Evidence map›Paper›PMID 36341174›Full record

ArticleJIMD reports2022

MicroRNA and metabolomics signatures for adrenomyeloneuropathy disease severity.

Bela Rui Turk, Laila Marie Poisson, Christina Linnea Nemeth, Jordan Goodman, Ann B Moser, Richard Owen Jones, Ali Fatemi, Jaspreet Singh

Abstract read
In one paragraph

Article in JIMD reports, 2022. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

8 authors.

Bela Rui TurkMoser Center for Leukodystrophies, Kennedy Krieger Institute Johns Hopkins Medical Institutions Baltimore Maryland USA.
Laila Marie PoissonDepartment of Public Health Sciences Henry Ford Health System Detroit Michigan USA.
Christina Linnea NemethMoser Center for Leukodystrophies, Kennedy Krieger Institute Johns Hopkins Medical Institutions Baltimore Maryland USA.
Jordan GoodmanMoser Center for Leukodystrophies, Kennedy Krieger Institute Johns Hopkins Medical Institutions Baltimore Maryland USA.
Ann B MoserMoser Center for Leukodystrophies, Kennedy Krieger Institute Johns Hopkins Medical Institutions Baltimore Maryland USA.
Richard Owen JonesMoser Center for Leukodystrophies, Kennedy Krieger Institute Johns Hopkins Medical Institutions Baltimore Maryland USA.
Ali FatemiMoser Center for Leukodystrophies, Kennedy Krieger Institute Johns Hopkins Medical Institutions Baltimore Maryland USA.
Jaspreet SinghDepartment of Neurology Henry Ford Health System Detroit Michigan USA.ORCID https://orcid.org/0000-0002-6563-5424

Funding

Sleep and Circadian Dysfunction, Brain and Neurobehavioral Development in AutismP50HD103538 · NICHD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI S. Ali Fatemi, Bradley L Schlaggar · 2020 to 2026
$9.9M
Use of IPSC to define role of astrocytes in specifying risk for onset of cerebral adrenoleukodystrophyR01NS114245 · NINDS · HENRY FORD HEALTH SYSTEM · PI SINGH, JASPREET · 2021 to 2024
$1.4M
Plasma biomarkers of cerebral disease in X-linked adrenoleukodystrophyR21NS104560 · NINDS · HENRY FORD HEALTH SYSTEM · PI SINGH, JASPREET · 2018 to 2019
$430k
NICHD NIH HHS P50 HD103538NINDS NIH HHS R01 NS114245NINDS NIH HHS R21 NS104560
6 · The paper itself

Abstract

Adrenomyeloneuropathy (AMN), the slow progressive phenotype of adrenoleukodystrophy (ALD), has no clinical plasma biomarker for disease progression. This feasibility study aimed to determine whether metabolomics and micro-RNA in blood plasma provide a potential source of biomarkers for AMN disease severity. Metabolomics and RNA-seq were performed on AMN and healthy human blood plasma. Biomarker discovery and pathway analyses were performed using clustering, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis, and regression against patient's clinical Expanded Disability Status Score (EDSS). Fourteen AMN and six healthy control samples were analyzed. AMN showed strong disease-severity-specific metabolic and miRNA clustering signatures. Strong, significant clinical correlations were shown for 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-HOCA) (

Indexed as

adrenoleukodystrophyadrenomyeloneuropathybiomarkerleukodystrophymetabolomicsmicro‐RNA

Identifiers

PMID36341174
PMCPMC9626672

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Registered trials

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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.