Evidence map›Paper›PMID 28400987›Full record

ArticleAging and disease2017

Serum Hepcidin Levels, Iron Dyshomeostasis and Cognitive Loss in Alzheimer's Disease.

Zohara Sternberg, Zihua Hu, Daniel Sternberg, Shayan Waseh, Joseph F Quinn, Katharine Wild, Kaye Jeffrey, Lin Zhao, Michael Garrick

Open access · goldAbstract read
In one paragraph

Article in Aging and disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Acidosis, Iron Dyshomeostasis and Inflammatory Injury.International journal of molecular sciences · 2026
    Review
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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

9 authors at 2 institutions in 1 country.

Zohara Sternberg1Department of Neurology, Stroke Center, Buffalo Medical Center, Buffalo, NY, USA.
Zihua Hu2Center for Computational Research, New York State Center for Excellence in Bioinformatics and Life Sciences, University at Buffalo, Buffalo, NY, USA.
Daniel Sternberg1Department of Neurology, Stroke Center, Buffalo Medical Center, Buffalo, NY, USA.
Shayan Waseh3Department of Biology, State University of New York at Buffalo, Buffalo, NY 14260 USA.
Joseph F Quinn4Layton Aging & Alzheimer's Research Center, Oregon Health and Science University, Portland, Oregon, USA.
Katharine Wild4Layton Aging & Alzheimer's Research Center, Oregon Health and Science University, Portland, Oregon, USA.
Kaye Jeffrey4Layton Aging & Alzheimer's Research Center, Oregon Health and Science University, Portland, Oregon, USA.
Lin Zhao5Department of Biochemistry, State University of New York at Buffalo, Buffalo, NY 14214 USA.
Michael Garrick5Department of Biochemistry, State University of New York at Buffalo, Buffalo, NY 14214 USA.; 6Department of Pediatrics, State University of New York at Buffalo, Buffalo, NY 14214 USA.
Oregon Health & Science University · USBuffalo State University · US

Funding

Outreach, Recruitment and Education CoreP30AG008017 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI KAYE, JEFFREY A · 1990 to 2019
$27.7M
NIA NIH HHS P30 AG008017
6 · The paper itself

Abstract

This pilot study examined the status of the master iron regulatory peptide, hepcidin, and peripheral related iron parameters in Alzheimer's disease (AD) and mild cognitive impairment patients, and evaluated the relationship between iron dyshomeostasis and amyloid-beta (Aβ), cognitive assessment tests, neuroimaging and clinical data. Frozen serum samples from the Oregon Tissue Bank were used to measure serum levels of hepcidin, ferritin, Aβ40, Aβ42 using enzyme-linked immunosorbent assay. Serum transferrin levels were determined indirectly as total iron binding capacity, serum iron was measured and the percent saturation of transferrin calculated. The study variables were correlated with the patients' existing cognitive assessment tests, neuroimaging, and clinical data. Hepcidin, and iron-related proteins tended to be higher in AD patients than controls, reaching statistical significance for ferritin, whereas Aβ40, Aβ42 serum levels tended to be lower. Patients with pure AD had three times higher serum hepcidin levels than controls; gender differences in hepcidin and iron-related proteins were observed. Patient stratification based on clinical dementia rating-sum of boxes revealed significantly higher levels of iron and iron-related proteins in AD patients in the upper 50% as compared to controls, suggesting that iron dyshomeostasis worsens as cognitive impairment increases. Unlike Aβ peptides, iron and iron-related proteins showed significant association with cognitive assessment tests, neuroimaging, and clinical data. Hepcidin and iron-related proteins comprise a group of serum biomarkers that relate to AD diagnosis and AD disease progression. Future studies should determine whether strategies targeted to diminishing hepcidin synthesis/secretion and improving iron homeostasis could have a beneficial impact on AD progression.

Indexed as

Alzheimer’s diseaseFerritinInflammationIron homeostasisMild cognitive impairmentPercent transferrin saturationSerum biomarker

Identifiers

PMID28400987
PMCPMC5362180
OpenAlexW2602222039

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.