Evidence map›Paper›PMID 26712713›Full record

ArticleLipids2016

Low Levels of HDL in Fragile X Syndrome Patients.

Małgorzata Z Lisik, Ewa Gutmajster, Aleksander L Sieroń

Open access · hybridAbstract read
In one paragraph

Article in Lipids, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Alteration of Fatty Acid Profile in Fragile X Syndrome.International journal of molecular sciences · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
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  12. Review
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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

3 authors at 1 institution in 2 countries.

Małgorzata Z LisikDepartment of Molecular Biology and Genetics, School of Medicine in Katowice ul., Medical University of Silesia, ul. Medyków 18, 40-752, Katowice, Poland. mlisik@sum.edu.pl.
Ewa GutmajsterDepartment of Molecular Biology and Genetics, School of Medicine in Katowice ul., Medical University of Silesia, ul. Medyków 18, 40-752, Katowice, Poland.
Aleksander L SierońDepartment of Molecular Biology and Genetics, School of Medicine in Katowice ul., Medical University of Silesia, ul. Medyków 18, 40-752, Katowice, Poland.
Medical University of Silesia · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fragile X syndrome (FXS) is the most common form of familial mental retardation and one of the leading known causes of autism. The mutation responsible for FXS is a large expansion of the CGG repeats in the promoter region of the FMR1 gene resulting in the transcriptional silencing of the gene in the pathophysiology of Fragile X syndrome was hypothesized. 23 male patients affected by Fragile X syndrome (full mutation in the FMR1 gene) and 24 controls were included in the study. The serum levels of HDL-C were lower in FXS patients (p < 0.001). The serum levels triacylglycerols were higher in FXS patients (p = 0.007) Further study involving larger samples are necessary to confirm the results and define the health implications for abnormal lipid levels in FXS patients.

Indexed as

AdultCholesterolFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeHumansLipoproteins, HDLLipoproteins, LDLMaleTriglyceridesCholesterolFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1Lipoproteins, HDLLipoproteins, LDLTriglyceridesGeneral area, HDLLipid biochemistryLipoproteinsLipoproteins, LDL

Identifiers

PMID26712713
PMCPMC4735238
OpenAlexW2284446072

What OpenQuestion holds

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LicenceCC BY
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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.