Evidence map›Paper›PMID 31917830›Full record

ArticleJournal of animal science2020

Characterization of metabolic and inflammatory profiles of transition dairy cows fed an energy-restricted diet.

Giulia Esposito, Emiliano Raffrenato, Somwe D Lukamba, Mounir Adnane, Pete C Irons, Paul Cormican, Taurai Tasara, Aspinas Chapwanya

Abstract readRandomized Controlled Trial, Veterinary
In one paragraph

Article in Journal of animal science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

8 authors.

Giulia EspositoDepartment of Animal Sciences, Faculty of Agricultural Science, Stellenbosch University, Stellenbosch, South Africa.
Emiliano RaffrenatoDepartment of Animal Sciences, Faculty of Agricultural Science, Stellenbosch University, Stellenbosch, South Africa.
Somwe D LukambaDepartment of Production Animal Studies, Faculty of Veterinary Science, University of Pretoria, Pretoria, South Africa.
Mounir AdnaneInstitute of Veterinary Sciences, Ibn-Khaldoun University, Tiaret, Algeria.
Pete C IronsDepartment of Production Animal Studies, Faculty of Veterinary Science, University of Pretoria, Pretoria, South Africa.
Paul CormicanDepartment of Animal and Grassland Research, Animal Bioscience Research Centre, Teagasc, Ireland.
Taurai TasaraInstitute for Food Safety and Hygiene, Vetsuisse Faculty, University of Zurich, Zürich, Switzerland.
Aspinas ChapwanyaDepartment of Production Animal Studies, Faculty of Veterinary Science, University of Pretoria, Pretoria, South Africa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periparturient diseases of dairy cows are caused by disproportionate energy metabolism, mineral imbalance, and perturbed immune function. The aim of the present study was to characterize metabolism, innate immune endometrial gene expression, and uterine microbial populations of transition animals receiving normal or restricted energy diets. Pregnant multiparous Holstein cows (n = 14) were randomly assigned to one of the two dietary treatments from 20 d prepartum until 35 d postpartum (DPP). One group was fed a diet providing 100% energy requirements (NE), whereas the other received an energy-restricted diet providing 80% energy requirements (RE). Feed intake, milk yield, body weight, body condition score, temperature, respiratory, and pulse rate were recorded. After calving, blood was collected weekly to analyze nonesterified fatty acids (NEFAs), β-hydroxybutyrate (BHB), and total cholesterol (TC). Endometrial cytobrushes were collected for gene expression analysis of inflammatory markers, microbial populations determination, and cytological evaluation. The restricted energy diet did not alter feed intake or milk yield but changed energy balance and metabolites levels (P < 0.05). In fact, RE animals had high NEFA and BHB levels, and low TC concentrations (P < 0.05). Moreover, RE animals had upregulated gene expression of serum amyloid A3 (SAA3) at 35 DPP (P < 0.05) and CXC chemokine receptor 2 (CXCR2) at 14 DPP (P < 0.01). Interleukin (IL) 1 and IL8 genes were downregulated 14 DPP but upregulated 35 DPP in RE animals, whereas IL6 and lipopolysaccharide-binding protein (LBP) genes were upregulated at 14 DPP (P ≤ 0.05). The most abundant phyla in RE animals (n = 3) were Bacteroidetes and Fusobacteria, whereas Proteobacteria was the least abundant at both 14 and 35 DPP. In conclusion, it can be speculated that energy balance is one of the main drivers for uterine inflammation by affecting metabolism, immune function, and uterine microbiota. However, these findings should be validated in a larger sample size.

Indexed as

CattleDietEnergy IntakeEnergy Metabolism3-Hydroxybutyric AcidAnimalsBacteriaBody WeightCholesterolFatty Acids, NonesterifiedFemaleLactationMicrobiotaMilkPostpartum PeriodPregnancy3-Hydroxybutyric AcidCholesterolFatty Acids, NonesterifiedRNA, Ribosomal, 16Senergy restricted dietgene expressioninflammatory markersmetabolitestransition cow

Identifiers

PMID31917830
PMCPMC6984754

What OpenQuestion 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 OpenQuestion graph.