Hyperphantasia
Hyperphantasia is the condition of having extremely vivid mental imagery.[1] It is the opposite condition to aphantasia, where mental visual imagery is not present.[2][3] The experience of hyperphantasia is more common than aphantasia[4][5] and has been described as being "as vivid as real seeing".[4] Hyperphantasia constitutes all five senses within vivid mental imagery, although literature on the subject is dominated by "visual" mental imagery research, with a lack of research on the other four senses.[6]
Research into hyperphantasia is most commonly completed by self-report questionnaires, such as the Vividness of Visual Imagery Questionnaire (VVIQ), developed by David Marks in 1973, which evaluates the vividness of an individual's mental imagery out of a score of 80.[6] Individuals scoring from 75 to 80 are deemed hyperphantasics and are estimated to constitute around 2.5% of the population.[2]
Mechanism
There is no reliably specific mental imagery cortical network; the formation of mental imagery involves many regions of the brain, as mental imagery shares many common brain regions with other cognitive functions.[7] Neurological evidence has shown that in the creation of imagery, neural activity spans prefrontal, parietal, temporal and visual areas.[6][8] Within the neuroscience of imagery, it is often split into three primary aspects: the triggering of imagery, its generation/manipulation, and the underlying vividness of the imagery.[6][9]
The mechanism underlying the vividness of imagery which may explain disorders like hyperphantasia is controversial amongst the literature.[10] The current findings of the mechanism of hyperphantasia are related to two regions of the brain: the early visual cortex and the frontal cortex.[9]
Recent research has shown the relationship between the size (surface area) of the early visual cortex (V1-V3), specifically V1 and to a lesser degree V2 (but not V3), negatively predicts imagery strength within individuals.[6][11] This relationship is evidenced across both clinical and non-clinical populations [see § Co-morbidity below].[6]
In contrast, there is a positive relationship between the surface area of the frontal cortex and visual imagery strength.[6][10] This aligns with the reciprocal relationship between the size of primary visual cortices and frontal cortices, with a smaller V1 correlating to a larger frontal cortex.[12] Within the general principle of human cortical organization, there is an anatomical trade-off between primary sensory cortices such as the primary visual cortex and frontal areas. Several lines of evidence suggest that the respective sizes of these areas within individuals predict their vividness of imagery.[6][12][11] Additionally, genetics play a part in determining the surface area of V1, suggesting that genetics may indirectly contribute to hyperphantasia.[6][12]
Beyond the size of these regions, there is evidence that lower resting activity and excitability levels within the primary visual cortex predicts stronger mental imagery and vice versa. This has been confirmed by artificially lowering the excitability of the visual cortex, which subsequently led to increased imagery strength.[8] The relationship between the frontal lobe and the visual cortex form an 'imagery network' where the ratio in size and excitability of these two areas relate to imagery strength amongst individuals.[8]
Neuroimaging studies using functional magnetic resonance imaging (fMRI) have additionally demonstrated that hyperphantasics have significantly stronger connectivity between their prefrontal cortices (Brodmann's Areas 9, 10, 11 in particular) and their visual cortex in comparison to aphantasics.[10]
The mechanism behind vivid imagery appears to come down to the size and excitability of the visual-occipital network and the frontal areas as well as the strength of connectivity between these brain regions. However, these factors can only explain the variations in mental imagery; the specific mechanisms that cause hyperphantasia are still not well documented.[10]
Impacts
Memory
Vivid mental imagery as observed in hyperphantasia impacts people's ability to “mental time travel”, or the ability to remember past events as well as imagine future events.[13] Hyperphantasics have reported more sensory details of episodic memories and future event constructions.[14][6][10]
Episodic and autobiographical memories are reliant on sensory-perceptual data such as visual imagery.[10][6] Concepts such as ‘flashbulb memories’ - which are powerful autobiographical memories that we often relive – are often built on vivid visual snapshots.[14] Evidence has shown that individuals exhibiting increased imagery vividness also often recall autobiographical memories with richer descriptions as well as with more fluency.[14] Additionally, disorders that affect vision and visual imagery such as aphantasia have been linked to autobiographical amnesia, depicting the importance of visual imagery to autobiographical recall.[13][14] This relationship of imagery vividness and improved autobiographical memory recall is evidenced across both clinical and non-clinical populations.[2]
There is a lack of research on the impacts of vivid mental imagery on imagining future events and possible scenarios (episodic future thinking); however, research has shown that increased vivid imagery will predict the “clarity of spatial context, the feeling of emotions, and the intensity and personal importance of the events”.[13] This implies that hyperphantasics may be better at planning for the future and predicting how events may impact them. Additionally, this explains why vivid imagery helps with perceptual acuity. Research has shown that higher VVIQ scores predict rapid and more precise decision-making in the face of a threat.[15]
Personality
Hyperphantasia has been shown to be associated with higher levels of ‘openness’ in the Big Five personality traits, using the NEO personality inventory. This entails more openness to "new experiences, broad interests, an active imagination and a likelihood of experiencing more positive and negative emotions more keenly than other people".[10]
Occupation
Research has shown that having hyperphantasia may impact the occupational preference of individuals. Hyperphantasics are significantly more likely to work in traditionally creative roles within "Arts, Design, Entertainment, Sports, and Media" in comparison to their aphantasic counterparts.[6][2] Hyperphantasia has been found to have a strong positive correlation between vividness and creativity, several study participants going as far as using their vividness in imagery to visualized 3D objects in their minds eye.[16]
Co-morbidity
Vivid imagery has been correlated to several mood disorders, particularly anxiety, major depressive disorder, and bipolar disorder, and having hyperphantasia may exacerbate symptoms of such disorders by subserving ruminating thoughts as well as acting as an “emotional amplifier”.[17][6] For example, vivid ‘flash forwards’ to suicidal acts may increase occurrences of suicide.[6]
The vividness of mental imagery has a key role in the development and continuation of intrusive memories, so for those with PTSD, having hyperphantasia is a substantial risk factor.[18] Both schizophrenia and Parkinson's disease also may be aggravated by hyperphantasia, as high levels of vivid imagery predict the severity of visual hallucinations.[6] In fact, it is possible that hyperphantasia is a ‘trait maker’ for schizophrenia, with both disorders being associated with a smaller primary visual cortex. Individuals with schizophrenia have a 25% volume reduction of their primary visual cortex (V1) and its total number of neurons.[19]
Additionally, a 2008 study found a connection between hyperphantasia and synesthesia. Sampling a large group of synesthetes, they found that individuals with synesthesia reported more vivid mental images than control groups.[20]
See also
References
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- Keogh, Rebecca; Pearson, Joel; Zeman, Adam (2021), Aphantasia: The science of visual imagery extremes, Handbook of Clinical Neurology, vol. 178, Elsevier, pp. 277–296, doi:10.1016/b978-0-12-821377-3.00012-x, ISBN 978-0-12-821377-3, PMID 33832681, S2CID 233193117, retrieved 2023-05-09
- Zeman A (4 May 2020). "An update on 'extreme imagination' – aphantasia / hyperphantasia". The Eye's Mind. University of Exeter. Retrieved 13 March 2021.
- Maddox L (14 November 2019). "Aphantasia: what it's like to live with no mind's eye". BBC Science Focus Magazine. Retrieved 2021-03-14.
- Pearson J (October 2019). "The human imagination: the cognitive neuroscience of visual mental imagery". Nature Reviews. Neuroscience. 20 (10): 624–634. doi:10.1038/s41583-019-0202-9. PMID 31384033. S2CID 199449027.
- Mellet E, Petit L, Mazoyer B, Denis M, Tzourio N (August 1998). "Reopening the mental imagery debate: lessons from functional anatomy". NeuroImage. 8 (2): 129–139. doi:10.1006/nimg.1998.0355. PMID 9740756. S2CID 44704704.
- Keogh R, Bergmann J, Pearson J (May 2020). "Cortical excitability controls the strength of mental imagery". eLife. 9: e50232. doi:10.7554/eLife.50232. PMC 7200162. PMID 32369016.
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- Milton F, Fulford J, Dance C, Gaddum J, Heuerman-Williamson B, Jones K, et al. (2021-04-01). "Behavioral and Neural Signatures of Visual Imagery Vividness Extremes: Aphantasia versus Hyperphantasia". Cerebral Cortex Communications. 2 (2): tgab035. doi:10.1093/texcom/tgab035. PMC 8186241. PMID 34296179.
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- D'Argembeau A, Van der Linden M (June 2006). "Individual differences in the phenomenology of mental time travel: The effect of vivid visual imagery and emotion regulation strategies". Consciousness and Cognition. 15 (2): 342–350. doi:10.1016/j.concog.2005.09.001. hdl:2268/2916. PMID 16230028. S2CID 10299410.
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- Imbriano G, Sussman TJ, Jin J, Mohanty A (December 2020). "The role of imagery in threat-related perceptual decision making". Emotion. 20 (8): 1495–1501. doi:10.1037/emo0000610. PMC 6908763. PMID 31192666.
- Hart, E.; Hay, L. (May 2022). "Do You See What I See? Exploring Vividness of Visual Mental Imagery in Product Design Ideation". Proceedings of the Design Society. 2: 881–890. doi:10.1017/pds.2022.90. ISSN 2732-527X. S2CID 249047429.
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