Biopsychosocial Perspectives on Healthy Brain Aging: A Narrative Review
Abstract
1. Introduction
Approaches to Brain Aging
2. Materials and Methods
Critical Analysis
3. Results
4. Discussion
4.1. Practical Recommendations/Policy Implications
4.2. Limitations
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Psychosocial Biomarkers | Psychosocial Factor | Mechanism of Action | Morphological Impact | Author(s) |
---|---|---|---|---|
Eating Behavior | Leptin synthesized by adipose tissue elevates Brain-Derived Neurotrophic Factor (BDNF) levels, involved in the formation of new memories related to episodic and semantic memory. Omega-3 fatty acids, flavonoids, and B- vitamins. Gut microbiome and its influence on certain dietary factors are generating promising evidence that promotes healthy brain aging. | Elevates BDNF levels, essential for neuroplasticity and memory formation. Dietary manipulation of the gut microbiota can enhance brain functions during aging. Affect the slowing of brain atrophy (Hippocampus and entorhinal cortex) and generate a lower risk of dementia associated with the APOEε4 genotype. | Affects dendritic morphology of the hippocampus and hypothalamus, positively influencing overall brain plasticity. Protect the brain by improving neuronal integrity and synaptic plasticity, reducing inflammation and damage from beta-amyloid, and improving cerebral blood flow. The gut–brain axis directly influences brain function and mood, based on levels of available serotonin linked to a range of neurodegenerative conditions, including dementia. | O’Malley et al., 2007 [35]. Amadieu et al., 2017 [36]. Flanagan et al., 2020 [37]. |
Physical Activity | Engaging in moderate and intense physical activity generates earlier and broader neuro-electrical potentials. | Enhances neuronal transmission, improving working memory, attention, and executive control. | Increases white matter (WM) volume in critical regions (e.g., corona radiata, fornix, corpus callosum) with more neuronal connections in the prefrontal cortex, reduces cortical thinning, preserves frontotemporal sulci. | San Martín et al., 2023 [38]; Vecchio et al., 2018 [39]. |
Quality of Sleep | Adequate restful sleep (7–8 h. per night) leads to positive changes in working memory processes, attention, and cognitive flexibility. Poor sleep quality tends to interfere with memory consolidation and the clearing of brain toxins, such as β-amyloid (protein), that accumulate during wakefulness. | Functional changes are linked to sex steroid-dependent receptor activity in the suprachiasmatic nuclei of the hypothalamus. Homeostatic mechanisms responsible for regulating the elimination of free radicals, cortical electrical activity, synaptic homeostasis, and memory consolidation are altered, regulated by the preoptic area of the hypothalamus based on Acetylcholine (ACh) and Serotonin (5 HT). | Supports improved cognitive functions and emotional stability, associated with increased structural health of relevant brain regions. Poor sleep quality is associated with decreased functional and structural connectivity of different networks, overlapping in the right superior temporal pole, left mid-temporal regions, and left inferior occipital region. | Madrid-Valero et al., 2017 [40]. Amorim et al., 2018 [41]. |
Social Participation | Pursuing meaningful activities enhances emotional intelligence and cognitive learning. | Activates the ventromedial prefrontal cortex (VMPFC) and limbic system, crucial for social cognition. | Engages multiple brain regions involving impulse control, emotional processing, and overall cognitive flexibility. | Van der Velpen et al., 2022 [42]; Piolatto et al., 2022 [43]. |
Quality of Life | Strong emotional regulation influences perceived physical health and discomfort. Strictly related to the physiology of brain activity, cognition, emotion, and stress. | Involves activation of brain areas such as the anterior insula and ventrolateral prefrontal cortex (VLPFC). Based on the optimization of Serotonin, improving cerebral blood flow and reducing inflammation and oxidative stress. | Increases functional connectivity and structural integrity in the corpus callosum, corona radiata, and cingulate regions, promoting cognitive health. A higher quality of life related to physical health and overall health perception was associated with increased gray matter volume in the anterior cingulate cortex, medial prefrontal cortex, insular cortex, and precuneus. | Ourry et al., 2021 [44]. Hahm et al., 2019 [45]. |
Subjective Well-being | A sense of happiness and optimism significantly impacts overall life satisfaction. The association between subjective well-being and the integrity of brain structures is supported by the limbic-thalamic-cortical pathway involved in emotional regulation. | Changes in grey matter (GM) volume of medial temporal lobes, including the parahippocampal gyrus. Favoring the integrity of white matter involved in emotional regulation by communicating the main regions of the brain. | Alters brain structure contributing to emotional regulation and cognitive efficiency. Happiness was correlated with integrity, especially in the internal capsule, corona radiata, posterior thalamic radiation, cingulum, and superior longitudinal fasciculus. | Kong et al., 2015 [46]. Kokubun et al., 2022 [47]. |
Marital Status | Marital status correlates with cognitive resilience; individuals never married often exhibit poorer brain health. Marriage is generally associated with a reduced risk of cognitive decline and dementia, while being single, divorced, or widowed is linked to a higher risk. | Situational cognitive reserves generated from problem-solving in partnerships enhance cognitive functioning. Marital status is significantly predictive of cognitive decline among older adults, and those with a spouse exhibited better cognitive functioning based on social support received throughout the life cycle. | Participants never married show reduced cortical thickness compared to those living with others, indicating possible protective effects of social bonds. Studies based on mean fractional anisotropy (MFA) demonstrate the integrity of the anterior rostral cingulate cortex, insular cortex, and precuneus in older individuals as measured by gray matter (GM) volume. | Lee et al., 2024 [48]. Zhang et al., 2024 [49]. |
Biological Biomarkers | Type | Description | Morphological Manifestation | Author(s) |
---|---|---|---|---|
Epigenetic Clocks (Current) | Molecular Aging Predictors | Epigenetic clocks assess the molecular alterations that signify the onset of aging at both physiological and phenotypic levels, particularly through analyzing DNA methylation (mDNA) across the human genome. | Specific biological age estimations include DNA methylation assessments in saliva, mitochondrial DNA (mtDNA) analysis in blood, and various measures of mDNA related to plasma proteins. | Higgins-Chen et al., 2021 [50]. |
Blood Epigenetic Clock | Biomarkers of Cognitive Risks DNAm PhenoAge | This biomarker encompasses one of the well-studied indicators of brain aging and is significantly associated with increased risks for Alzheimer’s disease, cognitive impairments, and dementia. Being a strong predictor of various aging-related outcomes such as physical functioning and Alzheimer’s disease. | Higher epigenetic age correlates with a decrease in brain volumetrics and white matter integrity, as well as an increase in vascular lesions and cortical thinning. An increase in epigenetic markers is associated with heightened activity in pro-inflammatory pathways and interferon, as well as decreased transcriptional activity in response to DNA damage and the subsequent mitochondrial activity. | Hodgson et al., 2017 [51]. Levine et al., 2018 [52]. |
Epigenetic Brain Clock | Molecular Measure of Brain Aging | This approach offers a direct molecular measurement of brain aging, shedding light on the physiological mechanisms by which aging occurs. This clock enables cellular and mitotic signal assessments related to neuronal attrition with age. | There is a documented link between brain epigenetic age (BAG) and various pathologies, including an accelerated BAG in conditions like bipolar disorder (BD) and Alzheimer’s disease (AD). The lipid elongation enzyme (ELOVL2) hypermethylation serves as a notable age predictor. | Garagnani et al., 2012 [53]; Slieker et al., 2018 [54]. |
Proteomic Changes | Age-Related Protein Dynamics | Research has identified 1128 age-related proteins that change across various tissues, primarily focusing on plasma proteomics associated with alterations in brain function. | Accelerated proteomic aging is linked to cognitive functions, including reduced executive function, processing speed, visuospatial skills, and overall physical capabilities. Proteins such as beta-2-microglobulin (B2M) and vascular cell adhesion protein 1 (VCAM-1) disproportionately influence neurogenesis and cognitive performance post-age 50. | Smith et al., 2015 [55]; Yousef et al., 2019 [56]; Nikolakopoulou et al., 2019 [57]. |
Neuroimaging-Based Age Markers | Structural and Functional Imaging Techniques Predictive “brain age” biomarker, using structural neuroimaging. | Structural and functional magnetic resonance imaging (fMRI) is critical in assessing risks associated with mortality, cognitive decline, and diseases such as Alzheimer’s disease (AD). Having a predictive brain image indicating an older-appearing brain is associated with reduced grip strength, lower pulmonary function, decreased fluid intelligence, and higher mortality risk. | Neuroimaging findings can predict transitions from cognitive decline to Alzheimer’s disease more effectively than other measures, suggesting pivotal links between vascular aging and processing velocity. This suggests that neuroimaging data related to epigenetic aging markers provide significant insights into brain health and function. | Cole et al., 2017 [58]. Cole et al., 2018 [59]. |
Other Types of Biomarkers | Metabolic and Microbiome Markers | Fatty acid metabolism has been identified as a crucial pathway compromised in the context of brain aging, mortality, and Alzheimer’s disease. The human gut microbiome is emerging as an influential biomarker in central nervous system aging. | The plasma metabolome can be employed as a novel predictor of biological aging among humans. The gut microbiome interacts with the central nervous system through various signaling pathways, including those from the enteric nervous system, blood metabolites, and immune responses. | Galkin et al., 2020 [60]; Yang et al., 2025 [61]. |
Brain Age Gap (BAG) | Age Discrepancy Measurement | The BAG quantifies the difference between an individual’s estimated biological age and their chronological age, offering insights into cognitive health and resilience against aging-related impairments. | Assessing the BAG can provide useful insights into biological aging and potential risks for neurodegenerative diseases, thereby facilitating individualized approaches to cognitive health interventions. | Proskovec et al., 2020 [62]. |
New study perspectives based on non-invasive biomarkers | Study via Optical Coherence Tomography (OCT) and retinal angiography. | Reliable retinal biomarkers have been demonstrated for non-invasive screening and monitoring of Alzheimer’s disease (AD). | Evidence indicates a relationship between changes in the retina and brain tissue based on a peripapillary reduction in retinal nerve fiber layer (RNFL) and ganglion cell layer (GCL), correlating with cognitive function decline and the risk of developing AD. | Koronyo et al., 2023 [63]. |
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San Martín, C.; Rojas, C.; Sandoval, Y.; Vicente, B. Biopsychosocial Perspectives on Healthy Brain Aging: A Narrative Review. J. Ageing Longev. 2025, 5, 44. https://doi.org/10.3390/jal5040044
San Martín C, Rojas C, Sandoval Y, Vicente B. Biopsychosocial Perspectives on Healthy Brain Aging: A Narrative Review. Journal of Ageing and Longevity. 2025; 5(4):44. https://doi.org/10.3390/jal5040044
Chicago/Turabian StyleSan Martín, Claudio, Carlos Rojas, Yasna Sandoval, and Benjamín Vicente. 2025. "Biopsychosocial Perspectives on Healthy Brain Aging: A Narrative Review" Journal of Ageing and Longevity 5, no. 4: 44. https://doi.org/10.3390/jal5040044
APA StyleSan Martín, C., Rojas, C., Sandoval, Y., & Vicente, B. (2025). Biopsychosocial Perspectives on Healthy Brain Aging: A Narrative Review. Journal of Ageing and Longevity, 5(4), 44. https://doi.org/10.3390/jal5040044