Evidence map›Paper›PMID 33400141›Full record

ArticleInternational journal of hematology2021

Glycosylated ferritin as an improved marker for post-transfusion iron overload.

Ayako Ishihara, Tsuyuko Yamauchi, Katsuyoshi Ikeda, Yoko Fukuyoshi, Toshiro Yokoyama, Yuji Yonemura, Mitsuhiro Uchiba, Hirotaka Matsui

Abstract read
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2021. 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
0.4field-weighted citation impact, top 40% 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, 3 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

8 authors at 2 institutions in 1 country.

Ayako IshiharaDepartment of Clinical Laboratory Medicine, Kumamoto University Hospital, Kumamoto University, Kumamoto, Japan.
Tsuyuko YamauchiDepartment of Clinical Laboratory Medicine, Kumamoto University Hospital, Kumamoto University, Kumamoto, Japan.
Katsuyoshi IkedaDepartment of Medical Technology, Kumamoto Health Science University, Kumamoto, Japan.
Yoko FukuyoshiDepartment of Clinical Laboratory Medicine, Kumamoto University Hospital, Kumamoto University, Kumamoto, Japan.
Toshiro YokoyamaDepartment of Clinical Laboratory Medicine, Kumamoto University Hospital, Kumamoto University, Kumamoto, Japan.
Yuji YonemuraDepartment of Transfusion Medicine and Cell Therapy, Kumamoto University Hospital, Kumamoto University, Kumamoto, Japan.
Mitsuhiro UchibaDepartment of Transfusion Medicine and Cell Therapy, Kumamoto University Hospital, Kumamoto University, Kumamoto, Japan.
Hirotaka MatsuiDepartment of Clinical Laboratory Medicine, Kumamoto University Hospital, Kumamoto University, Kumamoto, Japan. hmatsui@kumamoto-u.ac.jp.ORCID http://orcid.org/0000-0002-6266-3227
Kumamoto University Hospital · JPKumamoto Health Science University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Red blood cell (RBC) transfusion is an effective therapy for anemia, but repeated transfusions may cause iron overload-related damage to various organs. Iron chelation therapy, now widely available for patients who have received transfusions, is expected to reduce organ damage even in patients who received many transfusions. Therefore, determining when to start iron chelation therapy is important. In guidelines for iron chelation therapy, the serum ferritin level has been widely accepted as a practical marker for estimating iron overload. However, guidelines recommend multiple measurements of serum ferritin, because levels often fluctuate. Here, we investigated the usefulness of glycosylated ferritin as a marker of iron overload using a cohort consisted of 103 patients who had a total ferritin value over 1000 ng/mL. We found that the volume of RBCs transfused was clearly associated with the glycosylated ferritin level. We also found that acute inflammation, as represented by C-reactive protein values, was associated with increased non-glycosylated ferritin and that patients with hematopoietic diseases had higher glycosylated ferritin levels, possibly because of repeated RBC transfusions. We thus conclude that glycosylated ferritin may be an improved marker for predicting iron overload status.

Indexed as

BiomarkersAgedBlood TransfusionComorbidityErythrocyte TransfusionFemaleFerritinsGlycoproteinsHumansIron OverloadMaleMiddle AgedPrognosisBiomarkersFerritinsGlycoproteinsglycosylated ferritinErythrocyte transfusionGlycosylated ferritinIron chelation therapy

Identifiers

PMID33400141
OpenAlexW3119854449

What OpenQuestion holds

Textmetadata
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.