Evidence mapPaperPMID 36904100Full record

ArticleNutrients2023

Metabolomic Diversity of Human Milk Cells over the Course of Lactation-A Preliminary Study.

Isabel Ten-Doménech, Mari Merce Cascant-Vilaplana, Víctor Navarro-Esteve, Birgit Felderer, Alba Moreno-Giménez, Iván Rienda, María Gormaz, Marta Moreno-Torres, David Pérez-Guaita, Guillermo Quintás and 1 more

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Article in Nutrients, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

11 authors.

Isabel Ten-DoménechNeonatal Research Group, Health Research Institute Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0002-4883-7948
Mari Merce Cascant-VilaplanaNeonatal Research Group, Health Research Institute Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0002-6680-2773
Víctor Navarro-EsteveNeonatal Research Group, Health Research Institute Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0002-1844-9848
Birgit FeldererNeonatal Research Group, Health Research Institute Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.
Alba Moreno-GiménezNeonatal Research Group, Health Research Institute Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.
Iván RiendaServicio de Anatomía Patológica, University & Polytechnic Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0002-3254-7372
María GormazNeonatal Research Group, Health Research Institute Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.
Marta Moreno-TorresUnidad de Hepatología Experimental y Trasplante Hepático, Health Research Institute Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0001-6684-8731
David Pérez-GuaitaDepartment of Analytical Chemistry, University of Valencia, Dr. Moliner 50, 46100 Burjassot, Spain.
Guillermo QuintásHealth and Biomedicine, Leitat Technological Center, Carrer de la Innovació, 2, 08225 Terrassa, Spain.
Julia KuligowskiNeonatal Research Group, Health Research Institute Hospital La Fe, Avda Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0001-6979-2235

Funding

Generalitat Valenciana GV/2021/186Instituto de Salud Carlos III CD19/00037; CD19/00176; CPII21/00003Ministerio de Ciencia e Innovación PRE2021-098833; RYC2019-026556-I; RPID2020-119326RA-I00; PID2021-125573OB-I00; RYC2021-031346-I
6 · The paper itself

Abstract

Human milk (HM) is a complex biofluid containing a wide cell variety including epithelial cells and leukocytes. However, the cellular compositions and their phenotypic properties over the course of lactation are poorly understood. The aim of this preliminary study was to characterize the cellular metabolome of HM over the course of lactation. Cells were isolated via centrifugation and the cellular fraction was characterized via cytomorphology and immunocytochemical staining. Cell metabolites were extracted and analyzed using ultra-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry (UPLC-QqTOF-MS) in the positive and negative electrospray ionization modes. Immunocytochemical analysis revealed a high variability of the number of detected cells with relative median abundances of 98% of glandular epithelial cells, 1% of leukocytes, and 1% of keratinocytes. Significant correlations between the milk postnatal age with percentage of epithelial cells and leukocytes, and with total cell count were observed. Results from the Hierarchical Cluster Analysis of immunocytochemical profiles were very similar to those observed in the analysis of the metabolomic profiles. In addition, metabolic pathway analysis showed alterations in seven metabolic pathways correlating with postnatal age. This work paves the way for future investigations on changes in the metabolomic fraction of the cellular compartment of HM.

Indexed as

LactationMilk, HumanBreast FeedingChromatography, High Pressure LiquidFemaleHumansMass SpectrometryMetabolomeMetabolomicshuman milk cellsinfant nutritionmetabolomicspreterm infantultra-performance liquid chromatography–mass spectrometry (UPLC-MS)

Identifiers

PMID36904100
PMCPMC10005050

What Socratic holds

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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 Socratic graph.