Home > Documents in Process > Apraxic deficits in Alzheimer's disease are associated with altered dynamic connectivity in praxis-related networks. > print

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024 7 _ |a 10.1016/j.neurobiolaging.2025.09.007
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024 7 _ |a 0197-4580
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024 7 _ |a 1558-1497
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037 _ _ |a DZNE-2025-01296
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Kuzu, Taylan D
|b 0
245 _ _ |a Apraxic deficits in Alzheimer's disease are associated with altered dynamic connectivity in praxis-related networks.
260 _ _ |a Amsterdam [u.a.]
|c 2026
|b Elsevier Science
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336 7 _ |a ARTICLE
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520 _ _ |a Apraxia is a common symptom in Alzheimer's disease (AD) that reduces autonomy and quality of life. However, the neural basis underlying apraxia in AD, for example, reflected by functional connectivity (FC) alterations, remains unexplored. We investigated static and dynamic FC using resting-state functional imaging in 14 patients with biomarker-confirmed AD pathology and 14 matched healthy participants. FC was estimated as average (static) and short-term (dynamic) connectivity strengths between motor- and praxis-related functional networks. Recurring connectivity patterns were clustered into dynamic states to compute temporal connectivity measures. Connectivity measures were used for correlations with apraxic deficits. In AD patients, static connectivity between visual and inferior parietal networks correlated with apraxic imitation (r = 0.762, PFDR = 0.043) and arm/hand gesture deficits (r = 0.848, PFDR = 0.020), while dynamic connectivity between these networks correlated with apraxic imitation deficits (r = 0.851, PFDR = 0.020). Dynamic FC analysis revealed a segregated and integrated state. AD patients spent more time overall (fraction time, PFDR < 0.001) and remained longer without switching (dwell time, PFDR = 0.004) in the segregated state. Both fraction (ρ = -0.858, PFDR = 0.015) and dwell time (ρ = -0.914, PFDR = 0.003) correlated with apraxic imitation deficits. Connectivity strengths between visual and inferior parietal networks and fraction time in the segregated state predicted apraxic imitation deficits (adjusted R2 = 0.782, P < 0.001). We conclude that apraxia in AD patients is associated with altered FC in praxis-related networks, suggesting FC as a potential clinical indicator for predicting motor-cognitive deficits.
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650 _ 7 |a Aging
|2 Other
650 _ 7 |a Alzheimer’s disease
|2 Other
650 _ 7 |a Cologne apraxia screening (KAS)
|2 Other
650 _ 7 |a Functional magnetic resonance imaging
|2 Other
650 _ 7 |a Motor system
|2 Other
650 _ 7 |a Praxis
|2 Other
650 _ 7 |a Resting-state
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650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Alzheimer Disease: complications
|2 MeSH
650 _ 2 |a Alzheimer Disease: physiopathology
|2 MeSH
650 _ 2 |a Alzheimer Disease: psychology
|2 MeSH
650 _ 2 |a Alzheimer Disease: diagnostic imaging
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Aged
|2 MeSH
650 _ 2 |a Apraxias: etiology
|2 MeSH
650 _ 2 |a Apraxias: physiopathology
|2 MeSH
650 _ 2 |a Apraxias: diagnostic imaging
|2 MeSH
650 _ 2 |a Nerve Net: physiopathology
|2 MeSH
650 _ 2 |a Aged, 80 and over
|2 MeSH
650 _ 2 |a Magnetic Resonance Imaging
|2 MeSH
650 _ 2 |a Middle Aged
|2 MeSH
650 _ 2 |a Brain: physiopathology
|2 MeSH
700 1 _ |a Brinkmann, Elena
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700 1 _ |a Bonkhoff, Anna K
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700 1 _ |a Wunderle, Veronika
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700 1 _ |a Bischof, Gérard N
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700 1 _ |a Giehl, Kathrin
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700 1 _ |a Schmieschek, Maximilian H T
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700 1 _ |a Onur, Oezguer A
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700 1 _ |a Jessen, Frank
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700 1 _ |a Fink, Gereon R
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700 1 _ |a Drzezga, Alexander
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700 1 _ |a Weiss, Peter H
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773 _ _ |a 10.1016/j.neurobiolaging.2025.09.007
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