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

Publication ,  Journal Article
Garrett, ME; Le, B; Bourassa, KJ; Dennis, MF; Hatch, D; Yang, Q; Tanabe, P; Shah, N; Luyster, FS; Oyedeji, C; Strouse, JJ; Cohen, HJ ...
Published in: J Gerontol A Biol Sci Med Sci
November 1, 2024

BACKGROUND: Sickle 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. METHODS: We utilized the DunedinPACE measure to compare the epigenetic pace of aging in 131 Black Americans with SCD to 1391 Black American veterans without SCD. RESULTS: SCD 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). CONCLUSIONS: These 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.

Duke Scholars

Patrick Shields Calhoun
Author Patrick Shields Calhoun Psychiatry & Behavioral Sciences, Behavioral Medicine & Neur ...
Rajendra A. Morey
Author Rajendra A. Morey Psychiatry, Child & Family Mental Health & Community Psychia ...
Jennifer C. Naylor
Author Jennifer C. Naylor Psychiatry, Child & Family Mental Health & Community Psychia ...
Eric Bradley Elbogen
Author Eric Bradley Elbogen Psychiatry & Behavioral Sciences, Behavioral Medicine & Neur ...
Jason David Kilts
Author Jason David Kilts Psychiatry, Child & Family Mental Health & Community Psychia ...
Scott Daniel Moore
Author Scott Daniel Moore Psychiatry & Behavioral Sciences, Adult Psychiatry & Psychol ...
Elizabeth E. Van Voorhees
Author Elizabeth E. Van Voorhees Psychiatry & Behavioral Sciences, Behavioral Medicine & Neur ...
Henry Ryan Wagner II
Author Henry Ryan Wagner II Psychiatry, Child & Family Mental Health & Community Psychia ...
Eric Dedert
Author Eric Dedert Psychiatry & Behavioral Sciences, Behavioral Medicine & Neur ...
Christine Elizabeth Marx
Author Christine Elizabeth Marx Psychiatry, Child & Family Mental Health & Community Psychia ...
Mitchell Knisely
Author Mitchell Knisely School of Nursing
Charity Oyedeji
Author Charity Oyedeji Medicine, Hematology
Marilyn Jo Telen
Author Marilyn Jo Telen Medicine, Hematology
Nirmish Ramesh Shah
Author Nirmish Ramesh Shah Medicine, Hematology
Paula J Tanabe
Author Paula J Tanabe School of Nursing
Qing Yang
Author Qing Yang School of Nursing
Jean Crowell Beckham
Author Jean Crowell Beckham Psychiatry & Behavioral Sciences, Behavioral Medicine & Neur ...
Harvey Jay Cohen
Author Harvey Jay Cohen Medicine, Geriatrics and Palliative Care
Nathan Andrew Kimbrel
Author Nathan Andrew Kimbrel Psychiatry & Behavioral Sciences, Behavioral Medicine & Neur ...
John J. Strouse
Author John J. Strouse Medicine, Hematology
Kyle Bourassa
Author Kyle Bourassa  
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Published In

J Gerontol A Biol Sci Med Sci

DOI

EISSN

1758-535X

Publication Date

November 1, 2024

Volume

79

Issue

11

Location

United States

Related Subject Headings

  • Veterans
  • United States
  • Middle Aged
  • Male
  • Humans
  • Gerontology
  • Female
  • Epigenesis, Genetic
  • Black or African American
  • Anemia, Sickle Cell
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Garrett, M. E., Le, B., Bourassa, K. J., Dennis, M. F., Hatch, D., Yang, Q., … VA Mid-Atlantic MIRECC Workgroup. (2024). Black Americans With Sickle Cell Disease (SCD) Demonstrate Accelerated Epigenetic Pace of Aging Compared to Black Americans Without SCD. J Gerontol A Biol Sci Med Sci, 79(11). https://doi.org/10.1093/gerona/glae230
Garrett, Melanie E., Brandon Le, Kyle J. Bourassa, Michelle F. Dennis, Daniel Hatch, Qing Yang, Paula Tanabe, et al. “Black Americans With Sickle Cell Disease (SCD) Demonstrate Accelerated Epigenetic Pace of Aging Compared to Black Americans Without SCD.J Gerontol A Biol Sci Med Sci 79, no. 11 (November 1, 2024). https://doi.org/10.1093/gerona/glae230.
Garrett ME, Le B, Bourassa KJ, Dennis MF, Hatch D, Yang Q, et al. Black Americans With Sickle Cell Disease (SCD) Demonstrate Accelerated Epigenetic Pace of Aging Compared to Black Americans Without SCD. J Gerontol A Biol Sci Med Sci. 2024 Nov 1;79(11).
Garrett, Melanie E., et al. “Black Americans With Sickle Cell Disease (SCD) Demonstrate Accelerated Epigenetic Pace of Aging Compared to Black Americans Without SCD.J Gerontol A Biol Sci Med Sci, vol. 79, no. 11, Nov. 2024. Pubmed, doi:10.1093/gerona/glae230.
Garrett ME, Le B, Bourassa KJ, Dennis MF, Hatch D, Yang Q, Tanabe P, Shah N, Luyster FS, Oyedeji C, Strouse JJ, Cohen HJ, Kimbrel NA, Beckham JC, Knisely MR, Telen MJ, Ashley-Koch AE, VA Mid-Atlantic MIRECC Workgroup. Black Americans With Sickle Cell Disease (SCD) Demonstrate Accelerated Epigenetic Pace of Aging Compared to Black Americans Without SCD. J Gerontol A Biol Sci Med Sci. 2024 Nov 1;79(11).
Journal cover image

Published In

J Gerontol A Biol Sci Med Sci

DOI

EISSN

1758-535X

Publication Date

November 1, 2024

Volume

79

Issue

11

Location

United States

Related Subject Headings

  • Veterans
  • United States
  • Middle Aged
  • Male
  • Humans
  • Gerontology
  • Female
  • Epigenesis, Genetic
  • Black or African American
  • Anemia, Sickle Cell