Evidence map›Paper›PMID 32382074›Full record

ArticleEuropean journal of clinical nutrition2020

Placental expression of leptin: fetal sex-independent relation with human placental growth.

P Kochhar, C Manikandan, G Ravikumar, P Dwarkanath, C N Sheela, S George, A Thomas, J Crasta, T Thomas, A V Kurpad and 1 more

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Article in European journal of clinical nutrition, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
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

11 authors at 2 institutions in 1 country.

P KochharDivision of Nutrition, St. John's Research Institute, St. John's National Academy of Health Sciences, Bangalore, India.
C ManikandanDivision of Nutrition, St. John's Research Institute, St. John's National Academy of Health Sciences, Bangalore, India.
G RavikumarDepartment of Pathology, St John's Medical College Hospital, Bangalore, India.
P DwarkanathDivision of Nutrition, St. John's Research Institute, St. John's National Academy of Health Sciences, Bangalore, India.
C N SheelaDepartment of Obstetrics and Gynaecology, St John's Medical College Hospital, Bangalore, India.
S GeorgeDepartment of Obstetrics and Gynaecology, St John's Medical College Hospital, Bangalore, India.
A ThomasDepartment of Obstetrics and Gynaecology, St John's Medical College Hospital, Bangalore, India.
J CrastaDepartment of Pathology, St John's Medical College Hospital, Bangalore, India.
T ThomasDepartment of Biostatistics, St. John's Medical College Hospital, Bangalore, India.ORCID http://orcid.org/0000-0002-1786-6076
A V KurpadDivision of Nutrition, St. John's Research Institute, St. John's National Academy of Health Sciences, Bangalore, India.
A MukhopadhyayDivision of Nutrition, St. John's Research Institute, St. John's National Academy of Health Sciences, Bangalore, India. arpitam@sjri.res.in.ORCID http://orcid.org/0000-0001-8260-5385
St.John's Medical College Hospital · INSt. John's National Academy of Health Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesLeptin (LEP) is a vital placental hormone that is known to affect different aspects of placental function and fetal development. The present study aimed to determine the association of placental LEP transcript abundance with maternal, placental, and newborn parameters. SUBJECTS/

methodsIn this retrospective case-control study, placental samples (n = 105) were collected from small (SGA) and appropriate (AGA) for gestational age full-term singleton pregnancies (n = 44 SGA and n = 61 AGA). Placental transcript abundance of LEP was assessed by real-time quantitative PCR after normalization to a reference gene panel. LEP methylation was measured using a quantitative MethyLight assay in a subset of samples (n = 54).

resultsPlacental LEP transcript abundance was negatively and significantly associated with placental weight (β = -3.883, P = 0.015). This association continued to be significant in the SGA group (β = -10.332, P = 0.001), both in female (β = -15.423, P = 0.021) and male births (β = -10.029, P = 0.007). LEP transcript abundance was not associated with LEP methylation levels (Spearman's ρ = 0.148, P = 0.287).

conclusionWe conclude that placental upregulation of LEP is an integral and fetal sex-independent component of placental growth restriction, which can be potentially targeted through maternal dietary modifications to improve fetoplacental growth.

Indexed as

LeptinPlacentaCase-Control StudiesFemaleGestational AgeHumansInfant, NewbornInfant, Small for Gestational AgeMalePregnancyRetrospective StudiesLeptin

Identifiers

PMID32382074
OpenAlexW3023421894

What OpenQuestion holds

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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.