Evidence map›Paper›PMID 37652816›Full record

ReviewPediatric neurology2023

Impoverished Conceptions of Gene Causation and Therapy in Developmental Neurology.

Juan M Pascual, Vikram Jakkamsetti, Ignacio Málaga, Denis Noble

Abstract readReview
In one paragraph

Review in Pediatric neurology, 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.

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

4 authors.

Juan M PascualRare Brain Disorders Program, Department of Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas; Department of Physiology, The University of Texas Southwestern Medical Center, Dallas, Texas; Department of Pediatrics, The University of Texas Southwestern Medical Center, Dallas, Texas; Eugene McDermott Center for Human Growth & Development/Center for Human Genetics, The University of Texas Southwestern Medical Center, Dallas, Texas. Electronic address: Juan.Pascual@UTSouthwestern.edu.
Vikram JakkamsettiRare Brain Disorders Program, Department of Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas.
Ignacio MálagaRare Brain Disorders Program, Department of Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas.
Denis NobleDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.

Funding

Dietary treatment of Glut1 deficiency (G1D) - Revision - 1R01NS094257 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI PASCUAL, JUAN M. · 2016 to 2021
$4.0M
Pyruvate dehydrogenase encephalopathy: mechanisms and therapyR01NS102588 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI PASCUAL, JUAN M. · 2017 to 2021
$1.8M
Modulation of neural function in energy failureR01NS077015 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI PASCUAL, JUAN M. · 2012 to 2016
$1.7M
NINDS NIH HHS R01 NS077015NINDS NIH HHS R01 NS094257NINDS NIH HHS R01 NS102588
6 · The paper itself

Abstract

We offer a primer to the modifiability of genetic neurological disease, particularly during development. One goal is to harness several unexpected observations made in the course of experimental gene modification or therapy into an explanatory conceptual context based on biological first principles. To this end, we anchor growing, disparate reports of unusual or untoward effects to a plausible framework wherein genes exhibit different degrees of modifiability and may result, when mutated or therapeutically modified, in unsuspected consequences. We propose that genetic pathogenic variant effects and modifiability depend on the number and complexity of associated protein-protein or higher-order interactions. Thus, gene malleability may range from that characteristic of the favorably modifiable primarily structural genes that subserve relatively invariant or circumscribed phenomena such as cell shape to that typical of some transcription factors, which are less functionally predictable when altered. The latter may be expressed developmentally, in compartmentalized manner, or only intermittently and yet exert vastly ramified influences sometimes circumscribed only to select species. We also argue that genetic diseases may steer the organism toward often poorly understood biological end points and co-opt multiple processes into hardly modifiable biology. Addition or modification of genes to approximate a normal state not previously experienced by the organism may lead to further aberration due to extraneous interference with the native biology of the disease state. Therefore, an understanding as perspicuous as possible of gene function, regulation, modifiability, and biological directionality down to seemingly minute but disease-relevant consequences is a prerequisite to intervention. Although we provide some groundwork steps to such an understanding, this may occasionally prove unattainable.

Indexed as

AntisenseGene therapyGenetic diseasePhenotype

Identifiers

PMID37652816
PMCPMC12918051

What OpenQuestion holds

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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.