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000283093 0247_ $$2ISSN$$a1552-5279
000283093 037__ $$aDZNE-2025-01500
000283093 041__ $$aEnglish
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000283093 1001_ $$0P:(DE-2719)9001692$$aMarquardt, Jonas$$b0$$eFirst author
000283093 1112_ $$aAlzheimer’s Association International Conference$$cToronto$$d2025-07-27 - 2025-07-31$$gAAIC 25$$wCanada
000283093 245__ $$aHippocampal vascularization is associated with greater efficiency during a remote real world wayfinding training in older adults
000283093 260__ $$c2025
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000283093 520__ $$aAlzheimer's Disease (AD) pathology accumulates early in the medial temporal lobe (MTL), crucial for spatial navigation. As spatial navigation is among the first cognitive functions affected by AD, it may benefit from targeted behavioral interventions. We investigated the potential of a novel smartphone-assisted real-world wayfinding training, tailored for healthy older adults, to improve their spatial abilities and explored associations with hippocampal vascularization and AD biomarkers.38 cognitively healthy older adults (62-84 years; 18 females) participated in a 3-week navigation training, using our smartphone application 'Explore' (Figure 1). Training involved finding several locations displayed on a map in the medical campus area of Magdeburg, Germany, while GPS data were recorded. Pre- and post-training, participants underwent fMRI, performed a pointing task in a virtual campus version, and completed the VWLT. At pre-assessment, AD pathology was characterized by plasma sampling (Abeta1-42/1-40, Ptau217) and [18F]PI-2620 PET in a subsample. Hippocampal vascularization was assessed by 7T angiography. Performance in the virtual pointing task and a map drawing test was compared to a control group (n = 20) who performed a walking task of equal length without a navigational component. Additionally, changes in different mobile wayfinding performance indicators and their associations with AD biomarkers and hippocampal vascularization (i.e., mean distance of hippocampus to surrounding vessels) were examined.Performance in the pointing task and map drawing, but not in the VWLT (p = .321), significantly improved due to the training (all p <.001; Figure 2A C). The control group showed no improvements in navigation. Training benefits were also evident in the mobile data (all p ≤.017; Figure 3A-E). Better wayfinding efficiency was associated with less vessel distance to hippocampus, r=.44, p = .012, and the number of orientation stops was negatively related to pTau217, r=-.38, p = .019 (Figure 3F).We provide evidence that a remotely administered real-world wayfinding training enhances wayfinding abilities and improves spatial memory in older adults. Importantly, hippocampal vascularization may benefit wayfinding efficiency. Higher pTau217 was related to fewer orientation stops during navigation. As a next step, potential mediating effects between vascularization and AD pathology on wayfinding performance will be investigated.
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000283093 650_7 $$2NLM Chemicals$$aAmyloid beta-Peptides
000283093 650_7 $$2NLM Chemicals$$aBiomarkers
000283093 650_2 $$2MeSH$$aHumans
000283093 650_2 $$2MeSH$$aFemale
000283093 650_2 $$2MeSH$$aAged
000283093 650_2 $$2MeSH$$aMale
000283093 650_2 $$2MeSH$$aHippocampus: diagnostic imaging
000283093 650_2 $$2MeSH$$aHippocampus: blood supply
000283093 650_2 $$2MeSH$$aAged, 80 and over
000283093 650_2 $$2MeSH$$aMiddle Aged
000283093 650_2 $$2MeSH$$aMagnetic Resonance Imaging
000283093 650_2 $$2MeSH$$aAlzheimer Disease
000283093 650_2 $$2MeSH$$aSpatial Navigation: physiology
000283093 650_2 $$2MeSH$$aSmartphone
000283093 650_2 $$2MeSH$$aAmyloid beta-Peptides: blood
000283093 650_2 $$2MeSH$$aPositron-Emission Tomography
000283093 650_2 $$2MeSH$$aBiomarkers: blood
000283093 650_2 $$2MeSH$$aMobile Applications
000283093 650_2 $$2MeSH$$aDementia
000283093 650_2 $$2MeSH$$aNeuropsychological Tests
000283093 7001_ $$0P:(DE-2719)9000804$$aVockert, Niklas$$b1
000283093 7001_ $$0P:(DE-2719)9002133$$aBehrenbruch, Niklas$$b2
000283093 7001_ $$0P:(DE-2719)9002320$$aSchumann-Werner, Beate$$b3
000283093 7001_ $$0P:(DE-2719)2812346$$aHochkeppler, Anne$$b4
000283093 7001_ $$0P:(DE-2719)9001800$$aBuechel, Anna-Therese$$b5
000283093 7001_ $$0P:(DE-2719)9002180$$aMolloy, Eóin N.$$b6
000283093 7001_ $$0P:(DE-2719)9000379$$aSchwarck, Svenja$$b7
000283093 7001_ $$0P:(DE-2719)9002356$$aFischer, Larissa$$b8
000283093 7001_ $$0P:(DE-2719)9001517$$aIncesoy, Enise I$$b9
000283093 7001_ $$0P:(DE-2719)2812734$$aGarcia-Garcia, Berta$$b10
000283093 7001_ $$0P:(DE-2719)9002178$$aMattern, Hendrik$$b11
000283093 7001_ $$0P:(DE-2719)9003591$$aMarcos Morgado, Barbara$$b12
000283093 7001_ $$aEsselmann, Hermann$$b13
000283093 7001_ $$aStephens, Andrew W$$b14
000283093 7001_ $$aSchildan, Andreas$$b15
000283093 7001_ $$aBarthel, Henryk$$b16
000283093 7001_ $$0P:(DE-2719)2814810$$aSabri, Osama$$b17
000283093 7001_ $$0P:(DE-2719)2811317$$aWiltfang, Jens$$b18
000283093 7001_ $$0P:(DE-2719)2812799$$aKreissl, Michael C$$b19
000283093 7001_ $$0P:(DE-2719)2000005$$aDüzel, Emrah$$b20
000283093 7001_ $$0P:(DE-2719)9001179$$aKuehn, Esther$$b21
000283093 7001_ $$0P:(DE-2719)2812631$$aSchreiber, Stefanie$$b22
000283093 7001_ $$0P:(DE-2719)2811815$$aMaass, Anne$$b23
000283093 7001_ $$0P:(DE-2719)2811077$$aDiersch, Nadine$$b24$$eLast author
000283093 773__ $$0PERI:(DE-600)2201940-6$$a10.1002/alz70863_110578$$gVol. 21 Suppl 9, no. Suppl 9, p. e110578$$nSuppl 9$$pe110578$$tAlzheimer's and dementia$$v21$$x1552-5260$$y2025
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