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Dalby, C.

Publications and source records attributed to Dalby, C..

2 recordsLinked to original sources

Diagnostic Labels and Measurement Timing Drive Systematic Inconsistency in ADNI Neuroimaging Data

The Alzheimer's Disease Neuroimaging Initiative (ADNI) is widely used to train machine learning models for Alzheimer's disease, yet whether it provides consistent ground truth for predictive modeling has not been systematically tested. In this paper, we showed that ADNI contains three interacting sources of bias with direct implications for machine learning: (a) diagnostic label inconsistency, (b) technical measurement drift, and (c) longitudinal survivor bias. A substantial proportion of cases, particularly within intermediate stages, fall outside ADNI's own diagnostic thresholds. MRI field strength and evolving processing pipelines introduce significant technical variability in hippocampal volume, while cohort survivor bias arising from differential retention of participants across phases further distorts longitudinal estimates of disease progression. These findings indicated that ADNI does not provide the stable, internally consistent labels often required in machine learning applications. We proposed a practical framework for diagnostic validation, feature harmonization, and cohort accounting, offering guidance for building more robust and biologically meaningful predictive models from large-scale neuroimaging cohorts.

neuroscience↗

Delineating In-Vivo T1-Weighted Intensity Profiles Within the Human Insula Cortex Using 7-Tesla MRI

The integral role of the insula cortex in sensory and cognitive function has been well documented in humans, and fine anatomical details characterising the insula have been extensively investigated ex-vivo in both human and non-human primates. However, in-vivo studies of insula anatomy in humans (in general), and within-insula parcellation (in particular) have been limited. The current study leverages 7 Tesla magnetic resonance imaging to delineate cortical depth intensity profiles within the human cortex. Our analysis revealed two separate clusters of relatively high and low signal intensity across the insula cortex located in three distinct compartments within the posterior, anterior-inferior, and middle insula. The posterior and anterior-inferior compartments are characterised by elevated T1-weighted signal intensities, contrasting with lower intensity observed in the middle insular compartment, compatible with ex-vivo studies. Importantly, the detection of the high T1-weighted anterior cluster is determined by the choice of brain atlas employed to define the insular ROI. We obtain reliable in-vivo within-insula parcellation at the individual and group levels, across two separate cohorts acquired in two separate sites (n1 = 21, Glasgow, UK; n2 = 101, Amsterdam, NL). Results are further confirmed by deriving cortical depth dependent profiles from T1Map and R1Map images. These results reflect new insights into the insula anatomical structure, in-vivo, while highlighting the use of 7 Tesla in neuroimaging with potential implications for individualised medicine approaches. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=125 SRC="FIGDIR/small/605123v3_ufig1.gif" ALT="Figure 1"> View larger version (51K): org.highwire.dtl.DTLVardef@1c27244org.highwire.dtl.DTLVardef@dbd256org.highwire.dtl.DTLVardef@1ce44f6org.highwire.dtl.DTLVardef@11183d0_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗