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Clinical Associations with Telomere Length in Chronic Spinal Cord Injury

STUDY DESIGN: Cross-sectional study OBJECTIVES: To determine clinical factors associated with telomere length in persons with chronic spinal cord injury (SCI). SETTING: Veterans Affairs Medical Center, Boston, MA. METHODS: 278 participants with chronic SCI provided blood samples for measurement of C...

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Autores principales: Monroe, David, Goldstein, Rebekah L., Teylan, Merilee, Hart, Jaime E., DeVivo, Immaculata, Orr, Esther, Garshick, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940383/
https://www.ncbi.nlm.nih.gov/pubmed/31383950
http://dx.doi.org/10.1038/s41393-019-0336-7
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author Monroe, David
Goldstein, Rebekah L.
Teylan, Merilee
Hart, Jaime E.
DeVivo, Immaculata
Orr, Esther
Garshick, Eric
author_facet Monroe, David
Goldstein, Rebekah L.
Teylan, Merilee
Hart, Jaime E.
DeVivo, Immaculata
Orr, Esther
Garshick, Eric
author_sort Monroe, David
collection PubMed
description STUDY DESIGN: Cross-sectional study OBJECTIVES: To determine clinical factors associated with telomere length in persons with chronic spinal cord injury (SCI). SETTING: Veterans Affairs Medical Center, Boston, MA. METHODS: 278 participants with chronic SCI provided blood samples for measurement of C-reactive protein (CRP), interleukin-6 (IL-6), and telomere length, completed respiratory health questionnaires, underwent dual x-ray absorptiometry (DXA) to assess body fat, and completed spirometry. High-throughput real-time PCR assays were used to assess telomere length in leukocyte genomic DNA. Linear regression models were used to assess cross-sectional associations with telomere length. RESULTS: Telomere length was inversely related to age (p<0.0001). In age-adjusted models, gender, race, injury duration, %-total and %-trunk fat, body mass index (BMI), %-predicted forced vital capacity (FVC) and forced expiratory volume in one second (FEV(1)), chronic cough or phlegm, CRP, IL-6, wheeze, smoking, diabetes, heart disease, chronic obstructive pulmonary disease (COPD), skin ulcer, urinary tract infection (UTI), or chest illness history were not significantly associated with telomere length. There was a suggestive age-adjusted association between persons with the most severe SCI (cervical motor complete and AIS C) and shorter telomere length (p=0.055), an effect equivalent to approximately 8.4 years of premature aging. There were similar age-adjusted associations with telomere length between persons using a wheelchair (p=0.059) and persons with chronic urinary catheter use (p=0.082) compared to persons without these characteristics. CONCLUSIONS: Our results suggest that clinical characteristics such as decreased mobility and bladder dysfunction that are common in individuals with more severe SCI are associated with shorter telomere length.
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spelling pubmed-69403832020-02-05 Clinical Associations with Telomere Length in Chronic Spinal Cord Injury Monroe, David Goldstein, Rebekah L. Teylan, Merilee Hart, Jaime E. DeVivo, Immaculata Orr, Esther Garshick, Eric Spinal Cord Article STUDY DESIGN: Cross-sectional study OBJECTIVES: To determine clinical factors associated with telomere length in persons with chronic spinal cord injury (SCI). SETTING: Veterans Affairs Medical Center, Boston, MA. METHODS: 278 participants with chronic SCI provided blood samples for measurement of C-reactive protein (CRP), interleukin-6 (IL-6), and telomere length, completed respiratory health questionnaires, underwent dual x-ray absorptiometry (DXA) to assess body fat, and completed spirometry. High-throughput real-time PCR assays were used to assess telomere length in leukocyte genomic DNA. Linear regression models were used to assess cross-sectional associations with telomere length. RESULTS: Telomere length was inversely related to age (p<0.0001). In age-adjusted models, gender, race, injury duration, %-total and %-trunk fat, body mass index (BMI), %-predicted forced vital capacity (FVC) and forced expiratory volume in one second (FEV(1)), chronic cough or phlegm, CRP, IL-6, wheeze, smoking, diabetes, heart disease, chronic obstructive pulmonary disease (COPD), skin ulcer, urinary tract infection (UTI), or chest illness history were not significantly associated with telomere length. There was a suggestive age-adjusted association between persons with the most severe SCI (cervical motor complete and AIS C) and shorter telomere length (p=0.055), an effect equivalent to approximately 8.4 years of premature aging. There were similar age-adjusted associations with telomere length between persons using a wheelchair (p=0.059) and persons with chronic urinary catheter use (p=0.082) compared to persons without these characteristics. CONCLUSIONS: Our results suggest that clinical characteristics such as decreased mobility and bladder dysfunction that are common in individuals with more severe SCI are associated with shorter telomere length. 2019-08-05 2019-12 /pmc/articles/PMC6940383/ /pubmed/31383950 http://dx.doi.org/10.1038/s41393-019-0336-7 Text en 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
Monroe, David
Goldstein, Rebekah L.
Teylan, Merilee
Hart, Jaime E.
DeVivo, Immaculata
Orr, Esther
Garshick, Eric
Clinical Associations with Telomere Length in Chronic Spinal Cord Injury
title Clinical Associations with Telomere Length in Chronic Spinal Cord Injury
title_full Clinical Associations with Telomere Length in Chronic Spinal Cord Injury
title_fullStr Clinical Associations with Telomere Length in Chronic Spinal Cord Injury
title_full_unstemmed Clinical Associations with Telomere Length in Chronic Spinal Cord Injury
title_short Clinical Associations with Telomere Length in Chronic Spinal Cord Injury
title_sort clinical associations with telomere length in chronic spinal cord injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940383/
https://www.ncbi.nlm.nih.gov/pubmed/31383950
http://dx.doi.org/10.1038/s41393-019-0336-7
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