Evidence map›Paper›PMID 42281581›Full record

ArticleHealth science reports2026

Relationship of Genetic Variability (

Mohammad Pouya Samiee, Azita Chegini, Majid Shahabi, Amir Teimourpour

Abstract read
In one paragraph

Article in Health science reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Mohammad Pouya SamieeHematology and Blood Banking, Blood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran Iran.
Azita CheginiAnesthesiology. Assistant Professor of Blood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran Iran.ORCID https://orcid.org/0000-0002-7715-5591
Majid ShahabiBiotechnology, Blood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran Iran.ORCID https://orcid.org/0000-0003-2755-1921
Amir TeimourpourBiostatics, Biological Products and Blood Safety Research Center High Institute for Research and Education in Transfusion Medicine Tehran Iran.ORCID https://orcid.org/0000-0002-6986-1314

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Frequent blood donation can significantly increase the risk of iron deficiency, influenced by demographic, dietary, environmental, and genetic factors. This study aims to evaluate the association between iron deficiency and specific genetic variations ( Methods: This cross-sectional study was conducted at the Iranian Blood Transfusion Organization (IBTO) between March and September 2023, targeting male donors registered as regular donors in the database (with a minimum of two donations in the past year and at least five donations over the past 3 years) aged 18-65. Strict inclusion criteria were applied to minimize potential confounding variables. To investigate genetic polymorphisms, we utilized techniques such as Sanger sequencing, allele-specific PCR, and high-resolution melt (HRM) analysis. Iron status was assessed by measuring key biochemical indicators-serum ferritin, Iron, transferrin saturation (TSAT), and total iron-binding capacity (TIBC)-through ELISA and colorimetric assays. Statistical analyses were performed using R software (version 4.1.1). Methods included one-way ANOVA, the Kruskal-Wallis test, the Shapiro-Wilk test, and independent samples Results: The rs11549465 polymorphism in Conclusion: Genetic screening for the rs11549465 polymorphism could be integrated into donor management programs to personalize strategies for mitigating Iron deficiency risks. Additional research involving larger and more diverse groups is necessary to investigate interactions between genetic, dietary, and environmental factors.

Indexed as

blood donorsGene polymorphismHIF1Airon deficiency anemiaTMPRSS6

Identifiers

PMID42281581
PMCPMC13250472

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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.