4.6 Article

Characterization of structural and functional network organization after focal prefrontal lesions in humans in proof of principle study

Journal

BRAIN STRUCTURE & FUNCTION
Volume 227, Issue 9, Pages 3027-3041

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00429-022-02570-2

Keywords

Lesion; Superior frontal gyrus; Inferior frontal gyrus; Neuroimaging

Funding

  1. Canadian Institutes of Health Research
  2. Biotechnology and Biological Sciences Research Council UK [BB/N019814/1]
  3. Netherlands Organization for Scientific Research [452-13-015]
  4. Wellcome Trust [203129/Z/16/Z]
  5. Fonds de Recherche en Sante du Quebec (Chercheur-Boursier Award)
  6. McGill University's Healthy Brains for Healthy Lives Canada First Research Excellence Fund
  7. National Institutes of Health
  8. Sidney Baer Foundation

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Lesion research not only focuses on the directly injured brain region, but also considers distant effects. In this study, multiple MRI imaging modalities were used to investigate network organization in patients with chronic focal damage and healthy controls. The results suggest widespread grey matter loss in distal regions, but relatively preserved white matter and resting state networks. Lesions to the prefrontal region had a similar impact on both structural and functional networks.
Lesion research classically maps behavioral effects of focal damage to the directly injured brain region. However, such damage can also have distant effects that can be assessed with modern imaging methods. Furthermore, the combination and comparison of imaging methods in a lesion model may shed light on the biological basis of structural and functional networks in the healthy brain. We characterized network organization assessed with multiple MRI imaging modalities in 13 patients with chronic focal damage affecting either superior or inferior frontal gyrus (SFG, IFG) and 18 demographically matched healthy Controls. We first defined structural and functional network parameters in Controls and then investigated grey matter (GM) and white matter (WM) differences between patients and Controls. Finally, we examined the differences in functional coupling to large-scale resting state networks (RSNs). The results suggest lesions are associated with widespread within-network GM loss at distal sites, yet leave WM and RSNs relatively preserved. Lesions to either prefrontal region also had a similar relative level of impact on structural and functional networks. The findings provide initial evidence for causal contributions of specific prefrontal regions to brain networks in humans that will ultimately help to refine models of the human brain.

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