Evidence map›Paper›PMID 27578511›Full record

ArticleAnnals of laboratory medicine2016

Abnormalities in Chromosomes 1q and 13 Independently Correlate With Factors of Poor Prognosis in Multiple Myeloma.

Miyoung Kim, Young Su Ju, Eun Jin Lee, Hee Jung Kang, Han Sung Kim, Hyoun Chan Cho, Hyo Jung Kim, Jung Ah Kim, Dong Soon Lee, Young Kyung Lee

Open access · diamondAbstract read
In one paragraph

Article in Annals of laboratory medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 30% of its field
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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Establishment and Validation for Predicting the Death of Multiple Myeloma among Whites.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  3. Article
  4. Article
  5. 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

10 authors at 2 institutions in 1 country.

Miyoung KimDepartment of Laboratory Medicine, Hallym University College of Medicine, Anyang, Korea.
Young Su JuDepartment of Occupational and Environmental Medicine, Hallym University College of Medicine, Anyang, Korea.
Eun Jin LeeDepartment of Laboratory Medicine, Hallym University College of Medicine, Anyang, Korea.
Hee Jung KangDepartment of Laboratory Medicine, Hallym University College of Medicine, Anyang, Korea.
Han Sung KimDepartment of Laboratory Medicine, Hallym University College of Medicine, Anyang, Korea.
Hyoun Chan ChoDepartment of Laboratory Medicine, Hallym University College of Medicine, Anyang, Korea.
Hyo Jung KimDepartment of Internal Medicine, Hallym University College of Medicine, Anyang, Korea.
Jung Ah KimDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Dong Soon LeeDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Young Kyung LeeDepartment of Laboratory Medicine, Hallym University College of Medicine, Anyang, Korea. lyoungk@hallym.or.kr.
Hallym University · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe comprehensively profiled cytogenetic abnormalities in multiple myeloma (MM) and analyzed the relationship between cytogenetic abnormalities of undetermined prognostic significance and established prognostic factors.

methodsThe karyotype of 333 newly diagnosed MM cases was analyzed in association with established prognostic factors. Survival analysis was also performed.

resultsMM with abnormal karyotypes (41.1%) exhibited high international scoring system (ISS) stage, frequent IgA type, elevated IgG or IgA levels, elevated calcium levels, elevated creatine (Cr) levels, elevated β2-microglobulin levels, and decreased Hb levels. Structural abnormalities in chromosomes 1q, 4, and 13 were independently associated with elevated levels of IgG or IgA, calcium, and Cr, respectively. Chromosome 13 abnormalities were associated with poor prognosis and decreased overall survival.

conclusionsThis is the first study to demonstrate that abnormalities in chromosomes 1q, 4, and 13 are associated with established factors for poor prognosis, irrespective of the presence of other concurrent chromosomal abnormalities. Chromosome 13 abnormalities have a prognostic impact on overall survival in association with elevated Cr levels. Frequent centromeric breakpoints appear to be related to MM pathogenesis.

Indexed as

Chromosome AberrationsAdolescentAdultAgedAged, 80 and overCalciumChromosomes, Human, Pair 1Chromosomes, Human, Pair 13Chromosomes, Human, Pair 4CreatineFemaleHemoglobinsHumansImmunoglobulin AImmunoglobulin GKaryotypingCalciumCreatineHemoglobinsImmunoglobulin AImmunoglobulin GChromosomeMyelomaPrognosis

Identifiers

PMID27578511
PMCPMC5011111
OpenAlexW2515013642

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.