diet, and encountering new people. Such a design was based on an effort to minimize non-meditation factors, but our results suggest that the intervention also causes neural and behavioral changes. These changes may imply a “vacation effect,” as reported in previous studies (de Bloom et al., 2009; Epel et al., 2016). The vacation effect refers to the temporary improvements in health and psychological well-being after taking a vacation, which soon fades after work resumption. The absence of the maintenance effect of psychological measures in the control group also supports this definition. Unfortunately, we are unable to identify the exact factor that caused the changes in the rsFC of the control group after intervention because of the lack of any correlation with psychological measures. Moreover, randomized controlled studies to clarify the effect of vacation on neural levels, especially in resting-state connectivity, are very rare. In further studies, it will be necessary to explore the rsFC changes in the control group in more depth with various psychological measures, larger sample size and more follow-up time points.

We suspect a few possible few causes for the rsFC changes detected in the control group after the intervention. First, detachment from stress and everyday life may cause participants to feel relieved, which eventually led to changes in self-reported questionnaires and rsFC. Previous studies reported reduced rACC-temporal gyrus rsFC in veterans whether the individuals had PTSD or not (Kennis et al., 2015). The study suggested that experiencing stressful situations may alter the neural network. Unfortunately, we are unable to support the further explanation of the increased the rACC-temporal gyrus in the control because of the lack of correlation with psychological variables, but we suspect that the changes in the neural network were related to stress relief. Second, we cautiously assume that the diary writing in the control group might have enhanced language-related connectivity after the intervention. Some studies also demonstrated the effects of diary training at the cognitive and behavioral levels (Ho et al., 2011; Travers, 2011). The fronto-temporal rsFC has been known for its role in the language network; in particular, decoupling between ACC-temporal gyrus connectivity is associated with auditory hallucinations in individuals with schizophrenia (Stamatakis et al., 2005). However, it might be premature to suggest that writing in diaries account for the rsFC changes in the control group since previous studies used weeks of diary training. In the current study, further explanations of the rsFC changes in the control group are limited, but we suggest that these changes are due to the environmental modifications, including residence, diet, and other lifestyles.

The present study exhibits several strengths in exploring the effect of meditation exclusively. First, we recruited participants without prior experience in meditation or Templestay; therefore, all participants underwent the same period of intervention. Second, this study was designed as a longitudinal study and a randomized controlled trial to reduce possible pre-existing individual differences in the characteristics and brains of the participants. Third, we included an active control group to reduce the expectation effect on the participants. Finally, all of the participants, regardless of their group, were exposed to the same environment and diet in a retreat format to minimize any non-meditation-related factors.

When compared with previous studies, although the present study exhibits the above strengths, it also presents some potential limitations that should be noted. First, the individual level of mindfulness and resilience were assessed using self-reported questionnaires. Therefore, the scores may include some subjective bias. However, these scores have been used in many studies, and no objective tool for measuring these factors has been invented to date. Second, some participants’ religion was Buddhism, and there is a possibility that their religion may have an effect on the result, even though they reported a lack of prior experience in meditation or Templestay. However, our statistical analyses support that the effect of religion was not statistically significant at either the baseline or in the changes in self-reported questionnaires or in the rsFC. Third, even though we assessed self-reported questionnaires at three time points (baseline, an immediate follow-up after the intervention, and a 3-month follow-up), we acquired brain imaging data only at baseline and at the immediate follow-up due to the participants’ schedules and financial issues. For these reasons, it is unknown whether the change in neural connectivity was also maintained after 3 months. Further studies are needed to confirm the maintenance of neural changes and their relationships with other beneficial effects of meditation. In addition, more refined parcellation of ACC is recommended for the future studies, especially those with mental health conditions. Many recent studies suggest a distinct role of subgenual region and pregenual region of perigenual cingulate cortex, and different degrees of deficits in individuals with various psychiatric disorders (Davey et al., 2012; Zeng et al., 2014a). Adaptation of more elaborated ROI may clarify the effect of meditation in the neural level.

In conclusion, our highly controlled residential trial involving 4 days of meditation practice generated findings worthy of further study. Our study indicates that changes in the rACC-dmPFC rsFC may mediate improvement in and maintenance of individuals’ resilience via short-term meditation. Given that resilience is a crucial factor in mental health conditions, our results may contribute to intervention and prevention programs for individuals at risk of psychiatric disorders. Moreover, the rACC-dmPFC rsFC may be a potential neural target for future adjunctive therapies.

Data Availability

The datasets generated for this study are available on request to the corresponding author.

Author Contributions

SK: acquisition of data, analysis, manuscript interpretation, making figures, revision and final approval of the article, agreement to be accountable for all aspects of the work. TL, WJ and J-WH: interpretation, critical comments on manuscript, revision and final approval of the article, agreement to be accountable for all aspects of the work. DB, KC and WH: acquisition of data, revision and final approval of the article, agreement to be accountable for all aspects of the work. K-OL, S-YK, HP and JK: acquiring fund, conception and design of the work, interpretation, critical comments on manuscript, revision and final approval of the article, agreement to be accountable for all aspects of the work.

Funding

This work was supported by the Basic Science Research Program of the National Research Foundation of Korea (NRF), which is funded by the Ministry of Science, ICT and Future Planning (Grant no. 2016R1E1A1A02921618) and Jogye Order of Korean Buddhism supported this research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Footnotes

  1. ^ https://fsl.fmrib.ox.ac.uk/fsl/
  2. ^ http://github.com/canlab/MediationToolbox

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnhum.2019.00101/full#supplementary-material

References

Andrews-Hanna, J. R., Smallwood, J., and Spreng, R. N. (2014). The default network and self-generated thought: component processes, dynamic control and clinical relevance. Ann. N Y Acad. Sci. 1316, 29–52. doi: 10.1111/nyas.12360

PubMed Abstract | CrossRef Full Text | Google Scholar

Brewer, J. A., Worhunsky, P. D., Gray, J. R., Tang, Y. Y., Weber, J., and Kober, H. (2011). Meditation experience is associated with differences in default mode network activity and connectivity. Proc. Natl. Acad. Sci. U S A 108, 20254–20259. doi: 10.1073/pnas.1112029108

PubMed Abstract | CrossRef Full Text | Google Scholar

Bush, G., Luu, P., and Posner, M. I. (2000). Cognitive and emotional influences in anterior cingulate cortex. Trends Cogn. Sci. 4, 215–222. doi: 10.1016/s1364-6613(00)01483-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Creswell, J. D., and Lindsay, E. K. (2014). How does mindfulness training affect health? A mindfulness stress buffering account. Curr. Dir. Psychol. Sci. 23, 401–407. doi: 10.1177/0963721414547415

CrossRef Full Text | Google Scholar

Davey, C. G., Harrison, B. J., Yucel, M., and Allen, N. B. (2012). Regionally specific alterations in functional connectivity of the anterior cingulate cortex in major depressive disorder. Psych. Med. 42, 2071–2081. doi: 10.1017/s0033291712000323

PubMed Abstract | CrossRef Full Text | Google Scholar

de Bloom, J., Kompier, M., Geurts, S., de Weerth, C., Taris, T., and Sonnentag, S. (2009). Do we recover from vacation? Meta-analysis of vacation effects on health and well-being. J. Occup. Health 51, 13–25. doi: 10.1539/joh.k8004

PubMed Abstract | CrossRef Full Text | Google Scholar

Destrieux, C., Fischl, B., Dale, A., and Halgren, E. (2010). Automatic parcellation of human cortical gyri and sulci using standard anatomical nomenclature. Neuroimage 53, 1–15. doi: 10.1016/j.neuroimage.2010.06.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Epel, E. S., Puterman, E., Lin, J., Blackburn, E. H., Lum, P. Y., Beckmann, N. D., et al. (2016). Meditation and vacation effects have an impact on disease-associated molecular phenotypes. Transl. Psychiatry 6:e880. doi: 10.1038/tp.2016.164

PubMed Abstract | CrossRef Full Text | Google Scholar

Farb, N. A. S., Segal, Z. V., Mayberg, H., Bean, J., McKeon, D., Fatima, Z., et al. (2007). Attending to the present: mindfulness meditation reveals distinct neural modes of self-reference. Soc. Cogn. Affect. Neurosci. 2, 313–322. doi: 10.1093/scan/nsm030

PubMed Abstract | CrossRef Full Text | Google Scholar

Fava, G. A., and Tomba, E. (2009). Increasing psychological well-being and resilience by psychotherapeutic methods. J. Pers. 77, 1903–1934. doi: 10.1111/j.1467-6494.2009.00604.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Feldman, G., Hayes, A., Kumar, S., Greeson, J., and Laurenceau, J. P. (2007). Mindfulness and emotion regulation: the development and initial validation of the cognitive and affective mindfulness scale-revised (CAMS-R). J. Psychopathol. Behav. 29, 177–190. doi: 10.1007/s10862-006-9035-8

CrossRef Full Text | Google Scholar

Ferreira, L. K., and Busatto, G. F. (2013). Resting-state functional connectivity in normal brain aging. Neurosci. Biobehav. Rev. 37, 384–400. doi: 10.1016/j.neubiorev.2013.01.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Fox, K. C. R., Dixon, M. L., Fijeboer, S., Gim, M., Floman, J. L., Lifshitz, M., et al. (2016). Functional neuroanatomy of meditation: a review and meta-analysis of 78 functional neuroimaging investigations. Neurosci. Biobehav. Rev. 65, 208–228. doi: 10.1016/j.neubiorev.2016.03.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Fox, M. D., Zhang, D. Y., Snyder, A. Z., and Raichle, M. E. (2009). The global signal and observed anticorrelated resting state brain networks. J. Neurophysiol. 101, 3270–3283. doi: 10.1152/jn.90777.2008

PubMed Abstract | CrossRef Full Text | Google Scholar

Garrison, K. A., Santoyo, J. F., Davis, J. H., Thornhilll, T. A. IV., Kerr, C. E., and Judson, A. B. (2013). Effortless awareness: using real time neurofeedback to investigate correlates of posterior cingulate cortex activity in meditators’ self-report. Front. Hum. Neurosci. 7:440. doi: 10.3389/fnhum.2013.00440

PubMed Abstract | CrossRef Full Text | Google Scholar

Goyal, M., Singh, S., Sibinga, E. M. S., Gould, N. F., Rowland-Seymour, A., Sharma, R., et al. (2014). Meditation programs for psychological stress and well-being. JAMA Intern. Med. 174, 357–368. doi: 10.1001/jamainternmed.2013.13018

PubMed Abstract | CrossRef Full Text | Google Scholar

Habas, C. (2009). Functional connectivity of the human rostral and caudal cingulate motor areas in the brain resting state at 3T. Neuroradiology 52, 47–59. doi: 10.1007/s00234-009-0572-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Hasenkamp, W., Wilson-Mendenhall, C. D., Duncan, E., and Barsalou, L. W. (2012). Mind wandering and attention during focused meditation: a fine-grained temporal analysis of fluctuating cognitive states. Neuroimage 59, 750–760. doi: 10.1016/j.neuroimage.2011.07.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Ho, J., Epps, A., Parry, L., Poole, M., and Lah, S. (2011). Rehabilitation of everyday memory deficits in paediatric brain injury: self-instruction and diary training. Neuropsychol. Rehabil. 21, 183–207. doi: 10.1080/09602011.2010.547345

PubMed Abstract | CrossRef Full Text | Google Scholar

Hoge, E. A., Bui, E., Marques, L., Metcalf, C. A., Morris, L. K., Robinaugh, D. J., et al. (2013). Randomized controlled trial of mindfulness meditation for generalized anxiety disorder. J. Clin. Psychiatry 74, 786–792. doi: 10.4088/JCP.12m08083

PubMed Abstract | CrossRef Full Text | Google Scholar

Hölzel, B. K., Ott, U., Hempel, H., Hackl, A., Wolf, K., Stark, R., et al. (2007). Differential engagement of anterior cingulate and adjacent medial frontal cortex in adept meditators and non-meditators. Neurosci. Lett. 421, 16–21. doi: 10.1016/j.neulet.2007.04.074

PubMed Abstract | CrossRef Full Text | Google Scholar

Hwang, W. J., Lee, T. Y., Lim, K. O., Bae, D., Kwak, S., Park, H. Y., et al. (2017). The effects of four days of intensive mindfulness meditation training (Templestay program) on resilience to stress: a randomized controlled trial. Psychol. Health Med. 23, 497–504. doi: 10.1080/13548506.2017.1363400

PubMed Abstract | CrossRef Full Text | Google Scholar

Jang, J. H., Jung, W. H., Kang, D. H., Byun, M. S., Kown, S. J., Choi, C. H., et al. (2011). Increased default mode network connectivity associated with meditation. Neurosci. Lett. 487, 358–362. doi: 10.1016/j.neulet.2010.10.056

PubMed Abstract | CrossRef Full Text | Google Scholar

Kang, D. H., Jo, H. J., Jung, W. H., Kim, S. H., Jung, Y. H., Choi, C. H., et al. (2012). The effect of meditation on brain structure: cortical thickness mapping and diffusion tensor imaging. Soc. Cogn. Affect. Neurosci. 8, 27–33. doi: 10.1093/scan/nss056

PubMed Abstract | CrossRef Full Text | Google Scholar

Kennis, M., Rademaker, A. R., van Rooij, S. J., Kahn, R. S., and Geuze, E. (2015). Resting state functional connectivity of the anterior cingulate cortex in veterans with and without post-traumatic stress disorder. Hum. Brain Mapp. 36, 99–109. doi: 10.1002/hbm.22615

PubMed Abstract | CrossRef Full Text | Google Scholar

Koriat, A. (2000). The feeling of knowing: some metatheoretical implications for consciousness and control. Conscious. Cogn. 9, 149–171. doi: 10.1006/ccog.2000.0433

PubMed Abstract | CrossRef Full Text | Google Scholar

Lazar, S. W., Kerr, C. E., Wasswerman, R. H., Gray, J. R., Greve, D. N., Treadway, M. T., et al. (2005). Meditation experience is associated with increased cortical thickness. Neuroreport 16, 1893–1897. doi: 10.1097/01.wnr.0000186598.66243.19

PubMed Abstract | CrossRef Full Text | Google Scholar

Lombardo, M. V., Chakrabarti, B., Bullmore, E. T., Wheelwright, S. J., Sadek, S. A., Suckling, J., et al. (2010). Shared neural circuits for mentalizing about the self and others. J. Cogn. Neurosci. 22, 1623–1635. doi: 10.1162/jocn.2009.21287

PubMed Abstract | CrossRef Full Text | Google Scholar

Ludwig, D. S., and Kabat-Zinn, J. (2008). Mindfulness in medicine. JAMA 300, 1350–1352. doi: 10.1001/jama.300.11.1350

PubMed Abstract | CrossRef Full Text | Google Scholar

Margulies, D. S., Kelly, A. M. C., Uddin, L. Q., Biswal, B. B., Castellanos, F. X., and Milham, M. P. (2007). Mapping the functional connectivity of anterior cingulate cortex. Neuroimage 37, 579–588. doi: 10.1016/j.neuroimage.2007.05.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Milham, M. P., and Banich, M. T. (2005). Anterior cingulate cortex: an fMRI analysis of conflict specificity and functional differentiation. Hum. Brain Mapp. 25, 328–335. doi: 10.1002/hbm.20110

PubMed Abstract | CrossRef Full Text | Google Scholar

Mohanty, A., Engels, A. S., Herrington, J. D., Heller, W., Ho, M. R., Banich, M. T., et al. (2007). Differential engagement of anterior cingulate cortex subdivisions for cognitive and emotional function. Psychophysiology 44, 343–351. doi: 10.1111/j.1469-8986.2007.00515.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Murphy, K., Birn, R. M., Handwerker, D. A., Jones, T. B., and Bandettini, P. A. (2009). The impact of global signal regression on resting state correlations: are anti-correlated networks introduced? Neuroimage 44, 893–905. doi: 10.1016/j.neuroimage.2008.09.036

PubMed Abstract | CrossRef Full Text | Google Scholar

Padesky, C. A., and Mooney, K. A. (2012). Strengths-based cognitive-behavioural therapy: a four-step model to build resilience. Clin. Psychol. Psychother. 19, 283–290. doi: 10.1002/cpp.1795

PubMed Abstract | CrossRef Full Text | Google Scholar

Prakash, R. S., De Leon, A. A., Klatt, M., Malarkey, W., and Patterson, B. (2012). Mindfulness disposition and default-mode network connectivity in older adults. Soc. Cogn. Affect. Neurosci. 8, 112–117. doi: 10.1093/scan/nss115

PubMed Abstract | CrossRef Full Text | Google Scholar

Reivich, K., and Shatté, A. (2002). The Resilience Factor: 7 Essential Skills for Overcoming Life’s Inevitable Obstacles. New York, NY: Broadway Books.

Google Scholar

Rubia, K. (2009). The neurobiology of meditation and its clinical effectiveness in psychiatric disorders. Biol. Psychol. 82, 1–11. doi: 10.1016/j.biopsycho.2009.04.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Segal, Z. V., Bieling, P., Young, T., MacQueen, G., Cooke, R., Martin, L., et al. (2010). Antidepressant monotherapy vs. sequential pharmacotherapy and mindfulness-based cognitive therapy, or placebo, for relapse prophylaxis in recurrent depression. J. Consult. Clin. Psychol. 67, 1256–1264. doi: 10.1001/archgenpsychiatry.2010.168

PubMed Abstract | CrossRef Full Text | Google Scholar

Sharma, A., Barrett, M. S., Cucchiara, A. J., Gooneratne, N. S., and Thase, M. E. (2016). A breathing-based meditation intervention for patients with major depressive disorder following inadequate response to antidepressants. J. Clin. Psychiatry 78, e59–e63. doi: 10.4088/JCP.16m10819

PubMed Abstract | CrossRef Full Text | Google Scholar

Stamatakis, E. A., Marslen-Wilson, W. D., Tyler, L. K., and Fletcher, P. C. (2005). Cingulate control of fronto-temporal integration reflects linguistic demands: a three-way interaction in functional connectivity. Neuroimage 28, 115–121. doi: 10.1016/j.neuroimage.2005.06.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Stein, H. (2006). Handbook of Mentalization-Based Treatment. Chichester: John Wiley and Sons.

Google Scholar

Tang, Y. Y., Hölzel, B. K., and Posner, M. I. (2015). The neuroscience of mindfulness meditation. Nat. Rev. Neurosci. 16, 213–225. doi: 10.1038/nrn3916

PubMed Abstract | CrossRef Full Text | Google Scholar

Tang, Y. Y., Ma, Y., Wang, J., Fan, Y., Feng, S., Lu, Q., et al. (2007). Short-term meditation training improves attention and self-regulation. Proc. Natl. Acad. Sci. U S A 104, 17152–17156. doi: 10.1073/pnas.0707678104

PubMed Abstract | CrossRef Full Text | Google Scholar

Taren, A. A., Gianaros, P. J., Greco, C. M., Lindsay, E. K., Fairgrieve, R., Braon, K. W., et al. (2015). Mindfulness meditation training alters stress-related amygdala resting state functional connectivity: a randomized controlled trial. Soc. Cogn. Affect. Neurosci. 10, 1758–1768. doi: 10.1093/scan/nsv066

PubMed Abstract | CrossRef Full Text | Google Scholar

Taylor, V. A., Daneault, V., Grant, J., Scavone, G., Breton, E., Roffe-vidal, S., et al. (2012). Impact of meditation training on the default mode network during a restful state. Soc. Cogn. Affect. Neurosci. 8, 4–14. doi: 10.1093/scan/nsr087

PubMed Abstract | CrossRef Full Text | Google Scholar

Travers, C. (2011). Unveiling a reflective diary methodology for exploring the lived experiences of stress and coping. J. Vocat. Behav. 79, 204–216. doi: 10.1016/j.jvb.2010.11.007

CrossRef Full Text | Google Scholar

van der Velden, A. M., and Roepstorff, A. (2015). Neural mechanisms of mindfulness meditation: bridging clinical and neuroscience investigations. Nat. Rev. Neurosci. 16:439. doi: 10.1038/nrn3916-c1

PubMed Abstract | CrossRef Full Text | Google Scholar

van der Werff, S. J. A., van den Berg, S. M., Pannekoek, J. N., Elzinga, B. M., and van der Wee, N. J. A. (2013). Neuroimaging resilience to stress: a review. Front. Behav. Neurosci. 7:39. doi: 10.3389/fnbeh.2013.00039

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Dijk, K. R. A., Sabuncu, M. R., and Buckner, R. L. (2012). The influence of head motion on intrinsic functional connectivity MRI. Neuroimage 59, 431–438. doi: 10.1016/j.neuroimage.2011.07.044

PubMed Abstract | CrossRef Full Text | Google Scholar

Vanhove, A. J., Herian, M. N., Perez, A. L. U., Harms, P. D., and Lester, P. B. (2015). Can resilience be developed at work? A meta-analytic review of resilience-building programme effectiveness. J. Occup. Organ. Psychol. 89, 278–307. doi: 10.1111/joop.12123

CrossRef Full Text | Google Scholar

Waugh, C. E., and Koster, E. H. W. (2015). A resilience framework for promoting stable remission from depression. Clin. Psychol. Rev. 41, 49–60. doi: 10.1016/j.cpr.2014.05.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Xue, S., Tang, Y. Y., and Posner, M. I. (2011). Short-term meditation increases network efficiency of the anterior cingulate cortex. Neuroreport 22, 570–574. doi: 10.1097/wnr.0b013e328348c750

PubMed Abstract | CrossRef Full Text | Google Scholar

Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., et al. (2011). The organization of the human cerebral cortex estimated by intrinsic functional connectivity. J. Neurophysiol. 106, 1125–1165. doi: 10.1152/jn.00338.2011

PubMed Abstract | CrossRef Full Text | Google Scholar

Zeng, L. L., Shen, H., Liu, L., and Hu, D. (2014a). Unsupervised classification of major depression using functional connectivity MRI. Hum. Brain Mapp. 35, 1630–1641. doi: 10.1002/hbm.22278

PubMed Abstract | CrossRef Full Text | Google Scholar

Zeng, L. L., Wang, D., Fox, M. D., Sabuncu, M., Hu, D., Ge, M., et al. (2014b). Neurobiological basis of head motion in brain imaging. Proc. Natl. Acad. Sci. U S A 111, 6058–6062. doi: 10.1073/pnas.1317424111

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: resilience, meditation, mindfulness training, templestay, resting-state functional connectivity

Citation: Kwak S, Lee TY, Jung WH, Hur J-W, Bae D, Hwang WJ, Cho KIK, Lim K-O, Kim S-Y, Park HY and Kwon JS (2019) The Immediate and Sustained Positive Effects of Meditation on Resilience Are Mediated by Changes in the Resting Brain. Front. Hum. Neurosci. 13:101. doi: 10.3389/fnhum.2019.00101

Received: 14 November 2018; Accepted: 05 March 2019;
Published: 26 March 2019.

Edited by:

Björn H. Schott, Leibniz Institute for Neurobiology (LG), Germany

Reviewed by:

Shijia Li, East China Normal University, China
Ling-Li Zeng, National University of Defense Technology, China

Copyright © 2019 Kwak, Lee, Jung, Hur, Bae, Hwang, Cho, Lim, Kim, Park and Kwon. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jun Soo Kwon, kwonjs@snu.ac.kr

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.