Evidence map›Paper›PMID 34489410›Full record

ArticleNature communications2021

BMP8 and activated brown adipose tissue in human newborns.

Adela Urisarri, Ismael González-García, Ánxela Estévez-Salguero, María P Pata, Edward Milbank, Noemi López, Natalia Mandiá, Carmen Grijota-Martinez, Carlos A Salgado, Rubén Nogueiras and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

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  20. An updated view on human neonatal thermogenesis.Nature reviews. Endocrinology · 2022
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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

15 authors at 5 institutions in 1 country.

Adela Urisarri *Neonatology Service, Department of Pediatrics, University Clinical Hospital of Santiago de Compostela, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), CIBER Enfermedades Raras (CIBERER), Travesia Choupana, Santiago de Compostela, Spain.
Ismael González-García *Department of Physiology, CIMUS, University of Santiago de Compostela-Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-5545-5841
Ánxela Estévez-SalgueroDepartment of Physiology, CIMUS, University of Santiago de Compostela-Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
María P PataBiostatech Advice, Training and Innovation in Biostatistics, S.L. Santiago de Compostela, Spain.
Edward MilbankDepartment of Physiology, CIMUS, University of Santiago de Compostela-Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
Noemi LópezNeonatology Service, Department of Pediatrics, University Clinical Hospital of Santiago de Compostela, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), CIBER Enfermedades Raras (CIBERER), Travesia Choupana, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-7759-3735
Natalia MandiáNeonatology Service, Department of Pediatrics, University Clinical Hospital of Santiago de Compostela, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), CIBER Enfermedades Raras (CIBERER), Travesia Choupana, Santiago de Compostela, Spain.
Carmen Grijota-MartinezDepartment of Cell Biology, Faculty of Biology, Complutense University, Madrid, Spain.ORCID http://orcid.org/0000-0003-2656-9062
Carlos A SalgadoInstituto Galego de Física de Altas Enerxías (IGFAE), University of Santiago de Compostela, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0003-4586-2758
Rubén NogueirasDepartment of Physiology, CIMUS, University of Santiago de Compostela-Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-9976-9930
Carlos DiéguezDepartment of Physiology, CIMUS, University of Santiago de Compostela-Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
Francesc VillarroyaCIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0003-1266-9142
José-Manuel Fernández-RealCIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-7442-9323
María L CouceNeonatology Service, Department of Pediatrics, University Clinical Hospital of Santiago de Compostela, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), CIBER Enfermedades Raras (CIBERER), Travesia Choupana, Santiago de Compostela, Spain. Maria.Luz.Couce.Pico@sergas.es.
Miguel LópezDepartment of Physiology, CIMUS, University of Santiago de Compostela-Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Santiago de Compostela, Spain. m.lopez@usc.es.ORCID http://orcid.org/0000-0002-7823-1648
Universidade de Santiago de Compostela · ESCentro de Investigación Biomédica en Red · ESInstitut d'Investigació Biomèdica de Girona · ESInstituto de Salud Carlos III · ESUniversidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The classical dogma states that brown adipose tissue (BAT) plays a major role in the regulation of temperature in neonates. However, although BAT has been studied in infants for more than a century, the knowledge about its physiological features at this stage of life is rather limited. This has been mainly due to the lack of appropriate investigation methods, ethically suitable for neonates. Here, we have applied non-invasive infrared thermography (IRT) to investigate neonatal BAT activity. Our data show that BAT temperature correlates with body temperature and that mild cold stimulus promotes BAT activation in newborns. Notably, a single short-term cold stimulus during the first day of life improves the body temperature adaption to a subsequent cold event. Finally, we identify that bone morphogenic protein 8B (BMP8B) is associated with the BAT thermogenic response in neonates. Overall, our data uncover key features of the setup of BAT thermogenesis in newborns.

Indexed as

Adipose Tissue, BrownBirth WeightBlood GlucoseBody TemperatureBone Morphogenetic ProteinsCold TemperatureFibroblast Growth FactorsHormonesHumansInfant, NewbornThermogenesisBlood GlucoseBMP8B protein, humanBone Morphogenetic ProteinsFGF21 protein, humanFibroblast Growth FactorsHormones

Identifiers

PMID34489410
PMCPMC8421355
OpenAlexW3196933545

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.