Evidence map›Paper›PMID 32620712›Full record

ArticleAging2020

Aging affects sex- and organ-specific trace element profiles in mice.

Kristina Lossow, Johannes F Kopp, Maria Schwarz, Hannah Finke, Nicola Winkelbeiner, Kostja Renko, Xheni Meçi, Christiane Ott, Wiebke Alker, Julian Hackler and 5 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

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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 7 institutions in 1 country.

Kristina LossowDepartment of Molecular Nutritional Physiology, Institute of Nutritional Sciences, Friedrich Schiller University Jena, Jena, Germany.
Johannes F KoppDepartment of Food Chemistry, Institute of Nutritional Science, University of Potsdam, Nuthetal, Germany.
Maria SchwarzDepartment of Molecular Nutritional Physiology, Institute of Nutritional Sciences, Friedrich Schiller University Jena, Jena, Germany.
Hannah FinkeDepartment of Food Chemistry, Institute of Nutritional Science, University of Potsdam, Nuthetal, Germany.
Nicola WinkelbeinerDepartment of Food Chemistry, Institute of Nutritional Science, University of Potsdam, Nuthetal, Germany.
Kostja RenkoInstitute for Experimental Endocrinology, Charité University Medical School Berlin, Berlin, Germany.
Xheni MeçiInstitute for Experimental Endocrinology, Charité University Medical School Berlin, Berlin, Germany.
Christiane OttGerman Institute of Human Nutrition, Nuthetal, Germany.
Wiebke AlkerTraceAge-DFG Research Unit on Interactions of Essential Trace Elements in Healthy and Diseased Elderly, Potsdam-Berlin-Jena, Germany.
Julian HacklerTraceAge-DFG Research Unit on Interactions of Essential Trace Elements in Healthy and Diseased Elderly, Potsdam-Berlin-Jena, Germany.
Tilman GruneGerman Institute of Human Nutrition, Nuthetal, Germany.
Lutz SchomburgTraceAge-DFG Research Unit on Interactions of Essential Trace Elements in Healthy and Diseased Elderly, Potsdam-Berlin-Jena, Germany.
Hajo HaaseTraceAge-DFG Research Unit on Interactions of Essential Trace Elements in Healthy and Diseased Elderly, Potsdam-Berlin-Jena, Germany.
Tanja SchwerdtleDepartment of Food Chemistry, Institute of Nutritional Science, University of Potsdam, Nuthetal, Germany.
Anna P KippDepartment of Molecular Nutritional Physiology, Institute of Nutritional Sciences, Friedrich Schiller University Jena, Jena, Germany.
German Institute of Human Nutrition · DEUniversity of Potsdam · DECharité - Universitätsmedizin Berlin · DEFriedrich Schiller University Jena · DEMSB Medical School Berlin · DETechnische Universität Berlin · DEFederal Institute for Risk Assessment · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A decline of immune responses and dynamic modulation of the redox status are observed during aging and are influenced by trace elements such as copper, iodine, iron, manganese, selenium, and zinc. So far, analytical studies have focused mainly on single trace elements. Therefore, we aimed to characterize age-specific profiles of several trace elements simultaneously in serum and organs of adult and old mice. This allows for correlating multiple trace element levels and to identify potential patterns of age-dependent alterations. In serum, copper and iodine concentrations were increased and zinc concentration was decreased in old as compared to adult mice. In parallel, decreased copper and elevated iron concentrations were observed in liver. The age-related reduction of hepatic copper levels was associated with reduced expression of copper transporters, whereas the increased hepatic iron concentrations correlated positively with proinflammatory mediators and Nrf2-induced ferritin H levels. Interestingly, the age-dependent inverse regulation of copper and iron was unique for the liver and not observed in any other organ. The physiological importance of alterations in the iron/copper ratio for liver function and the aging process needs to be addressed in further studies.

Indexed as

AdultAgedAgingAnimalsBiomarkersFemaleHumansInflammation MediatorsLiverMaleMiceModels, AnimalOxidation-ReductionOxidative StressSex FactorsTrace ElementsBiomarkersInflammation MediatorsTrace Elementsagingbiomarkersepigenetic markershomeostasistrace elements

Identifiers

PMID32620712
PMCPMC7377894
OpenAlexW3040239450

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.