Evidence map›Paper›PMID 36014934›Full record

ArticleNutrients2022

Nutrigenetic Interaction of Spontaneously Hypertensive Rat Chromosome 20 Segment and High-Sucrose Diet Sensitizes to Metabolic Syndrome.

Ondřej Šeda, Kristýna Junková, Hana Malinska, Adéla Kábelová, Martina Hüttl, Michaela Krupková, Irena Markova, František Liška, Lucie Šedová

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2022. 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
0.3field-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

1 citing paper in PubMed, 2 citations in OpenAlex.

  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

9 authors at 2 institutions in 1 country.

Ondřej ŠedaInstitute of Biology and Medical Genetics, The First Faculty of Medicine, Charles University and the General University Hospital in Prague, 128 00 Prague, Czech Republic.ORCID 0000-0001-8498-5895
Kristýna JunkováInstitute of Biology and Medical Genetics, The First Faculty of Medicine, Charles University and the General University Hospital in Prague, 128 00 Prague, Czech Republic.
Hana MalinskaCentre for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.ORCID 0000-0002-9076-3399
Adéla KábelováInstitute of Biology and Medical Genetics, The First Faculty of Medicine, Charles University and the General University Hospital in Prague, 128 00 Prague, Czech Republic.
Martina HüttlCentre for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.ORCID 0000-0002-2484-3630
Michaela KrupkováInstitute of Biology and Medical Genetics, The First Faculty of Medicine, Charles University and the General University Hospital in Prague, 128 00 Prague, Czech Republic.
Irena MarkovaCentre for Experimental Medicine, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.ORCID 0000-0002-4331-7636
František LiškaInstitute of Biology and Medical Genetics, The First Faculty of Medicine, Charles University and the General University Hospital in Prague, 128 00 Prague, Czech Republic.ORCID 0000-0002-9588-806X
Lucie ŠedováInstitute of Biology and Medical Genetics, The First Faculty of Medicine, Charles University and the General University Hospital in Prague, 128 00 Prague, Czech Republic.
Charles University · CZInstitute of Clinical and Experimental Medicine · CZ

Funding

Charles University SVV 260516, Cooperatio Program - Medical Diagnostics and Basic Medical SciencesMinistry of Health of the Czech Republic RVO64165
6 · The paper itself

Abstract

Several corresponding regions of human and mammalian genomes have been shown to affect sensitivity to the manifestation of metabolic syndrome via nutrigenetic interactions. In this study, we assessed the effect of sucrose administration in a newly established congenic strain BN.SHR20, in which a limited segment of rat chromosome 20 from a metabolic syndrome model, spontaneously hypertensive rat (SHR), was introgressed into Brown Norway (BN) genomic background. We mapped the extent of the differential segment and compared the genomic sequences of BN vs. SHR within the segment in silico. The differential segment of SHR origin in BN.SHR20 spans about 9 Mb of the telomeric portion of the short arm of chromosome 20. We identified non-synonymous mutations e.g., in

Indexed as

Cation Transport ProteinsHypertensionMetabolic SyndromeAnimalsApolipoproteins MChromosomes, Human, Pair 20FastingFatty AcidsGenome-Wide Association StudyHumansMaleMammalsNutrigenomicsRatsRats, Inbred BNRats, Inbred SHRApolipoproteins MApom protein, ratCation Transport ProteinsFatty AcidsSLC39A7 protein, humanSucroseanimal modelcongenic ratmetabolic syndromenutrigenetics

Identifiers

PMID36014934
PMCPMC9416443
OpenAlexW4292566755

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.