Evidence map›Paper›PMID 39297703›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2024

Black Americans With Sickle Cell Disease (SCD) Demonstrate Accelerated Epigenetic Pace of Aging Compared to Black Americans Without SCD.

Melanie E Garrett, Brandon Le, Kyle J Bourassa, Michelle F Dennis, Daniel Hatch, Qing Yang, Paula Tanabe, Nirmish Shah, Faith S Luyster, Charity Oyedeji and 8 more

Abstract readComparative Study
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Frailty phenotype in adults with sickle cell disease.The journals of gerontology. Series A, Biological sciences and medical sciences · 2026
    Article
  5. Chronic pain in the aging adult with sickle cell disease.Frontiers in pain research (Lausanne, Switzerland) · 2026
    Review
  6. Review
  7. 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

18 authors.

Melanie E GarrettDuke Molecular Physiology Institute, Duke University Medical Center, Durham, North Carolina, USA.ORCID 0000-0003-2302-6150
Brandon LeDuke Molecular Physiology Institute, Duke University Medical Center, Durham, North Carolina, USA.
Kyle J BourassaVA Mid-Atlantic Mental Illness Research, Education, and Clinical Center, Durham VA Health Care System, Durham, North Carolina, USA.
Michelle F DennisVA Mid-Atlantic Mental Illness Research, Education, and Clinical Center, Durham VA Health Care System, Durham, North Carolina, USA.
Daniel HatchDuke University School of Nursing, Durham, North Carolina, USA.
Qing YangDuke University School of Nursing, Durham, North Carolina, USA.
Paula TanabeDuke University School of Nursing, Durham, North Carolina, USA.
Nirmish ShahDivision of Hematology, Department of Medicine, and Duke Comprehensive Sickle Cell Center, Duke University Medical Center, Durham, North Carolina, USA.
Faith S LuysterSchool of Nursing, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Charity OyedejiDivision of Hematology, Department of Medicine, and Duke Comprehensive Sickle Cell Center, Duke University Medical Center, Durham, North Carolina, USA.
John J StrouseDivision of Hematology, Department of Medicine, and Duke Comprehensive Sickle Cell Center, Duke University Medical Center, Durham, North Carolina, USA.
Harvey J CohenCenter for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina, USA.
Nathan A KimbrelVA Mid-Atlantic Mental Illness Research, Education, and Clinical Center, Durham VA Health Care System, Durham, North Carolina, USA.
Jean C BeckhamVA Mid-Atlantic Mental Illness Research, Education, and Clinical Center, Durham VA Health Care System, Durham, North Carolina, USA.
Mitchell R KniselyDuke University School of Nursing, Durham, North Carolina, USA.
Marilyn J TelenDivision of Hematology, Department of Medicine, and Duke Comprehensive Sickle Cell Center, Duke University Medical Center, Durham, North Carolina, USA.
Allison E Ashley-KochDuke Molecular Physiology Institute, Duke University Medical Center, Durham, North Carolina, USA.
VA Mid-Atlantic MIRECC Workgroup

Funding

Support for QA/QC for Prior Approval ProcessUL1TR002553 · NCATS · DUKE UNIVERSITY · PI LI, JENNIFER S, MCNAMARA, JAMES O. · 2018 to 2023
$58.5M
Pulmonary Hypertension in SCDR01HL079915 · NHLBI · DUKE UNIVERSITY · PI TELEN, MARILYN J · 2005 to 2008
$6.7M
Improving SCD Care using Web-based Guidelines, Nurse Care Managers and Peer Mentors in Primary Care and Emergency Departments in Central North CarolinaU01HL133964 · NHLBI · DUKE UNIVERSITY · PI SHAH, NIRMISH R, TANABE, PAULA · 2016 to 2021
$4.8M
Outcome Modifying Genes in Sickle Cell DiseaseR01HL068959 · NHLBI · DUKE UNIVERSITY · PI TELEN, MARILYN J · 2001 to 2005
$3.6M
Genetics and Genomics Training GrantT32GM136627 · NIGMS · DUKE UNIVERSITY · PI ALLISON E ASHLEY-KOCH · 2020 to 2026
$3.1M
Epigenetic Age Acceleration and Psychoneurological Symptoms in Sickle Cell DiseaseR21NR020017 · NINR · DUKE UNIVERSITY · PI ASHLEY-KOCH, ALLISON E, KNISELY, MITCHELL ROBERT · 2022 to 2023
$443k
Genetic and Epigenetic Dissection of PTSD in African American VeteransI01BX002577 · VA · DURHAM VA MEDICAL CENTER · PI BECKHAM, JEAN C. · 2015 to 2018
–
Gene x Environment Effects on PTSDIK2CX000525 · VA · OLIN TEAGUE VETERANS CENTER · PI KIMBREL, NATHAN A. · 2012 to 2016
–
Biomedical Laboratory Research and Development (BLR&D) Service I01BX002577BLRD VA I01 BX002577Clinical Science Research and Development (CSR&D) Service of VA ORD IK2CX002694CSRD VA IK2 CX000525CSRD VA IK2 CX002694CSRD VA IK6 CX002767Department of Psychiatry and Behavioral Sciences at the Duke University School of MedicineDurham VA Geriatrics Research, Education, and Clinical CenterMental Health and Research Services of the Durham VA Healthcare SystemNational Center for Advancing Translational Sciences of the National Institutes of Health UL1TR002553NCATS NIH HHS UL1 TR002553NHLBI NIH HHS R01 HL068959NHLBI NIH HHS R01 HL079915NHLBI NIH HHS R01HL68959NHLBI NIH HHS U01 HL133964NIGMS NIH HHS T32 GM136627NINR NIH HHS R21 NR020017NINR NIH HHS R21NR020017VA Mid-Atlantic Mental Illness Research, Education and Clinical Center
6 · The paper itself

Abstract

backgroundSickle cell disease (SCD) is a chronic medical condition characterized by red blood cell sickling, vaso-occlusion, hemolytic anemia, and subsequently, end-organ damage and reduced survival. Because of this significant pathophysiology and early mortality, we hypothesized that patients with SCD are experiencing accelerated biological aging compared with individuals without SCD.

methodsWe utilized the DunedinPACE measure to compare the epigenetic pace of aging in 131 Black Americans with SCD to 1391 Black American veterans without SCD.

resultsSCD patients displayed a significantly accelerated pace of aging (DunedinPACE mean difference of 0.057 points) compared with the veterans without SCD, whereby SCD patients were aging ≈0.7 months more per year than those without SCD (p = 4.49 × 10-8). This was true, even though the SCD patients were significantly younger according to chronological age than the individuals without SCD, making the epigenetic aging discrepancy even more apparent. This association became stronger when we removed individuals with posttraumatic stress disorder from the non-SCD group (p = 2.18 × 10-9), and stronger still when we restricted the SCD patients to those with hemoglobin SS and Sβ0 thalassemia genotypes (p = 1.61 × 10-10).

conclusionsThese data support our hypothesis that individuals with SCD experience accelerated biological aging as measured by global epigenetic variation. The assessment of epigenetic measures of biological aging may prove useful to identify which SCD patients would most benefit from clinical interventions to reduce mortality.

Indexed as

AgingAnemia, Sickle CellBlack or African AmericanEpigenesis, GeneticAdultAgedFemaleHumansMaleMiddle AgedUnited StatesVeteransChronic disease pathologyDNA methylationHemoglobinopathy

Identifiers

PMID39297703
PMCPMC11511909

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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.