Evidence map›Paper›PMID 37543633›Full record

ArticleScientific reports2023

Mapping brain networks in MPS I mice and their restoration following gene therapy.

Wei Zhu, Li Ou, Lin Zhang, Isaac H Clark, Ying Zhang, Xiao-Hong Zhu, Chester B Whitley, Perry B Hackett, Walter C Low, Wei Chen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 37% of its field
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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Advances in Therapies for Mucopolysaccharidoses.Current issues in molecular biology · 2026
    Review
  2. Article
  3. Review
  4. Review
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

10 authors at 2 institutions in 2 countries.

Wei ZhuCenter for Magnetic Resonance Research, University of Minnesota, Minneapolis, MN, 55455, USA.
Li OuDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, 55455, USA.
Lin ZhangDivision of Biostatistics, University of Minnesota, Minneapolis, MN, 55455, USA.
Isaac H ClarkBiomedical Engineering Graduate Program, University of Minnesota, Minneapolis, MN, 55455, USA.
Ying ZhangMinnesota Supercomputing Institute, University of Minnesota, Minneapolis, MN, 55455, USA.
Xiao-Hong ZhuCenter for Magnetic Resonance Research, University of Minnesota, Minneapolis, MN, 55455, USA.
Chester B WhitleyDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, 55455, USA.
Perry B HackettDepartment of Genetics, Cell Biology Development, University of Minnesota, Minneapolis, MN, 55455, USA.
Walter C LowBiomedical Engineering Graduate Program, University of Minnesota, Minneapolis, MN, 55455, USA. lowwalt@umn.edu.
Wei ChenCenter for Magnetic Resonance Research, University of Minnesota, Minneapolis, MN, 55455, USA. chenx075@umn.edu.
University of Minnesota · USResonance Research (United States) · US

Funding

TRD4 - Ultrahigh Field Engineering and SafetyP41EB027061 · NIBIB · UNIVERSITY OF MINNESOTA · PI Mehmet Akcakaya · 2019 to 2026
$11.7M
Breaking Spatiotemporal Barriers of MR Imaging Technologies to Study Human Brain Function and NeuroenergeticsU01EB026978 · NIBIB · UNIVERSITY OF MINNESOTA · PI CHEN, WEI, ZHU, XIAO-HONG · 2018 to 2022
$6.4M
Integrated fMRI Methods to Study Neurophysiology and Circuit Dynamics at Laminar and Columnar LevelR01MH111413 · NIMH · UNIVERSITY OF MINNESOTA · PI CHEN, WEI · 2016 to 2020
$4.4M
Advancing simultaneous fMRI-multiphoton imaging technique to study brain function and connectivity across different scales at ultrahigh fieldR01NS118330 · NINDS · UNIVERSITY OF MINNESOTA · PI CHEN, WEI, CUI, MENG · 2020 to 2024
$2.7M
Establishing translational neuroimaging tools for quantitative assessment of energy metabolism and metabolic reprogramming in healthy and diseased human brain at 7TR01NS133006 · NINDS · UNIVERSITY OF MINNESOTA · PI Wei Chen, XIAO-HONG ZHU · 2023 to 2026
$2.5M
NIBIB NIH HHS U01 EB026978NIH HHS R01 NS118330NIMH NIH HHS R01 MH111413NINDS NIH HHS R01 NS118330NINDS NIH HHS R01 NS133006
6 · The paper itself

Abstract

Mucopolysaccharidosis type I (MPS I) is an inherited lysosomal disorder that causes syndromes characterized by physiological dysfunction in many organs and tissues. Despite the recognizable morphological and behavioral deficits associated with MPS I, neither the underlying alterations in functional neural connectivity nor its restoration following gene therapy have been shown. By employing high-resolution resting-state fMRI (rs-fMRI), we found significant reductions in functional neural connectivity in the limbic areas of the brain that play key roles in learning and memory in MPS I mice, and that adeno-associated virus (AAV)-mediated gene therapy can reestablish most brain connectivity. Using logistic regression in MPS I and treated animals, we identified functional networks with the most alterations. The rs-fMRI and statistical methods should be translatable into clinical evaluation of humans with neurological disorders.

Indexed as

Mucopolysaccharidosis IAnimalsBrainBrain MappingGenetic TherapyHumansMagnetic Resonance ImagingMice

Identifiers

PMID37543633
PMCPMC10404260
OpenAlexW4385606616

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.