Evidence map›Paper›PMID 32212788›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2020

Chromosomal Abnormalities in Myelodysplastic Syndrome Patients in Upper Northern Thailand.

Suphitcha Phrommin, Adisak Tantiworawit, Thanawat Rattanathammethee, Chaniporn Puaninta, Nathaporn Pangjaidee, Sirinda Aungsuchawan, Kanokkan Bumroongkit

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 54% of its field
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

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Suphitcha PhromminDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Adisak TantiworawitDivision of Hematology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Thanawat RattanathammetheeDivision of Hematology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Chaniporn PuanintaDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Nathaporn PangjaideeDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Sirinda AungsuchawanDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Kanokkan BumroongkitDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Chiang Mai University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveChromosome detection is important in the diagnosis and prognosis of Myelodysplastic syndrome (MDS) patients. About 50% of MDS patients have chromosomal abnormalities. Moreover, chromosome 5 and 7 are common genetic abnormalities in MDS patients and use to identify prognosis risk group and the proper treatment in MDS patients. The objective of this study was to evaluate chromosomal abnormalities and clinical features of MDS patients in upper northern Thailand.

methodsFifty bone marrow (BM) specimens were examined by conventional cytogenetic (CC) technique and fluorescence in situ hybridization (FISH) technique for detected chromosome 5 and 7 abnormalities. The clinical features were comparison between MDS patients with chromosomal abnormalities and those with normal karyotype.

resultsChromosomal abnormalities were detected in 8/50 MDS patients by CC and 17/50 cases by FISH technique. When the CC and FISH techniques were combined, chromosomal abnormalities increased to 21/50 cases.  Abnormalities of isolated chromosome 5 were found in 13 cases and were associated with lower level of percentage blast of BM (p = 0.003) and higher level of hemoglobin (p = 0.019). Moreover, abnormalities of chromosome 7 were found in 3 cases, 1 case of isolated del(7q) and 2 cases of -7 and del(7q) with complex abnormalities. These three cases were associated with higher level of percentage blast of BM (p = 0.010).

conclusionThis study showed the frequency and pattern of chromosomal abnormalities of MDS patients in upper northern Thailand were different from other populations. MDS with isolated chromosome 5 abnormalities had clinical characteristics corresponding with patients in good prognosis risk group. However, MDS patients with chromosome 7 and complex abnormalities showed higher percentage blast of BM which high risk to progression to acute myeloid leukemia (AML). Combined CC and FISH techniques detect chromosomal abnormalities with greater frequency than when either technique is used alone.<br />.

Indexed as

Chromosome AberrationsAdultAgedAged, 80 and overChromosomes, Human, Pair 5Chromosomes, Human, Pair 7FemaleHumansIn Situ Hybridization, FluorescenceKaryotypingMaleMiddle AgedMyelodysplastic SyndromesThailandChromosomal abnormalitiesconventional cytogenetic techniqueFluorescence in Situ HybridizationMyelodysplastic syndromeupper Northern Thailand

Identifiers

PMID32212788
PMCPMC7437337
OpenAlexW3013760177

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LicenceCC BY
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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.