Evidence map›Paper›PMID 36531334›Full record

ArticleNature cardiovascular research2022

Oestrogen enforces the integrity of blood vessels in the bone during pregnancy and menopause.

Julia Rodrigues, Yi-Fang Wang, Amit Singh, Michelle Hendriks, Gopuraja Dharmalingam, Martine Cohen-Solal, Anjali P Kusumbe, Saravana K Ramasamy

Open access · hybridAbstract read
In one paragraph

Article in Nature cardiovascular research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
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  11. Targeting type H vessels in bone-related diseases.Journal of cellular and molecular medicine · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Type H vessels: functions in bone development and diseases.Frontiers in cell and developmental biology · 2023
    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

8 authors at 5 institutions in 3 countries.

Julia RodriguesInstitute of Clinical Sciences, Imperial College London, London, UK.
Yi-Fang WangBioinformatics and Computing Facility, MRC London Institute of Medical Sciences, Imperial College London, London, UK.
Amit SinghTissue and Tumor Microenvironments Group, MRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-9979-7221
Michelle HendriksInstitute of Clinical Sciences, Imperial College London, London, UK.
Gopuraja DharmalingamBioinformatics and Computing Facility, MRC London Institute of Medical Sciences, Imperial College London, London, UK.
Martine Cohen-SolalBioscar Inserm U1132 and Université de Paris, Hospital Lariboisiere, Paris, France.
Anjali P KusumbeTissue and Tumor Microenvironments Group, MRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Saravana K RamasamyInstitute of Clinical Sciences, Imperial College London, London, UK. s.ramasamy@imperial.ac.uk.ORCID http://orcid.org/0000-0003-2658-2945
MRC London Institute of Medical Sciences · GBHeidelberg University · DEInserm · FRNIHR Imperial Biomedical Research Centre · GBUniversity of Oxford · GB

Funding

Medical Research Council MC_UP_1605/1Wellcome Trust 202300
6 · The paper itself

Abstract

The mammalian skeletal system shows sex differences in structure, functions, ageing and disease incidences. The role of blood vessels in physiological, regenerative and pathological bone functions indicates the requisite to understanding their sex specificity. Here, we find oestrogen regulates blood vessel physiology during pregnancy and menopause through oestrogen receptor alpha (ERα) and G-protein coupled oestrogen receptor-1 (Gper1) but not ERβ-dependent signalling in mice. Oestrogen regulates BECs' lipid use and promotes lipolysis of adipocytes and FA uptake from the microenvironment. Low oestrogen conditions skew endothelial FA metabolism to accumulate lipid peroxides (LPO), leading to vascular ageing. High ferrous ion levels in female BECs intensify LPO accumulation and accelerate the ageing process. Importantly, inhibiting LPO generation using liproxstatin-1 in aged mice significantly improved bone heath. Thus, our findings illustrate oestrogen's effects on BECs and suggest LPO targeting could be an efficient strategy to manage blood and bone health in females.

Indexed as

Ageingblood vesselsoestrogenpostmenopausal bone losssex differences

Identifiers

PMID36531334
PMCPMC7613952
OpenAlexW4304777357

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.