Evidence map›Paper›PMID 24711860›Full record

ArticleJournal of chemical biology2014

Increased lipid droplet accumulation associated with a peripheral sensory neuropathy.

Lee L Marshall, Scott E Stimpson, Ryan Hyland, Jens R Coorssen, Simon J Myers

Open access · bronzeAbstract read
In one paragraph

Article in Journal of chemical biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Lee L MarshallNeuro-Cell Biology Laboratory, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; Molecular Medicine Research Group, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; School of Science and Health, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia.
Scott E StimpsonNeuro-Cell Biology Laboratory, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; Molecular Medicine Research Group, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; School of Science and Health, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia.
Ryan HylandNeuro-Cell Biology Laboratory, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; Molecular Medicine Research Group, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; School of Science and Health, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia.
Jens R CoorssenMolecular Physiology, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; Molecular Medicine Research Group, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; School of Science and Health, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; School of Medicine, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; University of Western Sydney, Office 30.2.15, Campbelltown campus, Locked Bag 1797, Penrith South DC, NSW 1797 Australia.
Simon J MyersMolecular Medicine Research Group, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; School of Science and Health, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; School of Medicine, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797 Australia ; University of Western Sydney, Office 21.1.05, Campbelltown campus, Locked Bag 1797, Penrith South DC, NSW 1797 Australia.
Western Sydney University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary sensory neuropathy type 1 (HSN-1) is an autosomal dominant neurodegenerative disease caused by missense mutations in the SPTLC1 gene. The SPTLC1 protein is part of the SPT enzyme which is a ubiquitously expressed, critical and thus highly regulated endoplasmic reticulum bound membrane enzyme that maintains sphingolipid concentrations and thus contributes to lipid metabolism, signalling, and membrane structural functions. Lipid droplets are dynamic organelles containing sphingolipids and membrane bound proteins surrounding a core of neutral lipids, and thus mediate the intracellular transport of these specific molecules. Current literature suggests that there are increased numbers of lipid droplets and alterations of lipid metabolism in a variety of other autosomal dominant neurodegenerative diseases, including Alzheimer's and Parkinson's disease. This study establishes for the first time, a significant increase in the presence of lipid droplets in HSN-1 patient-derived lymphoblasts, indicating a potential connection between lipid droplets and the pathomechanism of HSN-1. However, the expression of adipophilin (ADFP), which has been implicated in the regulation of lipid metabolism, was not altered in lipid droplets from the HSN-1 patient-derived lymphoblasts. This appears to be the first report of increased lipid body accumulation in a peripheral neuropathy, suggesting a fundamental molecular linkage between a number of neurodegenerative diseases.

Indexed as

ADFPHereditary sensory neuropathy type 1Lipid dropletsNile redSerine palmitoyltransferaseSerine palmitoyltransferase long chain subunit 1

Identifiers

PMID24711860
PMCPMC3976696
OpenAlexW2134894964

What OpenQuestion holds

Textmetadata
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.