Evidence map›Paper›PMID 32573970›Full record

ArticleMolecular genetics & genomic medicine2020

Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients.

Hasna Hamdaoui, Oumaima Benlarroubia, Oum Kaltoum Ait Boujmia, Hossein Mossafa, Karim Ouldim, Aziza Belkhayat, Imane Smyej, Houda Benrahma, Hind Dehbi, Fatima Chegdani

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 24% 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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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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Monoclonal Gammopathies in Africa.Clinical lymphoma, myeloma & leukemia · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Conventional Karyotyping and FluorescenceJournal of hematology · 2022
    Article
  8. Article
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  10. Article
  11. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Hasna HamdaouiNational Reference Laboratory, Mohammed VI University of Health Sciences (UM6SS), Casablanca, Morocco.ORCID 0000-0002-8267-8186
Oumaima BenlarroubiaNational Reference Laboratory, Mohammed VI University of Health Sciences (UM6SS), Casablanca, Morocco.
Oum Kaltoum Ait BoujmiaLaboratory of Cellular and Molecular Pathology, Faculty of Medicine and Pharmacy of Casablanca, University Hassan II, Casablanca, Morocco.ORCID 0000-0002-1014-9728
Hossein MossafaNational Reference Laboratory, Mohammed VI University of Health Sciences (UM6SS), Casablanca, Morocco.
Karim OuldimFaculty of Medicine and Pharmacy, Medical Genetics and Oncogenetics Unit, Sidi Mohamed Ben Abdellah University, Fes, Morocco.
Aziza BelkhayatNational Reference Laboratory, Mohammed VI University of Health Sciences (UM6SS), Casablanca, Morocco.
Imane SmyejNational Reference Laboratory, Mohammed VI University of Health Sciences (UM6SS), Casablanca, Morocco.
Houda BenrahmaNational Reference Laboratory, Mohammed VI University of Health Sciences (UM6SS), Casablanca, Morocco.
Hind DehbiLaboratory of Cellular and Molecular Pathology, Faculty of Medicine and Pharmacy of Casablanca, University Hassan II, Casablanca, Morocco.
Fatima ChegdaniLaboratory of Health and Environment, Faculty of Sciences Ain Chock, University Hassan II, Casablanca, Morocco.
Université Mohammed VI des Sciences et de la Santé · MAUniversity of Hassan II Casablanca · MASidi Mohamed Ben Abdellah University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple myeloma (MM) is a disease characterized by heterogeneous clinical presentations as well as complex genetic and molecular abnormalities. In MM, cytogenetic analysis is a challenge because of the low proliferation of malignant plasma cells. Thus, interphase fluorescence in situ hybridization (FISH), performed on sorted plasma cells detected abnormalities independently of a proliferative and infiltrative index. The purpose of this study was to explore, for the first time, the cytogenetic and molecular genetics features in Moroccan patients with multiple myeloma referred exclusively to National Reference Laboratory and to determine their risk stratification based on these features.

methodsWe performed cytogenetic analysis on 93 MM cases, all patients were subjected to FISH analysis, among which 45 patients have benefited from both FISH analysis and standard karyotype.

resultsKaryotype was normal in 78% (35/45) while, it was complex with varied structural and numerical abnormalities in 22% (10/45) of all patients, among which Hyperdiploid karyotype was found in 9% (n = 4 cases) and nonhyperdiploid in 13% (n = 6 cases). The most common numerical abnormalities were gains of chromosomes 3, 5, 9, 15, and 19. Whole chromosome losses were also frequent, affecting chromosomes X, 3, 14, 16 and 22. FISH analysis detected abnormalities in 50% of cases. The translocation t(4;14) and dup (1q) were the most frequent types of anomalies (14% and 13% respectively), followed by (17p) deletion and 14q32/IGH translocations with an undetermined origin (12% each) then the (1p) deletion (4%). For the normal karyotypes, FISH revealed chromosome abnormalities in 46%.

conclusionThis study compares the results of cytogenetic analysis of chromosomal abnormalities in the Moroccan population with other countries. ½ patient showed at least one type of molecular genetic abnormalities. Therefore, the introducing of the cytogenetic analysis is obligatory in the diagnosis of multiple myeloma.

Indexed as

Abnormal KaryotypeAdultAgedAged, 80 and overChromosome DeletionChromosome DuplicationFemaleHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedMultiple MyelomaTranslocation, Geneticconventional karyotypecytogeneticFISHmultiple myelomaplasma cells sorted

Identifiers

PMID32573970
PMCPMC7507047
OpenAlexW3037394792

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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.