Evidence map›Paper›PMID 39114232›Full record

ReviewCureus2024

The Genetic Diagnostics of Hemochromatosis: Disparities in Low- Versus High-Income Countries.

Sol Villa Nogueyra, María F Trujillo Rodríguez, María L Garcia Oliva, Andrea Vidal-Gallardo, Amanda Ramírez Leal, Jose Beltran Hernandez, Andres Manuel Vargas Beltran, José D Guillen Sandoval, David Arriaga Escamilla, Marily Martinez Ramirez

Abstract readReview
In one paragraph

Review in Cureus, 2024. 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
–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

1 citing paper in PubMed.

  1. Antimicrobial peptides: from discovery to developmental applications.Applied and environmental microbiology · 2025
    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

10 authors.

Sol Villa NogueyraGeneral Practice, Universidad de Buenos Aires, Buenos Aires, ARG.
María F Trujillo RodríguezGeneral Practice, Universidad Nacional Autonoma de Mexico, Mexico City, MEX.
María L Garcia OlivaGeneral Practice, Universidad de Buenos Aires, Buenos Aires, ARG.
Andrea Vidal-GallardoGeneral Practice, Universidad de los Andes, Merida, VEN.
Amanda Ramírez LealFaculty of Medicine, Universidad Nacional Autónoma de México, Mexico City, MEX.
Jose Beltran HernandezGeneral Practice, Centro de Estudios Universitarios Xochicalco, Mexicali, MEX.
Andres Manuel Vargas BeltranGeneral Practice, Benemerita Universidad Autonoma de Puebla, Puebla, MEX.
José D Guillen SandovalGeneral Practice, Universidad Nacional Autonoma de Mexico, Mexico City, MEX.
David Arriaga EscamillaInternal Medicine, Universidad Justo Sierra, Mexico City, MEX.
Marily Martinez RamirezInternal Medicine, Universidad Nacional Autonoma de Mexico, Mexico City, MEX.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study provides a comprehensive overview of hereditary hemochromatosis (HH), a genetic condition characterized by iron overload due to excessive iron absorption. It elucidates diverse inheritance patterns and clinical manifestations by exploring mutations in critical genes such as HFE (hemochromatosis), HJV (hemojuvelin), HAMP (hepcidin antimicrobial peptide), TfR2 (transferrin receptor 2), and FP (ferroportin). The significance of early screening, diagnosis, and personalized management strategies based on genetic classification is emphasized, particularly in terms of high-income vs. low-income countries. Addressing challenges in diagnosis, genetic testing accessibility, and healthcare disparities, the study highlights the importance of early detection, cost-effective screening strategies, and enhancing healthcare outcomes globally. Advanced genetic testing in high-income countries facilitates early diagnosis and management, reducing complications such as liver disease and cardiomyopathy. In contrast, low-income populations face several barriers, including limited access to genetic testing, high costs, and inadequate healthcare infrastructure. Cost-effective serum ferritin (SF) and transferrin saturation (TS) tests and emerging point-of-care (POC) tests offer affordable diagnostic options for low-resource settings. Additionally, the ongoing development of hepcidin measurement methods holds promise for enhancing diagnostic capabilities. Implementing these strategies can aid healthcare providers in improving global HH management and reducing the burden of iron overload complications. Furthermore, the study underscores the need for public health initiatives to raise awareness about HH, promote routine screenings, and advocate for equitable healthcare policies. Collaborative efforts between governments, healthcare organizations, and research institutions are crucial in addressing the global burden of HH. By fostering international cooperation and resource-sharing, it is possible to bridge the gap between high-income and low-income countries, ensuring all individuals have access to the necessary diagnostic and treatment options. This holistic approach can ultimately lead to better health outcomes and improved quality of life for individuals affected by HH worldwide. This comprehensive examination of HH not only illuminates the genetic and clinical aspects of the condition but also provides a roadmap for addressing the multifaceted challenges associated with its diagnosis and management.

Indexed as

accessgenetic diagnostic approacheshereditary hemochromatosis (hh)high-income countrieslow-income countries

Identifiers

PMID39114232
PMCPMC11305073

What Socratic 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 Socratic graph.