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Mirror-touch synaesthesia: the role of shared ... - UCL Discovery

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159<br />

Chapter 9<br />

Ramachandran, 2005; Rouw and Scholte, 2007). Cross-activation accounts have<br />

tended to focus on adjacent brain regions (e.g. in <strong>the</strong> case <strong>of</strong> grapheme-colour<br />

<strong>synaes<strong>the</strong>sia</strong> - between visual grapheme and colour processing areas in <strong>the</strong> fusiform<br />

gyrus) and suggest that activation in <strong>the</strong> region responsible for processing <strong>the</strong><br />

synaes<strong>the</strong>tic inducer (e.g. <strong>the</strong> grapheme in grapheme-colour <strong>synaes<strong>the</strong>sia</strong>) leads to<br />

activation in <strong>the</strong> adjacent region for processing <strong>the</strong> synaes<strong>the</strong>tic concurrent (e.g.<br />

colour in grapheme-colour <strong>synaes<strong>the</strong>sia</strong>). It is not entirely clear how <strong>the</strong> principle <strong>of</strong><br />

adjacency can be applied to mirror-<strong>touch</strong> <strong>synaes<strong>the</strong>sia</strong>, and an alternative mechanism<br />

which may bias individuals to this type <strong>of</strong> <strong>synaes<strong>the</strong>sia</strong> is <strong>the</strong> normal architecture for<br />

multi-sensory interactions (Sagiv and Ward, 2006). For example, <strong>the</strong>re is good<br />

evidence for an observed-<strong>touch</strong> mirror system in non-synaes<strong>the</strong>tes (Keysers, Wicker,<br />

Gazzola, Anton, Fogassi, and Gallese, 2004; Blakemore et al., 2005; Ebisch, Perrucci,<br />

Ferretti, Del Gratta, Romani, and Gallese, 2008) and mirror-<strong>touch</strong> <strong>synaes<strong>the</strong>sia</strong> has<br />

been suggested to reflect over-activity within this network (Blakemore et al., 2005).<br />

Future studies will aim to address <strong>the</strong> similarities and differences in <strong>the</strong> neural<br />

basis <strong>of</strong> different subtypes <strong>of</strong> <strong>synaes<strong>the</strong>sia</strong> by investigating structural and functional<br />

correlates <strong>of</strong> different variants <strong>of</strong> <strong>synaes<strong>the</strong>sia</strong> (e.g. grapheme-colour, tone-colour,<br />

mirror-<strong>touch</strong>, and number-space <strong>synaes<strong>the</strong>sia</strong>). For example, previous DTI findings<br />

indicate that grapheme-colour <strong>synaes<strong>the</strong>sia</strong> is linked with increased structural<br />

connectivity in right inferior-temporal, right parietal, and bilateral frontal regions<br />

(Rouw and Scholte, 2007), and research in progress indicates that tone-colour<br />

<strong>synaes<strong>the</strong>sia</strong> is linked to increased cortical thickness (a marker <strong>of</strong> cortical morphology<br />

and neurodevelopment; MacDonald, Kabani, Avis, and Evans, 2000; Shaw et al.,<br />

2006) in similar right inferior temporal regions (Banissy, Stewart, Ward, Walsh, and<br />

Kanai, in prep). I am also starting a combined fMRI-DTI study <strong>of</strong> mirror-<strong>touch</strong>

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