Evidence map›Paper›PMID 42464613›Full record

SynthesisCancer2026

Excess risk for cardiovascular and noncardiovascular comorbidities and multimorbidity among patients with myelodysplastic syndrome: A systematic review and meta-analysis.

Konstantinos Liapis, Vasileios Papadopoulos, Iliana Stamatiou, Dimitrios Koparanis, Lydia Inglezou, Emmanouil Panagiotopoulos, Bouse Malkots, Georgios Vrachiolias, Theodoros Spyropoulos, Ioannis Kotsianidis

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Konstantinos LiapisDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.
Vasileios PapadopoulosLaboratory of Anatomy, Democritus University of Thrace School of Medicine, Alexandroupolis, Greece.
Iliana StamatiouDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.ORCID https://orcid.org/0009-0007-6458-8201
Dimitrios KoparanisDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.
Lydia InglezouDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.
Emmanouil PanagiotopoulosDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.
Bouse MalkotsDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.ORCID https://orcid.org/0009-0007-0156-9484
Georgios VrachioliasDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.
Theodoros SpyropoulosDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.
Ioannis KotsianidisDepartment of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The authors performed a systematic review and meta-analysis to estimate the prevalence of comorbidities among patients with myelodysplastic syndrome (MDS) by pooling results from 28 studies and 71,400 patients. In conducting this research, the authors observed that individuals with MDS have a high rate of cardiovascular disease that is 6.2 times greater than that in the general population. A remarkably high prevalence of heart failure (between 10.4% and 18.6%) was observed, indicating that heart failure is a major issue that warrants urgent attention in MDS. The prevalence of chronic kidney disease, chronic liver disease, and solid tumors was also higher in patients with MDS. The results of this analysis indicate a much higher prevalence of multimorbidity in patients who have MDS compared with the general population (79.1% vs. 63.4%; p < .0001). Furthermore, the data demonstrate that the association between MDS and noncommunicable diseases remains strong in both high-income and low-income regions, the comorbidity burden increases with higher scores on the revised International Prognostic Scoring System, patients with multimorbidity are twice as likely to die as those without multimorbidity, and a high burden of comorbidities emerges as a common problem in MDS, occurring in 35% of patients. These findings suggest that a focus on multimorbidity and a holistic, multidisciplinary, and patient-centered approach to address the challenge of common chronic diseases could significantly improve outcomes for patients with MDS.

Indexed as

Cardiovascular DiseasesMultimorbidityMyelodysplastic SyndromesComorbidityHeart FailureHumansNeoplasmsPrevalenceRenal Insufficiency, ChronicRisk Factorsage‐related diseasescardiovascular diseasesclonal hematopoiesis of indeterminate potential (CHIP)comorbiditiesmultimorbiditymyelodysplastic neoplasms (MDS)

Identifiers

PMID42464613
PMCPMC13377009

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.