Evidence map›Paper›PMID 41450978›Full record

ArticleBrain, behavior, & immunity - health2025

Early brain changes in Lyme disease are associated with clinical outcomes.

Cherie L Marvel, Alison W Rebman, Kylie H Alm, Pegah Touradji, Arnold Bakker, Prianca A Nadkarni, Deeya Bhattacharya, Owen P Morgan, Amy Mistri, Christopher C Sandino and 6 more

Abstract read
In one paragraph

Article in Brain, behavior, & immunity - health, 2025. 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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Cherie L MarvelDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Alison W RebmanDivision of Rheumatology, Department of Medicine, Lyme Disease Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Kylie H AlmDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Pegah TouradjiDeparment of Physical Medicine and Rehabilitation, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Arnold BakkerDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Prianca A NadkarniDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Deeya BhattacharyaDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Owen P MorganDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Amy MistriDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Christopher C SandinoDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Jonathan A EckerDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Erica A KozeroDivision of Rheumatology, Department of Medicine, Lyme Disease Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Arun VenkatesanDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Abhay MoghekarDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
Ashar A KeeysDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.
John N AucottDivision of Rheumatology, Department of Medicine, Lyme Disease Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, United States of America.

Funding

Institute for Clinical and Translational Research (UL1)UL1RR025005 · NCRR · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2007 to 2011
$75.8M
State of the Art 3T Research ScannerS10OD021648 · OD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI VAN ZIJL, PETER CM · 2016 to 2016
$2.0M
NCRR NIH HHS UL1 RR025005NIH HHS S10 OD021648
6 · The paper itself

Abstract

In Lyme disease (LD), 10-20 % of patients develop persistent symptoms following antibiotic treatment (i.e., post-treatment Lyme disease (PTLD)), which often includes neurological symptoms. This study tested the hypothesis that physiological brain changes occur early in LD and influence outcomes. Task-based functional MRI (fMRI) and health surveys were administered to patients with acute LD (n = 20) after treatment and six months later. Demographically matched healthy controls (HC; n = 19) were also assessed six months apart. The LD group was categorized at six months into those who had returned to health (RTH, n = 11) or reported persistent symptoms (sPTLD, n = 9). FMRI data from both LD subgroups were compared to each other and HC at both time points. FMRI-guided regions of interest (ROI) values were compared to health surveys. Baseline brain activity in RTH was elevated in fronto-parietal regions relative to sPTLD (p < .0025) and HC (p < .001). Notably, 64 % of activation clusters in RTH were in white matter, confirmed by segmentation analysis. FMRI-guided ROI values from RTH vs. HC correlated with higher health survey scores. At 6-months, few group differences remained. By contrast, sPTLD vs. HC fMRI comparisons yielded few activation differences at either time point or correlations with health survey scores. Robust brain activity in early LD was associated with future RTH. By contrast, the absence of early brain activity was associated with persistent symptoms, suggesting that failure to mount an early response contributes to PTLD. Understanding how brain activity relates to recovery in LD can aid prognosis and guide treatment.

Indexed as

AstrocyteLyme diseaseMRIPTLDTickborneWhite matter

Identifiers

PMID41450978
PMCPMC12731907

What OpenQuestion holds

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LicenceCC BY-NC
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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.