Evidence map›Paper›PMID 40935825›Full record

ArticleLeukemia2025

Estimating the burden of chronic stress through allostatic load in patients with chronic myeloid leukemia.

Marisol Miranda-Galvis, Kellen C Tjioe, Muhannad Sharara, McKenzie Maloney, Amany R Keruakous, Anand Jillella, Vamsi Kota, Avirup Guha, Jorge E Cortes

Abstract read
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In one paragraph

Article in Leukemia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

9 authors.

Marisol Miranda-GalvisGeorgia Cancer Center, Augusta University, Augusta, GA, USA.ORCID 0000-0003-4798-584X
Kellen C TjioeGeorgia Cancer Center, Augusta University, Augusta, GA, USA.ORCID 0000-0003-4145-0684
Muhannad ShararaGeorgia Cancer Center, Augusta University, Augusta, GA, USA.ORCID 0000-0002-2840-5646
McKenzie MaloneyMedical College of Georgia, Augusta University, Augusta, GA, USA.
Amany R KeruakousGeorgia Cancer Center, Augusta University, Augusta, GA, USA.
Anand JillellaGeorgia Cancer Center, Augusta University, Augusta, GA, USA.
Vamsi KotaGeorgia Cancer Center, Augusta University, Augusta, GA, USA.ORCID 0000-0002-5290-9289
Avirup GuhaCardio-Oncology Program, Medical College of Georgia at Augusta University, Augusta, GA, USA.ORCID 0000-0003-0253-1174
Jorge E CortesGeorgia Cancer Center, Augusta University, Augusta, GA, USA. jorge.cortes@augusta.edu.ORCID 0000-0002-8636-1071

Funding

American Heart Association (American Heart Association, Inc.) #847740, #863620U.S. Department of Defense (United States Department of Defense) HT94252310158
6 · The paper itself

Abstract

Despite advances in tyrosine kinase inhibitor (TKI) therapy, outcomes in chronic myeloid leukemia remain (CML) highly variable, underscoring the need to explore determinants beyond conventional clinical indicators. This study examined the relationship between allostatic load (AL), a biomarker-based index of cumulative chronic stress, social determinants of health (SDH), and treatment outcomes. In a retrospective cohort of 194 patients, AL was calculated using 23 biomarkers spanning cardiovascular, metabolic, hematologic, renal, and hepatic systems. Higher AL was associated with adverse SDH and behavioral factors, including greater extreme poverty (p = 0.02), limited transportation access (p = 0.02), reliance on public health coverage (p = 0.03), and physical inactivity (p = 0.05). Each unit increase in AL reduced the odds of achieving optimal molecular response by 18% (p = 0.02). All 11 disease progressions to advanced CML and all 9 deaths occurred in the high AL group, who also had higher rates of composite adverse events, including loss of molecular response, TKI failure, disease progression, and mortality (p = 0.03). These findings position AL as a promising integrative biomarker to identify high-risk patients facing combined physiological stress burden and social disadvantage, enabling oncology practices to refine risk stratification and implement personalized, multidisciplinary interventions.

Indexed as

AllostasisLeukemia, Myelogenous, Chronic, BCR-ABL PositiveStress, PsychologicalAdultAgedDisease ProgressionFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisProtein Kinase InhibitorsRetrospective StudiesProtein Kinase Inhibitors

Identifiers

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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.