TY - JOUR
T1 - Multivariate lesion-behavior mapping of general cognitive ability and its psychometric constituents
AU - Bowren, Mark
AU - Adolphs, Ralph
AU - Bruss, Joel
AU - Manzel, Kenneth
AU - Corbetta, Maurizio
AU - Tranel, Daniel
AU - Boes, Aaron D.
N1 - Publisher Copyright:
© 2020 the authors
PY - 2020/11/11
Y1 - 2020/11/11
N2 - General cognitive ability, or general intelligence (g), is central to cognitive science, yet the processes that constitute it remain unknown, in good part because most prior work has relied on correlational methods. Large-scale behavioral and neuroanatomical data from neurologic patients with focal brain lesions can be leveraged to advance our understanding of the key mechanisms of g, as this approach allows inference on the independence of cognitive processes along with elucidation of their respective neuroanatomical substrates. We analyzed behavioral and neuroanatomical data from 402 humans (212 males; 190 females) with chronic, focal brain lesions. Structural equation models (SEMs) demonstrated a psychometric isomorphism between g and working memory in our sample (which we refer to as g/Gwm), but not between g and other cognitive abilities. Multivariate lesion-behavior mapping analyses indicated that g and working memory localize most critically to a site of converging white matter tracts deep to the left temporo-parietal junction. Tractography analyses demonstrated that the regions in the lesion-behavior map of g/Gwm were primarily associated with the arcuate fasciculus. The anatomic findings were validated in an independent cohort of acute stroke patients (n = 101) using model-based predictions of cognitive deficits generated from the Iowa cohort lesion-behavior maps. The neuroanatomical localization of g/ Gwm provided the strongest prediction of observed g in the new cohort (r = 0.42, p, 0.001), supporting the anatomic specificity of our findings. These results provide converging behavioral and anatomic evidence that working memory is a key mechanism contributing to domain-general cognition.
AB - General cognitive ability, or general intelligence (g), is central to cognitive science, yet the processes that constitute it remain unknown, in good part because most prior work has relied on correlational methods. Large-scale behavioral and neuroanatomical data from neurologic patients with focal brain lesions can be leveraged to advance our understanding of the key mechanisms of g, as this approach allows inference on the independence of cognitive processes along with elucidation of their respective neuroanatomical substrates. We analyzed behavioral and neuroanatomical data from 402 humans (212 males; 190 females) with chronic, focal brain lesions. Structural equation models (SEMs) demonstrated a psychometric isomorphism between g and working memory in our sample (which we refer to as g/Gwm), but not between g and other cognitive abilities. Multivariate lesion-behavior mapping analyses indicated that g and working memory localize most critically to a site of converging white matter tracts deep to the left temporo-parietal junction. Tractography analyses demonstrated that the regions in the lesion-behavior map of g/Gwm were primarily associated with the arcuate fasciculus. The anatomic findings were validated in an independent cohort of acute stroke patients (n = 101) using model-based predictions of cognitive deficits generated from the Iowa cohort lesion-behavior maps. The neuroanatomical localization of g/ Gwm provided the strongest prediction of observed g in the new cohort (r = 0.42, p, 0.001), supporting the anatomic specificity of our findings. These results provide converging behavioral and anatomic evidence that working memory is a key mechanism contributing to domain-general cognition.
KW - Brain networks
KW - General cognitive ability
KW - General intelligence
KW - Lesion method
KW - Psychometrics
KW - Working memory
UR - https://www.scopus.com/pages/publications/85096044950
U2 - 10.1523/JNEUROSCI.1415-20.2020
DO - 10.1523/JNEUROSCI.1415-20.2020
M3 - Article
C2 - 33046547
AN - SCOPUS:85096044950
SN - 0270-6474
VL - 40
SP - 8924
EP - 8937
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 46
ER -