Evidence map›Paper›PMID 35955788›Full record

ArticleInternational journal of molecular sciences2022

Harnessing the Power of Purple Sweet Potato Color and

Synneva Hagen-Lillevik, Joshua Johnson, Anwer Siddiqi, Jes Persinger, Gillian Hale, Kent Lai

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Reshaping the Treatment Landscape of a Galactose Metabolism Disorder.Journal of inherited metabolic disease · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. Inositol in Disease and Development: Roles of Catabolism viaInternational journal of molecular sciences · 2023
    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

6 authors at 4 institutions in 1 country.

Synneva Hagen-LillevikDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT 84108, USA.ORCID 0000-0003-2316-7228
Joshua JohnsonDivision of Reproductive Sciences, Aurora, CO 80045, USA.ORCID 0000-0002-6016-8089
Anwer SiddiqiCollege of Medicine, University of Florida, Jacksonville, FL 32209, USA.
Jes PersingerEcology and Evolutionary Biology, University of Colorado, Boulder, CO 80302, USA.
Gillian HaleDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
Kent LaiDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT 84108, USA.
University of Utah · USThe Medical Center of Aurora · USUniversity of Colorado Boulder · USUniversity of Florida · US

Funding

CRR LIGAND ASSAY AND ANALYSIS CORER24HD102061 · NICHD · UNIVERSITY OF VIRGINIA · PI HAISENLEDER, DANIEL J. · 2019 to 2023
$2.2M
Towards Improved Therapy for Classic GalactosemiaR01HD089933 · NICHD · UNIVERSITY OF UTAH · PI LAI, KENT · 2017 to 2019
$948k
Agilent 6550 QTOF system for U of UtahS10OD016232 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2013 to 2013
$578k
Q-ToF Mass Spectrometer for the University of Utah MS and Proteomics CoreS10OD018210 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2015 to 2015
$530k
Agilent 7200 GC/Q-TOF for the University of UtahS10OD021505 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2016 to 2016
$401k
NICHD NIH HHS R01 HD089933NICHD NIH HHS R24 HD102061NIH HHS R01HD089933NIH HHS S10 OD016232NIH HHS S10 OD018210NIH HHS S10 OD021505The Galactosemia Foundation 10060162
6 · The paper itself

Abstract

Classic Galactosemia (CG) is a devastating inborn error of the metabolism caused by mutations in the GALT gene encoding the enzyme galactose-1 phosphate uridylyltransferase in galactose metabolism. Severe complications of CG include neurological impairments, growth restriction, cognitive delays, and, for most females, primary ovarian insufficiency. The absence of the GALT enzyme leads to an accumulation of aberrant galactose metabolites, which are assumed to be responsible for the sequelae. There is no treatment besides the restriction of dietary galactose, which does not halt the development of the complications; thus, additional treatments are sorely needed. Supplements have been used in other inborn errors of metabolism but are not part of the therapeutic regimen for CG. The goal of this study was to test two generally recognized as safe supplements (purple sweet potato color (PSPC) and

Indexed as

GalactosemiasIpomoea batatasAnimalsColorFemaleGalactoseInositolMiceUTP-Hexose-1-Phosphate UridylyltransferaseGalactoseInositolUTP-Hexose-1-Phosphate UridylyltransferaseantioxidantcerebellumClassic Galactosemiaeukaryotic initiation Factor 2 alpha (eIF2ɑ)hepatocyte balloon-cell changeIntegrated Stress Responsemyo-inositolprimary ovarian insufficiencypurple sweet potato colorsupplements

Identifiers

PMID35955788
PMCPMC9369367
OpenAlexW4289745384

What Socratic 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 Socratic graph.