Reduced Vitamin K Status as a Potentially Modifiable Risk Factor of Severe Coronavirus Disease 2019. (27th August 2020)
- Record Type:
- Journal Article
- Title:
- Reduced Vitamin K Status as a Potentially Modifiable Risk Factor of Severe Coronavirus Disease 2019. (27th August 2020)
- Main Title:
- Reduced Vitamin K Status as a Potentially Modifiable Risk Factor of Severe Coronavirus Disease 2019
- Authors:
- Dofferhoff, Anton S M
Piscaer, Ianthe
Schurgers, Leon J
Visser, Margot P J
van den Ouweland, Jody M W
de Jong, Pim A
Gosens, Reinoud
Hackeng, Tilman M
van Daal, Henny
Lux, Petra
Maassen, Cecile
Karssemeijer, Esther G A
Vermeer, Cees
Wouters, Emiel F M
Kistemaker, Loes E M
Walk, Jona
Janssen, Rob - Abstract:
- Abstract: Background: Respiratory failure and thromboembolism are frequent in severe acute respiratory syndrome coronavirus 2–infected patients. Vitamin K activates both hepatic coagulation factors and extrahepatic endothelial anticoagulant protein S, required for thrombosis prevention. In times of vitamin K insufficiency, hepatic procoagulant factors are preferentially activated over extrahepatic proteins. Vitamin K also activates matrix Gla protein (MGP), which protects against pulmonary and vascular elastic fiber damage. We hypothesized that vitamin K may be implicated in coronavirus disease 2019 (COVID-19), linking pulmonary and thromboembolic disease. Methods: A total of 135 hospitalized COVID-19 patients were compared with 184 historic controls. Inactive vitamin K–dependent MGP (desphospho-uncarboxylated [dp-uc] MGP) and prothrombin (PIVKA-II) were measured inversely related to extrahepatic and hepatic vitamin K status, respectively. Desmosine was measured to quantify the rate of elastic fiber degradation. Arterial calcification severity was assessed using computed tomography. Results: dp-ucMGP was elevated in COVID-19 patients compared with controls ( P < .001), with even higher dp-ucMGP in patients with poor outcomes ( P < .001). PIVKA-II was normal in 82.1% of patients. dp-ucMGP was correlated with desmosine ( P < .001) and with coronary artery ( P = .002) and thoracic aortic ( P < .001) calcification scores. Conclusions: dp-ucMGP was severely increased inAbstract: Background: Respiratory failure and thromboembolism are frequent in severe acute respiratory syndrome coronavirus 2–infected patients. Vitamin K activates both hepatic coagulation factors and extrahepatic endothelial anticoagulant protein S, required for thrombosis prevention. In times of vitamin K insufficiency, hepatic procoagulant factors are preferentially activated over extrahepatic proteins. Vitamin K also activates matrix Gla protein (MGP), which protects against pulmonary and vascular elastic fiber damage. We hypothesized that vitamin K may be implicated in coronavirus disease 2019 (COVID-19), linking pulmonary and thromboembolic disease. Methods: A total of 135 hospitalized COVID-19 patients were compared with 184 historic controls. Inactive vitamin K–dependent MGP (desphospho-uncarboxylated [dp-uc] MGP) and prothrombin (PIVKA-II) were measured inversely related to extrahepatic and hepatic vitamin K status, respectively. Desmosine was measured to quantify the rate of elastic fiber degradation. Arterial calcification severity was assessed using computed tomography. Results: dp-ucMGP was elevated in COVID-19 patients compared with controls ( P < .001), with even higher dp-ucMGP in patients with poor outcomes ( P < .001). PIVKA-II was normal in 82.1% of patients. dp-ucMGP was correlated with desmosine ( P < .001) and with coronary artery ( P = .002) and thoracic aortic ( P < .001) calcification scores. Conclusions: dp-ucMGP was severely increased in COVID-19 patients, indicating extrahepatic vitamin K insufficiency, which was related to poor outcome; hepatic procoagulant factor II remained unaffected. These data suggest pneumonia-induced extrahepatic vitamin K depletion leading to accelerated elastic fiber damage and thrombosis in severe COVID-19 due to impaired activation of MGP and endothelial protein S, respectively. Abstract : Indirectly quantified extrahepatic vitamin K status is severely reduced in COVID-19. Data suggest pneumonia-induced vitamin K depletion leading to elastic fiber damage and thrombosis due to impaired vitamin K–dependent activation of matrix Gla protein and endothelial protein S, respectively. … (more)
- Is Part Of:
- Clinical infectious diseases. Volume 73:Number 11(2021)
- Journal:
- Clinical infectious diseases
- Issue:
- Volume 73:Number 11(2021)
- Issue Display:
- Volume 73, Issue 11 (2021)
- Year:
- 2021
- Volume:
- 73
- Issue:
- 11
- Issue Sort Value:
- 2021-0073-0011-0000
- Page Start:
- e4039
- Page End:
- e4046
- Publication Date:
- 2020-08-27
- Subjects:
- COVID-19 -- elastic fibers -- factor II -- matrix Gla protein -- vitamin K
Communicable diseases -- Periodicals
616.905 - Journal URLs:
- http://cid.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://www.journals.uchicago.edu/CID/journal ↗
http://www.jstor.org/journals/10584838.html ↗ - DOI:
- 10.1093/cid/ciaa1258 ↗
- Languages:
- English
- ISSNs:
- 1058-4838
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.293860
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- 20236.xml