Evidence map›Paper›PMID 37693412›Full record

ArticlebioRxiv : the preprint server for biology2023

Myelin dystrophy in the aging prefrontal cortex leads to impaired signal transmission and working memory decline: a multiscale computational study.

Sara Ibañez, Nilapratim Sengupta, Jennifer I Luebke, Klaus Wimmer, Christina M Weaver

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Sara IbañezDepartment of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA USA 02118.
Nilapratim SenguptaDepartment of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA USA 02118.
Jennifer I LuebkeDepartment of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA USA 02118.
Klaus WimmerCentre de Recerca Matemàtica, Edifici C, Campus Bellaterra, 08193 Bellaterra, Spain.
Christina M WeaverDepartment of Mathematics, Franklin and Marshall College, Lancaster, PA, USA 17604.
Boston University · USCentre de Recerca Matemàtica · ESFranklin & Marshall College · US

Funding

Mechanisms of Age-related Cognitive Decline in the Rhesus MonkeyR01AG059028 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HOF, PATRICK R, LUEBKE, JENNIFER I · 2018 to 2022
$3.5M
CRCNS: Age-related changes to cortical dynamics underlying working memoryR01AG071230 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LUEBKE, JENNIFER I · 2020 to 2022
$553k
NIA NIH HHS R01 AG059028NIA NIH HHS R01 AG071230
6 · The paper itself

Abstract

Normal aging leads to myelin alternations in the rhesus monkey dorsolateral prefrontal cortex (dlPFC), which are often correlated with cognitive impairment. It is hypothesized that remyelination with shorter and thinner myelin sheaths partially compensates for myelin degradation, but computational modeling has not yet explored these two phenomena together systematically. Here, we used a two-pronged modeling approach to determine how age-related myelin changes affect a core cognitive function: spatial working memory. First we built a multicompartment pyramidal neuron model fit to monkey dlPFC data, with axon including myelinated segments having paranodes, juxtaparanodes, internodes, and tight junctions, to quantify conduction velocity (CV) changes and action potential (AP) failures after demyelination and subsequent remyelination in a population of neurons. Lasso regression identified distinctive parameter sets likely to modulate an axon's susceptibility to CV changes following demyelination versus remyelination. Next we incorporated the single neuron results into a spiking neural network model of working memory. While complete remyelination nearly recovered axonal transmission and network function to unperturbed levels, our models predict that biologically plausible levels of myelin dystrophy, if uncompensated by other factors, can account for substantial working memory impairment with aging. The present computational study unites empirical data from electron microscopy up to behavior on aging, and has broader implications for many demyelinating conditions, such as multiple sclerosis or schizophrenia.

Identifiers

PMID37693412
PMCPMC10491254
OpenAlexW4386353271

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.