Functional connectivity (FC) is known to be individually unique and to reflect cognitive variability. Although FC can serve as a valuable correlate and potential predictor of (patho-) physiological nervous function in high-risk constellations, such as preterm birth, templates for individualized FC analysis are lacking, and knowledge about the capacity of the premature brain to develop FC variability is limited. In a cohort of prospectively recruited, preterm-born infants undergoing magnetic resonance imaging close to term-equivalent age, we show that the overall pattern could be reliably detected with a broad range of interindividual FC variability in regions of higher-order cognitive functions (e.g., association cortices) and less interindividual variability in unimodal regions (e.g., visual and motor cortices). However, when comparing the preterm and adult brains, some brain regions showed a marked shift in variability toward adulthood. This shift toward greater variability was strongest in cognitive networks like the attention and frontoparietal networks and could be partially predicted by developmental cortical expansion. Furthermore, FC variability was reflected by brain tissue characteristics indicating cortical maturation. Brain regions with high functional variability (e.g., the inferior frontal gyrus and temporoparietal junction) displayed lower cortical maturation at birth compared with somatosensory cortices. In conclusion, the overall pattern of interindividual variability in FC is already present preterm; however, some brain regions show increased variability toward adulthood, identifying characteristic patterns, such as in cognitive networks. These changes are related to postnatal cortical expansion and maturation, allowing for environmental and developmental factors to translate into marked individual differences in FC.
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http://dx.doi.org/10.1073/pnas.1907892117 | DOI Listing |
Alzheimers Dement
December 2024
Washington University in St. Louis, Saint Louis, MO, USA.
Background: Alzheimer disease (AD) is a chronic progressive neurodegenerative disorder that presents with cognitive dysfunction, memory loss, language difficulties, emotion dysregulation, and the eventual loss of motor function and death. Magnetic resonance imaging (MRI) shows early atrophy in the medial temporal lobes, which then spreads to the posterior temporal lobe, parietal lobe, and finally the frontal lobe with relative sparing of the sensorimotor cortex. Social disadvantage has been shown to have potentially additive impacts on aging trajectories.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Universidad de La Laguna, Santa Cruz de Tenerife, Spain.
Background: The brain undergoes structural changes during aging, such as gray matter loss, enlarged ventricles, and sulcal widening. However, previous studies have primarily investigated these changes in isolation, without describing the complex spatial relationships between overall brain shape and regions. Here, we tested how gradients of expansion and compression of the global shape of the brain as well as between homologous brain regions across hemispheres are affected by age, and whether these changes further contribute to clinical impairment and cognitive deficits in older adults.
View Article and Find Full Text PDFBackground: Recent advancements in molecular positron emission tomography (PET) enable precise tracking of tau pathology in Alzheimer's disease (AD). Tau pathology typically begins focally in the medial temporal lobe, rapidly expanding due to amyloid-β (Aβ) influence. This expansion may lead to neurodegeneration along connected pathways to the tau epicenters, resulting in cognitive decline.
View Article and Find Full Text PDFBackground: Cortical brain atrophy is an excellent marker of clinical decline and can support future clinical course prediction in cognitive impairment. We used a U-Net image-generation deep learning network to predict future cortical atrophy rates in elderly populations, with initial T1-weighted (T1w-) MRI or baseline amyloid-PET serving as inputs to the model.
Method: MRI and PET data were retrospectively collected from Alzheimer's Disease Imaging Initiative (ADNI) and all participants had two serial T1w-MRI scans (Figure 1A,B).
Alzheimers Dement
December 2024
University of Texas Medical Branch, Galveston, TX, USA.
Background: Chronically reactivating Herpes Simplex Virus Type 1 (HSV1) infection has been shown to produce key molecular and behavioral markers of Alzheimer's disease (AD). Most notably, the accumulation of neurotoxic tau isoforms, neurofibrillary tangles (NFTs), and Amyloid-beta plaques. Our study takes a unique approach to the systematic characterization of HSV1 biomarkers within the brain.
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