Evidence map›Paper›PMID 40613022›Full record

ArticleCureus2025

Outcomes in Patients With Multiple Myeloma and Prescribed Urate-Lowering Therapy: A Propensity-Matched Study.

Sarah Eidbo, Maxim Barnett, Diego Lema Rodriguez, Nanuka Tsibadze, Alexander Pappas, Mohibur Shah, Abhishek Shah, Ryan Mayo

Abstract read
In one paragraph

Article in Cureus, 2025. 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

8 authors.

Sarah EidboInternal Medicine, Jefferson Einstein Philadelphia Hospital, Philadelphia, USA.
Maxim BarnettInternal Medicine, Jefferson Einstein Philadelphia Hospital, Philadelphia, USA.
Diego Lema RodriguezInternal Medicine, Jefferson Einstein Philadelphia Hospital, Philadelphia, USA.
Nanuka TsibadzeInternal Medicine, Einstein Healthcare Network, Philadelphia, USA.
Alexander PappasInternal Medicine, Jefferson Einstein Philadelphia Hospital, Philadelphia, USA.
Mohibur ShahInternal Medicine, Jefferson Einstein Philadelphia Hospital, Philadelphia, USA.
Abhishek ShahInternal Medicine, Jefferson Einstein Philadelphia Hospital, Philadelphia, USA.
Ryan MayoHematology and Oncology, Jefferson Einstein Philadelphia Hospital, Philadelphia, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Multiple myeloma or MM is a plasma cell dyscrasia that causes monoclonal immunoglobulin accumulation and is associated with manifestations including hypercalcemia, anemia, bone pain, and renal dysfunction. Gout is also associated with electrolyte derangements that result in similar end-organ dysfunction. There is little information on outcomes in patients with both diagnoses. Methods Adult patients with MM were propensity-score matched according to age at index event, sex, demographics, and comorbidities. Patients were identified using the International Classification of Diseases (ICD)-10 codes through TriNetX's US Collaborative Network and sorted into cohorts based on the prescription of urate-lowering therapies (ULTs). Three ULTs, allopurinol, febuxostat, and rasburicase, were studied individually. Cohorts of patients with MM and any ULT and those with MM but no ULT were also included. Outcomes were followed for five years to assess the rates of acute kidney injury (AKI), dialysis initiation (HD), seizures, atrial fibrillation/atrial flutter (AF/AFL), ventricular fibrillation/ventricular tachycardia (VF/VT), and all-cause mortality.  Results When compared to patients with MM with any ULT, the cohort of patients with MM and no ULT demonstrated significantly lower rates of HD (HR 0.74, 95% CI 0.671-0.815, p<0.0001), AF/AFL (HR 0.99, 95% CI 0.924-1.061, p<0.0001), VF/VT (HR 0.853, 95% CI 0.752-0.968, p=0.0066), and mortality (HR 1.012, 95% CI 0.965-1.065, p<0.0001). The MM with no allopurinol group demonstrated significantly reduced rates of AKI (HR 0.901, 95% CI 0.839-0.968, p=0.0007), HD (HR 0.715, 95% CI 0.633-0.807, p<0.0001), seizures (HR 1.029, 95% CI 0.868-1.219, p=0.0012), AF/AFL (HR 1.006, 95% CI 0.921-1.098, p<0.0001), VF/VT (HR 0.837, 95% CI 0.718-0.975, p=0.0024), and mortality (HR 0.919, 95% CI 0.868-0.974, p<0.0001) compared to the MM with allopurinol cohort. The MM with no febuxostat cohort showed significantly reduced rates of AF/AFL (HR 1.009, 95% CI 0.762-1.335, p=0.004) compared to the MM cohort with febuxostat. The MM with no rasburicase cohort had significantly reduced risk of AF/AFL (HR 0.861, 95% CI 0.582-1.275, p=0.0381) compared to the MM with rasburicase cohort.  Conclusion ULTs may increase the risk of requiring HD, developing cardiac arrhythmia, and potentially mortality in patients with MM. There appear to be some ULT-specific relationships that warrant further exploration. These findings could be related to the electrolyte disturbances and end-organ dysfunction of MM being compounded by those of gout. Further research should be conducted to elucidate any relationship between these diagnoses.

Indexed as

databasegoutmultiple myelomatrinetxurate lowering therapy

Identifiers

PMID40613022
PMCPMC12225964

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.