Circadian rhythms of hemostatic factors in tetraplegia: a double-blind, randomized, placebo-controlled cross-over study of melatonin
Study design: This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia. Objectives: Tetraplegic patients have an increased risk of venous thrombosis despite prophylaxis, blunted variations in melatonin and altered circadian variation of several hem...
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Published in: | Spinal cord Vol. 53; no. 4; pp. 285 - 290 |
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Abstract | Study design:
This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia.
Objectives:
Tetraplegic patients have an increased risk of venous thrombosis despite prophylaxis, blunted variations in melatonin and altered circadian variation of several hemostatic markers. To examine whether melatonin could modify the regulation of hemostasis, we measured plasma melatonin and several markers of hemostasis in tetraplegic subjects with or without melatonin supplement.
Setting:
The study was conducted in the Section for Spinal Cord Injury, Sunnaas Hospital, Nesoddtangen, Norway.
Methods:
Six subjects with long-standing complete tetraplegia were included in this cross-over study with 2 mg of melatonin or placebo given 4 days before sampling. We also included six able-bodied men without any intervention. Plasma samples were then collected frequently during a 24-h awake/sleep cycle. The plasma concentrations of melatonin and the various markers were analyzed using linear mixed models.
Results:
The 24-h profiles of prothrombin fragment 1+2 and von Willebrand factor, but not D-dimer, activated FVII, tissue factor pathway inhibitor and plasminogen activator inhibitor type 1, differed (
P
<0.05) between tetraplegic patients and able-bodied subjects. The absolute plasma concentration of activated FVII was higher (
P
<0.05) among the able-bodied compared with the tetraplegic groups. Supplementation of melatonin had no impact on these findings.
Conclusions:
We found differences in circadian variation of several hemostatic markers between able-bodied and tetraplegics. These differences were apparently unrelated to fluctuations in the melatonin concentrations, suggesting little or no role of melatonin in the regulation of hemostasis in tetraplegia.
Sponsorship:
Financial support was provided from the Throne Holst Foundation. |
---|---|
AbstractList | Study design: This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia.
Objectives: Tetraplegic patients have an increased risk of venous thrombosis despite prophylaxis, blunted variations in melatonin and
altered circadian variation of several hemostatic markers. To examine whether melatonin could modify the regulation of hemostasis,
we measured plasma melatonin and several markers of hemostasis in tetraplegic subjects with or without melatonin supplement.
Setting: The study was conducted in the Section for Spinal Cord Injury, Sunnaas Hospital, Nesoddtangen, Norway.
Methods: Six subjects with long-standing complete tetraplegia were included in this cross-over study with 2 mg of melatonin or
placebo given 4 days before sampling. We also included six able-bodied men without any intervention. Plasma samples were then
collected frequently during a 24-h awake/sleep cycle. The plasma concentrations of melatonin and the various markers were analyzed
using linear mixed models.
Results: The 24-h profiles of prothrombin fragment 1+2 and von Willebrand factor, but not D-dimer, activated FVII, tissue factor
pathway inhibitor and plasminogen activator inhibitor type 1, differed (Po0.05) between tetraplegic patients and able-bodied subjects.
The absolute plasma concentration of activated FVII was higher (Po0.05) among the able-bodied compared with the tetraplegic
groups. Supplementation of melatonin had no impact on these findings.
Conclusions: We found differences in circadian variation of several hemostatic markers between able-bodied and tetraplegics. These
differences were apparently unrelated to fluctuations in the melatonin concentrations, suggesting little or no role of melatonin in the
regulation of hemostasis in tetraplegia. Study design:This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia. Objectives: Tetraplegic patients have an increased risk of venous thrombosis despite prophylaxis, blunted variations in melatonin and altered circadian variation of several hemostatic markers. To examine whether melatonin could modify the regulation of hemostasis, we measured plasma melatonin and several markers of hemostasis in tetraplegic subjects with or without melatonin supplement.Setting:The study was conducted in the Section for Spinal Cord Injury, Sunnaas Hospital, Nesoddtangen, Norway. Methods: Six subjects with long-standing complete tetraplegia were included in this cross-over study with 2 mg of melatonin or placebo given 4 days before sampling. We also included six able-bodied men without any intervention. Plasma samples were then collected frequently during a 24-h awake/sleep cycle. The plasma concentrations of melatonin and the various markers were analyzed using linear mixed models. Results: The 24-h profiles of prothrombin fragment 1+2 and von Willebrand factor, but not D-dimer, activated FVII, tissue factor pathway inhibitor and plasminogen activator inhibitor type 1, differed (P<0.05) between tetraplegic patients and able-bodied subjects. The absolute plasma concentration of activated FVII was higher (P<0.05) among the able-bodied compared with the tetraplegic groups. Supplementation of melatonin had no impact on these findings. Conclusions: We found differences in circadian variation of several hemostatic markers between able-bodied and tetraplegics. These differences were apparently unrelated to fluctuations in the melatonin concentrations, suggesting little or no role of melatonin in the regulation of hemostasis in tetraplegia.Sponsorship:Financial support was provided from the Throne Holst Foundation. STUDY DESIGNThis is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia.OBJECTIVESTetraplegic patients have an increased risk of venous thrombosis despite prophylaxis, blunted variations in melatonin and altered circadian variation of several hemostatic markers. To examine whether melatonin could modify the regulation of hemostasis, we measured plasma melatonin and several markers of hemostasis in tetraplegic subjects with or without melatonin supplement.SETTINGThe study was conducted in the Section for Spinal Cord Injury, Sunnaas Hospital, Nesoddtangen, Norway.METHODSSix subjects with long-standing complete tetraplegia were included in this cross-over study with 2 mg of melatonin or placebo given 4 days before sampling. We also included six able-bodied men without any intervention. Plasma samples were then collected frequently during a 24-h awake/sleep cycle. The plasma concentrations of melatonin and the various markers were analyzed using linear mixed models.RESULTSThe 24-h profiles of prothrombin fragment 1+2 and von Willebrand factor, but not D-dimer, activated FVII, tissue factor pathway inhibitor and plasminogen activator inhibitor type 1, differed (P<0.05) between tetraplegic patients and able-bodied subjects. The absolute plasma concentration of activated FVII was higher (P<0.05) among the able-bodied compared with the tetraplegic groups. Supplementation of melatonin had no impact on these findings.CONCLUSIONSWe found differences in circadian variation of several hemostatic markers between able-bodied and tetraplegics. These differences were apparently unrelated to fluctuations in the melatonin concentrations, suggesting little or no role of melatonin in the regulation of hemostasis in tetraplegia.SPONSORSHIPFinancial support was provided from the Throne Holst Foundation. Study design: This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia. Objectives: Tetraplegic patients have an increased risk of venous thrombosis despite prophylaxis, blunted variations in melatonin and altered circadian variation of several hemostatic markers. To examine whether melatonin could modify the regulation of hemostasis, we measured plasma melatonin and several markers of hemostasis in tetraplegic subjects with or without melatonin supplement. Setting: The study was conducted in the Section for Spinal Cord Injury, Sunnaas Hospital, Nesoddtangen, Norway. Methods: Six subjects with long-standing complete tetraplegia were included in this cross-over study with 2 mg of melatonin or placebo given 4 days before sampling. We also included six able-bodied men without any intervention. Plasma samples were then collected frequently during a 24-h awake/sleep cycle. The plasma concentrations of melatonin and the various markers were analyzed using linear mixed models. Results: The 24-h profiles of prothrombin fragment 1+2 and von Willebrand factor, but not D-dimer, activated FVII, tissue factor pathway inhibitor and plasminogen activator inhibitor type 1, differed ( P <0.05) between tetraplegic patients and able-bodied subjects. The absolute plasma concentration of activated FVII was higher ( P <0.05) among the able-bodied compared with the tetraplegic groups. Supplementation of melatonin had no impact on these findings. Conclusions: We found differences in circadian variation of several hemostatic markers between able-bodied and tetraplegics. These differences were apparently unrelated to fluctuations in the melatonin concentrations, suggesting little or no role of melatonin in the regulation of hemostasis in tetraplegia. Sponsorship: Financial support was provided from the Throne Holst Foundation. This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia. Tetraplegic patients have an increased risk of venous thrombosis despite prophylaxis, blunted variations in melatonin and altered circadian variation of several hemostatic markers. To examine whether melatonin could modify the regulation of hemostasis, we measured plasma melatonin and several markers of hemostasis in tetraplegic subjects with or without melatonin supplement. The study was conducted in the Section for Spinal Cord Injury, Sunnaas Hospital, Nesoddtangen, Norway. Six subjects with long-standing complete tetraplegia were included in this cross-over study with 2 mg of melatonin or placebo given 4 days before sampling. We also included six able-bodied men without any intervention. Plasma samples were then collected frequently during a 24-h awake/sleep cycle. The plasma concentrations of melatonin and the various markers were analyzed using linear mixed models. The 24-h profiles of prothrombin fragment 1+2 and von Willebrand factor, but not D-dimer, activated FVII, tissue factor pathway inhibitor and plasminogen activator inhibitor type 1, differed (P<0.05) between tetraplegic patients and able-bodied subjects. The absolute plasma concentration of activated FVII was higher (P<0.05) among the able-bodied compared with the tetraplegic groups. Supplementation of melatonin had no impact on these findings. We found differences in circadian variation of several hemostatic markers between able-bodied and tetraplegics. These differences were apparently unrelated to fluctuations in the melatonin concentrations, suggesting little or no role of melatonin in the regulation of hemostasis in tetraplegia. Financial support was provided from the Throne Holst Foundation. |
Author | Dahm, A E A Østerud, B Kostovski, E Mowinckel, M C Stranda, A Skretting, G Iversen, P O Sandset, P M |
Author_xml | – sequence: 1 givenname: E surname: Kostovski fullname: Kostovski, E organization: Sunnaas Hospital – sequence: 2 givenname: A E A surname: Dahm fullname: Dahm, A E A organization: Akershus University Hospital, Institute of Clinical Medicine, University of Oslo – sequence: 3 givenname: M C surname: Mowinckel fullname: Mowinckel, M C organization: Institute of Clinical Medicine, University of Oslo, Research Institute of Internal Medicine, Oslo University Hospital – sequence: 4 givenname: A surname: Stranda fullname: Stranda, A organization: Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo – sequence: 5 givenname: G surname: Skretting fullname: Skretting, G organization: Institute of Clinical Medicine, University of Oslo, Research Institute of Internal Medicine, Oslo University Hospital – sequence: 6 givenname: B surname: Østerud fullname: Østerud, B organization: Institute of Medical Biology, Faculty of Health Sciences, The Arctic University of Norway – sequence: 7 givenname: P M surname: Sandset fullname: Sandset, P M organization: Institute of Clinical Medicine, University of Oslo, Research Institute of Internal Medicine, Oslo University Hospital, Department of Hematology, Oslo University Hospital – sequence: 8 givenname: P O surname: Iversen fullname: Iversen, P O email: p.o.iversen@medisin.uio.no organization: Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Department of Hematology, Oslo University Hospital |
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CitedBy_id | crossref_primary_10_1080_10790268_2018_1543925 crossref_primary_10_1080_07420528_2022_2080557 crossref_primary_10_1160_TH15_05_0396 crossref_primary_10_1080_10790268_2018_1505312 crossref_primary_10_1016_j_dhjo_2016_12_002 crossref_primary_10_1016_j_sleep_2018_07_008 crossref_primary_10_1038_s41393_018_0176_x |
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Copyright | The Author(s) 2015 Copyright Nature Publishing Group Apr 2015 info:eu-repo/semantics/openAccess Copyright © 2015 International Spinal Cord Society 2015 International Spinal Cord Society |
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This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia.
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Tetraplegic patients... This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia. Tetraplegic patients have an increased risk of... Study design:This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia.Objectives:Tetraplegic patients have... STUDY DESIGNThis is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia.OBJECTIVESTetraplegic patients have an... Study design:This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia. Objectives: Tetraplegic patients... Study design: This is a double-blind, randomized, placebo-controlled cross-over study of melatonin in complete tetraplegia. Objectives: Tetraplegic patients... |
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SubjectTerms | 631/443/1338/567 692/699/75/567 Adult Anatomy Biomedical and Life Sciences Biomedicine Central Nervous System Agents - blood Central Nervous System Agents - therapeutic use Cervical Cord - injuries Circadian Rhythm - physiology Cross-Over Studies Double-Blind Method Human Physiology Humans Male Melatonin - blood Melatonin - therapeutic use Middle Aged Neurochemistry Neuropsychology Neurosciences Norway Original original-article Quadriplegia - blood Quadriplegia - drug therapy Quadriplegia - etiology Spinal Cord Injuries - blood Spinal Cord Injuries - complications Spinal Cord Injuries - drug therapy |
Title | Circadian rhythms of hemostatic factors in tetraplegia: a double-blind, randomized, placebo-controlled cross-over study of melatonin |
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