Evidence map›Paper›PMID 29176728›Full record

ArticleScientific reports2017

Similarities between acylcarnitine profiles in large for gestational age newborns and obesity.

Paula Sánchez-Pintos, Maria-Jose de Castro, Iria Roca, Segundo Rite, Miguel López, Maria-Luz Couce

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

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  11. Carnitine and Depression.Frontiers in nutrition · 2022
    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

6 authors at 2 institutions in 1 country.

Paula Sánchez-PintosDiagnosis and Treatment of Congenital Metabolic Diseases Unit (UDyTEMC). Neonatology Service. Department of Pediatrics. Hospital Clínico Universitario. University of Santiago de Compostela. Institute of Clinical Research of Santiago de Compostela (IDIS). CIBERER, Santiago de Compostela, Spain. paula.sanchez.pintos@sergas.es.
Maria-Jose de CastroDiagnosis and Treatment of Congenital Metabolic Diseases Unit (UDyTEMC). Neonatology Service. Department of Pediatrics. Hospital Clínico Universitario. University of Santiago de Compostela. Institute of Clinical Research of Santiago de Compostela (IDIS). CIBERER, Santiago de Compostela, Spain.
Iria RocaDiagnosis and Treatment of Congenital Metabolic Diseases Unit (UDyTEMC). Neonatology Service. Department of Pediatrics. Hospital Clínico Universitario. University of Santiago de Compostela. Institute of Clinical Research of Santiago de Compostela (IDIS). CIBERER, Santiago de Compostela, Spain.
Segundo RiteNeonatology Unit. University Hospital Miguel Servet, Zaragoza, Spain.
Miguel LópezNeurObesity Group. Department of Physiology, CIMUS. University of Santiago de Compostela. Institute of Clinical Research of Santiago de Compostela (IDIS), Santiago de Compostela, 15782, Spain.
Maria-Luz CouceDiagnosis and Treatment of Congenital Metabolic Diseases Unit (UDyTEMC). Neonatology Service. Department of Pediatrics. Hospital Clínico Universitario. University of Santiago de Compostela. Institute of Clinical Research of Santiago de Compostela (IDIS). CIBERER, Santiago de Compostela, Spain.
Universidade de Santiago de Compostela · ESHospital Universitario Miguel Servet · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large for gestational age (LGA) newborns have an increased risk of obesity, insulin resistance, and metabolic syndrome. Acylcarnitine profiles in obese children and adults are characterized by increased levels of C3, C5, and certain medium-chain (C12) and long-chain (C14:1 and C16) acylcarnitines. C2 is also increased in insulin-resistant states. In this 1-year observational study of 2514 newborns (246 LGA newborns, 250 small for gestational age (GA) newborns, and 2018 appropriate for GA newborns), we analyzed and compared postnatal acylcarnitine profiles in LGA newborns with profiles described for obese individuals. Acylcarnitine analysis was performed by tandem mass spectrometry on dried-blood spots collected on day 3 of life. LGA newborns had higher levels of total short-chain acylcarnitines (p < 0.001), C2 (p < 0.01) and C3 (p < 0.001) acylcarnitines, and all C12, C14, and C16 acylcarnitines except C12:1. They also had a higher tendency towards carnitine insufficiency (p < 0.05) and carnitine deficiency (p < 0.001). No significant differences were observed between LGA newborns born to mothers with or without a history of gestational diabetes. This novel study describes a postnatal acylcarnitine profile in LGA with higher levels of C2, C3, total acylcarnitines, and total short-chain acylcarnitines that is characteristic of childhood and adult obesity and linked to an unhealthy metabolic phenotype.

Indexed as

CardiomyopathiesCarnitineFemaleGestational AgeHumansHyperammonemiaInfant, NewbornInfant, Small for Gestational AgeMaleMuscular DiseasesObesityPregnancyacylcarnitineCarnitine

Identifiers

PMID29176728
PMCPMC5701125
OpenAlexW2769712620

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.