Current Biology Vol 17 No 24 R1042

Correspondences

Impaired parietal magnitude processing in developmental dyscalculia Gavin R. Price1, Ian Holloway2, Pekka Räsänen3, Manu Vesterinen1 and Daniel Ansari2 Developmental dyscalculia (DD) is a specific learning disability affecting the acquisition of school- level mathematical abilities in the context of otherwise normal academic achievement, with prevalence estimates in the order of 3–6% [1] . Behavioural studies show deficits in elementary numerical processing among individuals with pure DD [2,3], indicating that deficits in higher-level mathematical skills may stem from impaired representation and processing of basic numerical magnitude. Adult neuropsychological and neuroimaging research points to the intraparietal sulcus as a key region for the representation and processing of numerical magnitude [4]. This raises the possibility of a parietal dysfunction as a root cause of DD [5]. We show that, in children with pure DD, the right intraparietal sulcus is not modulated in response to numerical processing demands to the same degree as in typically developing children. This finding provides the first direct evidence for a specific impairment of parietal magnitude systems in DD during non-symbolic numerosity processing. We used functional magnetic resonance imaging (fMRI) to investigate the neural correlates of basic numerical processing in children with pure DD in comparison to their typically developing peers. Numerosity comparison becomes increasingly difficult as the numerical distance between the comparators is decreased; suggesting an underlying, approximate

representation of numerosity. This ‘numerical distance effect’ [6] has been shown to modulate brain activity in bilateral parietal areas in both adults [7] and children [8]. In the present study, therefore, the numerical distance between stimuli was systematically varied (see Supplemental data available on-line with this issue for details of the experimental procedures). Eight right-handed children diagnosed with DD on the basis of standardised math scores of at least 1.5 standard deviations below the average, in the absence of any other cognitive or learning disabilities (Table S1), were compared to eight right- handed, typically developing, age- matched peers. Participants were required to select which of two simultaneously presented sets of squares contained the larger number of items. Set pairs were assigned to either close (1–3) or far distance (5–8) groups (Figure S1). Behavioural performance data (see Table S2) were analyzed by a 2 x 2 mixed design analysis of variance (ANOVA), with distance (close versus far) as a within- subjects factor and group (control versus DD) as a betweensubjects factor. This analysis revealed a main effect of distance on reaction time (F(1,14) = 115.75, p < 0.001, η2 = 0.89) with longer response times for close distance trials, but no distance by group interaction (F(1,14) = 2.13, p > 0.1, η2 = 0.13). A significant main effect of distance (F(1,14) = 85.58, p < 0.001, η2 = 0.86) on the number of errors was found, with more errors in the close distance condition. Additionally, a significant group by distance interaction was found (F(1,14) = 5.09, p < 0.05, η2 = 0.27), with DD subjects showing a greater effect of distance on response accuracy. To assess which brain regions were differentially modulated by distance between groups, we carried out a random- effects, whole brain, voxel-wise analysis testing for group x distance interactions. Significant interactions were observed at cluster corrected threshold of p < 0.05 (cluster-level threshold calculated on the basis of

interaction t-map thresholded at p < 0.005, uncorrected: see Supplemental data for details) in the right intraparietal sulcus (IPS; BA7; 33, −50, 52; k = 222 mm3; Figure 1 ), left fusiform gyrus (FG; BA37; −36, −54, −13; k = 323 mm3;, Figure S2), and left medial prefrontal cortex (MPFC; BA11; −13, 54, −2; k = 199 mm3; Figure S3). As can be seen from the Bar chart in Figure 1, the interaction in the IPS was characterized by a stronger distance effect in the control group than in the DD group, suggesting a lack of modulation of parietal numerical processing mechanisms in response to increasing numerical task demands in DD children. The same pattern was observed in the FG, suggesting a deficient neural response in DD to the increased demand for visual segmentation of the displays as the numerical distance between the two sets of squares decreases [9]. The interaction in the MPFC region, on the other hand, was characterized by a greater deactivation in the DD group for close versus far distances, while showing equal positive activations in the control group. This may reflect greater deactivation of the so-called resting state network for DD children in response to greater subjective task difficulty [10]. These data suggest specific abnormalities in the functional neuroanatomy underlying numerical magnitude processing in DD. Furthermore, these results provide evidence for a link between brain mechanisms underlying basic numerical magnitude processing and the development of higher level mathematical skills, which are impaired in DD. To date, only one neuroimaging study has investigated pure DD in children who were otherwise typically developing [11], finding no anatomically specific impairment of brain activation during nonsymbolic magnitude comparison. The contradiction between those and our new results may stem from the differences in stimulus controls between the studies. The present results are therefore the first

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Supplemental data Supplemental data are available at http://www.current-biology.com/cgi/ content/full/17/24/R1042/DC1 Acknowledgments This work was supported by grant MRTN-CT-2003-504927 NUMBRA of The European Community. Finnish Center of Excellence Grant 44858. We would like to thank Olesja Severin for her help with data collection, members of the Jyvaskyla Longitudinal study for help with subject recruitment, and Lucia van Eimeren for her assistance with the figures. References

Figure 1. Interaction of group X distance in the right intraparietal sulcus. Statistical map showing interaction of group x distance (p < 0.05, corrected at the cluster level) overlaid on an average image of all participants’ high-resolution structural MRI scans level. The bar chart shows the parameter estimates for this region for both groups. Error bars represent the standard error of the mean. (NSC, Nonsymbolic Close Distance; NSF. Nonsymbolic Far Distance.)

to reveal atypical activation in the right intraparietal sulcus, during a non-symbolic, numerical magnitude processing task, in children with pure DD. The observed group by distance interaction in the right IPS falls within areas previously associated with processing of numerical magnitude in typically developing children [8] and adults [7], as well as within close proximity to a region referred to as the horizontal segment of the intraparietal sulcus (hIPS). The hIPS has been identified in a meta-analysis [4] of neuroimaging studies of numerical processing as being involved in the representation and processing of numerical quantity (mean Talairach coordinates for hIPS:41, –47, 48; standard deviations for these mean coordinates: 7, 7, 5). The present results, therefore, suggest either a weakened parietal representation of numerical magnitude in DD and/or a reduced ability

to access and manipulate numerical quantities. This basic numerical capacity, for which a brain-level impairment in DD is revealed here, appears to be a necessary foundation on which the development of higher level arithmetical skills is scaffolded. A recent study [12] showed that transcranial magnetic stimulation of the right parietal lobe produces behavioural patterns similar to those found in adult dyscalculics, providing a simulation of DD, and providing further evidence for the key role played by the right intraparietal sulcus in basic numerical magnitude processing. Our results, however, provide direct evidence of parietal dysfunction in pure developmental dyscalculia and thereby strengthen the hypothesis that dyscalculia is caused by ontogenetic disruption of the neural circuitry that supports fundamental representation of numerical magnitude.

1. Shalev, R.S., and Gross-Tsur, V. (2001). Developmental dyscalculia. Pediatric Neurol. 24, 337–342. 2. Landerl, K., Bevan, A., and Butterworth, B. (2004). Developmental dyscalculia and basic numerical capacities: a study of 8-9-year-old students. Cognition 93, 99–125. 3. Rousselle, L., and Noel, M.P. (2007). Basic numerical skills in children with mathematics learning disabilities: A comparison of symbolic vs non-symbolic number magnitude processing. Cognition 102, 361–395. 4. Dehaene, S., Piazza, M., Pinel, P., and Cohen, L. (2003). Three parietal circuits for number processing. Cogn. Neuropsychol. 20, 487–506. 5. Butterworth, B. (1999). The Mathematical Brain (London: Macmillan). 6. Moyer, R.S., and Landauer, T.K. (1967). Time required for judgements of numerical inequality. Nature 215, 1519–1520. 7. Pinel, P., Dehaene, S., Riviere, D., and LeBihan, D. (2001). Modulation of parietal activation by semantic distance in a number comparison task. Neuroimage 14, 1013–1026. 8. Ansari, D., and Dhital, B. (2006). Agerelated changes in the activation of the intraparietal sulcus during nonsymbolic magnitude processing: An event-related functional magnetic resonance imaging study. J. Cogn. Neurosci. 18, 1820–1828. 9. Reddy, L., and Kanwisher, N. (2006). Coding of visual objects in the ventral stream. Curr. Opin. Neurobiol. 16, 408–414. 10. Gusnard, D.A., and Raichle, M.E. (2001). Searching for a baseline: Functional imaging and the resting human brain. Nat. Rev. Neurosci. 2, 685–694. 11. Kucian, K., Loenneker, T., Dietrich, T., Dosch, M., Martin, E., and von Aster, M. (2006). Impaired neural networks for approximate calculation in dyscalculic children: a functional MRI study. Behav. Brain Funct. 2, 31. 12. Kadosh, R.C., Kadosh, K.C., Schuhmann, T., Kaas, A., Goebel, R., Henik, A., and Sack, A.T. (2007). Virtual dyscalculia induced by parietal-lobe TMS impairs automatic magnitude processing. Curr. Biol. 17, 689–693. 1Agora

Center, Department of Psychology, University of Jyvaskyla, Finland. 2Department of Psychology and Graduate Program in Neuroscience, University of Western Ontario, Canada. 3Niilo Maki Institute, Jyvaskyla, Finland. E-mail: [email protected]

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