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Altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome

Abnormal clot microstructure plays a pivotal role in the pathophysiology of thromboembolic diseases. Assessing the viscoelastic properties of clot microstructure using novel parameters, Time to Gel Point (T(GP)), Fractal Dimension (d(f)) and clot elasticity (G׳(GP)) could explain the increased cardi...

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Autores principales: D׳Silva, Lindsay, Wilczynska, Maria, Lewis, Keir, Lawrence, Matthew, Hawkins, Karl, Williams, Rhodri, Stanford, Sophia, Davidson, Simon, Morris, Keith, Evans, Adrian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867923/
https://www.ncbi.nlm.nih.gov/pubmed/27226818
http://dx.doi.org/10.1016/j.slsci.2016.02.175
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author D׳Silva, Lindsay
Wilczynska, Maria
Lewis, Keir
Lawrence, Matthew
Hawkins, Karl
Williams, Rhodri
Stanford, Sophia
Davidson, Simon
Morris, Keith
Evans, Adrian
author_facet D׳Silva, Lindsay
Wilczynska, Maria
Lewis, Keir
Lawrence, Matthew
Hawkins, Karl
Williams, Rhodri
Stanford, Sophia
Davidson, Simon
Morris, Keith
Evans, Adrian
author_sort D׳Silva, Lindsay
collection PubMed
description Abnormal clot microstructure plays a pivotal role in the pathophysiology of thromboembolic diseases. Assessing the viscoelastic properties of clot microstructure using novel parameters, Time to Gel Point (T(GP)), Fractal Dimension (d(f)) and clot elasticity (G׳(GP)) could explain the increased cardiovascular and thromboembolic events in patients with Obstructive Sleep Apnoea Hypopnea Syndrome (OSAHS). We wanted to compare T(GP), d(f), and G׳(GP) and their diurnal variation in OSAHS and symptomatic comparators. thirty six patients attending a sleep disturbed breathing clinic with symptoms of OSAHS were recruited. T(GP), d(f) and G׳(GP) were measured alongside standard coagulation screening, thrombin generation assays, and platelet aggregometry at 16:00 h and immediately after an in-patient sleep study at 07:30 h. OSAHS group had significantly lower afternoon d(f) than comparators (1.705±0.033 vs. 1.731±0.031, p<0.05). d(f) showed diurnal variation and only in the OSAHS group, being significantly lower in the afternoon than morning (p<0.05). Diurnal changes in d(f) correlated with 4% DR, even after controlling for BMI (r=0.37, p=0.02). The lower d(f) in the afternoon in OSAHS suggests a partial compensatory change that may make up for other pro-clotting abnormalities/hypertension during the night. The change to the thrombotic tendency in the afternoon is biggest in severe OSAHS. d(f) Shows promise as a new microstructural indicator for abnormal haemostasis in OSAHS.
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spelling pubmed-48679232016-05-25 Altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome D׳Silva, Lindsay Wilczynska, Maria Lewis, Keir Lawrence, Matthew Hawkins, Karl Williams, Rhodri Stanford, Sophia Davidson, Simon Morris, Keith Evans, Adrian Sleep Sci Full Length Article Abnormal clot microstructure plays a pivotal role in the pathophysiology of thromboembolic diseases. Assessing the viscoelastic properties of clot microstructure using novel parameters, Time to Gel Point (T(GP)), Fractal Dimension (d(f)) and clot elasticity (G׳(GP)) could explain the increased cardiovascular and thromboembolic events in patients with Obstructive Sleep Apnoea Hypopnea Syndrome (OSAHS). We wanted to compare T(GP), d(f), and G׳(GP) and their diurnal variation in OSAHS and symptomatic comparators. thirty six patients attending a sleep disturbed breathing clinic with symptoms of OSAHS were recruited. T(GP), d(f) and G׳(GP) were measured alongside standard coagulation screening, thrombin generation assays, and platelet aggregometry at 16:00 h and immediately after an in-patient sleep study at 07:30 h. OSAHS group had significantly lower afternoon d(f) than comparators (1.705±0.033 vs. 1.731±0.031, p<0.05). d(f) showed diurnal variation and only in the OSAHS group, being significantly lower in the afternoon than morning (p<0.05). Diurnal changes in d(f) correlated with 4% DR, even after controlling for BMI (r=0.37, p=0.02). The lower d(f) in the afternoon in OSAHS suggests a partial compensatory change that may make up for other pro-clotting abnormalities/hypertension during the night. The change to the thrombotic tendency in the afternoon is biggest in severe OSAHS. d(f) Shows promise as a new microstructural indicator for abnormal haemostasis in OSAHS. Elsevier 2016 2016-02-23 /pmc/articles/PMC4867923/ /pubmed/27226818 http://dx.doi.org/10.1016/j.slsci.2016.02.175 Text en © 2016 Brazilian Association of Sleep. Production and Hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
D׳Silva, Lindsay
Wilczynska, Maria
Lewis, Keir
Lawrence, Matthew
Hawkins, Karl
Williams, Rhodri
Stanford, Sophia
Davidson, Simon
Morris, Keith
Evans, Adrian
Altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome
title Altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome
title_full Altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome
title_fullStr Altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome
title_full_unstemmed Altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome
title_short Altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome
title_sort altered clot microstructure detected in obstructive sleep apnoea hypopnoea syndrome
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867923/
https://www.ncbi.nlm.nih.gov/pubmed/27226818
http://dx.doi.org/10.1016/j.slsci.2016.02.175
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