- Research article
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Regionally accentuated reversible brain grey matter reduction in ultra marathon runners detected by voxel-based morphometry
BMC Sports Science, Medicine and Rehabilitationvolume 6, Article number: 4 (2014)
During the 4,487 km ultra marathon TransEurope-FootRace 2009 (TEFR09), runners showed catabolism with considerable reduction of body weight as well as reversible brain volume reduction. We hypothesized that ultra marathon athletes might have developed changes to grey matter (GM) brain morphology due to the burden of extreme physical training. Using voxel-based morphometry (VBM) we undertook a cross sectional study and two longitudinal studies.
Prior to the start of the race 13 runners volunteered to participate in this study of planned brain scans before, twice during, and 8 months after the race. A group of matched controls was recruited for comparison. Twelve runners were able to participate in the scan before the start of the race and were taken into account for comparison with control persons. Because of drop-outs during the race, VBM could be performed in 10 runners covering the first 3 time points, and in 7 runners who also had the follow-up scan after 8 months. Volumetric 3D datasets were acquired using an MPRAGE sequence. A level of p < 0.05, family-wise corrected for multiple comparisons was the a priori set statistical threshold to infer significant effects from VBM.
Baseline comparison of TEFR09 participants and controls revealed no significant differences regarding GM brain volume. During the race however, VBM revealed GM volume decreases in regionally distributed brain regions. These included the bilateral posterior temporal and occipitoparietal cortices as well as the anterior cingulate and caudate nucleus. After eight months, GM normalized.
Contrary to our hypothesis, we did not observe significant differences between TEFR09 athletes and controls at baseline. If this missing difference is not due to small sample size, extreme physical training obviously does not chronically alter GM.
However, during the race GM volume decreased in brain regions normally associated with visuospatial and language tasks. The reduction of the energy intensive default mode network as a means to conserve energy during catabolism is discussed. The changes were reversible after 8 months.
Despite substantial changes to brain composition during the catabolic stress of an ultra marathon, the observed differences seem to be reversible and adaptive.
In 2009 (April 19th to June 21st) the TransEurope-FootRace 2009 (TEFR09) took place. It was the second European transcontinental multistage ultra marathon race and covered 4487 km (2788 miles) from Bari in the south of Italy to the North Cape. A group of 68 endurance runners with a mean age of 50.5 years ranging from 26 to 74 and encompassing 11 women and 57 men from 12 nations met the challenge. Their goal was to run the distance in 64 days without a day rest. Thus, they expected to complete an average distance of 70.1 km daily, that is 1.7 marathon distances per day (minimum: 44 km/d, maximum: 95.1 km/d) for 64 consecutive days without any day rest . The race and the research project  as well as some results have been described elsewhere [3–5].
Brain anatomy is not static and changes due to structural plasticity have been described in several previous studies [6, 7]. For example, hand inactivity related volume loss of the motorcortex has been observed to be reversible after reuse of the hand . Sport related grey matter (GM) volume increase has been demonstrated in premotor and parietal regions of golfers  and has also been reported to correlate with aerobic capacity .
Contrary to the described activities, walking and running is challenging only during the period of learning it. The process of running is highly automated after childhood  without relevant challenges for motor coordination or intellectual capabilities. Functional magnetic resonance imaging (fMRI) studies have shown that the control of running is associated with activity in spinal motor generators under supraspinal (e.g. cerebellar) control [12, 13] but with only marginal cortical involvement. Thus, gross plastic structural changes of brain regions relevant to the motor aspects of running could not be expected from participation in an ultra marathon.
Rather we speculated that participation in the TEFR09 would prove challenging for other brain functions such as pain suppression with possible activation of amygdala – hippocampal or perigenicular cingulate areas [14–16] or for sheer will power with possible activation of prefrontal areas .
To observe cerebral effects of sustained metabolic and functional challenges in TEFR09 participants, we had planned a voxel based morphometry (VBM)  study to investigate voxel-wise differences of brain anatomy between TEFR09 participants and controls at baseline, and also a longitudinal study to observe changes in brain anatomy due to the participation in the TEFR09.
After approval of the local ethics committee (University of Ulm, decision 78/08-UBB/se) and in accordance with the Declaration of Helsinki, 13 athletes without any contraindications to MRI were recruited signing informed consent. We had planned to perform brain scans before, twice during, and 8 months after the race. Due to the strong challenge and ensuing phenomena of fatigue, compliance of runners to participate in MR imaging in the evening after a day of running was limited and resulted in drop-outs such that data of a reduced number of runners could be included into the analysis of the longitudinal data. We carried out a cross sectional comparison of athletes and controls with 12 subjects (one of the 13 participating athletes was not able to participate in the baseline scan). We also performed a longitudinal VBM analysis with ten runners covering 3 time points and a second analysis with seven runners who were able to attend a follow-up scan after 8 months at time point 4. All included TEFR09 participants were men, aged 31 to 67 years with a mean of 50.2 (SD 9.7) years. In the year before the race, they had trained 12.9 hours/week (SD 3.4).
We individually matched 12 men aged 30 to 70 years with mean age of 49.5 (SD 10.6) years into the control group. Inclusion criteria for the control group were matched sex, handedness and age (± 3 years). Exclusion criteria were a chronic pain disorder (neurological interview) and any participation in long distance runs (e.g. marathon runs) during the previous five years. The controls had performed sports for 2.5 hours/week (SD 1.4).
MR acquisition protocol
Scanning was performed on three identical 1.5 T Siemens (Erlangen, Germany) MAGNETOM Avanto® MR scanners with identical sequence parameters. Two scanners were located at our university. The third was a mobile MRI unit mounted on a truck escorting the runners during the race. Volumetric 3D datasets were acquired using an MPRAGE sequence with the following sequence parameters: Time of repetition/echo/inversion TR/TE/TI was 2100/4.8/1060 ms, flip angle FA 15° and isotropic voxel-size of 1 mm. Direction of acquisition was sagittal with 192 slices covering the entire brain of each participant.
Cross sectional design
Scanning was performed on one scanner for all participants except one TEFR09 participant who was scanned on the mobile unit. The TEFR09 participants were scanned before the race, the controls within three months after starting the race.
The first examination (time point 1, t1) took place before the start of the race (same data as used in the cross sectional design). Time points 2 and 3 (t2 and t3) were planned at 2400 and 4000 km and the follow-up was performed on average 8 months after the end of the race.
Scanning data from 10 runners were available for the analysis comparing time points t3-t1, t2-t1 and t3-t2. Seven runners were available for time point 4 (t4) follow-up scan and were contrasted to time points t1, t2 and t3, respectively.
In a previous analysis, we had shown that the sample of 10 subjects attending 3 examinations and the sample of 7 subjects attending all 4 examinations did not differ with respect to biometrical data, and both groups were representative of the whole group of TEFR09 participants . Furthermore, we had shown that the physical load of the multi stage ultra marathon had resulted in profound changes of body weight and total brain volume  and that both samples of athletes exhibited similar changes.
Data preprocessing and analysis was performed with the VBM8 toolbox (http://dbm.neuro.uni-jena.de/vbm), which is incorporated in the SPM8 software (http://www.fil.ion.ucl.ac.uk/spm/) running on MATLAB® (Mathworks). Within the same generative model, images were corrected for bias-field inhomogeneities, registered using linear (12-parameter affine) and nonlinear transformations using DARTEL (Diffeomorphic Anatomical Registration Through Exponentiated Lie Algebra) , and tissue-classified into GM, white matter (WM), and CSF. This “new segmentation” procedure was further refined by accounting for partial volume effects , by applying adaptive maximum a posteriori estimations , and by applying a hidden Markov random field model  as described by Gaser et al. .
Cross sectional design
Data were preprocessed using the standard batch for cross-sectional data as described above (including modulation). Finally, segmentations were smoothed using a 10 mm full-width at half maximum (FWHM) Gaussian kernel. A two-sample t-test was performed to test for local volume differences between athletes and controls in both directions. Statistical threshold was set to p < 0.05, and corrected for multiple comparisons using family wise error (FWE). Only cluster exceeding a size of more than 15 voxels are reported. To avoid possible edge effects between different tissue types, all voxels with GM values of < 0.2 were excluded (absolute threshold masking).
The preprocessing of the imaging data before the statistical analysis was carried out using a specific batch for longitudinal data as implemented in VBM8 (there was no modulation used because it is not necessary in longitudinal designs where the focus is on relative differences between the same objects). Individual T1w images were first aligned to a T1 template in MNI-space (Montreal Neurological Institute) in order to bring them in a common reference frame with respect to translation and rotation. A mean image was calculated from these realigned images and a first realignment of raw data followed enclosing this mean image as a reference. At this stage individual images were bias-corrected to account for signal inhomogeneities. The resulting mean image was segmented into grey matter (GM), white matter (WM) and cerebrospinal fluid (CSF) using the segmentation approach described above. The segmented GM was normalized using DARTEL (to the same template as in the cross sectional design). The resulting normalization parameters were applied to the realigned and bias-corrected single images. Afterwards, these images were segmented and a second realignment followed. Smoothing of GM segments was done using a 10 mm FWHM Gaussian kernel (suitable for small samples sizes ) and data were passed to the statistical analysis.
We used an ANOVA with a flexible factorial design with factors ‘subject’ and ‘time’. In the first longitudinal study with the 10 runners group, one model was set up with 10 runners and GM segments at 3 time points. The factorial design for 10 runners was masked as described below to exclude scanner effects, so no covariate was needed. For the second longitudinal study, we used the 7 runners group with 4 time points including the follow up. The model for 7 runners considered the fact that data were obtained from three different scanners using a covariate coding for each MR scanner.
Again, an absolute threshold masking with a threshold of 0.2 was applied to avoid possible edge effects between different tissue types. To infer a significant decrease over time in the factorial design comprising three time points a t-contrast was formulated comparing GM segments at time point 3 against those of baseline (time point 1 minus time point 3). Statistical threshold for this contrast was set to level of p < 0.05, family-wise corrected to account for multiple comparisons.
To ascertain a true linear trend and to exclude possible systematic errors due to different scanner types, this contrast was further inclusively masked by the conjunction of two additional t-contrasts inferring significant differences between time points 2 and 1, and between time points 3 and 2. Voxels were included only if the conjunction of both contrasts passed a significance level of p < 0.001 (uncorrected) to account for the one-sidedness of these t-contrasts. The inverted main contrast (time point 3 minus time point 1) was assessed for the sake of completeness (no significant results). The factorial design including 7 runners was mainly used to contrast time points 1–4 and 4–1 in order to test whether there were significant changes in GM segments before and 8 months after the end of TEFR 2009, but the contrasts of the other time points are also reported.
The resulting coordinates of significant voxels were transformed from MNI space into Talairach space using GingerAle 2.1 incorporating the Lancaster transformation . The anatomical analysis was conducted with Talairach Client Version 2.4.2 . Significant effects were projected on a mean image of all 10 runners from time point 1. 3D rendering was performed with MRIcron Version April 2010 .
Cross sectional comparison
There were no significant grey matter volume differences between runners in preparation for an endurance run and controls.
At time point 2 the runners had finished 2475 km on average, and 4001 km at time point 3. The average time elapsed between the end of the race and the follow-up measurement was 256 days.
Regional VBM GM volume changes
The ANOVA with the flexible factorial design comprising three time points in 10 runners revealed a highly significant effect of time, and showed a strong linear decrease of regional GM volumes in anatomical locations summarized in Table 1 (p < 0.05 FWE). Due to the inclusive masking procedure outlined in the Methods section this linearly decreasing trend was further characterized by significant (p < 0.001) decreases between consecutive time points (t2-t1 and t3-t2). Significant clusters were located mainly bilaterally in the posterior temporal and occipitoparietal cortices as well as in anterior cingulate cortex and right ventral caudate nucleus (see Table 1 and Figures 1 and 2).
The ANOVA computed with the second factorial design of the 7 runners investigated at four time points (now including the follow-up) showed the same linearly decreasing effect (p < 0.001 for masking with t2-t1 and t3-t2 and p < 0.05 FWE for t3-t1) from t1 to t3 as observed in the investigation of the ten runners at 3 time points. Comparing regional GM volumes obtained at t1 with those obtained at follow-up did not show any significant differences. Interestingly, all regions that had demonstrated a significant decrease from t1 to t3 showed a significant increase from t3 to t4 at a level of p < 0.05 FWE (no masking).
The main findings of our study were GM volume decreases mainly located in bilateral posterior temporal and occipitoparietal brain regions, in the anterior cingulate cortex and in the right ventral caudate nucleus during participation in an ultra marathon. These changes were accompanied by decreasing body weight and global GM matter reduction during the race . All changes reversed to baseline when measured eight months after finishing the race.
In a cross sectional comparison we found no significant differences of regional grey matter distribution between our rather moderately physically active controls and the TEFR09 participants. This is at first surprising given the fact that both groups practise sports differently  and could be associated with low sensitivity due to our small sample sizes . Still, repetitive running might not activate specific brain areas enough - in contrast to e.g. juggling  - to induce local structural plasticity despite tremendous differences in training load. Therefore we could not elucidate any predispositions for or consequences of ultra marathon training regarding brain plasticity. In a previous study  we have already shown that substantial structural brain lesions did not occur during the TEFR09 participation. Together with the present results one might therefore conclude that ultra marathon training does not permanently alter brain anatomy.
However, our previous longitudinal analyses have already shown that a reversible global volume loss of brain grey matter occurred during the TEFR09 . We are now able to add that this global GM volume loss is not evenly distributed but has a specific spatial distribution. As a putative mechanism of action for global GM loss catabolism with likely loss of proteins has been described which is further supported by the apparently strong parallel variation of body weight and GM volume which both returned to baseline after eight months in our previous study . Other reports on multi stage endurance events also showed catabolism [28, 29].
In the present longitudinal analyses focussing on localized GM volume changes we found four different brain regions with significant GM reduction: the bilateral posterior temporoparietal cortex, bilateral occipitotemporal cortex, bilateral anterior cingulate cortex and adjacent prefrontal cortex, and the head of the right caudate nucleus.
Recently, a series of studies have reported changes of GM that were associated with behavioural changes. For example, regional changes of GM indicating structural plasticity with reversible (upon treatment) GM decrease have been shown with VBM for pathologic states such as immobilization , pain syndromes , obsessive compulsive disease , but also action induced GM increase for sports like juggling  and playing golf . However, these studies differ from the present one since the behaviour under investigation could be experimentally varied so that variations of behaviour could be related to structural brain changes. This was not the case with the present naturalistic study. Therefore any attempt to give an explanation for the present distribution of regional GM changes is speculative and great caution in discussion is necessary . Nevertheless, some of the authors of the present study accompanied the race and were therefore in the position to experience the uniformity and monotony of daily running such long distances. Thus, some of the decreases of GM volume in different brain areas can be discussed under the assumption of mental underload. For example, the bilateral occipitotemporal cortex (encompassing Brodmann’s Area (BA) 18, 19, 39 and 7) are well known to serve visual and visuospatial processing [33–35]. Therefore, one might assume that daily running on streets in straight lines may impose only little needs on detailed visual processing. This assumption might be supported by vertigo imaging studies, which have repetitively shown that the parietooccipital cortex is deactivated when visual acuity is not necessary . Similarly, GM volume reductions in bilateral posterior temporal cortex and parietal lobe (BA 20–22, 37, 40 and 42), which include auditory association areas [33, 37, 38], might be related to running the entire day in isolation with reduced auditory stimulation. The anterior cingulate gyrus (BA 24, 31) together with prefrontal cortices (BA 8–11) is thought to play a crucial role in attentional and inhibitory control  and more generally in cognitively demanding tasks . All these skills are less demanded during daily running and therefore these areas may have received less priority in maintenance under conditions of severe catabolism . The caudate nucleus has been implicated in motor planning, especially in demanding conditions  which were also absent during the run.
Yet another interpretation of regional GM volume reductions can be derived when considering the similarity between their anatomical distribution and those brain areas that belong to the so called default mode network (DMN). Essentially, the DMN comprises the temporoparietal junction, the inferior parietal lobule, posterior cingulate cortex and lateral temporal cortices. This network of brain areas is thought to be associated with self oriented thinking, and is deactivated during externally oriented attention [43, 44]. It has been calculated that roughly 60-80% of the brain’s high energy consumption is used in baseline activity , possibly permitting faster responses in cases of functional challenges than a truly resting brain without activity . During ultra marathon running most of the day a resting state system might be less important so that a reduction of GM volume could result. However, an important area of the DMN, the posterior cingulate cortex PCC  was not involved in GM reduction, and the caudate nucleus (showing volume decrease in our data) has not been reported as a member of the DMN so far.
Limiting factors and technical considerations
One of the major limiting factors of the present study is small sample size, which could condition false negative results (mainly the negative results in the cross sectional study) . Although a larger sample of athletes willing to participate in our examinations could be recruited at the beginning of the race, the rather time consuming examinations as an add-on to the already tight time schedule for athletes performing at their limits has prohibited inclusion of more subjects.
We did not perform modulation in the preprocessing of our VBM data in the longitudinal studies because it has recently been shown that unmodulated images improve sensitivity  to detect mesoscopic changes, such as cortical thinning, which are probably those expected in longitudinal VBM comparisons. However, in the cross sectional study modulation was performed.
Since the MRI scanner mounted on the truck was available only for the run, scanning before the race and during follow-up had to be performed on different scanners. A third scanner became necessary due to the long follow-up interval. MRI scanners were identical models and used identical sequence parameters. Usually, great care has to be taken to avoid systematic errors in longitudinal VBM comparisons, so that data acquisition should not be performed on different scanners. However, we could already show that the use of different identical scanners did not affect the global volume changes in our setting . For the present investigation with regional volume changes we have tried to protect the longitudinal analyses against putative influences from the use of different scanner types by the inclusive masking procedure designed to accept only changes verified on same scanner comparisons. By this masking operation, inference of significant volume changes from t1 to t3 was constrained by significant changes between t2 and t3 for which the data had been scanned on the same truck mounted scanner only. Since the relevant contrast of t3 against t1 could only infer significant results for those voxels significant in the t3 to t2 comparison (same scanner), present results were deemed to not having been influenced by a systematic bias stemming from different scanner types.
The accentuated and regionally distributed GM volume reduction in our study may be associated with decreased demands during daily running of very long distances in areas responsible for higher brain functions. Furthermore, the need for energy conservation may drive the reduction of high energy consuming default mode network circuits. As possible mechanism of action catabolic processes appear as candidates who should be addressed in future investigations. Extreme running may serve as model to better understand mechanisms involved in transient regional brain volume reductions. It may show mechanisms of the brain to cope with extreme catabolic demands encountered also in cancer and its treatment. The reversibility of the changes at follow-up supports the finding that GM changes in chronic diseases like chronic pain are not related to structural atrophy or neuronal loss but are functional and reversible . Accordingly relevant and persisting long term effects on the brain’s integrity in ultra-marathon runners are less likely to occur. Still, this conclusion awaits further research and replications.
Diffeomorphic anatomical registration through exponentiated lie algebra
Magnetic resonance imaging
Time point 1
Time point 2 et cetera
A contrast involving the comparison of t1 and t2, showing regions significantly larger at t1 than at t2
Voxel based morphometry
Schulze I: TransEurope-FootRace 2009. Bari-Nordkap - 4.487,7 km in 64 Tagesetappen. 2010, Engelsdorfer Verlag: Leipzig, Germany
Schuetz UH, Schmidt-Trucksäss A, Knechtle B, Machann J, Wiedelbach H, Erhardt M, Freund W, Gröninger S, Brunner H, Schulze I, Brambs HJ, Billich C: The Transeurope Footrace Project: longitudinal data acquisition in a cluster randomized mobile MRI observational cohort study on 44 endurance runners at a 64-stage 4,486 km transcontinental ultramarathon. BMC Med. 2012, 10: 78-10.1186/1741-7015-10-78.
Freund W, Faust S, Birklein F, Gaser C, Wunderlich AP, Muller M, Billich C, Juchems MS, Schmitz BL, Gron G, Schutz UH: Substantial and reversible brain gray matter reduction but no acute brain lesions in ultramarathon runners: experience from the TransEurope-FootRace Project. BMC Med. 2012, 10: 170-10.1186/1741-7015-10-170.
Freund W, Weber F, Billich C, Birklein F, Breimhorst M, Schuetz UH: Ultra-marathon runners are different: investigations into pain tolerance and personality traits of participants of the TransEurope FootRace 2009. Pain Pract. 2013, doi: 10.1111/papr.12039. [Epub ahead of print]
Freund W, Weber F, Billich C, Schuetz UH: The foot in multistage ultra-marathon runners: experience in a cohort study of 22 participants of the Trans Europe Footrace Project with mobile MRI. BMJ Open. 2012, 2: 1-8.
Draganski B, Gaser C, Busch V, Schuierer G, Bogdahn U, May A: Neuroplasticity: changes in grey matter induced by training. Nature. 2004, 427: 311-312. 10.1038/427311a.
Driemeyer J, Boyke J, Gaser C, Buchel C, May A: Changes in gray matter induced by learning–revisited. PLoS One. 2008, 3: e2669-10.1371/journal.pone.0002669.
Granert O, Peller M, Gaser C, Groppa S, Hallett M, Knutzen A, Deuschl G, Zeuner KE, Siebner HR: Manual activity shapes structure and function in contralateral human motor hand area. Neuroimage. 2010, 54: 32-41.
Jäncke L, Koeneke S, Hoppe A, Rominger C, Hänggi J: The architecture of the golfer’s brain. PLoS One. 2009, 4: e4785-10.1371/journal.pone.0004785.
Peters J, Dauvermann M, Mette C, Platen P, Franke J, Hinrichs T, Daum I: Voxel-based morphometry reveals an association between aerobic capacity and grey matter density in the right anterior insula. Neuroscience. 2009, 163 (4): 1102-1108. 10.1016/j.neuroscience.2009.07.030.
Zwergal A, Linn J, Xiong G, Brandt T, Strupp M, Jahn K: Aging of human supraspinal locomotor and postural control in fMRI. Neurobiol Aging. 2010, 33 (6): 1073-1084.
Ivanenko YP, Poppele RE, Lacquaniti F: Distributed neural networks for controlling human locomotion: lessons from normal and SCI subjects. Brain Res Bull. 2009, 78: 13-21. 10.1016/j.brainresbull.2008.03.018.
Jahn K, Deutschlander A, Stephan T, Strupp M, Wiesmann M, Brandt T: Brain activation patterns during imagined stance and locomotion in functional magnetic resonance imaging. Neuroimage. 2004, 22: 1722-1731. 10.1016/j.neuroimage.2004.05.017.
Freund W, Klug R, Weber F, Stuber G, Schmitz B, Wunderlich AP: Perception and suppression of thermally induced pain: a fMRI study. Somatosens Mot Res. 2009, 26: 1-10. 10.1080/08990220902738243.
Freund W, Stuber G, Wunderlich AP, Schmitz B: Cortical correlates of perception and suppression of electrically induced pain. Somatosens Mot Res. 2007, 24: 203-212. 10.1080/08990220701723636.
Freund W, Wunderlich AP, Stuber G, Mayer F, Steffen P, Mentzel M, Schmitz B, Weber F: The role of periaqueductal grey and cingulate cortex during suppression of pain in complex regional pain syndrome. Clin J Pain. 2011, 27: 796-804. 10.1097/AJP.0b013e31821d9063.
Price JL: Free will versus survival: brain systems that underlie intrinsic constraints on behavior. J Comp Neurol. 2005, 493: 132-139. 10.1002/cne.20750.
Ashburner J: Computational anatomy with the SPM software. Magn Reson Imaging. 2009, 27: 1163-1174. 10.1016/j.mri.2009.01.006.
Ashburner J: A fast diffeomorphic image registration algorithm. Neuroimage. 2007, 38: 95-113. 10.1016/j.neuroimage.2007.07.007.
Tohka J, Zijdenbos A, Evans A: Fast and robust parameter estimation for statistical partial volume models in brain MRI. Neuroimage. 2004, 23: 84-97. 10.1016/j.neuroimage.2004.05.007.
Rajapakse JC, Giedd JN, Rapoport JL: Statistical approach to segmentation of single-channel cerebral MR images. IEEE Trans Med Imaging. 1997, 16: 176-186. 10.1109/42.563663.
Cuadra MB, Cammoun L, Butz T, Cuisenaire O, Thiran JP: Comparison and validation of tissue modelization and statistical classification methods in T1-weighted MR brain images. IEEE Trans Med Imaging. 2005, 24: 1548-1565.
VBM8 Toolbox. http://dbm.neuro.uni-jena.de/vbm/download/.
Shen S, Sterr A: Is DARTEL-based voxel-based morphometry affected by width of smoothing kernel and group size? A study using simulated atrophy. J Magn Reson Imaging. 2013, 37: 1468-1475. 10.1002/jmri.23927.
Eickhoff SB, Bzdok D, Laird AR, Kurth F, Fox PT: Activation likelihood estimation meta-analysis revisited. Neuroimage. 2012, 59: 2349-2361. 10.1016/j.neuroimage.2011.09.017.
Laird AR, Robinson JL, McMillan KM, Tordesillas-Gutierrez D, Moran ST, Gonzales SM, Ray KL, Franklin C, Glahn DC, Fox PT, Lancaster JL: Comparison of the disparity between Talairach and MNI coordinates in functional neuroimaging data: validation of the Lancaster transform. Neuroimage. 2010, 51: 677-683. 10.1016/j.neuroimage.2010.02.048.
Rorden C, Karnath HO, Bonilha L: Improving lesion-symptom mapping. J Cogn Neurosci. 2007, 19: 1081-1088. 10.1162/jocn.2007.19.7.1081.
Knechtle B, Knechtle P, Schuck R, Andonie JL, Kohler G: Effects of a Deca Iron Triathlon on body composition: a case study. Int J Sports Med. 2008, 29: 343-351. 10.1055/s-2007-965354.
Knechtle B, Salas Fraire O, Andonie JL, Kohler G: Effect of a multistage ultra-endurance triathlon on body composition: World Challenge Deca Iron Triathlon 2006. Br J Sports Med. 2008, 42: 121-125. discussion 125
Rodriguez-Raecke R, Niemeier A, Ihle K, Ruether W, May A: Brain gray matter decrease in chronic pain is the consequence and not the cause of pain. J Neurosci. 2009, 29: 13746-13750. 10.1523/JNEUROSCI.3687-09.2009.
Lazaro L, Bargallo N, Castro-Fornieles J, Falcon C, Andres S, Calvo R, Junque C: Brain changes in children and adolescents with obsessive-compulsive disorder before and after treatment: a voxel-based morphometric MRI study. Psychiatry Res. 2009, 172: 140-146. 10.1016/j.pscychresns.2008.12.007.
Poldrack RA: Inferring mental states from neuroimaging data: from reverse inference to large-scale decoding. Neuron. 2011, 72: 692-697. 10.1016/j.neuron.2011.11.001.
Strotzer M: One century of brain mapping using Brodmann areas. Clin Neuroradiol. 2009, 19: 179-186. 10.1007/s00062-009-9002-3.
Bowyer SM, Hsieh L, Moran JE, Young RA, Manoharan A, Liao CC, Malladi K, Yu YJ, Chiang YR, Tepley N: Conversation effects on neural mechanisms underlying reaction time to visual events while viewing a driving scene using MEG. Brain research. 2009, 1251: 151-161.
Urakawa T, Inui K, Yamashiro K, Tanaka E, Kakigi R: Cortical dynamics of visual change detection based on sensory memory. Neuroimage. 2010, 52: 302-308. 10.1016/j.neuroimage.2010.03.071.
Bense S, Bartenstein P, Lochmann M, Schlindwein P, Brandt T, Dieterich M: Metabolic changes in vestibular and visual cortices in acute vestibular neuritis. Ann Neurol. 2004, 56: 624-630. 10.1002/ana.20244.
Booth JR, Burman DD, Meyer JR, Gitelman DR, Parrish TB, Mesulam MM: Functional anatomy of intra- and cross-modal lexical tasks. Neuroimage. 2002, 16: 7-22. 10.1006/nimg.2002.1081.
Maess B, Herrmann CS, Hahne A, Nakamura A, Friederici AD: Localizing the distributed language network responsible for the N400 measured by MEG during auditory sentence processing. Brain Res. 2006, 1096: 163-172. 10.1016/j.brainres.2006.04.037.
Horton JE, Crawford HJ, Harrington G, Downs JH: Increased anterior corpus callosum size associated positively with hypnotizability and the ability to control pain. Brain. 2004, 127: 1741-1747. 10.1093/brain/awh196.
Milham MP, Banich MT: Anterior cingulate cortex: an fMRI analysis of conflict specificity and functional differentiation. Hum Brain Mapp. 2005, 25: 328-335. 10.1002/hbm.20110.
Schuetz UH, Billich C, Konig K, Wurslin C, Wiedelbach H, Brambs HJ, Machann J: Characteristics, changes and influence of body composition during a 4486 km transcontinental ultramarathon: results from the Transeurope Footrace mobile whole body MRI-project. BMC Med. 2013, 11: 122-10.1186/1741-7015-11-122.
Wan X, Nakatani H, Ueno K, Asamizuya T, Cheng K, Tanaka K: The neural basis of intuitive best next-move generation in board game experts. Science. 2011, 331: 341-346. 10.1126/science.1194732.
Otti A, Gundel H, Wohlschlager A, Zimmer C, Sorg C, Noll-Hussong M: Default mode network of the brain : neurobiology and clinical significance. Nervenarzt. 2012, 83: 16-24. 10.1007/s00115-011-3307-6.
Raichle ME, MacLeod AM, Snyder AZ, Powers WJ, Gusnard DA, Shulman GL: A default mode of brain function. Proc Natl Acad Sci U S A. 2001, 98: 676-682. 10.1073/pnas.98.2.676.
Raichle ME, Mintun MA: Brain work and brain imaging. Annu Rev Neurosci. 2006, 29: 449-476. 10.1146/annurev.neuro.29.051605.112819.
Raichle ME, Snyder AZ: A default mode of brain function: a brief history of an evolving idea. Neuroimage. 2007, 37: 1083-1090. 10.1016/j.neuroimage.2007.02.041. discussion 1097–1089
Fransson P, Marrelec G: The precuneus/posterior cingulate cortex plays a pivotal role in the default mode network: Evidence from a partial correlation network analysis. Neuroimage. 2008, 42: 1178-1184. 10.1016/j.neuroimage.2008.05.059.
Radua J, Canales-Rodriguez EJ, Pomarol-Clotet E, Salvador R: Validity of modulation and optimal settings for advanced voxel-based morphometry. Neuroimage. 2013, Epub doi: 10.1016/j.neuroimage.2013.07.084
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/2052-1847/6/4/prepub
This project was mainly supported by the German Research Association (DFG: ‘Deutsche Forschungsgemeinschaft’), under grants SCHU 2514/1-1 and SCHU 2514/1-2. Other non-public funds were received from Siemens medical and the Medical Faculty of the University of Ulm. All funding was unrestricted. None of the funding bodies had any role in the study design, data collection, data analysis, data interpretation, manuscript preparation or decision to publish. Heike Wiedelbach and Martin Erhard participated in data acquisition.
The authors declare that they have no competing interests.
WF proposed and designed the study, worked on the statistical analysis, interpreted the results and wrote the report. SF planned the statistical analysis of the volumetric data and performed it, and wrote parts of the report. CG revised the methodology of the statistical analysis and wrote parts of the paper. GG contributed to the statistical analyses of the brain and non-brain data and wrote parts of the report. FB helped to conceive and plan the study and wrote parts of the paper. APW planned the study and the physical properties of the used sequences and wrote part of the manuscript. MM took part in the statistical analysis and revised the paper. CB planned the study and sampled data. UHS planned the TEFR09 project and this study and sampled data and read the images. All authors critically revised and approved the final manuscript.