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Sleep Quality Following Hematopoietic Stem Cell Transplantation: Longitudinal Trajectories and Biobehavioral Correlates

The present study examined changes in sleep quality following hematopoietic stem cell transplantation (HSCT) and investigated associations with biobehavioral factors. Individuals undergoing HSCT for hematologic malignancies (N=228) completed measures of sleep quality and psychological symptoms pre-t...

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Autores principales: Nelson, Ashley M., Coe, Christopher L., Juckett, Mark B., Rumble, Meredith E., Rathouz, Paul J., Hematti, Peiman, Costanzo, Erin S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221490/
https://www.ncbi.nlm.nih.gov/pubmed/25133898
http://dx.doi.org/10.1038/bmt.2014.179
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author Nelson, Ashley M.
Coe, Christopher L.
Juckett, Mark B.
Rumble, Meredith E.
Rathouz, Paul J.
Hematti, Peiman
Costanzo, Erin S.
author_facet Nelson, Ashley M.
Coe, Christopher L.
Juckett, Mark B.
Rumble, Meredith E.
Rathouz, Paul J.
Hematti, Peiman
Costanzo, Erin S.
author_sort Nelson, Ashley M.
collection PubMed
description The present study examined changes in sleep quality following hematopoietic stem cell transplantation (HSCT) and investigated associations with biobehavioral factors. Individuals undergoing HSCT for hematologic malignancies (N=228) completed measures of sleep quality and psychological symptoms pre-transplant and 1, 3, 6, and 12 months post-transplant. Circulating inflammatory cytokines (IL-6, TNF-α) were also assessed. Sleep quality was poorest at one month post-transplant, improving and remaining relatively stable after 3 months post-transplant. However, approximately half of participants continued to experience significant sleep disturbance at 6 and 12 months post-transplant. Mixed-effects linear regression models indicated that depression and anxiety were associated with poorer sleep quality, while psychological well-being was associated with better sleep. Higher circulating levels of IL-6 were also linked with poorer sleep. Subject-level fixed effects models demonstrated that among individual participants, changes in depression, anxiety, and psychological well-being were associated with corresponding changes in sleep after covarying for the effects of time since transplant. Sleep disturbance was most severe when depression and anxiety were greatest, and psychological well-being was lowest. Findings indicate that sleep disturbance is a persistent problem during the year following HSCT. Patients experiencing depression or anxiety and those with elevated inflammation may be at particular risk for poor sleep.
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spelling pubmed-42214902015-05-01 Sleep Quality Following Hematopoietic Stem Cell Transplantation: Longitudinal Trajectories and Biobehavioral Correlates Nelson, Ashley M. Coe, Christopher L. Juckett, Mark B. Rumble, Meredith E. Rathouz, Paul J. Hematti, Peiman Costanzo, Erin S. Bone Marrow Transplant Article The present study examined changes in sleep quality following hematopoietic stem cell transplantation (HSCT) and investigated associations with biobehavioral factors. Individuals undergoing HSCT for hematologic malignancies (N=228) completed measures of sleep quality and psychological symptoms pre-transplant and 1, 3, 6, and 12 months post-transplant. Circulating inflammatory cytokines (IL-6, TNF-α) were also assessed. Sleep quality was poorest at one month post-transplant, improving and remaining relatively stable after 3 months post-transplant. However, approximately half of participants continued to experience significant sleep disturbance at 6 and 12 months post-transplant. Mixed-effects linear regression models indicated that depression and anxiety were associated with poorer sleep quality, while psychological well-being was associated with better sleep. Higher circulating levels of IL-6 were also linked with poorer sleep. Subject-level fixed effects models demonstrated that among individual participants, changes in depression, anxiety, and psychological well-being were associated with corresponding changes in sleep after covarying for the effects of time since transplant. Sleep disturbance was most severe when depression and anxiety were greatest, and psychological well-being was lowest. Findings indicate that sleep disturbance is a persistent problem during the year following HSCT. Patients experiencing depression or anxiety and those with elevated inflammation may be at particular risk for poor sleep. 2014-08-18 2014-11 /pmc/articles/PMC4221490/ /pubmed/25133898 http://dx.doi.org/10.1038/bmt.2014.179 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Nelson, Ashley M.
Coe, Christopher L.
Juckett, Mark B.
Rumble, Meredith E.
Rathouz, Paul J.
Hematti, Peiman
Costanzo, Erin S.
Sleep Quality Following Hematopoietic Stem Cell Transplantation: Longitudinal Trajectories and Biobehavioral Correlates
title Sleep Quality Following Hematopoietic Stem Cell Transplantation: Longitudinal Trajectories and Biobehavioral Correlates
title_full Sleep Quality Following Hematopoietic Stem Cell Transplantation: Longitudinal Trajectories and Biobehavioral Correlates
title_fullStr Sleep Quality Following Hematopoietic Stem Cell Transplantation: Longitudinal Trajectories and Biobehavioral Correlates
title_full_unstemmed Sleep Quality Following Hematopoietic Stem Cell Transplantation: Longitudinal Trajectories and Biobehavioral Correlates
title_short Sleep Quality Following Hematopoietic Stem Cell Transplantation: Longitudinal Trajectories and Biobehavioral Correlates
title_sort sleep quality following hematopoietic stem cell transplantation: longitudinal trajectories and biobehavioral correlates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221490/
https://www.ncbi.nlm.nih.gov/pubmed/25133898
http://dx.doi.org/10.1038/bmt.2014.179
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