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MINI REVIEW article

Front. Cell. Neurosci., 05 June 2023
Sec. Non-Neuronal Cells
Volume 17 - 2023 | https://doi.org/10.3389/fncel.2023.1198657

Physical activity and the brain myelin content in humans

Mariusz J. Kujawa1* Anna B. Marcinkowska1,2 Małgorzata Grzywińska3 Monika Waśkow4 Alexander Romanowski5 Edyta Szurowska1 Paweł J. Winklewski1,6 Arkadiusz Szarmach1
  • 12nd Department of Radiology, Medical University of Gdańsk, Gdańsk, Poland
  • 2Applied Cognitive Neuroscience Lab, Department of Neurophysiology, Neuropsychology and Neuroinformatics, Medical University of Gdańsk, Gdańsk, Poland
  • 3Neuroinformatics and Artificial Intelligence Lab, Department of Neurophysiology, Neuropsychology and Neuroinformatics, Medical University of Gdańsk, Gdańsk, Poland
  • 4Institute of Health Sciences, Pomeranian University in Słupsk, Słupsk, Poland
  • 5Department of Psychiatry and Psychotherapy, Helios Klinik, Hettstedt, Germany
  • 6Department of Neurophysiology, Neuropsychology and Neuroinformatics, Medical University of Gdańsk, Gdańsk, Poland

New imaging sequences and biophysical models allow adopting magnetic resonance imaging (MRI) for in vivo myelin mapping in humans. Understanding myelination and remyelination processes in the brain is fundamental from the perspective of proper design of physical exercise and rehabilitation schemes that aim to slow down demyelination in the aging population and to induce remyelination in patients with neurodegenerative diseases. Therefore, in this review we strive to provide a state-of-the art summary of the existing MRI studies in humans focused on the effects of physical activity on myelination/remyelination. We present and discuss four cross-sectional and four longitudinal studies and one case report. Physical activity and an active lifestyle have a beneficial effect on the myelin content in humans. Myelin expansion can be induced in humans throughout the entire lifespan by intensive aerobic exercise. Additional research is needed to determine (1) what exercise intensity (and cognitive novelty, which is embedded in the exercise scheme) is the most beneficial for patients with neurodegenerative diseases, (2) the relationship between cardiorespiratory fitness and myelination, and (3) how exercise-induced myelination affect cognitive abilities.

1. Introduction

New imaging sequences and biophysical models hold promise for the ability to adopt magnetic resonance imaging (MRI) for in vivo myelin mapping in humans. Hopefully, MRI will allow for large, longitudinal, painless and non-invasive studies focused on tracking of the cellular composition of neuronal and extra-neuronal brain tissue (Paquola and Hong, 2023). The mean correlation between MRI and histology is good, with R2 = 0.54 [standard deviation (SD) = 0.30] for animal studies, and R2 = 0.54 (SD = 0.18) for human studies. Moreover, the reproducibility for the various MRI methods seems acceptable [interclass correlation coefficient (ICC) = 0.75–0.93, R2 = 0.90–0.98, coefficient of variance = 1.3–27%], except for the magnetization transfer ratio (ICC = 0.05–0.51) (van der Weijden et al., 2021). Due to its three-dimensional nature, MRI offers the potential ability to visualize myeloarchitecture in three dimensions, along with biologically meaningful anatomical axes, compared with two-dimensional scans offered by classical histology. Finally, MRI delivers the unique possibility to assess the contribution of region-specific myelination to large-scale organization, offering a tool to unveil how myelination affects global brain networks (Paquola and Hong, 2023).

Myelin is a lipid-rich membrane that sheathes axons, speeds up information transfer embodied in action potentials, provides protection and metabolic support to covered neurons, and is indispensable for the proper cognitive functioning and motor tasks undertaken by the nervous system (Saab and Nave, 2017; Bechler et al., 2018; Elazar et al., 2019). Myelination development over the lifespan resembles an inverted U-shape curve, with the highest brain myelin content from 30 to 60 years of age, and subsequent decline after 60 years of age (Naumburg et al., 2012; Grydeland et al., 2013; Aviv et al., 2014; Bouhrara et al., 2021; Sui et al., 2022). Demyelination is at the core of neurodegenerative disorders and cognitive decline in physiological aging. It is increasingly recognized that abnormalities associated with the brain myelin content are not limited to information transfer speed within individual axons; they also affect the synchrony of network circuits (Bartzokis, 2004, 2005). Consequently, there is a constant search for novel pharmacological and non-pharmacological interventions to slow down and possibly revert demyelination processes.

Animal studies provide a quite complex scheme with regard to myelination and remyelination. There are two terms that have been coined to describe the underlying mechanisms behind myelination physiology and pathophysiology: adaptive myelination and remyelination (Bloom et al., 2022). Adaptive myelination refers to the expansion of already existing myelin sheaths or the addition of supplementary myelin to myelinated brain regions. Remyelination is understood as the covering of demyelinated axons with a new myelin (Bloom et al., 2022). Adaptive myelination is triggered by novel learning experiences—for example, when an animal acquires a novel motor task (McKenzie et al., 2014; Zhou et al., 2016). It is believed that the first 24 h following exposure to novel motor tasks are critical and actually define the opportunity window for adaptive myelination (Bloom et al., 2022). It remains unclear if, in animals, voluntary exercise not associated with novel learning may result in adaptive myelination. In contrast, remyelination is distinct from adaptive myelination and might be induced by voluntary exercise not associated with novel motor task learning (Bloom et al., 2022).

It remains unknown if the same scheme applies to humans. In their excellent review, Bloom et al. (2022) suggest that such direct translation may exist. Nevertheless, to support their reasoning, they cite only diffusion tensor imaging (DTI) studies in humans, referring to fractional anisotropy as a main marker of white matter integrity. Fractional anisotropy, however, is a marker that reflects the entire complexity of the neuronal tissue microstructure (Jones and Cercignani, 2010; Winklewski et al., 2018). Consequently, it is likely that fractional anisotropy does not detect subtle changes in myelination. The topic is of fundamental significance from the perspective of proper design of physical exercise and rehabilitation schemes to slow down demyelination in the aging population and to induce remyelination in patients with neurodegenerative diseases.

Therefore, in this review we strived to provide a state-of-the art summary of the existing MRI studies in humans focused on the effects of physical activity on myelination/remyelination. Electronic databases PubMed and Scopus were searched for relevant studies; last search was performed on 23 March 2023. The reference lists of included studies were hand-searched for additional references. A two-step approach was used to select articles. Firstly, titles and abstracts of all search results were screened for the following characteristics (1) original article and (2) published in English. Secondly, full-text articles were obtained from the selected studies and were reviewed on the following inclusion criteria (1) performed physical activity intervention and (2) performed MRI assessment of myelin. Two researchers independently reviewed titles, abstracts, full texts and extracted data. The following search terms were used: myelin AND exercise OR physical activity AND MRI. To date, there are only nine publications in this field (four cross-sectional studies, four longitudinal studies, and one case report; Table 1). Nevertheless, some initials conclusions can be drawn and recommendations for future direction in the research in this area may be formulated.

TABLE 1
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Table 1. Summary of MRI studies investigating the brain myelin content in humans.

2. Cross-sectional studies

Bracht et al. (2016) recruited 33 healthy participants (19 women, 14 men; 25.5 ± 4.2 years of age). All volunteers were right handed and were either undergoing or had previously completed a university degree course. They excluded professional athletes, musicians and subjects involved in amateur sport at competitive levels. The authors used multicomponent driven equilibrium single pulse observation of T1 and T2 (McDESPOT) to visualize whole brain estimated myelin water fraction maps. They found a selective positive correlation between activity level and myelin water fraction in the right parahippocampal cingulum (r = 0.482, p = 0.007). Importantly, they found no correlations between DTI fractional anisotropy and physical activity. Therefore, the authors concluded that the water myelin fraction “not only represents a more specific marker for myelination but is also a more sensitive marker than fractional anisotropy for detecting associations between white matter microstructure and physical activity.”

Greeley et al. (2022) investigated patients with chronic stroke (>6 months) and matched older healthy controls (the ages from 40 to 85 years). Myelin asymmetry ratios, calculated as a ratio of contralesional to ipsilesional myelin water fraction was analyzed in patients and healthy volunteers with high and low level of physical activity. Physical activity was assessed using accelerometers fixed on the subjects’ wrists for 3 consecutive days (72 h). The water myelin content was defined as the sum of the amplitudes within a short T2 signal (15–40 ms) divided by the sum of the amplitudes for the total T2 distribution. Asymmetries in water myelin content were investigated in the following motor regions of interest (chosen a priori): superior corona radiata, posterior corona radiata, cerebral peduncle, anterior limb of internal capsule and posterior limb of the internal capsule. Patients in the high physical activity stroke group had myelin content asymmetry comparable to that noted in older healthy adults. In contrast, the low physical activity stroke patients exhibited greater myelin content asymmetry compared to older healthy controls. Moreover, myelin content in the anterior limb of internal capsule, posterior corona radiata and superior corona radiata was positively linked to wrist movement activity across all participants.

Shao et al. (2022) included 55 adults: 28 golf players (20 men and 8 women; 24.61 ± 5.20 years old) and 27 non-players (19 men and 8 women; 24.56 ± 4.68 years old). All the participants were right handed, physically and neurologically healthy with normal or corrected-to-normal vision. The authors generated maps of macromolecular tissue volume and quantitative T1 for each participant from spoiled gradient echo images and spin-echo inversion recovery images. They processed the obtained images by using the mrQ software package.1 They found augmented myelin content in the left temporal pole in elite golf players compared with the non-players. Importantly, they found that increased microstructural plasticity was positively linked to golfing proficiency.

Boa Sorte Silva et al. (2023) enrolled 102 community-dwelling older adults (63.7% women; 74.7 ± 5.5 years old) with cerebral small vessel disease (diagnosed with MRI), and mild cognitive impairment defined as scoring <26 on the Montreal Cognitive Assessment. None of participants had a significant functional impairment or a prior diagnosis of dementia. They calculated the myelin water fraction as the fraction of signal with T2 < 40 ms over the entire T2 distribution. Then, they developed voxel-wise myelin water fraction maps for each participant and extracted data for whole-brain and tract-specific white matter. They found that active lifestyle (including physical activity) is associated with a higher myelin water fraction in the whole-brain white matter and in the following tracts: the anterior corona radiata, the genu of the corpus callosum and the sagittal stratum. Because the associations were independent of age, sex, body mass index, education and white matter volume, the authors concluded that physical activity may slow down myelin loss in adults with cerebral small vessel disease and mild cognitive impairment.

To conclude, the cross-sectional studies have demonstrated that more physically active adults have better myeloarchitecture profiles compared with less active adults. Importantly, this association remains valid throughout the entire adult lifespan, from the early 20 s to past the 70 s, in men and women. High physical activity profile seems to be neuroprotective in stroke patients. The authors used various MRI modalities to visualize the brain myelin content while the association between physical activity and estimated myelination remained clearly visible.

3. Longitudinal studies

Casella et al. (2020) investigated eight patients with Huntington’s disease (48.5 ± 15.62 years old, range 22–68 years) and nine matched controls (52.6 ± 14.56 years old, range 22–68 years). Six patients were at an early stage of the disease and two were at a more advanced stage. The participants performed drumming training: 15 min per day, 5 times per week, for 2 months. The drumming pattern was based on one of the following rhythms: Brazilian samba, Spanish rumba, West-African kuku and Cuban son (Metzler-Baddeley et al., 2014). The authors investigated changes in the white matter microstructure with DTI-based metrics, the fraction of restricted diffusion from the composite hindered and restricted model of diffusion, and the macromolecular proton fraction from quantitative magnetization transfer imaging. The drumming exercise resulted in significantly higher training-induced macromolecular proton fraction (myelin plasticity marker) changes within the corpus callosum (CCII and CCIII) and the pathways linking the right supplementary motor areas and the putamen in patients with Huntington’s disease compared with controls. Myelin plasticity did not change in the control group. The authors described the macromolecular proton fraction changes in patients relative to controls as a “catch-up effect to the better baseline status of the control group.”

Rowley et al. (2020) evaluated MRI scans from 47 healthy subjects: 22 in the passive control group (9 women; 72.8 ± 5.4 years old) and 25 in exercise group (15 women; 76.8 ± 8.0 years old). The exercise intervention comprised 12 weeks of supervised cycle ergometer training with three 30-min sessions per week. They visualized changes by examining myelin quantitative T1 and proton density maps with B1 correction for cortical segmentation and R1 images calculated as R1 = 1/T1. There was a significant difference in R1 between the groups, with R1 augmentation in the cycling group in the leg region of the motor cortex. The authors indicated that “aerobic cycling exercise promotes the maintenance and growth of the myelin sheaths in this region in the elderly.” In the control group, they reported a correlation between ventilatory threshold (equivalent to 64 ± 9% VO2max) and myelin content. Importantly, the Rowley et al. (2020) publication is the only one describing the longitudinal study focused on cortical myelination.

Mendez Colmenares et al. (2021) investigated 180 healthy older adults in three groups: control (43 participants, 26 women; 66.3 ± 4.5 years old), dance (51 participants, 37 women; 65.8 years ± 4.6 years old) and walking (86 participants, 54 women; 64.8 ± 4.2 years old). The active control consisted of exercises lasting 24 weeks and aiming at improvement in flexibility, strength and balance and involved some yoga mats and blocks, chairs and resistance bands. All exercised were adjusted for individuals ≥60 years old. The walking intervention aimed at augmenting cardiorespiratory fitness. It started with walking sessions at 50–60% of the maximal heart rate, then the walking duration was prolonged from 20 to 40 min during the first 6 weeks of the programme. During the last 18 weeks, the volunteers walked during each session for 40 min at 60–75% of their maximal heart rate. The dance intervention delivered combined cognitive and social enrichment associated with aerobic physical exercise. The dance choreography was increasingly challenging during the 6-month course. The authors calculated the T1-/T2-weighted (T1W/T2W) ratio from calibrated T1- to T2-weighted images to detect white matter integrity/myelin content. The effects of the aerobic exercise (both walking and dancing) on the T1W/T2W signal was significant for the mean of all white matter voxels. Moreover, regional analyses indicated a specific effect in the late myelinating regions containing association and commissural fibers: the genu and splenium of the corpus callosum, the forceps minor and the cingulum. There were no associations between augmented cardiorespiratory fitness and change in the T1W/T2W signal. This signal diminished during the 6-month period in the majority of white matter brain regions in the active control group.

Kirby et al. (2022) enrolled twelve healthy, right-handed subjects (seven women) who performed a 2-week motor-training schedule consisting of a visual-motor maze task with significant level of difficulty. Both non-dominant and dominant hands were trained and examined. There was no control group. The volunteers were young adults: mean age of 25.8 ± 3.7 years. The water myelin fraction was obtained using a 32 echo gradient and spin echo (GRASE) sequence T2 scan. Myelin water fraction was defined as the fraction of the geometric mean T2 distribution with 10 ms < T2 < 25 ms over the total geometric mean T2 distribution. The authors associated the water myelin content with structural (DTI fractional anisotropy) and functional (blood oxygen level dependent signal low frequency oscillations) to conclude that the higher myelin content the better axonal transmission in corticospinal tract.

In summary, the longitudinal studies have clearly shown that intense aerobic exercise (such as walking, cycling or dancing) can induce myelination in specific regions associated with particular activity (i.e., motor cortex) or late myelinating regions that are particularly vulnerable to demyelination with aging. Exposure to physical training of high complexity seems to result in higher myelin content and improved axonal transmission. There seems to be no relation between favorable changes in cardiorespiratory fitness evoked by intense aerobic exercise and myelin expansion. The link between aerobic fitness and myelin content is seen sometimes in control groups (so a similar finding like in cross-over studies). Physical activity of low intensity (such as drumming or exercise designed to improve flexibility, strength and balance) did not produce a favorable effect (in terms of myelin content augmentation) in healthy subjects. Nevertheless, drumming appeared to be very effective in remyelination in patients with Huntington disease.

4. Case report

Central pontine myelinolysis is a rare neurological complication that occurs after rapid correction of hyponatremia in patients with malnutrition, alcoholism and severe burns. The main pathophysiological process is symmetric demyelination of the central pons (Singh et al., 2014). A 44-year-old man with a past history of chronic alcoholism had an abnormality typical for central pontine myelinolysis in the central pons detected on axial MRI (high-signal area resembling a piglet sign in diffusion-weighted images; not clear in T2W and T1W images). The central pontine piglet sign was clearly defined in T2W and T1W images 11 weeks after disease onset. The diagnosis was based on radiological examination (MRI) and clinical signs and symptoms (Tobiume et al., 2022). Rehabilitation was not particularly specific or sophisticated, as no specialized equipment was used (commonly available aids such as a chair, parallel bars, a walker and a cane were applied), but it was regular (about 1 h daily). The patient was completely paraplegic on admission (but with contact, could express “Yes” or “No” either by blinking or moving his eyes). After half a year, the patient was discharged with only slightly slurred speech and minor muscle weakness in his right hand. Unfortunately, the remyelination process was not confirmed by MRI examination. Consequently, we can only infer from clinical picture that such process most likely occurred.

5. Discussion

Based on the available literature, it seems that two relatively firm conclusions can be made: (1) an active lifestyle is associated with augmented myelin content in the human brain and (2) with the use of intense aerobic exercise myelin expansion can be achieved in healthy subjects throughout the entire adult lifespan. One small study in patients with Huntington’s disease (Casella et al., 2020) and a case report describing a subject with central pontine myelinolysis (Tobiume et al., 2022) may suggest that even not very intensive but regular physical activity can result in remyelination in the brain areas affected by demyelination. Active life style also seems to be neuroprotective in stroke patients (Greeley et al., 2022). However, this very positive finding needs to be confirmed in larger studies. Less intense physical activity could represent a very valuable option for patients with neurodegenerative diseases associated with demyelination. It is quite surprising that to date, there is no study in patients with multiple sclerosis.

Less intense physical activity does not seem to cause myelin expansion in healthy subjects (Casella et al., 2020; Mendez Colmenares et al., 2021). This is an interesting finding and suggests that in humans as in animals (rodents) there are two different patterns with regard to myelination and remyelination processes (Bloom et al., 2022). Overall, such a pattern is consistent with the wider consensus that exercise intensity to induce neuronal plasticity can be scalable in healthy individuals but not necessarily in patients with neurological conditions (Hortobágyi et al., 2022). Additional research is needed to determine how humans (in terms of myelin content) respond to physical exercise associated with novelty. Kirby et al. (2022) study may suggest that physical training of high complexity augments myelination and improve axonal transmission in involved brain structures.

The relationship between cardiorespiratory fitness and myelination remains unclear. An active lifestyle is usually associated with better cardiorespiratory performance (Castells-Sánchez et al., 2021). However, the relationship between the cardiorespiratory profile and brain myelin content has not yet been investigated in cross-sectional studies. The only longitudinal study where the authors considered this relationship showed no relation between favorable changes in cardiorespiratory fitness evoked by intense aerobic exercise and myelin expansion (Mendez Colmenares et al., 2021). This finding is somewhat contradictory to the belief that exercise-induced changes in cardiovascular performance represent a key element in cognitive improvement (Aczel et al., 2022; Maleki et al., 2022; Renke et al., 2022).

The main weakness of the presented studies is that all of them, except of Rowley et al. (2020), refer to myelin content in white matter. The latest study by Sandrone et al. (2023) comparing MRI T1W/T2 sequences with ex vivo post-mortem histology suggests that MRI T1W/T2W sequences correlate well with myelin content in the cortical gray matter, but may not be a specific method to map myelin density in the callosal white matter. This limitation particularly refers to Bracht et al. (2016) and Mendez Colmenares et al. (2021) studies. In contrast, T1 or 1/T1 is very related to brain water content (Lee et al., 2021; Paquola and Hong, 2023). Brain water content, in turn, is affected by pathophysiological processes such as neuroinflammation or edema which generally makes white matter integrity assessment in MRI settings more complex (Winklewski et al., 2018). Nevertheless, in the reviewed studies the T1 and 1/T1 sequences were used in young healthy subjects (Rowley et al., 2020; Shao et al., 2022).

It should be emphasized that the authors of the reviewed articles used various MRI techniques, including MTV (Myelin Volume Fraction), MWF (Myelin Water Fraction), mcDESPOT MWF (Multi-Component Driven Equilibrium Single Pulse Observation of T1 and T2 with Myelin Water Fraction), and MPF (Magnetization Transfer Ratio Pool Size Ratio). These are all practical MRI techniques for quantifying tissue properties but have some limitations (Lee et al., 2021; Zhou et al., 2023). Firstly, these techniques are limited by their spatial resolution, making it difficult to accurately measure tissue properties in small structures or regions of interest. It can be particularly challenging for techniques like mcDESPOT MWF, which require high spatial resolution to accurately distinguish between different tissue compartments (Deoni and Kolind, 2015). Secondly, the accuracy and reproducibility of MRI techniques can be highly dependent on the specific acquisition parameters used, such as the magnetic field strength, sequence type, and imaging parameters. It can create difficulties in comparing results across different studies or institutions (Lee et al., 2021). Thirdly, MRI signal is inherently noisy, limiting the accuracy and precision of quantitative measurements. Techniques like mcDESPOT MWF, which require multiple scans with different acquisition parameters, can be susceptible to noise (Alonso-Ortiz et al., 2018). Additionally, tissue properties can vary widely between individuals, making it problematic to establish normative values or detect subtle changes in disease states. It can pose significant difficulties for techniques like MPF, which rely on comparing different tissue compartments (Khodanovich et al., 2017). While these techniques are valuable tools for studying tissue microstructure, they should be interpreted cautiously and in the context of other clinical and imaging data (van der Weijden et al., 2023).

Finally, future research should examine how changes in myelin content evoked by physical activity translate into cognitive improvement in patients and healthy subjects. Thus, extensive neuropsychological testing should become a gold standard particularly in longitudinal studies.

6. Conclusion

Physical activity and an active lifestyle have a beneficial effect on the myelin content in humans. Myelin expansion can be induced in humans throughout the entire lifespan by intense aerobic exercise. Additional research is needed to determine what exercise intensity (and embedded in exercise scheme cognitive novelty) is the most beneficial for patients with neurodegenerative diseases. The relationship between cardiorespiratory fitness and myelination has yet to be established. Extensive neuropsychological testing is needed to determine how exercise-induced myelination affects cognitive abilities.

Author contributions

MK, AM, MG, PW, and AS: conceptualization. MK: methodology, investigation, writing—original draft preparation, and project administration. AM, MG, MW, AR, ES, PW, and AS: validation and supervision. MK, AM, and MG: formal analysis. ES, PW, and AS: resources. MK, ES, and AS: funding acquisition. All author: writing—review and editing, read, and agreed to the published version of the manuscript.

Conflict of interest

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.

Publisher’s note

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.

Footnotes

  1. ^ https://github.com/mezera/mrQ

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Keywords: myelin, magnetic resonance imaging (MRI), human brain, physical activity, myelination and remyelination

Citation: Kujawa MJ, Marcinkowska AB, Grzywińska M, Waśkow M, Romanowski A, Szurowska E, Winklewski PJ and Szarmach A (2023) Physical activity and the brain myelin content in humans. Front. Cell. Neurosci. 17:1198657. doi: 10.3389/fncel.2023.1198657

Received: 01 April 2023; Accepted: 19 May 2023;
Published: 05 June 2023.

Edited by:

Bo Hu, Houston Methodist Research Institute, United States

Reviewed by:

Irene Vavasour, The University of British Columbia, Canada

Copyright © 2023 Kujawa, Marcinkowska, Grzywińska, Waśkow, Romanowski, Szurowska, Winklewski and Szarmach. 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: Mariusz J. Kujawa, mariusz.kujawa@gumed.edu.pl

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