Evidence map›Paper›PMID 40017026›Full record

ArticleExperimental aging research

Identifying Biomarkers of Neuroplasticity Associated with Exercise-Induced Cognitive Change in Older Adults with MCI.

Adriana Savettiere, Peter Louras, Sarah Langdon, J Kaci Fairchild

Abstract read
In one paragraph

Article in Experimental aging research. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Adriana SavettiereDepartment of Psychology, Palo Alto University, Palo Alto, California, USA.
Peter LourasSierra Pacific Mental Illness Research Education and Clinical Center (MIRECC), Veteran's Affairs Palo Alto Health Care System, Palo Alto, California, USA.
Sarah LangdonDepartment of Psychology, Palo Alto University, Palo Alto, California, USA.
J Kaci FairchildSierra Pacific Mental Illness Research Education and Clinical Center (MIRECC), Veteran's Affairs Palo Alto Health Care System, Palo Alto, California, USA.

Funding

RRD VA I21 RX001884
6 · The paper itself

Abstract

objectivesThis exploratory study aimed to identify biomarkers of neuroplasticity that prevent cognitive decline. This study examined activity-dependent changes in the neurologic proteome that contributed to post-exercise improvements in processing speed in older adults with mild cognitive impairment (MCI).

methodsParticipants included 20 older adult Veterans with MCI recruited through the VA Palo Alto Health Care System (VAPAHCS) who participated in moderate-high intensity water-based activity thrice weekly for six months. Plasma protein concentration was measured using the Olink Target 96 Neurology Assay. Processing speed measures included the Trail Making Test Trial A (TMT-A), the Stroop Color (SC) and Word (SW) trials, and the Symbol Digit Modalities Test (SDMT).

resultsPreliminary analyses revealed two proteins of interest: neuropilin-2 (NRP2) and neuroblastoma suppressor of tumorigenicity 1 (NBL1). Primary analyses used mixed effects models to determine the impact of changes in neurologic-related proteins on changes in processing speed after exercise. Results indicated that decreased levels of NRP2 were associated with improved outcomes on the SDMT after exercise. In contrast, changes in NBL1 had no significant effect on the relationship between exercise and processing speed.

conclusionThese results support previous research linking NRP2 function to synaptic plasticity downscaling and present NRP2 as a potential target for cognitive intervention.

Indexed as

CognitionCognitive DysfunctionExerciseNeuronal PlasticityAgedAged, 80 and overBiomarkersFemaleHumansMaleVeteransBiomarkers

Identifiers

PMID40017026
PMCPMC12353216

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