Evidence map›Paper›PMID 28720890›Full record

ArticleScientific reports2017

Iron overload exacerbates age-associated cardiac hypertrophy in a mouse model of hemochromatosis.

Abitha Sukumaran, JuOae Chang, Murui Han, Shrutika Mintri, Ban-An Khaw, Jonghan Kim

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Targeting macro- and micro-nutrient regulation of HNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  3. Review
  4. Article
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  6. Article
  7. Article
  8. Article
  9. Review
  10. Inflammation alters iron distribution in bone and spleen in mice.Metallomics : integrated biometal science · 2023
    Article
  11. Carnitine-acylcarnitine translocase deficiency caused byThe Journal of international medical research · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Role of Iron in Aging Related Diseases.Antioxidants (Basel, Switzerland) · 2022
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Abitha SukumaranDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA.
JuOae ChangDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA.
Murui HanDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA.
Shrutika MintriDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA.
Ban-An KhawDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA.
Jonghan KimDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA. j.kim@neu.edu.
Northeastern University · US

Funding

Influence of HFE on metal pharmacokinetics and neurotoxicityR00ES017781 · NIEHS · NORTHEASTERN UNIVERSITY · PI KIM, JONGHAN · 2012 to 2014
$728k
Influence of HFE on metal pharmacokinetics and neurotoxicityK99ES017781 · NIEHS · HARVARD SCHOOL OF PUBLIC HEALTH · PI KIM, JONGHAN · 2010 to 2011
$177k
NIEHS NIH HHS K99 ES017781NIEHS NIH HHS R00 ES017781
6 · The paper itself

Abstract

Cardiac damage associated with iron overload is the most common cause of morbidity and mortality in patients with hereditary hemochromatosis, but the precise mechanisms leading to disease progression are largely unexplored. Here we investigated the effects of iron overload and age on cardiac hypertrophy using 1-, 5- and 12-month old Hfe-deficient mice, an animal model of hemochromatosis in humans. Cardiac iron levels increased progressively with age, which was exacerbated in Hfe-deficient mice. The heart/body weight ratios were greater in Hfe-deficient mice at 5- and 12-month old, compared with their age-matched wild-type controls. Cardiac hypertrophy in 12-month old Hfe-deficient mice was consistent with decreased alpha myosin and increased beta myosin heavy chains, suggesting an alpha-to-beta conversion with age. This was accompanied by cardiac fibrosis and up-regulation of NFAT-c2, reflecting increased calcineurin/NFAT signaling in myocyte hypertrophy. Moreover, there was an age-dependent increase in the cardiac isoprostane levels in Hfe-deficient mice, indicating elevated oxidative stress. Also, rats fed high-iron diet demonstrated increased heart-to-body weight ratios, alpha myosin heavy chain and cardiac isoprostane levels, suggesting that iron overload promotes oxidative stress and cardiac hypertrophy. Our findings provide a molecular basis for the progression of age-dependent cardiac stress exacerbated by iron overload hemochromatosis.

Indexed as

Disease Models, AnimalAge FactorsAnimalsCardiomegalyFibrosisHemochromatosisHemochromatosis ProteinHumansIronIron OverloadIsoprostanesMaleMice, 129 StrainMice, KnockoutMyocardiumRats, Sprague-DawleyHemochromatosis ProteinHfe protein, mouseIronIsoprostanes

Identifiers

PMID28720890
PMCPMC5516030
OpenAlexW2735561529

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.