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Published in: Journal of Inherited Metabolic Disease 2/2018

Open Access 01-03-2018 | Original Article

Coagulopathy in Zellweger spectrum disorders: a role for vitamin K

Authors: Sara Zeynelabidin, Femke C. C. Klouwer, Joost C. M. Meijers, Monique H. Suijker, Marc Engelen, Bwee Tien Poll-The, C. Heleen van Ommen

Published in: Journal of Inherited Metabolic Disease | Issue 2/2018

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Abstract

Introduction

Zellweger spectrum disorders (ZSDs) are caused by an impairment of peroxisome biogenesis, resulting in multiple metabolic abnormalities. This leads to a range of symptoms, including hepatic dysfunction and coagulopathy. This study evaluated the incidence and severity of coagulopathy and the effect of vitamin K supplementation orally and IV in ZSD.

Methods

Data were retrospectively retrieved from the medical records of 30 ZSD patients to study coagulopathy and the effect of vitamin K orally on proteins induced by vitamin K absence (PIVKA-II) levels. Five patients from the cohort with a prolonged prothrombin time, low factor VII, and elevated PIVKA-II levels received 10 mg of vitamin K IV. Laboratory results, including thrombin generation, at baseline and 72 h after vitamin K administration were examined.

Results

In the retrospective cohort, four patients (13.3%) experienced intracranial bleedings and 14 (46.7%) reported minor bleeding. No thrombotic events occurred. PIVKA-II levels decreased 38% after start of vitamin K therapy orally. In the five patients with a coagulopathy, despite treatment with oral administration of vitamin K, vitamin K IV caused an additional decrease (23%) of PIVKA-II levels and increased thrombin generation.

Conclusion

Bleeding complications frequently occur in ZSD patients due to liver disease and vitamin K deficiency. Vitamin K deficiency is partly corrected by vitamin K supplementation orally, and vitamin K administered IV additionally improves vitamin K status, as shown by further decrease of PIVKA-II and improved thrombin generation.
Literature
go back to reference Berendse K, Engelen M, Ferdinandusse S et al (2016) Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood. J Inherit Metab Dis 39:93–106CrossRefPubMed Berendse K, Engelen M, Ferdinandusse S et al (2016) Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood. J Inherit Metab Dis 39:93–106CrossRefPubMed
go back to reference Croffie JM, Gupta SK, Chong SK, Fitzgerald JF (1999) Tyrosinemia type 1 should be suspected in infants with severe coagulopathy even in the absence of other signs of liver failure. Pediatrics 103:675–678CrossRefPubMed Croffie JM, Gupta SK, Chong SK, Fitzgerald JF (1999) Tyrosinemia type 1 should be suspected in infants with severe coagulopathy even in the absence of other signs of liver failure. Pediatrics 103:675–678CrossRefPubMed
go back to reference El-Sayed R, El-Karaksy H, El-Raziky M et al (2013) Assessment of coagulation and fibrinolysis in children with chronic liver disease. Blood Coagul Fibrinolysis 24:113–117PubMed El-Sayed R, El-Karaksy H, El-Raziky M et al (2013) Assessment of coagulation and fibrinolysis in children with chronic liver disease. Blood Coagul Fibrinolysis 24:113–117PubMed
go back to reference Ferdinandusse S, Denis S, Dacremont G, Wanders RJA (2009) Toxicity of peroxisomal C27-bile acid intermediates. Mol Genet Metab 96:121–128CrossRefPubMed Ferdinandusse S, Denis S, Dacremont G, Wanders RJA (2009) Toxicity of peroxisomal C27-bile acid intermediates. Mol Genet Metab 96:121–128CrossRefPubMed
go back to reference Fischler B, Lamireau T (2014) Cholestasis in the newborn and infant. Clin Res Hepatol Gastroenterol 38:263–267CrossRefPubMed Fischler B, Lamireau T (2014) Cholestasis in the newborn and infant. Clin Res Hepatol Gastroenterol 38:263–267CrossRefPubMed
go back to reference Hemker HC, Giesen P, Al Dieri R et al (2003) Calibrated automated thrombin generation measurement in clotting plasma. Pathophysiol Haemost Thromb 33:4–15CrossRefPubMed Hemker HC, Giesen P, Al Dieri R et al (2003) Calibrated automated thrombin generation measurement in clotting plasma. Pathophysiol Haemost Thromb 33:4–15CrossRefPubMed
go back to reference Klouwer FCC, Berendse K, Ferdinandusse S et al (2015) Zellweger spectrum disorders: clinical overview and management approach. Orphanet J Rare Dis 10:151CrossRefPubMedPubMedCentral Klouwer FCC, Berendse K, Ferdinandusse S et al (2015) Zellweger spectrum disorders: clinical overview and management approach. Orphanet J Rare Dis 10:151CrossRefPubMedPubMedCentral
go back to reference Lisman T, Porte RJ (2011) Rebalanced hemostasis in patients with liver disease : evidence and clinical consequences. Liver 116:878–885 Lisman T, Porte RJ (2011) Rebalanced hemostasis in patients with liver disease : evidence and clinical consequences. Liver 116:878–885
go back to reference Magnusson M, Ignjatovic V, Hardikar W, Monagle P (2016) A conceptual and practical approach to haemostasis in paediatric liver disease. Arch Dis Child 101:854–859CrossRefPubMed Magnusson M, Ignjatovic V, Hardikar W, Monagle P (2016) A conceptual and practical approach to haemostasis in paediatric liver disease. Arch Dis Child 101:854–859CrossRefPubMed
go back to reference Mitchell LG, Male C (2011) Outcome measures in interventional trials for prevention or treatment of venous thrombosis in the pediatric population. Semin Thromb Hemost 37:840–847CrossRefPubMed Mitchell LG, Male C (2011) Outcome measures in interventional trials for prevention or treatment of venous thrombosis in the pediatric population. Semin Thromb Hemost 37:840–847CrossRefPubMed
go back to reference Pereira SP, Shearer MJ, Williams R, Mieli-Vergani G (2003) Intestinal absorption of mixed micellar phylloquinone (vitamin K 1 ) is unreliable in infants with conjugated hyperbilirubinaemia: implications for oral prophylaxis of vitamin K deficiency bleeding. Arch Dis Child Fetal Neonatal Ed 88:113–118CrossRef Pereira SP, Shearer MJ, Williams R, Mieli-Vergani G (2003) Intestinal absorption of mixed micellar phylloquinone (vitamin K 1 ) is unreliable in infants with conjugated hyperbilirubinaemia: implications for oral prophylaxis of vitamin K deficiency bleeding. Arch Dis Child Fetal Neonatal Ed 88:113–118CrossRef
go back to reference Pereira SP, Rowbotham D, Fitt S et al (2005) Pharmacokinetics and efficacy of oral versus intravenous mixed-micellar phylloquinone (vitamin K1) in severe acute liver disease. J Hepatol 42:365–370CrossRefPubMed Pereira SP, Rowbotham D, Fitt S et al (2005) Pharmacokinetics and efficacy of oral versus intravenous mixed-micellar phylloquinone (vitamin K1) in severe acute liver disease. J Hepatol 42:365–370CrossRefPubMed
go back to reference Preston RJS, Rawley O, Gleeson EM, O’Donnell JS (2013) Elucidating the role of carbohydrate determinants in regulating hemostasis: insights and opportunities. Blood 121:3801–3810CrossRefPubMed Preston RJS, Rawley O, Gleeson EM, O’Donnell JS (2013) Elucidating the role of carbohydrate determinants in regulating hemostasis: insights and opportunities. Blood 121:3801–3810CrossRefPubMed
go back to reference Wanders RJA, Waterham HR (2006) Biochemistry of mammalian peroxisomes revisited. Annu Rev Biochem 75:295–332CrossRefPubMed Wanders RJA, Waterham HR (2006) Biochemistry of mammalian peroxisomes revisited. Annu Rev Biochem 75:295–332CrossRefPubMed
Metadata
Title
Coagulopathy in Zellweger spectrum disorders: a role for vitamin K
Authors
Sara Zeynelabidin
Femke C. C. Klouwer
Joost C. M. Meijers
Monique H. Suijker
Marc Engelen
Bwee Tien Poll-The
C. Heleen van Ommen
Publication date
01-03-2018
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 2/2018
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-017-0113-8

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