Evidence map›Paper›PMID 36459297›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2022

Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium.

Hui-Qi Qu, Joseph Glessner, Jingchun Qu, Frank Mentch, Ian Campbell, Patrick Sleiman, John J Connolly, Hakon Hakonarson

Open access · hybridAbstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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 at 2 institutions in 1 country.

Hui-Qi QuThe Center for Applied Genomics, Children's Hospital of Philadelphia, 19104, Philadelphia, PA, USA.
Joseph GlessnerThe Center for Applied Genomics, Children's Hospital of Philadelphia, 19104, Philadelphia, PA, USA.
Jingchun QuThe Center for Applied Genomics, Children's Hospital of Philadelphia, 19104, Philadelphia, PA, USA.
Frank MentchThe Center for Applied Genomics, Children's Hospital of Philadelphia, 19104, Philadelphia, PA, USA.
Ian CampbellThe Center for Applied Genomics, Children's Hospital of Philadelphia, 19104, Philadelphia, PA, USA.
Patrick SleimanThe Center for Applied Genomics, Children's Hospital of Philadelphia, 19104, Philadelphia, PA, USA.
John J ConnollyThe Center for Applied Genomics, Children's Hospital of Philadelphia, 19104, Philadelphia, PA, USA.
Hakon HakonarsonThe Center for Applied Genomics, Children's Hospital of Philadelphia, 19104, Philadelphia, PA, USA. hakonarson@email.chop.edu.
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious study has shown that dyslipidemia is common in patients with Sickle cell disease (SCD) and is associated with more serious SCD complications.

methodsThis study investigated systematically dyslipidemia in SCD using a state-of-art nuclear magnetic resonance (NMR) metabolomics platform, including 147 pediatric cases with SCD and 1234 controls without SCD. We examined 249 metabolomic biomarkers, including 98 biomarkers for lipoprotein subclasses, 70 biomarkers for relative lipoprotein lipid concentrations, plus biomarkers for fatty acids and phospholipids.

resultsSpecific patterns of hypolipoproteinemia and hypocholesterolemia in pediatric SCD were observed in lipoprotein subclasses other than larger VLDL subclasses. Triglycerides are not significantly changed in SCD, except increased relative concentrations in lipoprotein subclasses. Decreased plasma FFAs (including total-FA, SFA, PUFA, Omega-6, and linoleic acid) and decreased plasma phospholipids were observed in SCD.

conclusionThis study scrutinized, for the first time, lipoprotein subclasses in pediatric patients with SCD, and identified SCD-specific dyslipidemia from altered lipoprotein metabolism. The findings of this study depict a broad panorama of lipid metabolism and nutrition in SCD, suggesting the potential of specific dietary supplementation of the deficient nutrients for the management of SCD.

Indexed as

Anemia, Sickle CellDyslipidemiasChildHumansMetabolomicsPlasmaTriglyceridesTriglyceridesDyslipidemiaFree fatty acidsHypocholesterolemiaLipoprotein subclassesNutrition therapyPhospholipidsSickle cell disease

Identifiers

PMID36459297
PMCPMC9718871
OpenAlexW4310777357

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.