» Articles » PMID: 38698168

Human Intraparietal Sulcal Morphology Relates to Individual Differences in Language and Memory Performance

Overview
Journal Commun Biol
Specialty Biology
Date 2024 May 2
PMID 38698168
Authors
Affiliations
Soon will be listed here.
Abstract

The sulco-gyral pattern is a qualitative feature of the cortical anatomy that is determined in utero, stable throughout lifespan and linked to brain function. The intraparietal sulcus (IPS) is a nodal associative brain area, but the relation between its morphology and cognition is largely unknown. By labelling the left and right IPS of 390 healthy participants into two patterns, according to the presence or absence of a sulcus interruption, here we demonstrate a strong association between the morphology of the right IPS and performance on memory and language tasks. We interpret the results as a morphological advantage of a sulcus interruption, probably due to the underlying white matter organization. The right-hemisphere specificity of this effect emphasizes the neurodevelopmental and plastic role of sulcus morphology in cognition prior to lateralisation processes. The results highlight a promising area of investigation on the relationship between cognitive performance, sulco-gyral pattern and white matter bundles.

Citing Articles

Variable Presence of an Evolutionarily New Brain Structure is Related to Trait Impulsivity.

Willbrand E, Maboudian S, Elliott M, Kellerman G, Johnson S, Weiner K bioRxiv. 2024; .

PMID: 39484399 PMC: 11527008. DOI: 10.1101/2024.10.23.619912.


Unique longitudinal contributions of sulcal interruptions to reading acquisition in children.

Bouhali F, Dubois J, Hoeft F, Weiner K bioRxiv. 2024; .

PMID: 39131390 PMC: 11312548. DOI: 10.1101/2024.07.30.605574.


Anchoring functional connectivity to individual sulcal morphology yields insights in a pediatric study of reasoning.

Hakkinen S, Voorhies W, Willbrand E, Willbrand E, Tsai Y, Gagnant T bioRxiv. 2024; .

PMID: 38659961 PMC: 11042283. DOI: 10.1101/2024.04.18.590165.

References
1.
Cachia A, Borst G, Tissier C, Fisher C, Plaze M, Gay O . Longitudinal stability of the folding pattern of the anterior cingulate cortex during development. Dev Cogn Neurosci. 2016; 19:122-7. PMC: 4912935. DOI: 10.1016/j.dcn.2016.02.011. View

2.
Unger N, Haeck M, Eickhoff S, Camilleri J, Dickscheid T, Mohlberg H . Cytoarchitectonic mapping of the human frontal operculum-New correlates for a variety of brain functions. Front Hum Neurosci. 2023; 17:1087026. PMC: 10336231. DOI: 10.3389/fnhum.2023.1087026. View

3.
Paus T, Tomaiuolo F, Otaky N, MacDonald D, Petrides M, ATLAS J . Human cingulate and paracingulate sulci: pattern, variability, asymmetry, and probabilistic map. Cereb Cortex. 1996; 6(2):207-14. DOI: 10.1093/cercor/6.2.207. View

4.
Galati G, Committeri G, Pitzalis S, Pelle G, Patria F, Fattori P . Intentional signals during saccadic and reaching delays in the human posterior parietal cortex. Eur J Neurosci. 2011; 34(11):1871-85. DOI: 10.1111/j.1460-9568.2011.07885.x. View

5.
Budisavljevic S, DellAcqua F, Rijsdijk F, Kane F, Picchioni M, McGuire P . Age-Related Differences and Heritability of the Perisylvian Language Networks. J Neurosci. 2015; 35(37):12625-34. PMC: 4571601. DOI: 10.1523/JNEUROSCI.1255-14.2015. View