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RESEARCH PRODUCT
Complexity analysis of cortical surface detects changes in future Alzheimer's disease converters
Víctor CostumeroVíctor CostumeroVíctor CostumeroJuan Ruiz De MirasJuan Ruiz De MirasJorge SepulcreCésar ÁVilaVicente BellochJoaquín Escuderosubject
0301 basic medicineRadiological and Ultrasound TechnologyDiseaseNeurological disorderHuman brainEntorhinal cortexmedicine.diseasebehavioral disciplines and activitiesTemporal lobeWhite matter03 medical and health sciences030104 developmental biology0302 clinical medicinemedicine.anatomical_structureNeurologyFrontal lobemental disordersmedicineRadiology Nuclear Medicine and imagingNeurology (clinical)AnatomyPsychologyGyrificationNeuroscience030217 neurology & neurosurgerydescription
Alzheimer's disease (AD) is a neurological disorder that creates neurodegenerative changes at several structural and functional levels in human brain tissue. The fractal dimension (FD) is a quantitative parameter that characterizes the morphometric variability of the human brain. In this study, we investigate spherical harmonic-based FD (SHFD), thickness, and local gyrification index (LGI) to assess whether they identify cortical surface abnormalities toward the conversion to AD. We study 33 AD patients, 122 mild cognitive impairment (MCI) patients (50 MCI converters and 29 MCI nonconverters), and 32 healthy controls (HC). SHFD, thickness, and LGI methodology allowed us to perform not only global level but also local level assessments in each cortical surface vertex. First, we found that global SHFD decreased in AD and future MCI converters compared to HC, and in MCI converters compared to MCI nonconverters. Second, we found that local white matter SHFD was reduced in AD compared to HC and MCI mainly in medial temporal lobe. Third, local white-matter SHFD was significantly reduced in MCI converters compared to MCI nonconverters in distributed areas, including the medial frontal lobe. Thickness and LGI metrics presented a reduction in AD compared to HC. Thickness was significantly reduced in MCI converters compared to healthy controls in entorhinal cortex and lateral temporal. In summary, SHFD was the only surface measure showing differences between MCI individuals that will convert or remain stable in the next 4 years. We suggest that SHFD may be an optimal complement to thickness loss analysis in monitoring longitudinal changes in preclinical and clinical stages of AD. Hum Brain Mapp 38:5905-5918, 2017. © 2017 Wiley Periodicals, Inc.
year | journal | country | edition | language |
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2017-08-30 | Human Brain Mapping |