Evidence map›Paper›PMID 41926751›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2026

Frailty phenotype in adults with sickle cell disease.

Charity I Oyedeji, Rania E Mohamed, Richard Faldowski, Teagan Callaway, Tamara Poole, Francyess Denis Oliva, Veronica Mathis, Arvind Subramaniam, Heather Whitson, Bryce B Reeve and 6 more

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

16 authors.

Charity I OyedejiDepartment of Medicine, Division of Hematology, Duke University School of Medicine, Durham, North Carolina, United States.ORCID 0000-0001-5179-7142
Rania E MohamedDepartment of Medicine, Division of Hematology, Duke University School of Medicine, Durham, North Carolina, United States.
Richard FaldowskiCenter for the Study of Aging and Human Development, Duke University School of Medicine, Durham, North Carolina, United States.
Teagan CallawayDepartment of Medicine, Division of Hematology, Duke University School of Medicine, Durham, North Carolina, United States.
Tamara PooleSchool of Nursing, Duke University, Durham, North Carolina, United States.
Francyess Denis OlivaSchool of Medicine, Duke University, Durham, North Carolina, United States.
Veronica MathisIndependent Consultant, Department of Medicine, Duke University, Durham, NC, United States.
Arvind SubramaniamBrody School of Medicine, East Carolina University, Greenville, North Carolina, United States.
Heather WhitsonClaude D. Pepper Older Americans Independence Center, Duke University, Durham, North Carolina, United States.ORCID 0000-0002-8417-4846
Bryce B ReeveDepartment of Population Health Sciences, Duke University School of Medicine, Durham, North Carolina, United States.
Carl PieperClaude D. Pepper Older Americans Independence Center, Duke University, Durham, North Carolina, United States.ORCID 0000-0003-4809-1725
Marilyn J TelenDepartment of Medicine, Division of Hematology, Duke University School of Medicine, Durham, North Carolina, United States.
Allison Ashley-KochDepartment of Medicine, Division of Hematology, Duke University School of Medicine, Durham, North Carolina, United States.
Harvey J CohenClaude D. Pepper Older Americans Independence Center, Duke University, Durham, North Carolina, United States.
Katherine HallClaude D. Pepper Older Americans Independence Center, Duke University, Durham, North Carolina, United States.ORCID 0000-0002-9834-2011
John J StrouseDepartment of Medicine, Division of Hematology, Duke University School of Medicine, Durham, North Carolina, United States.ORCID 0000-0003-0341-1457

Funding

Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI CATHLEEN S COLON-EMERIC, Susan Nicole Hastings · 2006 to 2026
$24.6M
PRIDE: Functional and Translational Genomics of Blood DisordersR25HL106365 · NHLBI · AUGUSTA UNIVERSITY · PI PACE, BETTY SUE · 2010 to 2024
$5.2M
Sickle Cell Disease Functional Assessment Validation and Exercise Pilot InterventionK01HL166369 · NHLBI · DUKE UNIVERSITY · PI OYEDEJI, CHARITY IBILOLA · 2023 to 2024
$397k
Characterizing Frailty in Older Adults with Sickle Cell Disease Using a Sickle Cell Frailty Index (FI-SCD)R03AG074054 · NIA · DUKE UNIVERSITY · PI OYEDEJI, CHARITY IBILOLA · 2021 to 2022
$322k
NHLBI NIH HHS K01 HL166369NHLBI NIH HHS R25 HL106365NIA NIH HHS P30 AG028716NIA NIH HHS R03 AG074054
6 · The paper itself

Abstract

backgroundPeople with sickle cell disease (SCD) are at risk for accelerated biological aging and functional decline due to both age and SCD-related stressors. Frailty is characterized by decreased physiologic reserve and increased vulnerability to stressors that can lead to disability and death. The purpose of this study was to evaluate frailty phenotype in adults with SCD and identify factors associated with frailty.

methodsFrailty was defined by meeting ≥3 of the following criteria: slowness, weakness, weight loss, low physical activity, and exhaustion. Participants meeting 1-2 criteria were prefrail and "robust" if no criteria were present.

resultsWe analyzed frailty in 137 adults (age ≥ 18) with SCD in a single-center cross-sectional study (mean age 45; range 19-82). Three (2%) participants were frail, 47% prefrail, and 51% robust. Compared to robust, frail/prefrail participants were more likely to have emergency department visits in the past year (66% vs 46%; p < .02), hypertension (42% vs 19%; p < .003), diabetes (16% vs 4%; p < .02), more SCD complications (2.8 vs 2.1; p < .02), and significantly worse socioeconomic status, cognitive function, depression, physical function, and disability in activities of daily living.

conclusionsThe prevalence of prefrailty in this sample of young and predominantly middle-aged adults with SCD was similar to older adults in the general population, further supporting that accelerated aging occurs in this population and emphasizing the need for early identification and initiation of interventions to prevent and attenuate frailty in SCD. In future studies, we will evaluate SCD-specific cutpoints for frailty components that predict clinically meaningful outcomes.

Indexed as

Anemia, Sickle CellFrailtyAdultAgedAged, 80 and overCross-Sectional StudiesFemaleHumansMaleMiddle AgedPhenotypeRisk FactorsYoung AdultBloodFrailtyMinority agingPhysical functionSickle cell anemia

Identifiers

PMID41926751
PMCPMC13118487

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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.