Evidence map›Paper›PMID 40642331›Full record

ArticlePeerJ2025

Utilizing loop-mediated isothermal amplification (LAMP) for detecting hemoglobin Constant Spring and hemoglobin Pakse mutations amidst the high prevalence and genetic heterogeneity of thalassemia in Thailand.

Kasama Wongprachum, Nichakan Thitipoomdecha, Phakkamon Ananratanakit, Wattanakit Prakobkul, Unchasa Angkuranak, Nitchagan Sawangkul, Prapaporn Panichchob, Rossarin Karnpean, Wittaya Jomoui

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Article in PeerJ, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  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

9 authors.

Kasama WongprachumNutritional Science, Dietetics and Food Safety Program, Faculty of Public Health, Mahasarakham University, Maha Sarakham, Thailand.
Nichakan ThitipoomdechaFaculty of Medicine, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.
Phakkamon AnanratanakitFaculty of Medicine, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.
Wattanakit PrakobkulFaculty of Medicine, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.
Unchasa AngkuranakFaculty of Medicine, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.
Nitchagan SawangkulFaculty of Medicine, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.
Prapaporn PanichchobDepartment of Pathology, Maha Chakri Sirindhorn Medical Center, Faculty of Medicine, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.
Rossarin KarnpeanDepartment of Pathology, Maha Chakri Sirindhorn Medical Center, Faculty of Medicine, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.
Wittaya JomouiDepartment of Pathology, Maha Chakri Sirindhorn Medical Center, Faculty of Medicine, Srinakharinwirot University, Ongkharak, Nakhon Nayok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thalassemia is a genetic disorder with significant prevalence in Southeast Asia, particularly in Thailand, where hemoglobin (Hb) Constant Spring (Hb CS) and hemoglobin Pakse (Hb PS) mutations are common. These mutations, resulting from stop codon alterations in the α2-globin gene, can lead to severe phenotypes such as non-deletional Hb H disease. This study aimed to develop and evaluate a novel colorimetric loop-mediated isothermal amplification (LAMP) assay for detecting Hb CS and Hb PS mutations. A total of 282 samples with several genotypes were recruited in the study. We developed LAMP assay, using a phenol red pH indicator, which provided visual detection of DNA amplification within 35 minutes at 65 °C. Both assays demonstrated a lower limit of detection of 0.625 ng/reaction and achieved 100% sensitivity and specificity across 282 DNA samples, validated against standard allele-specific polymerase chain reaction (PCR). Additionally, the assay's minimal equipment requirements and cost-effectiveness make it suitable for use in community hospitals and large-scale screenings. The LAMP assay offers a rapid, accurate, and affordable alternative for Hb CS and Hb PS detection, addressing the challenges of managing thalassemia in genetically diverse and resource-limited regions like Thailand.

Indexed as

Hemoglobins, AbnormalMolecular Diagnostic TechniquesMutationNucleic Acid Amplification TechniquesThalassemiaGenotypeHumansPrevalenceSensitivity and SpecificityThailandHemoglobin Constant SpringHemoglobins, AbnormalBiomedicalHb Constant SpringHb PakseLAMPThalassemia

Identifiers

PMID40642331
PMCPMC12244126

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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.