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Epigenetic Aging Associations With Psychoneurological Symptoms and Social Functioning in Adults With Sickle Cell Disease.

Publication ,  Journal Article
Knisely, MR; Masese, RV; Mathias, JG; Yang, Q; Hatch, D; Lê, BM; Luyster, F; Garrett, ME; Tanabe, PJ; Shah, NR; Ashley-Koch, A
Published in: Biol Res Nurs
October 2024

Objective: Sickle cell disease (SCD), the most common inherited blood disorder in the United States, is associated with severe psychoneurological symptoms. While epigenetic age acceleration has been linked to psychoneurological symptom burden in other diseases, this connection is unexplored in SCD. This study aimed to assess the association between epigenetic age acceleration and psychoneurological symptom burden in SCD. Methods: In this cross-sectional study, emotional impact, pain impact, sleep impact, social functioning, and cognitive function were assessed in 87 adults living with SCD. DNA methylation data were generated from blood specimens and used to calculate epigenetic age using five clocks (Horvath, Hannum, PhenoAge, GrimAge, & DunedinPACE). Associations between epigenetic age acceleration and symptoms were assessed. Results: The sample (N = 87) had a mean (SD) chronologic age was 30.6 (8.1) years. Epigenetic age acceleration was associated with several symptom outcomes. GrimAge age acceleration (β = -0.49, p = .03) and increased DunedinPACE (β = -2.23, p = .004) were associated with worse emotional impact scores. PhenoAge (β = -0.32, p = .04) and the GrimAge (β = -0.48, p = .05) age acceleration were associated with worse pain impact scores. Increased DunedinPACE (β = -2.07 p = .04) were associated with worse sleep impact scores. Increased DunedinPACE (β = -2.87, p = .005) was associated with worse social functioning scores. We did not find associations between epigenetic age acceleration and cognitive function in this sample. Conclusion: Epigenetic age acceleration was associated with worse symptom experiences, suggesting the potential for epigenetic age acceleration as a biomarker to aid in risk stratification or targets for intervention to mitigate symptom burden in SCD.

Duke Scholars

Published In

Biol Res Nurs

DOI

EISSN

1552-4175

Publication Date

October 2024

Volume

26

Issue

4

Start / End Page

508 / 517

Location

United States

Related Subject Headings

  • Nursing
  • Middle Aged
  • Male
  • Humans
  • Female
  • Epigenesis, Genetic
  • Cross-Sectional Studies
  • Anemia, Sickle Cell
  • Aging
  • Adult
 

Citation

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ICMJE
MLA
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Knisely, M. R., Masese, R. V., Mathias, J. G., Yang, Q., Hatch, D., Lê, B. M., … Ashley-Koch, A. (2024). Epigenetic Aging Associations With Psychoneurological Symptoms and Social Functioning in Adults With Sickle Cell Disease. Biol Res Nurs, 26(4), 508–517. https://doi.org/10.1177/10998004241250322
Knisely, Mitchell R., Rita V. Masese, Joacy G. Mathias, Qing Yang, Daniel Hatch, Brandon M. Lê, Faith Luyster, et al. “Epigenetic Aging Associations With Psychoneurological Symptoms and Social Functioning in Adults With Sickle Cell Disease.Biol Res Nurs 26, no. 4 (October 2024): 508–17. https://doi.org/10.1177/10998004241250322.
Knisely MR, Masese RV, Mathias JG, Yang Q, Hatch D, Lê BM, et al. Epigenetic Aging Associations With Psychoneurological Symptoms and Social Functioning in Adults With Sickle Cell Disease. Biol Res Nurs. 2024 Oct;26(4):508–17.
Knisely, Mitchell R., et al. “Epigenetic Aging Associations With Psychoneurological Symptoms and Social Functioning in Adults With Sickle Cell Disease.Biol Res Nurs, vol. 26, no. 4, Oct. 2024, pp. 508–17. Pubmed, doi:10.1177/10998004241250322.
Knisely MR, Masese RV, Mathias JG, Yang Q, Hatch D, Lê BM, Luyster F, Garrett ME, Tanabe PJ, Shah NR, Ashley-Koch A. Epigenetic Aging Associations With Psychoneurological Symptoms and Social Functioning in Adults With Sickle Cell Disease. Biol Res Nurs. 2024 Oct;26(4):508–517.
Journal cover image

Published In

Biol Res Nurs

DOI

EISSN

1552-4175

Publication Date

October 2024

Volume

26

Issue

4

Start / End Page

508 / 517

Location

United States

Related Subject Headings

  • Nursing
  • Middle Aged
  • Male
  • Humans
  • Female
  • Epigenesis, Genetic
  • Cross-Sectional Studies
  • Anemia, Sickle Cell
  • Aging
  • Adult