Effects of simvastatin on tissue factor pathway of blood coagulation in STATCOPE (Simvastatin in the prevention of COPD exacerbations) trial.
blood coagulation
chronic obstructive pulmonary disease
simvastatin
statin
tissue factor pathway
Journal
Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508
Informations de publication
Date de publication:
07 2021
07 2021
Historique:
revised:
23
12
2020
received:
06
08
2020
accepted:
13
01
2021
pubmed:
28
2
2021
medline:
10
8
2021
entrez:
27
2
2021
Statut:
ppublish
Résumé
Statins are widely used to lower lipids and reduce cardiovascular events. In vitro studies and small studies in patients with hyperlipidemias show statins inhibit tissue factor (TF) and blood coagulation mechanisms. We assessed the effects of simvastatin on TF and coagulation biomarkers in patients entered in STATCOPE, a multicenter, randomized, placebo-controlled trial of simvastatin (40 mg daily) versus placebo on exacerbation rates in patients with chronic obstructive pulmonary disease (COPD). In 227 patients (114 simvastatin, 113 placebo; mean [± standard error of the mean] age 62 ± 0.53 years, 44.5% women) we measured (baseline, and 6 and 12 months): whole blood membrane TF-procoagulant activity (TF-PCA) and plasma factors VIIa, VII, VIII, fibrinogen, TF antigen, tissue factor pathway inhibitor (TFPI), thrombin-antithrombin complexes (TAT), and D-dimer. We excluded patients with diabetes, cardiovascular disease, and those taking or requiring a statin. In the statin group, there was a small increase in TF-PCA (from 25.18 ± 1.08 to 30.36 ± 1.10 U/ml; p = .03) over 12 months; factors VIIa and VIII, fibrinogen, TAT, and D-dimer did not change. Plasma TFPI (from 52.4 ± 1.75 to 44.7 ± 1.78 ng/ml; p < .0001) and FVIIC (1.23 ± 0.04 to 1.15 ± 0.03 U/ml; p = .03) decreased and correlated with total cholesterol levels. No changes in biomarkers were observed with placebo. In contrast to previous studies on statins, in COPD patients without diabetes, cardiovascular disease, or requiring a statin treatment, simvastatin (40 mg per day) did not decrease TF or factors VIIa and VIII, fibrinogen, TAT, or D-dimer. The decreases in TFPI and factor VII reflect the decrease in serum lipids.
Sections du résumé
BACKGROUND
Statins are widely used to lower lipids and reduce cardiovascular events. In vitro studies and small studies in patients with hyperlipidemias show statins inhibit tissue factor (TF) and blood coagulation mechanisms. We assessed the effects of simvastatin on TF and coagulation biomarkers in patients entered in STATCOPE, a multicenter, randomized, placebo-controlled trial of simvastatin (40 mg daily) versus placebo on exacerbation rates in patients with chronic obstructive pulmonary disease (COPD).
METHODS
In 227 patients (114 simvastatin, 113 placebo; mean [± standard error of the mean] age 62 ± 0.53 years, 44.5% women) we measured (baseline, and 6 and 12 months): whole blood membrane TF-procoagulant activity (TF-PCA) and plasma factors VIIa, VII, VIII, fibrinogen, TF antigen, tissue factor pathway inhibitor (TFPI), thrombin-antithrombin complexes (TAT), and D-dimer. We excluded patients with diabetes, cardiovascular disease, and those taking or requiring a statin.
RESULTS
In the statin group, there was a small increase in TF-PCA (from 25.18 ± 1.08 to 30.36 ± 1.10 U/ml; p = .03) over 12 months; factors VIIa and VIII, fibrinogen, TAT, and D-dimer did not change. Plasma TFPI (from 52.4 ± 1.75 to 44.7 ± 1.78 ng/ml; p < .0001) and FVIIC (1.23 ± 0.04 to 1.15 ± 0.03 U/ml; p = .03) decreased and correlated with total cholesterol levels. No changes in biomarkers were observed with placebo.
CONCLUSIONS
In contrast to previous studies on statins, in COPD patients without diabetes, cardiovascular disease, or requiring a statin treatment, simvastatin (40 mg per day) did not decrease TF or factors VIIa and VIII, fibrinogen, TAT, or D-dimer. The decreases in TFPI and factor VII reflect the decrease in serum lipids.
Identifiants
pubmed: 33638931
doi: 10.1111/jth.15282
pmc: PMC8238804
mid: NIHMS1679776
pii: S1538-7836(22)01798-6
doi:
Substances chimiques
Thromboplastin
9035-58-9
Simvastatin
AGG2FN16EV
Factor VIIa
EC 3.4.21.21
Banques de données
ClinicalTrials.gov
['NCT01061671']
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1709-1717Subventions
Organisme : NHLBI NIH HHS
ID : U10 HL074416
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074424
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074428
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074439
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074408
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074407
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074441
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074418
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074409
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL074431
Pays : United States
Organisme : CIHR
ID : 115074
Pays : Canada
Organisme : NHLBI NIH HHS
ID : U10 HL074422
Pays : United States
Informations de copyright
© 2021 International Society on Thrombosis and Haemostasis.
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