The aging brain undergoes selective atrophy, mainly in the prefrontal cortices and medial temporal lobes [47, 48]. For instance, it has been reported that beginning at approximately age 50, the hippocampus shrinks 1 to 2% every year in healthy older adults . These decrements in volume have been linked to age-related decreases in memory and executive function [49, 50]. Decreased age-related atrophy has historically been implicated in explaining exercise-mediated improvements in cognitive performance for the older adult population .
Table 2 summarizes the results of studies that investigated the effects of exercise on brain volume. The 2 studies that examined the influence of short-term (12-week) moderate-intensity aerobic interventions on brain structure failed to find differences in whole-brain gray matter volume, either when exercise was compared to a waitlist control  or a stretching/muscle relaxation comparison . Although no between-group differences were found, a subanalysis in the Maass et al.  study demonstrated regional increases in the volume of the hippocampal head exclusively in those who exhibited improvements in fitness and hippocampal perfusion . Taken together, these results suggest that perhaps certain individuals who show mediatory gains in secondary outcome measures (such as cardiorespiratory fitness and hippocampal perfusion) may also exhibit benefits in exercise-induced changes in brain structure.
Medium length interventions may have greater impact in the regional brain structure however. Kleemeyer et al.  found that 26 weeks (i.e., 6 months) of both low and high aerobic exercise was associated with increased neuron density and volume in the hippocampus, and these 2 outcomes were correlated . Ruscheweyh et al.  found that both high-intensity exercise in the form of Nordic walking and low-intensity exercise in the form of gymnastics improved gray matter volume, mainly in prefrontal and cingulate cortices, when compared with a no-intervention control . In addition, a low- to moderate-intensity aerobic exercise was associated with increased regional brain volume in both gray and white matter areas relevant to the processing of attentional control and memory processes and shown to be implicated in age-related atrophy, when compared with stretching and toning . Namely, the most prominent increases in volume were found in the ACC, right superior temporal gyrus, right middle frontal gyrus, and anterior white matter. However, a more recent intervention delivered with similar dose and exercise mode (differing in total time per week 90-180 vs 180 min) did not find differences in frontal and hippocampus cortical thickness when compared with a stretching/toning group, despite an improvement in a composite cognitive score (episodic memory, processing speed, updating, task-switching, visuospatial reasoning) in the aerobic exercise group . The author discussed 2 possible reasons for these controversial findings, especially regarding brain volume. First, it is possible that an exercise intervention longer than 6 months may be required to achieve greater changes in brain volume. Second, the myriad cognitive improvements following a 6-month exercise intervention may be driven by other physiological processes, apart from macrostructural changes.
Furthermore, there is evidence suggesting differential structural effects according to exercise mode. For instance, individuals demonstrated increased brain volume in various frontal and temporal cortical areas following a 26-week dancing intervention, whereas individuals participating in a resistance training and flexibility group demonstrated increased brain volume in occipital and cerebellar regions . Interestingly, both groups had similar increased aerobic fitness and small changes in attention and visuospatial memory. It was hypothesized that the constant novelty and greater demand in attention and memory posed by the choreography in the dancing group created a greater challenge than the repetitive routine in the resistance training and flexibility group, possibly accounting for the larger improvements in brain volume.
The only study we found proposing moderate–high exposure to exercise (40 weeks) incorporated 2 distinct nonaerobic modalities, tai chi and social interaction, and made comparisons to light aerobic exercise and a no-exercise control group . Interestingly, only tai chi and social interaction were associated with increased whole-brain volume and improved processing speed and short-term memory. Contrary to previous findings in the literature, there were no differences between the light aerobic exercise and the control. We believe that this is possibly due to the fact that unlike the other studies that used light exercise interventions [15, 52], there was not a preferred intensity or a target zone, allowing the participants to walk at their self-selected pace. Although walking interventions are common in the literature, support for a potential floor effect in the aerobic exercise group comes from a subanalysis which revealed that faster walkers exhibited greater processing speed and short-term memory and lower brain tissue loss than slower walkers. Although there was no target intensity for the tai chi, this intervention requires a higher level of intellectual involvement and sustained attention compared to walking, which may have contributed to the results. Taken together, it is possible that aerobic exercise needs to be dosed at a minimum intensity and session time to achieve a threshold for structural gains, whereas other interventions such as tai chi, gymnastics, or social interaction may enlist distinct mechanisms due to the fact that they are more cognitively challenging.
The remainder of human studies examined high exercise exposure in yearlong interventions. Liu-Ambrose  assessed the effects of resistance training, either delivered 1×/week or 2×/week, and made comparisons with a balance and toning group delivered 2×/week. Interestingly, the authors found decreased whole-brain volume and increased executive function in the resistance groups when compared with the balance and toning group. The decreased whole-brain volume was unexpected but consistent with a mean of about 0.5% decreased annual whole-brain volume reported in healthy aging [57, 58]. A latter follow-up study performed 1 year after intervention demonstrated that neither group showed changes in whole-brain gray matter or hippocampal volume, but the 2×/week did show reduced cortical white matter atrophy . Additionally, both resistance training frequencies (1×/week and 2×/week) maintained their increased processing speed and attention, but the 2×/week group additionally demonstrated improved short-term memory . Thus, further research is needed to examine the relationship between structural brain changes and resistance training, especially given the improvements in certain cognitive abilities noted.
Both light to moderate aerobic exercise and a flexibility/toning/balance interventions were found to be associated with similar levels of white matter integrity in the frontal and temporal lobes, executive control, and short-term memory . A subanalysis revealed that individuals who made greater improvements in cardiovascular fitness made greater improvements in white matter integrity and short-term memory. An average increase in cardiovascular fitness of 8% following a moderate aerobic exercise intervention was associated with an average 2% increase in hippocampal volume, when compared with a yearlong stretching intervention . Similar increases in hippocampal volume have been reported with a coordination intervention . Interestingly however, aerobic exercise increased volume in the left hippocampus and the coordination group increased the volume of the right hippocampus. The authors attributed the differential effects to distinct demands posed by the 2 interventions; the right hippocampus is more highly engaged in spatial memory processes and, thus, theoretically more active during coordination exercises, whereas the left hippocampus is more engaged in verbal memory and highly associated with the increase in fitness level .
In the study proposing the highest exposure to exercise (2 years), a multimodal intervention consisting of moderate-intensity physical activity (walking, lower extremity resistance training, balance, stretching, and behavioral counseling) was associated with improved bilateral hippocampal and left cornu ammonis volumes, when compared with a control group consisting of healthy education and stretching. In addition, the authors reported that greater self-reported adherence to the intervention was associated with greater hippocampal volume .
In addition to structural changes, age-related cognitive decline is associated with impaired functional activation of neural networks. For example, older individuals with age-related cognitive decline have exhibited impaired neural interhemispheric communication between the frontal and posterior cortices  and disrupted frontotemporal activation during memory-related tasks [65,66,67]. The studies described herein measure the degree of connectivity (i.e., degree of simultaneous cortical activation) between spatially distant cortical areas either during resting state (when the individual is not engaged in a specific thought or task) or during the performance of a specific task.
Table 3 summarizes the results of studies that investigated changes in brain connectivity after exercise intervention. Short-term exposure (12 weeks) to moderate-intensity exercise has been associated with a reduction in the number of cortical areas active during the performance of a memory semantic task, which was attributed to a potential increase in the efficiency of neural networks . In addition, the same intervention delivered at a slightly higher dose (16 weeks) was associated with connectivity of the hippocampi and increased interconnectivity between the hippocampi and ACC, when compared with education and light stretching . The interconnections with the ACC are relevant as this structure has reciprocal connections with the prefrontal cortex and is active during tasks that require executive control .
Medium-term exposure (6 months) to light to moderate aerobic interventions (6 months) was also associated with improved connectivity. The authors found decreased activation of the ACC, which was associated with improved executive control. The authors attributed the improved executive control to a task-related increase in various areas in the attentional circuitry network (middle frontal gyrus, superior frontal gyrus, and superior parietal lobules) which in theory decreased the demand of the ACC during the task . The authors attributed these findings to an increase in cardiovascular fitness, not exhibited by the stretching/toning group. Taken together, these results suggest that a global increase in connectivity and increased focal connectivity in areas pertinent to executive control and memory are possible with approximately 3 to 6 months of moderate aerobic exercise.
Similar to these previously reported findings, long-term exposure to exercise was also shown to improve connectivity and executive control, but with differing patterns according to exercise mode . Specifically, 1 year of light to moderate aerobic exercise was associated with an improvement in the connectivity between areas within the default mode network and within the frontal executive network. On the other hand, the stretching/toning/balance intervention was associated with increased connectivity within areas of the DMN at 6 months and within the frontoparietal network. However, neither group showed differences in task-switching ability or spatial working memory . The default mode network, frontal executive network, and frontoparietal network are highly engaged during the performance of executive control and spatial memory tasks, and connectivity between these areas is impaired in age-related cognitive decline [72, 73].
Voelker-Rehage et al.  also found improved perceptual speed and executive functioning with different exercise modes and differential patterns of improved connectivity. The authors found that both moderate to high aerobic exercise and coordination: 1) improved neural efficiency during the performance of an executive control task and 2) improvements in executive attentional control and perceptual speed, albeit with differential patterns of connectivity. The aerobic group showed a decreased activation of left superior and middle frontal, bilateral medial frontal gyrus, the left ACC, the left parahippocampal gyrus, and the right superior and middle temporal gyrus. The coordination group showed increased activation of inferior frontal gyrus, superior parietal cortex, and thalamus and caudate. In addition to the differential connectivity patterns between the 2 intervention groups, the authors also found that the improved perceptual speed and executive functioning in the aerobic exercise was driven by an improvement in cardiovascular fitness. Taken together, these studies suggest that long-term exposure to different modes of exercise may be associated with certain cognitive benefits via distinct patterns of functional connectivity.
Neurogenesis and Synaptogenesis
Animal models enable the study of the microscopic changes in brain structure that support exercise-mediated cognitive benefits, such as the formation of new neurons (neurogenesis) and synapses (synaptogenesis) in the hippocampus. One of the strongest and earliest links between exercise and cognition was found on neurogenesis [75,76,77], which was 1 of the first hypotheses used to explain the neurobiological underpinnings of exercise-mediated cognitive performance benefits. However, when considering the generalizability of these microscopic findings to translational research in aging humans, it is pertinent to also consider how age might impact processes such as neurogenesis and synaptogenesis. For instance, older rodents (9 months) show hippocampal neurogenesis at half the rate of young adult rodents (6 weeks), and that by 24 months, the rate of neurogenesis is further decreased to 17% .
Despite the age-related decrease in hippocampal neurogenesis, it is encouraging that neurogenesis can be enhanced with exercise in aged rodents. For example, 1 month and half of voluntary wheel-running (VWR) was shown to revert the decline in neurogenesis in 19-month-old rodents by 50% and increase gliogenesis by 20%, an improvement that was paralleled with improved spatial learning, when compared with sedentary control rodents . Interestingly, the authors found no difference in the number of new cells or in fine morphology between older exercised and young mice, suggesting that exercise may have enhanced the capacity for conversion of precursor cells into neurons. The aged exercised mice showed increased rate of conversion by 3-fold when compared with the sedentary aged mice (25.6 vs 9.5%, respectively). Regarding the exercise dose necessary to induce such benefits, there is evidence to support that 10 to 28 days of VWR was sufficient to induce increases in precursor cell divisions associated with hippocampal neurogenesis [78, 80, 81]. However, 1 study found that 14 days of VWR in 22-month-old mice was associated with lower neurogenesis .
Neural stem cells (NSC), considered to support the regenerative function of the brain, are decreased to about 70% in 18-month-old mice and 90% in 24-month-old mice . Interestingly, 21 days of VWR exercise attenuated the age-dependent decrease in NSC proliferation in endogenous extrahippocampal areas by 67% in 18-month-old mice but failed to do so in 24-month-old mice . One study did find increased proliferation of hippocampal NSC in 24-month aged mice after 3 days of VWR . Taken together, it is possible that aerobic exercise may have differential effects in different types of NSC.
Other studies have shown that exercise may influence neurogenesis through different pathways. For instance, evidence suggests that exercise rescues the levels of enzymes TET1 and TET2 (Ten-eleven translocation 1 and 2), shown to be decreased in aging animals and act to regulate hippocampal neurogenesis . In addition, exercise has been shown to revert the toxic effect of lipopolysaccharide, a bacterial endotoxin shown to reduce hippocampal neurogenesis levels when expressed in 21-month-old mice . Furthermore, exercise decreased new microglia, immune cells linked to low-grade neuroinflammation that may contribute to decreased plasticity and increased new neuron survival .
Similarly, to neurogenesis, synaptogenesis is also decreased in aged rodents. For example, the number of presynaptic receptors in the hippocampus is decreased . Unfortunately, we could not find evidence of the impact of exercise in aged rodents, but studies suggest improvements in synaptogenesis in young exercised rodents. For instance, VWR is associated with increased synaptophysin, a marker of synaptogenesis in young rodents . In addition, nonaerobic exercise (walking through an obstacle course) was also associated with new synapses in other areas of the brain, mostly related with the control of motor activity .
As mentioned previously, animal studies show that the capacity for neurogenesis can be positively influenced by exercise. However, the generalizability of decreased neurogenesis found in aged mice needs to be carefully interpreted when applied to older adults. A recent cross-sectional study in postmortem healthy individuals from 14 to 79 years found that adult hippocampal neurogenesis may persist throughout the life span, including the 8th decade of life, despite the common clinical finding of age-related cognitive decline . Neurogenesis (measured by levels of intermediate neural progenitors, immature neurons, glia, and mature granule in the dentate gyrus) was found to be at similar levels in individuals from 14 to 80 years of age. The authors attributed the aspects of preserved cognitive performance in older adults to the maintenance of those levels of neurogenesis. However, in the comparison between young adults and older adults, the authors did find decreased angiogenesis, neuroplasticity markers of PSA-NCAM+ (polysialylated neural cell adhesion molecule) cells of different morphologies, and capacity for neurogenesis (assessed by the number of quiescent NSC), potentially implicated in the aspects of cognition that show decreases in the aging brain .
Several trophic factors have been identified to support cognition in aging adults. The most commonly discussed factors that are supportive of cognition include brain-derived neurotrophic factor (BDNF), vascular endothelial growth factor (VEGF), and insulin-like growth factor-1 (IGF-1). These trophic factors work in concerted fashion to modulate exercise-induced cognitive improvements . IGF-1 is important for vascular maintenance and remodeling. Both IGF-1 and VEGF are thought to mediate neurogenesis and angiogenesis and influence the induction of hippocampal BDNF.
BDNF supports neuronal development and has been demonstrated to be crucial for exercise-related improvements in cognitive function. Blocking BDNF annuls the cognitive improvements induced by exercise , demonstrating its significance for cognitive change. Additionally, running increases IGF-1 and VEGF in the hippocampus [93, 94], both of which are crucial to exercise-induced plasticity and cognitive improvements. IGF-1 is increased in the hippocampus following exercise, and blocking IGF-1 receptors reduces exercise-induced BDNF and inhibits exercise-related cognitive improvements . Similarly, blocking VEGF reverses running-induced hippocampal neurogenesis .
In aged animals (24 months), treadmill running has been shown to increase BDNF and IGF-1 after 4 weeks of intervention, and these changes were associated with improved spatial learning and memory . However, another study in aged animals showed that there was a transient increase in BDNF levels after 1 week of a wheel running that returned to baseline levels in subsequent weeks (2-4 weeks). In this study, it was found that aged animals did not increase their running distance each week whereas the other study utilized a treadmill which standardized the exercise exposure, which may account for the transient increase found in voluntary wheel-running. Furthermore, improvements in memory and increases in BDNF have been shown after 8 weeks of aerobic and strength training, showing possible benefits beyond aerobic exercise . Table 4 summarizes the results of studies investigating the effects of exercise on trophic factors in humans.
Three studies that utilized short-term exercise interventions (between 4 and 10 weeks) proposed moderate-load resistance training, either in isolation [98, 99] or combined with aerobic exercise . Moderate-load resistance training increased BDNF levels when compared with baseline , but not when compared with a control . The combined intervention also did not improve BDNF levels . These studies suggest that short-term exposure to resistance training may not be associated with increases in BDNF.
Many studies assessed the effects of various isolated modes of short-duration (12 or 16 weeks) exercise. None of the following moderate-intensity aerobic activities modulated BDNF levels: walking or running  and cycling  and light and moderate-load resistance training [101,102,103]. Four studies employed combined exercise programs that contained resistance training: high-intensity aerobic cycling followed by moderate level coordination/strength , high-intensity aerobic cycling followed by moderate level coordination/strength , moderate-load resistance training followed by moderate- to high-intensity aerobic training , and combined aerobic/strength/coordination . Of these, only the moderate-load resistance training followed by moderate- to high-intensity aerobic training and the combined aerobic/strength/coordination reported increased BDNF levels, and both reported improvements in short-term memory and processing speed [106, 107]. Taken together, these studies suggest that medium exposure to aerobic or resistance training delivered in isolation might not be sufficient to influence BDNF levels. In addition, the only 2 studies that demonstrated BDNF increases employed a combined intervention of approximately 2000 total intervention minutes (i.e., 32 h), and therefore, the additional load posed by a second intervention and the greater exposure to exercise could have contributed to the results.
Three studies investigated medium-duration exercise (6 months), employing various modes of exercise: high-intensity aerobic, moderate-intensity aerobic, and a dance-based intervention [15, 54, 108]. The studies that utilized moderate- or high-intensity aerobic exercise in isolation found no changes in BDNF levels [15, 108]. Rehfeld et al.  found that a dance-based intervention was associated with increased BDNF levels, when compared to an endurance/strength/flexibility group. The dance intervention required subjects to memorize routines, perform complex choreography, and was regularly changed throughout the study, whereas the comparison group utilized an unchanging exercise regimen, which may have been related to the increases in BDNF found in the intervention group. However, despite the discrepancies in BDNF findings, all studies demonstrated improvements in a range of cognitive abilities (processing speed, visuospatial memory, and episodic memory).
Three studies evaluated the effects of long-duration exercise in a 12-month moderate aerobic walking intervention compared to a stretching and toning group. It appears that these studies are from 1 larger sample, with each study reporting on a subset of the total sample: 92 subjects , 120 subjects , and 65 subjects . There were no changes in BDNF levels from before to after in the intervention groups in any of the cohorts. A secondary analysis performed by Leckie et al.  showed that when dividing the sample by age, younger and older than 65 years of age, the intervention group had an increase in BDNF levels, whereas the control group had a decrease in BDNF levels in individuals older than 65 years old. Both Erickson et al.  and Leckie et al.  assessed and reported improvements in spatial memory function and task-switching after the intervention. These findings are consistent with the previous results that suggest that only aerobic activity may not be sufficient to modulate BDNF levels. However, it is possible that in individuals over 65 who are susceptible to decreases in BDNF , that the prolonged effects of a year-long aerobic intervention may have a positive influence on BDNF levels whereas shorter duration interventions are potentially unable to have the same effect.
IGF and VEGF
Six studies utilized short-duration exercise (10-12 weeks) of various modes: moderate aerobic exercise [19, 111, 112], combined moderate- and high-intensity aerobic and resistance training [111, 113], and low or moderate resistance training [112, 114, 115]. The moderate-intensity aerobic exercise interventions had no effect on IGF-1 levels [19, 111, 112] or VEGF levels . In 2 studies utilizing combined aerobic and resistance training, 1 found within-group increases in IGF-1, regardless of intervention order , whereas the other found no changes when compared to a control group. In the studies utilizing resistance training, only 1 study utilizing moderate-intensity exercise found increases in IGF-1 , whereas the other 2 found no changes. Both studies that found increased IGF-1 after the intervention (combined or resistance) were in participants in their late 60s, whereas the studies that found no changes were in people 80 years old [114, 115] or 50 years old . These findings may suggest that short exposure to both a combined approach and moderate-intensity resistance training may increase IGF-1 levels, but there may be an optimal window with regard to age range (at approximately 60 years of age).
Three studies utilized medium-duration exercise (24 weeks) including moderate- to high-intensity aerobic  and moderate to high resistance training [116, 117]. The aerobic exercise showed no changes in IGF-1 , but the cognitive assessment revealed improvements in executive function (task-switching and visuospatial processing speed). Only 1 of 2 studies found moderate- and high-intensity resistance training to increase IGF-1 levels . A possible reason for the difference in findings is that Cassilhas et al.  achieved 72 h of total intervention compared to 48 h . Additionally, Cassilhas et al.  showed that the intervention group had improvements in visual processing and short-term memory. As such, in the medium term, resistance training, but not aerobic, associated with memory and attention improvements, possibly due to longer intervention duration, may lead to increases in IGF-1.
Three studies used long-duration exercise (52 weeks), employing moderate to vigorous aerobic [109, 118] and high-load resistance training . Neither aerobic exercise intervention demonstrated a change in IGF-1 when compared to a control or comparison group. Voss et al.  also looked at the effects of aerobic intervention on VEGF, finding no changes . High-load resistance training compared to a control group was found to increase IGF-1 and improve processing speed . Overall, these studies provide evidence that short, medium, and long exposure to moderate- to high-intensity resistance training may increase IGF-1 levels in aging adults; however, no consistent effects from aerobic exercise have been evidenced.
The Takeaway: Dose Effects of Exercise in Aging Adults
In this review, we have summarized the evidence on the effects of different intervals of exposure to exercise (short- [1 day-16 weeks], medium- [24-40 weeks], and long-term exercise [52 weeks and beyond]) on the most well-accepted mechanisms used to explain the link between the practice of regular exercise and the improvement in cognitive performance. Due to the heterogeneity in studies, it was not possible to report on domain-specific mechanistic changes. However, evidence from a large-scale systematic review and regression indicates that the most stable and consistent improvements in cognition following exercise occur in executive functions and processing speed . Therefore, we discussed changes in cerebral perfusion, synaptic neuroplasticity, brain structure (volume and connectivity), neurogenesis and synaptogenesis, and trophic factors (BDNF, IGF-1, and VEGF) following participation of exercise in older adults or aged rodents (if no human data was available), that would underlie these improvements in cognitive abilities. We refer to Fig. 1 for a time-guided discussion of the exercise-mediated improvements in mechanisms related to brain health in humans.
Short Term (1 Day to 16 Weeks)
Even with very short aerobic exercise interventions (i.e., just a few minutes as part of an incremental cycling test), there were increases in resting regional CBF and MCA velocity. Short-duration aerobic was the only exercise mode found to be effective at changing connectivity, primarily increasing neural efficiency in frontal and temporal areas, relevant to the processing of cognitive information. The finding of increased connectivity allied to increased brain perfusion is consistent with animal studies that have found that increased connectivity is among the first of exercise-mediated improvements at the brain level, which in turn promotes an increase in angiogenesis to support increased metabolism, ultimately leading to neurogenesis [76, 79]. The only other structural improvement also associated with aerobic exercise was increased hippocampal volume, which was associated with increased cerebral blood flow to the hippocampus. Despite all of the aforementioned beneficial structural brain changes, aerobic exercise did not seem to change neurobiological factors, as increases in BDNF and IGF-1 were only found with resistance training or combined aerobic and resistance training. Therefore, for the most global benefits from exercise, a combined approach utilizing both aerobic and resistance exercises with at least moderate intensity will contribute best to improved brain structure, cerebral blood flow, as well as improvements in neurobiological factors such as BDNF and IGF-1, in the short-term.
Medium Term (24 to 40 Weeks)
As the intervention time increased to medium exposure, there continued to be findings of increased connectivity with aerobic exercise. In addition, there were more consistent and diverse structural changes found in terms of increased white and gray matter and volumetric increases mainly in the in frontal and temporal areas (such as the hippocampus, cingulate, and frontal cortices). BDNF was only increased when individuals engaged in an aerobic dance intervention and IGF-1 was only increased when individuals engaged in moderate to high resistance training. We also found some patterns in the studies and identified 3 isolated characteristics that seemed to be associated with the greater likelihood of finding a benefit: including a progressive intervention that increased the exercise intensity from moderate to high, an exercise intervention with at least 150 weekly minutes, and constant novelty (a choreography or the combination of exercise modes).
Although the present review synthesizes results from healthy aging individuals, it is pertinent to also consider the role of commonly seen cardiovascular risk factors on the baseline level of risk for cognitive decline. Cardiovascular risk factors are also risk factors for cognitive impairment . Hypertension (present in 65% of adults older than 60) , diabetes mellitus (present in 25% of adults older than 65) , obesity (present in 40% of adults older than 60), smoking (present in 8% of adults 65 and over), and insufficient activity (present in 60% of adults older than 65) are all associated with poor cognitive health . Notably, age-related cognitive changes associated with vascular risk factors are likely mediated through small vessel disease, including white matter pathology. For example, in a sample of 113 aging adults, 67% of individuals who had white matter lesions also had cardiovascular diseases, which in turn was linked to greater impaired visual functions, mental flexibility, and attention . Favorably however, maintaining a regular exercise regimen for approximately 3 to 6 months can improve maximal aerobic capacity (the gold standard for cardiorespiratory fitness) in older adults . The increased cardiovascular fitness can have a role in modifying these risk factors, thus contributing to potential improvements in cognitive brain health and, additionally, enlisting neurohumoral processes controlling the cardiovascular and endothelial systems [123, 125].
Long Term (52 Weeks and Beyond)
Studies in long-term exercise included exercise modes beyond aerobic interventions. Aerobic, coordination, and combined exercise interventions were linked to increases in white matter integrity and increased hippocampal volume, which seemed to be driven by an improvement in cardiovascular fitness through moderate to high exercise intensities. In addition, these interventions were associated with increased neural efficiency. Resistance training was shown to be effective at increasing IGF-1. These studies have also provided evidence that different exercise modes exert benefits via distinct mechanisms, which further supports the suggestion that engaging in physical exercise of different modes will lead to the greatest benefits on brain health.