PLANCHE, Vincent; COUPE, Pierrick; HELMER, Catherine; LE GOFF, Melanie; AMIEVA, Helene; TISON, Francois; DARTIGUES, Jean-Francois; CATHELINE, Gwenaelle

doi:10.1016/j.neurobiolaging.2019.03.006

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PLANCHE, Vincent
Institut des Maladies Neurodégénératives [Bordeaux] [IMN]

COUPE, Pierrick
Laboratoire Bordelais de Recherche en Informatique [LaBRI]

HELMER, Catherine

Bordeaux population health [BPH]

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Neurobiology of aging. 2019-03-22, vol. 79, p. 22-29

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It is currently unknown whether brain atrophy subtypes defined in Alzheimer's disease are clinically relevant during aging. We investigated participants (n = 368) from a population-based cohort of nondemented older adults who received longitudinal neuropsychological assessments during 12 years. Magnetic resonance imaging scans at baseline and 4 years later were used to define participants with "hippocampal predominant atrophy," "cortical predominant atrophy," "homogenous atrophy," and "no evidence of brain subtype atrophy" based on the dynamics of hippocampal-to-cortical volume ratio evolution. After adjustment on age, gender, educational level, and ApoE4 genotype, participants with "hippocampal predominant atrophy" declined faster regarding global cognition, verbal fluency, and verbal episodic memory. In Cox proportional-hazards models, "hippocampal predominant atrophy" was associated with an increased risk of developing Alzheimer's clinical syndrome over time (hazard ratio = 5.73; 95% CI 2.71-12.15), independently of age and ApoE4 genotype, the 2 other significant predictive factors. As a possible surrogate of confined tauopathy and early Alzheimer's disease pathology, future studies should consider the definition of "hippocampal predominant atrophy" based on hippocampal-to-cortical volume ratio evolution rather than hippocampal volume alone.< Réduire

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Evolution of brain atrophy subtypes during aging predicts long-term cognitive decline and future Alzheimer's clinical syndrome

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