161 results on '"Reuter-Lorenz P"'
Search Results
2. Why do valence asymmetries emerge in value learning? A reinforcement learning account
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Hao, Chenxu, Cabrera-Haro, Lilian E., Lin, Ziyong, Reuter-Lorenz, Patricia A., and Lewis, Richard L.
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- 2023
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3. Dynamics of working memory process revealed by independent component analysis in an fMRI study
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Fafrowicz, Magdalena, Ceglarek, Anna, Olszewska, Justyna, Sobczak, Anna, Bohaterewicz, Bartosz, Ostrogorska, Monika, Reuter-Lorenz, Patricia, Lewandowska, Koryna, Sikora-Wachowicz, Barbara, Oginska, Halszka, Hubalewska-Mazgaj, Magdalena, and Marek, Tadeusz
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- 2023
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4. Age differences in functional network reconfiguration with working memory training.
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Iordan, Alexandru, Moored, Kyle, Katz, Benjamin, Cooke, Katherine, Buschkuehl, Martin, Jaeggi, Susanne, Polk, Thad, Peltier, Scott, Jonides, John, and Reuter-Lorenz, Patricia
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Sternberg task ,cingulo-opercular network ,global efficiency ,graph theory ,intrinsic activity ,participation coefficient ,task-related connectivity ,Adolescent ,Adult ,Age Factors ,Aged ,Aging ,Connectome ,Default Mode Network ,Female ,Humans ,Magnetic Resonance Imaging ,Male ,Memory ,Short-Term ,Middle Aged ,Nerve Net ,Practice ,Psychological ,Young Adult - Abstract
Demanding cognitive functions like working memory (WM) depend on functional brain networks being able to communicate efficiently while also maintaining some degree of modularity. Evidence suggests that aging can disrupt this balance between integration and modularity. In this study, we examined how cognitive training affects the integration and modularity of functional networks in older and younger adults. Twenty three younger and 23 older adults participated in 10 days of verbal WM training, leading to performance gains in both age groups. Older adults exhibited lower modularity overall and a greater decrement when switching from rest to task, compared to younger adults. Interestingly, younger but not older adults showed increased task-related modularity with training. Furthermore, whereas training increased efficiency within, and decreased participation of, the default-mode network for younger adults, it enhanced efficiency within a task-specific salience/sensorimotor network for older adults. Finally, training increased segregation of the default-mode from frontoparietal/salience and visual networks in younger adults, while it diffusely increased between-network connectivity in older adults. Thus, while younger adults increase network segregation with training, suggesting more automated processing, older adults persist in, and potentially amplify, a more integrated and costly global workspace, suggesting different age-related trajectories in functional network reorganization with WM training.
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- 2021
5. Neural correlates of working memory training: Evidence for plasticity in older adults.
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Iordan, Alexandru, Cooke, Katherine, Moored, Kyle, Katz, Benjamin, Buschkuehl, Martin, Jaeggi, Susanne, Polk, Thad, Peltier, Scott, Jonides, John, and Reuter-Lorenz, Patricia
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Aging ,Cognitive training ,Default-mode ,Executive functions ,Fronto-parietal ,Aged ,Aging ,Brain ,Brain Mapping ,Cognition ,Executive Function ,Female ,Humans ,Learning ,Magnetic Resonance Imaging ,Male ,Memory ,Short-Term ,Nerve Net ,Neural Pathways ,Neuronal Plasticity ,Psychomotor Performance ,Young Adult - Abstract
Brain activity typically increases with increasing working memory (WM) load, regardless of age, before reaching an apparent ceiling. However, older adults exhibit greater brain activity and reach ceiling at lower loads than younger adults, possibly reflecting compensation at lower loads and dysfunction at higher loads. We hypothesized that WM training would bolster neural efficiency, such that the activation peak would shift towards higher memory loads after training. Pre-training, older adults showed greater recruitment of the WM network than younger adults across all loads, with decline at the highest load. Ten days of adaptive training on a verbal WM task improved performance and led to greater brain responsiveness at higher loads for both groups. For older adults the activation peak shifted rightward towards higher loads. Finally, training increased task-related functional connectivity in older adults, both within the WM network and between this task-positive network and the task-negative/default-mode network. These results provide new evidence for functional plasticity with training in older adults and identify a potential signature of improvement at the neural level.
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- 2020
6. Investigating the Effects of Spacing on Working Memory Training Outcome: A Randomized, Controlled, Multisite Trial in Older Adults.
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Jaeggi, Susanne, Buschkuehl, Martin, Parlett-Pelleriti, Chelsea, Moon, Seung, Evans, Michelle, Kritzmacher, Alexandra, Reuter-Lorenz, Patricia, Shah, Priti, and Jonides, John
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Cognitive training ,Distributed learning ,Transfer ,Aged ,Appointments and Schedules ,Cognition ,Cognitive Aging ,Cognitive Dysfunction ,Female ,Humans ,Inhibition ,Psychological ,Learning ,Male ,Memory ,Short-Term ,Neuropsychological Tests ,Outcome Assessment ,Health Care ,Quality of Life ,Teaching ,Transfer ,Psychology - Abstract
OBJECTIVE: The majority of the population will experience some cognitive decline with age. Therefore, the development of effective interventions to mitigate age-related decline is critical for older adults cognitive functioning and their quality of life. METHODS: In our randomized controlled multisite trial, we target participants working memory (WM) skills, and in addition, we focus on the interventions optimal scheduling in order to test whether and how the distribution of training sessions might affect task learning, and ultimately, transfer. Healthy older adults completed an intervention targeting either WM or general knowledge twice per day, once per day, or once every-other-day. Before and after the intervention and 3 months after training completion, participants were tested in a variety of cognitive domains, including those representing functioning in everyday life. RESULTS: In contrast to our hypotheses, spacing seems to affect learning only minimally. We did observe some transfer effects, especially within the targeted cognitive domain (WM and inhibition/interference), which remained stable at the 3-month follow-up. DISCUSSION: Our findings have practical implications by showing that the variation in training schedule, at least within the range used here, does not seem to be a crucial element for training benefits.
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- 2020
7. Aging and Network Properties: Stability Over Time and Links with Learning during Working Memory Training
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Iordan, Alexandru D, Cooke, Katherine A, Moored, Kyle D, Katz, Benjamin, Buschkuehl, Martin, Jaeggi, Susanne M, Jonides, John, Peltier, Scott J, Polk, Thad A, and Reuter-Lorenz, Patricia A
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Biological Psychology ,Psychology ,Neurosciences ,Clinical Research ,Aging ,2.1 Biological and endogenous factors ,Aetiology ,1.2 Psychological and socioeconomic processes ,1.1 Normal biological development and functioning ,Underpinning research ,Neurological ,Mental health ,intrinsic activity ,functional connectivity ,graph theory ,reliability analysis ,intraclass correlation ,Biochemistry and Cell Biology ,Cognitive Sciences ,Biological psychology - Abstract
Growing evidence suggests that healthy aging affects the configuration of large-scale functional brain networks. This includes reducing network modularity and local efficiency. However, the stability of these effects over time and their potential role in learning remain poorly understood. The goal of the present study was to further clarify previously reported age effects on "resting-state" networks, to test their reliability over time, and to assess their relation to subsequent learning during training. Resting-state fMRI data from 23 young (YA) and 20 older adults (OA) were acquired in 2 sessions 2 weeks apart. Graph-theoretic analyses identified both consistencies in network structure and differences in module composition between YA and OA, suggesting topological changes and less stability of functional network configuration with aging. Brain-wide, OA showed lower modularity and local efficiency compared to YA, consistent with the idea of age-related functional dedifferentiation, and these effects were replicable over time. At the level of individual networks, OA consistently showed greater participation and lower local efficiency and within-network connectivity in the cingulo-opercular network, as well as lower intra-network connectivity in the default-mode network and greater participation of the somato-sensorimotor network, suggesting age-related differential effects at the level of specialized brain modules. Finally, brain-wide network properties showed associations, albeit limited, with learning rates, as assessed with 10 days of computerized working memory training administered after the resting-state sessions, suggesting that baseline network configuration may influence subsequent learning outcomes. Identification of neural mechanisms associated with learning-induced plasticity is important for further clarifying whether and how such changes predict the magnitude and maintenance of training gains, as well as the extent and limits of cognitive transfer in both younger and older adults.
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- 2018
8. Aging and Network Properties: Stability Over Time and Links with Learning during Working Memory Training.
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Iordan, Alexandru D, Cooke, Katherine A, Moored, Kyle D, Katz, Benjamin, Buschkuehl, Martin, Jaeggi, Susanne M, Jonides, John, Peltier, Scott J, Polk, Thad A, and Reuter-Lorenz, Patricia A
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functional connectivity ,graph theory ,intraclass correlation ,intrinsic activity ,reliability analysis ,Neurosciences ,Aging ,Clinical Research ,1.1 Normal biological development and functioning ,1.2 Psychological and socioeconomic processes ,2.1 Biological and endogenous factors ,Mental Health ,Neurological ,Biochemistry and Cell Biology ,Cognitive Sciences - Abstract
Growing evidence suggests that healthy aging affects the configuration of large-scale functional brain networks. This includes reducing network modularity and local efficiency. However, the stability of these effects over time and their potential role in learning remain poorly understood. The goal of the present study was to further clarify previously reported age effects on "resting-state" networks, to test their reliability over time, and to assess their relation to subsequent learning during training. Resting-state fMRI data from 23 young (YA) and 20 older adults (OA) were acquired in 2 sessions 2 weeks apart. Graph-theoretic analyses identified both consistencies in network structure and differences in module composition between YA and OA, suggesting topological changes and less stability of functional network configuration with aging. Brain-wide, OA showed lower modularity and local efficiency compared to YA, consistent with the idea of age-related functional dedifferentiation, and these effects were replicable over time. At the level of individual networks, OA consistently showed greater participation and lower local efficiency and within-network connectivity in the cingulo-opercular network, as well as lower intra-network connectivity in the default-mode network and greater participation of the somato-sensorimotor network, suggesting age-related differential effects at the level of specialized brain modules. Finally, brain-wide network properties showed associations, albeit limited, with learning rates, as assessed with 10 days of computerized working memory training administered after the resting-state sessions, suggesting that baseline network configuration may influence subsequent learning outcomes. Identification of neural mechanisms associated with learning-induced plasticity is important for further clarifying whether and how such changes predict the magnitude and maintenance of training gains, as well as the extent and limits of cognitive transfer in both younger and older adults.
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- 2017
9. Variability in the analysis of a single neuroimaging dataset by many teams
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Botvinik-Nezer, Rotem, Holzmeister, Felix, Camerer, Colin F., Dreber, Anna, Huber, Juergen, Johannesson, Magnus, Kirchler, Michael, Iwanir, Roni, Mumford, Jeanette A., Adcock, R. Alison, Avesani, Paolo, Baczkowski, Blazej M., Bajracharya, Aahana, Bakst, Leah, Ball, Sheryl, Barilari, Marco, Bault, Nadège, Beaton, Derek, Beitner, Julia, Benoit, Roland G., Berkers, Ruud M. W. J., Bhanji, Jamil P., Biswal, Bharat B., Bobadilla-Suarez, Sebastian, Bortolini, Tiago, Bottenhorn, Katherine L., Bowring, Alexander, Braem, Senne, Brooks, Hayley R., Brudner, Emily G., Calderon, Cristian B., Camilleri, Julia A., Castrellon, Jaime J., Cecchetti, Luca, Cieslik, Edna C., Cole, Zachary J., Collignon, Olivier, Cox, Robert W., Cunningham, William A., Czoschke, Stefan, Dadi, Kamalaker, Davis, Charles P., Luca, Alberto De, Delgado, Mauricio R., Demetriou, Lysia, Dennison, Jeffrey B., Di, Xin, Dickie, Erin W., Dobryakova, Ekaterina, Donnat, Claire L., Dukart, Juergen, Duncan, Niall W., Durnez, Joke, Eed, Amr, Eickhoff, Simon B., Erhart, Andrew, Fontanesi, Laura, Fricke, G. Matthew, Fu, Shiguang, Galván, Adriana, Gau, Remi, Genon, Sarah, Glatard, Tristan, Glerean, Enrico, Goeman, Jelle J., Golowin, Sergej A. E., González-García, Carlos, Gorgolewski, Krzysztof J., Grady, Cheryl L., Green, Mikella A., Guassi Moreira, João F., Guest, Olivia, Hakimi, Shabnam, Hamilton, J. Paul, Hancock, Roeland, Handjaras, Giacomo, Harry, Bronson B., Hawco, Colin, Herholz, Peer, Herman, Gabrielle, Heunis, Stephan, Hoffstaedter, Felix, Hogeveen, Jeremy, Holmes, Susan, Hu, Chuan-Peng, Huettel, Scott A., Hughes, Matthew E., Iacovella, Vittorio, Iordan, Alexandru D., Isager, Peder M., Isik, Ayse I., Jahn, Andrew, Johnson, Matthew R., Johnstone, Tom, Joseph, Michael J. E., Juliano, Anthony C., Kable, Joseph W., Kassinopoulos, Michalis, Koba, Cemal, Kong, Xiang-Zhen, Koscik, Timothy R., Kucukboyaci, Nuri Erkut, Kuhl, Brice A., Kupek, Sebastian, Laird, Angela R., Lamm, Claus, Langner, Robert, Lauharatanahirun, Nina, Lee, Hongmi, Lee, Sangil, Leemans, Alexander, Leo, Andrea, Lesage, Elise, Li, Flora, Li, Monica Y. C., Lim, Phui Cheng, Lintz, Evan N., Liphardt, Schuyler W., Losecaat Vermeer, Annabel B., Love, Bradley C., Mack, Michael L., Malpica, Norberto, Marins, Theo, Maumet, Camille, McDonald, Kelsey, McGuire, Joseph T., Melero, Helena, Méndez Leal, Adriana S., Meyer, Benjamin, Meyer, Kristin N., Mihai, Glad, Mitsis, Georgios D., Moll, Jorge, Nielson, Dylan M., Nilsonne, Gustav, Notter, Michael P., Olivetti, Emanuele, Onicas, Adrian I., Papale, Paolo, Patil, Kaustubh R., Peelle, Jonathan E., Pérez, Alexandre, Pischedda, Doris, Poline, Jean-Baptiste, Prystauka, Yanina, Ray, Shruti, Reuter-Lorenz, Patricia A., Reynolds, Richard C., Ricciardi, Emiliano, Rieck, Jenny R., Rodriguez-Thompson, Anais M., Romyn, Anthony, Salo, Taylor, Samanez-Larkin, Gregory R., Sanz-Morales, Emilio, Schlichting, Margaret L., Schultz, Douglas H., Shen, Qiang, Sheridan, Margaret A., Silvers, Jennifer A., Skagerlund, Kenny, Smith, Alec, Smith, David V., Sokol-Hessner, Peter, Steinkamp, Simon R., Tashjian, Sarah M., Thirion, Bertrand, Thorp, John N., Tinghög, Gustav, Tisdall, Loreen, Tompson, Steven H., Toro-Serey, Claudio, Torre Tresols, Juan Jesus, Tozzi, Leonardo, Truong, Vuong, Turella, Luca, van ‘t Veer, Anna E., Verguts, Tom, Vettel, Jean M., Vijayarajah, Sagana, Vo, Khoi, Wall, Matthew B., Weeda, Wouter D., Weis, Susanne, White, David J., Wisniewski, David, Xifra-Porxas, Alba, Yearling, Emily A., Yoon, Sangsuk, Yuan, Rui, Yuen, Kenneth S. L., Zhang, Lei, Zhang, Xu, Zosky, Joshua E., Nichols, Thomas E., Poldrack, Russell A., and Schonberg, Tom
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- 2020
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10. Session II: Mechanisms of Age-Related Cognitive Change and Targets for Intervention: Neural Circuits, Networks, and Plasticity
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DeCarli, Charles, Kawas, Claudia, Morrison, John H, Reuter-Lorenz, Patricia A, Sperling, Reisa A, and Wright, Clinton B
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Biomedical and Clinical Sciences ,Health Sciences ,Neurodegenerative ,Clinical Research ,Behavioral and Social Science ,Dementia ,Brain Disorders ,Neurosciences ,Acquired Cognitive Impairment ,Biomedical Imaging ,Aging ,1.1 Normal biological development and functioning ,1.2 Psychological and socioeconomic processes ,2.1 Biological and endogenous factors ,Neurological ,Mental health ,Aged ,Amyloid ,Animals ,Cognition Disorders ,Humans ,Memory ,Nerve Net ,Neuronal Plasticity ,Prefrontal Cortex ,cognitive changes ,aging ,Neural networks ,Clinical Sciences ,Gerontology ,Biomedical and clinical sciences ,Health sciences - Abstract
Age-related changes in neural circuits, neural networks, and their plasticity are central to our understanding of age changes in cognition and brain structure and function. This paper summarizes selected findings on these topics presented at the Cognitive Aging Summit II. Specific areas discussed were synaptic vulnerability and plasticity, including the role of different types of synaptic spines, and hormonal effects in the dorsolateral prefrontal cortex of nonhuman primates, the impact of both compensatory processes and dedifferentiation on demand-dependent differences in prefrontal activation in relation to age and performance, the role of vascular disease, indexed by white matter signal abnormalities, on prefrontal activation during a functional magnetic resonance imaging-based cognitive control paradigm, and the influence of amyloid-β neuropathology on memory performance in older adults and the networks of brain activity underlying variability in performance. A greater understanding of age-related changes in brain plasticity and neural networks in healthy aging and in the presence of underlying vascular disease or amyloid pathology will be essential to identify new targets for intervention. Moreover, this understanding will assist in promoting the utilization of existing interventions, such as lifestyle and therapeutic modifiers of vascular disease.
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- 2012
11. Harnessing neuroplasticity for clinical applications.
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Cramer, Steven C, Sur, Mriganka, Dobkin, Bruce H, O'Brien, Charles, Sanger, Terence D, Trojanowski, John Q, Rumsey, Judith M, Hicks, Ramona, Cameron, Judy, Chen, Daofen, Chen, Wen G, Cohen, Leonardo G, deCharms, Christopher, Duffy, Charles J, Eden, Guinevere F, Fetz, Eberhard E, Filart, Rosemarie, Freund, Michelle, Grant, Steven J, Haber, Suzanne, Kalivas, Peter W, Kolb, Bryan, Kramer, Arthur F, Lynch, Minda, Mayberg, Helen S, McQuillen, Patrick S, Nitkin, Ralph, Pascual-Leone, Alvaro, Reuter-Lorenz, Patricia, Schiff, Nicholas, Sharma, Anu, Shekim, Lana, Stryker, Michael, Sullivan, Edith V, and Vinogradov, Sophia
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Aging ,Animals ,Biomedical Research ,Brain Diseases: physiopathology ,therapy ,Cognition Disorders: etiology ,Humans ,Neuronal Plasticity: physiology ,Recovery of Function ,Stroke: pathology ,physiopathology ,therapy - Abstract
Neuroplasticity can be defined as the ability of the nervous system to respond to intrinsic or extrinsic stimuli by reorganizing its structure, function and connections. Major advances in the understanding of neuroplasticity have to date yielded few established interventions. To advance the translation of neuroplasticity research towards clinical applications, the National Institutes of Health Blueprint for Neuroscience Research sponsored a workshop in 2009. Basic and clinical researchers in disciplines from central nervous system injury/stroke, mental/addictive disorders, paediatric/developmental disorders and neurodegeneration/ageing identified cardinal examples of neuroplasticity, underlying mechanisms, therapeutic implications and common denominators. Promising therapies that may enhance training-induced cognitive and motor learning, such as brain stimulation and neuropharmacological interventions, were identified, along with questions of how best to use this body of information to reduce human disability. Improved understanding of adaptive mechanisms at every level, from molecules to synapses, to networks, to behaviour, can be gained from iterative collaborations between basic and clinical researchers. Lessons can be gleaned from studying fields related to plasticity, such as development, critical periods, learning and response to disease. Improved means of assessing neuroplasticity in humans, including biomarkers for predicting and monitoring treatment response, are needed. Neuroplasticity occurs with many variations, in many forms, and in many contexts. However, common themes in plasticity that emerge across diverse central nervous system conditions include experience dependence, time sensitivity and the importance of motivation and attention. Integration of information across disciplines should enhance opportunities for the translation of neuroplasticity and circuit retraining research into effective clinical therapies.
- Published
- 2011
12. Rehearsal of To-Be-Remembered Items Is Unnecessary to Perform Directed Forgetting within Working Memory: Support for an Active Control Mechanism
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Festini, Sara B. and Reuter-Lorenz, Patricia A.
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Directed forgetting tasks instruct people to forget targeted memoranda. In the context of working memory, people attempt to forget representations that are currently held in mind. Here, we evaluated candidate mechanisms of directed forgetting within working memory, by (a) testing the influence of articulatory suppression, a rehearsal-reducing and attention-demanding secondary task, on directed forgetting efficacy, and by (b) assessing the ability of people to perform forgetting in the absence of to-be-remembered competitors to rehearse. In Experiment 1, articulatory suppression interfered with directed forgetting, increasing the proportion of false alarms to to-be-forgotten probes in the working memory phase and decreasing the magnitude of the directed forgetting effect as assessed by an incidental long-term memory recognition test. Experiment 2 replicated the effects of articulatory suppression and tested whether the simultaneous requirement to retain, and presumably rehearse, to-be-remembered items was necessary for successful forgetting. The long-term directed forgetting effect was equivalent whether or not participants had to-be-remembered items to rehearse during the working memory phase. Experiment 3 included an additional comparison condition and confirmed that articulatory suppression interfered with directed forgetting and that participants were as efficient at directed forgetting with and without competitors to remember. In combination, these experiments suggest that directed forgetting in working memory requires an active control process that is limited by articulatory suppression, and that the demand to remember a concurrent memory set is unnecessary for this control process to operate.
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- 2017
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13. Maintenance, reserve and compensation: the cognitive neuroscience of healthy ageing
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Cabeza, Roberto, Albert, Marilyn, Belleville, Sylvie, Craik, Fergus I. M., Duarte, Audrey, Grady, Cheryl L., Lindenberger, Ulman, Nyberg, Lars, Park, Denise C., Reuter-Lorenz, Patricia A., Rugg, Michael D., Steffener, Jason, and Rajah, M. Natasha
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- 2018
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14. Misremembering What You See or Hear: Dissociable Effects of Modality on Short- and Long-Term False Recognition
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Olszewska, Justyna M., Reuter-Lorenz, Patricia A., Munier, Emily, and Bendler, Sara A.
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False working memories readily emerge using a visual item-recognition variant of the converging associates task. Two experiments, manipulating study and test modality, extended prior working memory results by demonstrating a reliable false recognition effect (more false alarms to associatively related lures than to unrelated lures) within seconds of encoding in either the visual or auditory modality. However, false memories were nearly twice as frequent when study lists were seen than when they were heard, regardless of test modality, although study-test modality mismatch was generally disadvantageous (consistent with encoding specificity). A final experiment that varied study-test modality using a hybrid short- and long-term memory test (Flegal, Atkins & Reuter-Lorenz, 2010) replicated the auditory advantage in the short term but revealed a reversal in the long term: The false memory effect was greater in the auditory study-test condition than in the visual study-test condition. Thus, the same encoding conditions gave rise to an opposite modality advantage depending on whether recognition was tested under short-term or long-term memory conditions. Although demonstrating continuity in associative processing across delay, the results indicate that delay condition affects the availability of modality-dependent features of the memory trace and, thus, distinctiveness, leading to dissociable patterns of short- and long-term memory performance.
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- 2015
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15. Cognitive dysfunction and symptom burden in women treated for breast cancer: a prospective behavioral and fMRI analysis
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Jung, Mi Sook, Zhang, Min, Askren, Mary K., Berman, Marc G., Peltier, Scott, Hayes, Daniel F., Therrien, Barbara, Reuter-Lorenz, Patricia A., and Cimprich, Bernadine
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- 2017
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16. Neural correlates of multi-day learning and savings in sensorimotor adaptation
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Ruitenberg, M. F. L., Koppelmans, V., De Dios, Y. E., Gadd, N. E., Wood, S. J., Reuter-Lorenz, P. A., Kofman, I., Bloomberg, J. J., Mulavara, A. P., and Seidler, R. D.
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- 2018
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17. Uncertainty and Promise: the Effects of Transcranial Direct Current Stimulation on Working Memory
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Jantz, Tiffany K., Katz, Ben, and Reuter-Lorenz, Patricia A.
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- 2016
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18. Emotion and reward are dissociable from error during motor learning
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Festini, Sara B., Preston, Stephanie D., Reuter-Lorenz, Patricia A., and Seidler, Rachael D.
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- 2016
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19. False Memories Seconds Later: The Rapid and Compelling Onset of Illusory Recognition
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Flegal, Kristin E., Atkins, Alexandra S., and Reuter-Lorenz, Patricia A.
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Distortions of long-term memory (LTM) in the converging associates task are thought to arise from semantic associative processes and monitoring failures due to degraded verbatim and/or contextual memory. Sensory-based coding is traditionally considered more prevalent than meaning-based coding in short-term memory (STM), whereas the converse is true of LTM, leading to the expectation that false memory phenomena should be less robust in a canonical STM task. These expectations were violated in 2 experiments in which participants were shown lists of 4 semantically related words and were probed immediately following a filled 3- to 4-s retention interval or approximately 20 min later in a surprise recognition test. Corrected false recognition rates, confidence ratings, and Remember/Know judgments reveal similar false memory effects across STM and LTM conditions. These results indicate that compelling false memory illusions can be rapidly instantiated and that, consistent with unitary models of memory, they originate from processes that are not specific to LTM tasks. (Contains 2 tables, 2 figures, and 2 footnotes.)
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- 2010
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20. Contributions of Spatial Working Memory to Visuomotor Learning
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Anguera, Joaquin A., Reuter-Lorenz, Patricia A., and Willingham, Daniel T.
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Previous studies of motor learning have described the importance of cognitive processes during the early stages of learning; however, the precise nature of these processes and their neural correlates remains unclear. The present study investigated whether spatial working memory (SWM) contributes to visuomotor adaptation depending on the stage of learning. We tested the hypothesis that SWM would contribute early in the adaptation process by measuring (i) the correlation between SWM tasks and the rate of adaptation, and (ii) the overlap between the neural substrates of a SWM mental rotation task and visuomotor adaptation. Participants completed a battery of neuropsychological tests, a visuomotor adaptation task, and an SWM task involving mental rotation, with the latter two tasks performed in a 3.0-T MRI scanner. Performance on a neuropsychological test of SWM (two-dimensional mental rotation) correlated with the rate of early, but not late, visuomotor adaptation. During the early, but not late, adaptation period, participants showed overlapping brain activation with the SWM mental rotation task, in right dorsolateral prefrontal cortex and the bilateral inferior parietal lobules. These findings suggest that the early, but not late, phase of visuomotor adaptation engages SWM processes.
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- 2010
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21. Reply to ‘Mechanisms underlying resilience in ageing’
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Cabeza, Roberto, Albert, Marilyn, Belleville, Sylvie, Craik, Fergus I. M, Duarte, Audrey, Grady, Cheryl L., Lindenberger, Ulman, Nyberg, Lars, Park, Denise C., Reuter-Lorenz, Patricia A., Rugg, Michael D., Steffener, Jason, and Rajah, M. Natasha
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- 2019
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22. Hemispheric Specialization and Interhemispheric Integration: Insights from Experiments with Commissurotomy Patients
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Tramo, M. J., Baynes, K., Fendrich, R., Mangun, G. R., Phelps, E. A., Reuter-Lorenz, P. A., Gazzaniga, M. S., Reeves, Alexander G., editor, and Roberts, David W., editor
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- 1995
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23. Neuromarkers of fatigue and cognitive complaints following chemotherapy for breast cancer: a prospective fMRI investigation
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Askren, Mary K., Jung, Misook, Berman, Marc G., Zhang, Min, Therrien, Barbara, Peltier, Scott, Ossher, Lynn, Hayes, Daniel F., Reuter-Lorenz, Patricia A., and Cimprich, Bernadine
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- 2014
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24. How Does it STAC Up? Revisiting the Scaffolding Theory of Aging and Cognition
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Reuter-Lorenz, Patricia A. and Park, Denise C.
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- 2014
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25. Get the gist? The effects of processing depth on false recognition in short-term and long-term memory
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Flegal, Kristin E. and Reuter-Lorenz, Patricia A.
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- 2014
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26. Cognitive control of familiarity: Directed forgetting reduces proactive interference in working memory
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Festini, Sara B. and Reuter-Lorenz, Patricia A.
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- 2014
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27. The Effects of Long Duration Bed Rest on Brain Functional Connectivity and Sensorimotor Functioning
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Cassady, K, Koppelmans, V, De Dios, Y, Stepanyan, V, Szecsy, D, Gadd, N, Wood, S, Reuter-Lorenz, P, Castenada, R. Riascos, Kofman, I, Bloomberg, J, Mulavara, A, and Seidler, R
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Aerospace Medicine ,Behavioral Sciences - Abstract
Long duration spaceflight has been associated with detrimental alterations in human sensorimotor functioning. Prolonged exposure to a head-down tilt (HDT) position during long duration bed rest can resemble several effects of the microgravity environment such as reduced sensory inputs, body unloading and increased cephalic fluid distribution. The question of whether microgravity affects other central nervous system functions such as brain functional connectivity and its relationship with behavior is largely unknown, but of importance to the health and performance of astronauts both during and post-flight. In the present study, we investigate the effects of prolonged exposure to HDT bed rest on resting state brain functional connectivity and its association with behavioral changes in 17 male participants. To validate that our findings were not due to confounding factors such as time or task practice, we also acquired resting state functional magnetic resonance imaging (rs-fMRI) and behavioral measurements from 14 normative control participants at four time points. Bed rest participants remained in bed with their heads tilted down six degrees below their feet for 70 consecutive days. Rs-fMRI and behavioral data were obtained at seven time points averaging around: 12 and 8 days prior to bed rest; 7, 50, and 70 days during bed rest; and 8 and 12 days after bed rest. 70 days of HDT bed rest resulted in significant increases in functional connectivity during bed rest followed by a reversal of changes in the post bed rest recovery period between motor cortical and somatosensory areas of the brain. In contrast, decreases in connectivity were observed between temporoparietal regions. Furthermore, post-hoc correlation analyses revealed a significant relationship between motor-somatosensory network connectivity and standing balance performance changes; participants that exhibited the greatest increases in connectivity strength showed the least deterioration in postural equilibrium with HDT bed rest. This suggests that neuroplastic processes may facilitate adaptation to the HDT bed rest environment. The findings from this study provide novel insights into the neurobiology and future risk assessments of long-duration spaceflight.
- Published
- 2016
28. Publisher Correction: Maintenance, reserve and compensation: the cognitive neuroscience of healthy ageing
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Cabeza, Roberto, Albert, Marilyn, Belleville, Sylvie, Craik, Fergus I. M., Duarte, Audrey, Grady, Cheryl L., Lindenberger, Ulman, Nyberg, Lars, Park, Denise C., Reuter-Lorenz, Patricia A., Rugg, Michael D., Steffener, Jason, and Rajah, M. Natasha
- Published
- 2018
- Full Text
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29. Author Correction: Maintenance, reserve and compensation: the cognitive neuroscience of healthy ageing
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Cabeza, Roberto, Albert, Marilyn, Belleville, Sylvie, Craik, Fergus I. M., Duarte, Audrey, Grady, Cheryl L., Lindenberger, Ulman, Nyberg, Lars, Park, Denise C., Reuter-Lorenz, Patricia A., Rugg, Michael D., Steffener, Jason, and Rajah, M. Natasha
- Published
- 2018
- Full Text
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30. Increased Brain Activation for Foot Movement During 70-Day 6 Deg Head-Down Bed Rest (HDBR): Evidence from Functional Magnetic Resonance Imaging (fMRI)
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Yuan, P, Koppelmans, V, Cassady, K, Cooke, K, De Dios, Y. E, Stepanyan, V, Szecsy, D, Gadd, N, Wood, S. J, Reuter‐Lorenz, P. A, Riascos‐Castaneda, R, Kofman, I, Bloomberg, J. J, Mulavara, A. P, and Seidler, R. D
- Subjects
Aerospace Medicine - Abstract
Bed rest has been widely used as a simulation of weightlessness in studying the effects of microgravity exposure on human physiology and cognition. Changes in muscle function and functional mobility have been reported to be associated with bed rest. Understanding the effect of bed rest on neural control of movement would provide helpful information for spaceflight. In the current study, we evaluated how the brain activation for foot movement changed as a function of bed rest. Eighteen healthy men (aged 25 to 39 years) participated in this HDBR study. They remained continuously in the 6deg head‐down tilt position for 70 days. Functional MRI was acquired during 1‐Hz right foot tapping, and repeated at 7 time points: 12 days pre‐, 8 days pre‐, 7 days in‐, 50 days in‐, 70 days in‐, 8 days post‐, and 12 days post‐ HDBR. In all 7 sessions, we observed increased activation in the left motor cortex, right cerebellum and right occipital cortex during foot movement blocks compared to rest. Compared to the pre‐HDBR baseline (1st and 2nd sessions), foot movement‐induced activation in the left hippocampus increased during HDBR. This increase emerged in the 4th session, enlarged in the 5th session, and remained significant in the 6th and 7th sessions. Furthermore, increased activation relative to the baseline in left precuneus was observed in the 5th, 6th and 7th sessions. In addition, in comparison with baseline, increased activation in the left cerebellum was found in the 4th and 5th sessions, whereas increased activation in the right cerebellum was observed in the 4th, 6th and 7th sessions. No brain region exhibited decreased activation during bed rest compared to baseline. The increase of foot movement related brain activation during HDBR suggests that in a long‐term head‐down position, more neural control is needed to accomplish foot movements. This change required a couple of weeks to develop in HDBR (between 3rd and 4th sessions), and did not return to baseline even 12 days after HDBR. The observed effect of bed rest on brain activation during a foot tapping task could be linked to HDBR related changes in brain structure that we have recently reported. The relationship between pre‐ and post‐ HDBR changes in brain activation and performance in a functional mobility test will also be presented.
- Published
- 2015
31. The Effects of Long Duration Bed Rest as a Spaceflight Analogue on Resting State Sensorimotor Network Functional Connectivity and Neurocognitive Performance
- Author
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Cassady, K, Koppelmans, V, Yuan, P, Cooke, K, De Dios, Y, Stepanyan, V, Szecsy, D, Gadd, N, Wood, S, Reuter-Lorenz, P, Castenada, R. Riascos, Kofman, I, Bloomberg, J, Mulavara, A, and Seidler, R
- Subjects
Aerospace Medicine ,Behavioral Sciences - Abstract
Long duration spaceflight has been associated with detrimental alterations in human sensorimotor systems and neurocognitive performance. Prolonged exposure to a head-down tilt position during long duration bed rest can resemble several effects of the microgravity environment such as reduced sensory inputs, body unloading and increased cephalic fluid distribution. The question of whether microgravity affects other central nervous system functions such as brain functional connectivity and its relationship with neurocognitive performance is largely unknown, but of potential importance to the health and performance of astronauts both during and post-flight. The aims of the present study are 1) to identify changes in sensorimotor resting state functional connectivity that occur with extended bed rest exposure, and to characterize their recovery time course; 2) to evaluate how these neural changes correlate with neurocognitive performance. Resting-state functional magnetic resonance imaging (rsfMRI) data were collected from 17 male participants. The data were acquired through the NASA bed rest facility, located at the University of Texas Medical Branch (Galveston, TX). Participants remained in bed with their heads tilted down six degrees below their feet for 70 consecutive days. RsfMRI data were obtained at seven time points: 7 and 12 days before bed rest; 7, 50, and 65 days during bed rest; and 7 and 12 days after bed rest. Functional connectivity magnetic resonance imaging (fcMRI) analysis was performed to measure the connectivity of sensorimotor networks in the brain before, during, and post-bed rest. We found a decrease in left putamen connectivity with the pre- and post-central gyri from pre bed rest to the last day in bed rest. In addition, vestibular cortex connectivity with the posterior cingulate cortex decreased from pre to post bed rest. Furthermore, connectivity between cerebellar right superior posterior fissure and other cerebellar regions decreased from pre bed rest to the last day in bed rest. In contrast, connectivity within the default mode network remained stable over the course of bed rest. We also utilized a battery of behavioral measures including spatial working memory tasks and measures of functional mobility and balance. These behavioral measurements were collected before, during, and after bed rest. We will report the preliminary findings of correlations observed between brain functional connectivity and behavioral performance changes. Our results suggest that sensorimotor brain networks exhibit decoupling with extended periods of reduced usage. The findings from this study could aid in the understanding and future design of targeted countermeasures to alleviate the detrimental health and neurocognitive effects of long-duration spaceflight.
- Published
- 2015
32. Brain and Behavioral Evidence for Reweighting of Vestibular Inputs with Long-Duration Spaceflight
- Author
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Hupfeld, K E, primary, McGregor, H R, additional, Koppelmans, V, additional, Beltran, N E, additional, Kofman, I S, additional, De Dios, Y E, additional, Riascos, R F, additional, Reuter-Lorenz, P A, additional, Wood, S J, additional, Bloomberg, J J, additional, Mulavara, A P, additional, and Seidler, R D, additional
- Published
- 2021
- Full Text
- View/download PDF
33. Cognitive function and breast cancer: promise and potential insights from functional brain imaging
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Reuter-Lorenz, Patricia A. and Cimprich, Bernadine
- Published
- 2013
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34. Configural representations in spatial working memory: modulation by perceptual segregation and voluntary attention
- Author
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Gmeindl, Leon, Nelson, James K., Wiggin, Timothy, and Reuter-Lorenz, Patricia A.
- Published
- 2011
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35. Resolving semantic and proactive interference in memory over the short-term
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Atkins, Alexandra S., Berman, Marc G., Reuter-Lorenz, Patricia A., Lewis, Richard L., and Jonides, John
- Published
- 2011
- Full Text
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36. Aging, Training, and the Brain: A Review and Future Directions
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Lustig, Cindy, Shah, Priti, Seidler, Rachael, and Reuter-Lorenz, Patricia A.
- Published
- 2009
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37. False working memories? Semantic distortion in a mere 4 seconds
- Author
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Atkins, Alexandra S. and Reuter-Lorenz, Patricia A.
- Published
- 2008
- Full Text
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38. Focal Gray Matter Plasticity as a Function of Long Duration Head-down Tilt Bed Rest
- Author
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Koppelmans, V, DeDios, Y. E, Wood, S. J, Reuter-Lorenz, P. A, Kofman, I, Bloomberg, J. J, and Mulavara, A. P
- Subjects
Life Sciences (General) ,Aerospace Medicine - Abstract
Long duration spaceflight (i.e., > or = 22 days) has been associated with changes in sensorimotor systems, resulting in difficulties that astronauts experience with posture control, locomotion, and manual control. The microgravity environment is an important causal factor for spaceflight induced sensorimotor changes. Whether these sensorimotor changes may be related to structural and functional brain changes is yet unknown. However, experimental studies revealed changes in the gray matter (GM) of the brain after simulated microgravity. Thus, it is possible that spaceflight may affect brain structure and thereby cognitive functioning and motor behavior. Long duration head-down tilt bed rest has been suggested as an exclusionary analog to study microgravity effects on the sensorimotor system. Bed rest mimics microgravity in body unloading and bodily fluid shifts. In consideration of the health and performance of crewmembers both in- and post-flight, we are conducting a prospective longitudinal 70-day bed rest study as an analog to investigate the effects of microgravity on the brain. VBM analysis revealed a progressive decrease from pre- to in- bed rest in GM volume in bilateral areas including the frontal medial cortex, the insular cortex and the caudate. Over the same time period, there was a progressive increase in GM volume in the cerebellum, occipital-, and parietal cortex, including the precuneus. The majority of these changes did not fully recover during the post-bed rest period. Analysis of lobular GM volumes obtained with BRAINS showed significantly increased volume from pre-bed rest to in-bed rest in GM of the parietal lobe and the third ventricle. Temporal GM volume at 70 days in bed rest was smaller than that at the first pre-bed rest measurement. Trend analysis showed significant positive linear and negative quadratic relationships between parietal GM and time, a positive linear relationship between third ventricle volume and time, and a negative linear relationship between cerebellar GM volume and time. FM performance improved from pre-bed rest session 1 to session 2. From the second pre-bed rest measure to the last-day-in-bed rest, there was a significant decrease in performance that only partially recovered post-bed rest. No significant association was observed between changes in brain volume and changes in functional mobility. Extended bed rest, which is an analog for microgravity, can result in local volumetric GM increase and decrease and adversely affect functional mobility. These changes in brain structure and performance were not related in this sample. Whether the effects of bed rest dissipate at longer times post-bed rest, and if they are associated with behavior are important questions that warrant further research including more subjects and longer follow-up times.
- Published
- 2014
39. Focal Gray Matter Plasticity as a Function of Long Duration Bedrest: Preliminary Results
- Author
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Koppelmans, V, Erdeniz, B, De Dios, Y. E, Wood, S. J, Reuter-Lorenz, P. A, Kofman, I, Bloomberg, J. J, Mulavara, A. P, and Seidler, R. D
- Subjects
Aerospace Medicine - Abstract
Long duration spaceflight (i.e., 22 days or longer) has been associated with changes in sensorimotor systems, resulting in difficulties that astronauts experience with posture control, locomotion, and manual control. It is unknown whether and how spaceflight impacts sensorimotor brain structure and function, and whether such changes may potentially underlie behavioral effects. Long duration head down tilt bed rest has been used repeatedly as an exclusionary analog to study microgravity effects on the sensorimotor system [1]. Bed rest mimics microgravity in body unloading and bodily fluid shifts. We are currently testing sensorimotor function, brain structure, and brain function pre and post a 70‐day bed rest period. We will acquire the same measures on NASA crewmembers starting in 2014. Here we present the results of the first eight bed rest subjects. Subjects were assessed at 12 and 7 days before‐, at 7, 30, and ~70 days in‐, and at 8 and 12 days post 70 days of bed rest at the NASA bed rest facility, UTMB, Galveston, TX, USA. At each time point structural MRI scans (i.e., high resolution T1‐weighted imaging and Diffusion Tensor Imaging (DTI)) were obtained using a 3T Siemens scanner. Focal changes over time in gray matter density were assessed using the voxel based morphometry 8 (VBM8) toolbox under SPM. Focal changes in white matter microstructural integrity were assessed using tract based spatial statistics (TBSS) as part of the FMRIB software library (FSL). TBSS registers all DTI scans to standard space. It subsequently creates a study specific white matter skeleton of the major white matter tracts. Non‐parametric permutation based t‐tests and ANOVA's were used for voxel‐wise comparison of the skeletons. For both VBM and TBSS, comparison of the two pre bed rest measurements did not show significant differences. VBM analysis revealed decreased gray matter density in bilateral areas including the frontal medial cortex, the insular cortex and the caudate nucleus from pre to in bed rest. Over the same time period, there was an increase in gray matter density in the cerebellum, occipital, and parietal cortices. The majority of these changes did not recover from during to post bed rest. TBSS analyses will also be presented. Extended bed rest, which is an analog for microgravity, can result in gray matter changes and potentially in microstructural white matter changes in areas that are important for neuromotor behavior and cognition. These changes did not recover at two weeks post bed rest. These results have significant public health implications, and will also aid in interpretation of our future data obtained pre and post spaceflight. Whether the effects of bed rest wear off at longer times post bed rest, and if they are associated with behavior are important questions that warrant further research.
- Published
- 2014
40. Focal Gray Matter Plasticity as a Function of Long Duration Head Down Tilted Bed Rest: Preliminary Results
- Author
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Koppelmans, V, Erdeniz, B, DeDios, Y. E, Wood, S. J, Reuter-Lorenz, P. A, Kofman, I, Bloomberg, J. J, Mulavara, A. P, and Seidler, R. D
- Subjects
Aerospace Medicine - Abstract
Long duration spaceflight (i.e., 22 days or longer) has been associated with changes in sensorimotor systems, resulting in difficulties that astronauts experience with posture control, locomotion, and manual control. The microgravity environment is an important causal factor for spaceflight induced sensorimotor changes. Whether these sensorimotor changes are solely related to peripheral changes from reduced vestibular stimulation, body unloading, body fluid shifts or that they may be related to structural and functional brain changes is yet unknown. However, a recent study reported associations between microgravity and flattening of the posterior eye globe and protrusion of the optic nerve [1] possibly as the result of increased intracranial pressure due to microgravity induced bodily fluid shifts [3]. Moreover, elevated intracranial pressure has been related to white matter microstructural damage [2]. Thus, it is possible that spaceflight may affect brain structure and thereby cognitive functioning. Long duration head down tilt bed rest has been suggested as an exclusionary analog to study microgravity effects on the sensorimotor system [4]. Bed rest mimics microgravity in body unloading and bodily fluid shifts. In consideration of the health and performance of crewmembers both in- and post-flight, we are conducting a prospective longitudinal 70-day bed rest study as an analog to investigate the effects of microgravity on brain structure [5]. Here we present results of the first six subjects. Six subjects were assessed at 12 and 7 days before-, at 7, 30, and ~70 days in-, and at 8 and 12 days post 70 days of bed rest at the NASA bed rest facility in UTMB, Galveston, TX, USA. At each time point structural MRI scans (i.e., high resolution T1-weighted imaging and Diffusion Tensor Imaging (DTI)) were obtained using a 3T Siemens scanner. Focal changes over time in gray matter density were assessed using the voxel based morphometry 8 (VBM8) toolbox under SPM. Longitudinal processing in VBM8 includes linear registration of each scan to the mean of the subject and subsequently transforming all scans in to MNI space by applying the warp from the mean subject to MNI to the individual gray matter segmentations. Modulation was applied so that all images represented the volume of the original structure in native space. Voxel wise analysis was carried out on the gray matter images after smoothing, using a flexible factorial design with family wise error correction. Focal changes in white matter microstructural integrity were assessed using tract based spatial statistics (TBSS) as part of FMRIB software library (FSL). TBSS registers all DTI scans to standard space. It subsequently creates a study specific white matter skeleton of the major white matter tracts. For each subject, for each DTI metric (i.e. fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD)), the maximum value in a line perpendicular to the skeleton tract is projected to the skeleton. Non-parametric permutation based t-tests and ANOVA's were used for voxel-wise comparison of the skeletons. For both VBM and TBSS, comparison of pre bed rest measurements did not show significant differences. VBM analysis revealed decreased gray matter density in bilateral areas including the frontal medial cortex, the insular cortex and the caudate (see Figure) from 'pre to in bed rest'. Over the same time period, there was an increase in gray matter density in the cerebellum, occipital-, and parietal cortex, including the precuneus (see Figure). The majority of these changes did not recover from 'during to post bed rest'. TBSS analysis did not reveal significant changes in white matter microstructural integrity after correction for multiple comparisons. Uncorrected analyses (p<.015) revealed an increase in RD in the cerebellum and brainstem from pre bed rest to the first week in bed rest that did not recover post bed rest. Extended bed rest, which is an analog for microgravity, can result in gray matter changes and potentially in microstructural white matter changes in areas that are important for neuro motor behavior and cognition. These changes did not recover at two weeks post bed rest. Whether the effects of bed rest wear off at longer times post bed rest, and if they are associated with behavior are important questions that warrant further research.
- Published
- 2014
41. Emotional category data on images from the international affective picture system
- Author
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Mikels, Joseph A., Fredrickson, Barbara L., Larkin, Gregory R., Lindberg, Casey M., Maglio, Sam J., and Reuter-Lorenz, Patricia A.
- Published
- 2005
- Full Text
- View/download PDF
42. Strategic modulation of the fixation-offset effect: dissociable effects of target probability on prosaccades and antisaccades
- Author
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Gmeindl, Leon, Rontal, Andrew, and Reuter-Lorenz, Patricia A.
- Published
- 2005
- Full Text
- View/download PDF
43. Exercise Effects on the Course of Gray Matter Changes Over 70 Days of Bed Rest
- Author
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Koppelmans, V, Ploutz-Snyder, L, DeDios, Y. E, Wood, S. J, Reuter-Lorenz, P. A, Kofman, I, Bloomberg, J. J, Mulavara, A. P, and Seidler, R. D
- Subjects
Life Sciences (General) ,Aerospace Medicine - Abstract
Long duration spaceflight affects posture control, locomotion, and manual control. The microgravity environment is an important causal factor for spaceflight induced sensorimotor changes through direct effects on peripheral changes that result from reduced vestibular stimulation and body unloading. Effects of microgravity on sensorimotor function have been investigated on earth using bed rest studies. Long duration bed rest serves as a space-flight analogue because it mimics microgravity in body unloading and bodily fluid shifts. It has been hypothesized that the cephalad fluid shift that has been observed in microgravity could potentially affect central nervous system function and structure, and thereby indirectly affect sensorimotor or cognitive functioning. Preliminary results of one of our ongoing studies indeed showed that 70 days of long duration head down-tilt bed rest results in focal changes in gray matter volume from pre-bed rest to various time points during bed rest. These gray matter changes that could reflect fluid shifts as well as neuroplasticity were related to decrements in motor skills such as maintenance of equilibrium. In consideration of the health and performance of crewmembers both inand post-flight we are currently conducting a study that investigates the potential preventive effects of exercise on gray matter and motor performance changes that we observed over the course of bed rest. Numerous studies have shown beneficial effects of aerobic exercise on brain structure and cognitive performance in healthy and demented subjects over a large age range. We therefore hypothesized that an exercise intervention in bed rest could potentially mitigate or prevent the effects of bed rest on the central nervous system. Here we present preliminary outcomes of our study.
- Published
- 2014
44. Spaceflight Effects on Neurocognitive Performance: Extent, Longevity, and Neural Bases (NeuroMapping)
- Author
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Seidler, R. D, Reuter-Lorenz, P. A, Mulavara, A. P, Bloomberg, J. J, Wood, S. J, and Kofman, I. S
- Subjects
Aerospace Medicine ,Life Sciences (General) - Published
- 2014
45. Brain and Behavioral Evidence for Reweighting of Vestibular Inputs with Long-Duration Spaceflight.
- Author
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Hupfeld, K E, McGregor, H R, Koppelmans, V, Beltran, N E, Kofman, I S, Dios, Y E De, Riascos, R F, Reuter-Lorenz, P A, Wood, S J, Bloomberg, J J, Mulavara, A P, and Seidler, R D
- Published
- 2022
- Full Text
- View/download PDF
46. Auditory cues and inhibition of return: the importance of oculomotor activation
- Author
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Reuter-Lorenz, Patricia A. and Rosenquist, James Niels
- Published
- 1996
- Full Text
- View/download PDF
47. Effects of warning signals and fixation point offsets on the latencies of pro- versus antisaccades: implications for an interpretation of the gap effect
- Author
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Reuter-Lorenz, P. A., Oonk, H. M., Barnes, L. L., and Hughes, H. C.
- Published
- 1995
- Full Text
- View/download PDF
48. Are microsaccades responsible for the gap effect?
- Author
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Kingstone, Alan, Reuter-Lorenz, Patricia A., Fendrich, Robert, and Wessinger, C. Mark
- Published
- 1995
- Full Text
- View/download PDF
49. Parallel and serial processes in the human oculomotor system: bimodal integration and express saccades
- Author
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Nozawa, G., Reuter-Lorenz, P. A., and Hughes, H. C.
- Published
- 1994
- Full Text
- View/download PDF
50. Bidirectional control of saccadic eye movements by the disconnected cerebral hemispheres
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Hughes, H. C., Reuter-Lorenz, P. A., Fendrich, R., and Gazzaniga, M. S.
- Published
- 1992
- Full Text
- View/download PDF
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