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Thromb Haemost 1995; 74(06): 1486-1490
DOI: 10.1055/s-0038-1649970
Original Articles
Coagulation
Schattauer GmbH Stuttgart

The Pharmacokinetics and Lipoprotein Fraction Distribution of Intramuscular vs. Oral Vitamin K1Supplementation in Women of Childbearing Age: Effects on Hemostasis

J Nathan Hagstrom
1   The Department of Pathology, University of Vermont, Burlington, Vermont, USA
,
Edwin G Bovill
1   The Department of Pathology, University of Vermont, Burlington, Vermont, USA
,
Roger F Soll
2   The Department of Pediatrics, University of Vermont, Burlington, Vermont, USA
,
Kenneth W Davidson
3   The Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts, USA
,
James A Sadowski
3   The Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts, USA
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Received29. Juni 1994

Accepted after resubmission 16. August 1995

Publikationsdatum:
10. Juli 2018 (online)

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Summary

Prenatal maternal vitamin K1 supplementation to improve the hemostatic status of the fetus may depend upon the route of administration and subsequent presentation at the placental barrier. We investigated intramuscular (IM) vs oral (PO) vitamin K1 supplementation in eight healthy, nonpregnant women of childbearing age. Pharmacokinetics were studied in each subject after a 5 mg IM dose and after a 5 mg oral dose of vitamin K1 approximately one month later. Plasma collected at the peak vitamin K level for each treatment was separated into very low density lipoproteins (VLDL), low density lipoprotein (LDL), high density lipoprotein (HDL) and lipoprotein-free fractions by density gradient ultracentrifugation. Vitamin K1 was measured in the plasma and lipoprotein fractions using HPLC. The concentration of vitamin K1, in plasma reached a peak 2 h after an IM dose and remained high throughout the 30 h course of the study. In contrast, the oral dose of vitamin K1 peaked at 4 h and rapidly decreased to near baseline by 18 to 30 h. The distribution of vitamin K1 in the lipid fractions was different for IM compared to PO. The percentage of vitamin K1 in the VLDL fraction at the peak for an oral dose was significantly higher than for an IM dose (80.8% ± 3.5 vs 10.8% ± 6.5, p <0.0001). After the oral absorption stage, the subjects took 5 mg of vitamin K1 orally, once a day, for 12 days. No significant differences were observed for the following coagulation proteins and hemostatic markers measured immediately before and after long-term oral vitamin K supplementation: factor II, factor VII, protein C, and thrombin-antithrombin III complex. In conclusion, physiological processing of supplemented vitamin K1 differs in the IM vs PO routes of administration and 12 days of oral vitamin K1does not alter the concentration of selected vitamin Independent coagulation proteins or thrombin-antithrombin complex generation

 

  • References

  • 1 Shearer MJ, Rahim S, Barkhan P, Stimmler L. Plasma vitamin K1 in mothers and their newborn babies. Lancet 1982; 2: 460-463
    CrossrefPubMedGoogle Scholar
  • 2 Sann L, Leclercq M, Troncy J, Guillaumond M, Berland M, Coeur P. Serum vitamin K1 concentration and vitamin K-dependent clotting factor activity in maternal and fetal cord blood. Am J Obstet Gynec 1985; 153: 771-774
    CrossrefPubMedGoogle Scholar
  • 3 McCarthy PT, Shearer MJ, Gau G, Crampton OE, Barkhan P. Vitamin K content in human liver at different ages. Haemostasis 1986; 16 Suppl (Suppl. 05) 83 abstr
    PubMedGoogle Scholar
  • 4 Greer FR, Mummah-Schendel LL, Marshall S, Suttie JW. Vitamin K1 (phylloquinone) and vitamin K2 menaquinone status in newborns during the first week of life. Pediatrics 1988; 81: 137-140
    PubMedGoogle Scholar
  • 5 Bovill EG, Soll RF, Lynch M, Bhushan F, Landesman Freije M, Church W, McAuliffe T, Davidson K, Sadowski J. Vitamin K1 metabolism and the production of des-carboxy prothrombin and protein C in the term and premature neonate. Blood 1993; 81: 77-83
    PubMedGoogle Scholar
  • 6 Bleyer WA, Hakami N, Shepard TH. The development of hemostasis in the human fetus and newborn infant. J Pediatr 1971; 79: 838-853
    CrossrefPubMedGoogle Scholar
  • 7 Hathaway WE, Bonnar J. Perinatal Coagulation. New York: Grime & Stratton; 1978
    Google Scholar
  • 8 Andrew M, Paes B, Johnston M. Development of the hemostatic system in the neonate and young infant. Am J Pediatr Hem Oncol 190 (12) 95-104
    PubMedGoogle Scholar
  • 9 Motohara K, Kuroki Y, Kan H, Endo F, Matsuda I. Detection of vitamin K deficiency by use of an enzyme-linked immunosorbent assay for circulating abnormal prothrombin. Pediatr Res 1985; 19: 354-357
    CrossrefPubMedGoogle Scholar
  • 10 Shapiro AD, Jacobson LJ, Armon ME, Manco-Johnson MJ, Hulae P, Lane PA, Hathaway WE. Vitamin K deficiency in the newborn infant: prevalence and perinatal risk factors. J Pediatr 1986; 109: 675-680
    CrossrefPubMedGoogle Scholar
  • 11 Motohara K, Endo F, Matsuda I. Screening for late neonatal vitamin K defieiency by acarboxyprothrombin in dried blood spots. Arch Dis Child 1987; 62: 370-375
    CrossrefPubMedGoogle Scholar
  • 12 Widdershoven J, Lambert W, Motohara K, Monnens L, de Leenheer A, Matsuda I, Endo F. Plasma concentrations of vitamin K1 and PIVKA-II in bottle fed infants with and without vitamin K prophylaxis at birth. Eur J Pediatr 1988; 148: 139-142
    CrossrefPubMedGoogle Scholar
  • 13 Kries RV, Becjer A, Göbel U. Vitamin K in the newborn: Influence of nutritional factors on acarboxy-prothrombin detectability and factor II and VII clotting activity. Eur J Pediatr 1987; 146: 123-127
    CrossrefPubMedGoogle Scholar
  • 14 Salmonsen L. On the prevention of haemorrhagic disease of the newborn by the administration of cow’s milk during the first two days of life. Acta Paediatr Scand 1940; 28: 1
    CrossrefPubMedGoogle Scholar
  • 15 Dam H, Dyggve H, Larsen H, Plum P. The relation of vitamin K deficiency to hemorrhagic disease of the newborn. Adv Pediatr 1952; 5: 129-153
    PubMedGoogle Scholar
  • 16 Sutherland JM, Glueck HI, Gleser G. Hemorrhagic disease of the newborn: Breast feeding as a necessary factor in the pathogenesis. Am J Dis Child 1967; 113: 524-533
    CrossrefPubMedGoogle Scholar
  • 17 McNinch AW, Orme RL, Tripp JH. Haemorrhagic disease of the newborn returns. Lancet 1983; 1: 1089-1090
    PubMedGoogle Scholar
  • 18 Lane PA, Hathaway WE. Vitamin K in infancy. J Pediatr 1985; 106: 351-359
    CrossrefPubMedGoogle Scholar
  • 19 Committee on Nutrition, American Academy of Pediatrics. Vitamin K compounds and the water soluble analogues: use in therapy and prophylaxis in pediatrics. Pediatrics 1961; 28: 501-507
    PubMedGoogle Scholar
  • 20 Mandelbrot L, Guillaumont M, Leclercq M, Lefrère JJ, Gozin D, Daffos F, Forestier F. Placental transfer of vitamin K1 and its implications in fetal hemostasis. Thromb Haemost 1988; 60: 39-43
    Artikel in Thieme ConnectPubMedGoogle Scholar
  • 21 Hamulyák K, de Boer-van den Berg MA G, Thijssen HH W, Hemker HC, Vermeer C. The placental transport of [3H| vitamin K1 in rats. Brit J Haem 1987; 65: 335
    CrossrefPubMedGoogle Scholar
  • 22 Hiraike H, Kimura M, Itokawa Y. Distribution of K vitamins (phylloquinone and menaquinones) in human placenta and maternal and umbilical cord plasma. Am J Obstet Gynecol 1988; 158: 564-569
    CrossrefPubMedGoogle Scholar
  • 23 Yang Y-M, Simon N, Maertens P, Brigham S, Liu P. Maternal-fetal transport of vitamin K1 and its effects on coagulation in premature infants. J Pediatr 1989; 115: 1009-1013
    CrossrefPubMedGoogle Scholar
  • 24 Kazzi NJ, Ilagan NB, Liang K-C, Kazzi GM, Grietsell LA, Brans YW. Placental transfer of vitamin K1 in preterm pregnancy. Obstet Gynecol 1990; 75: 334-337
    PubMedGoogle Scholar
  • 25 Pomerance JJ, Teal JG, Gogolok JF, Brown S, Stewart ME. Maternally administered antenatal vitamin K1: effect on neonatal prothrombin activity, partial thromboplastin time, and intraventricular hemorrhage. Obstet Gynecol 1987; 70: 235-241
    PubMedGoogle Scholar
  • 26 Morales WJ, Angel JL, O’Brien WF, Knuppel RA, Marsalisi F. The use of antenatal vitamin K in the prevention of early neonatal intraventricular hemorrhage. Am J Obstet Gynecol 1988; 159: 774-779
    CrossrefPubMedGoogle Scholar
  • 27 Kazzi NJ, Ilagan NB, Liang K-C, Kazzi GM, Poland RL, Grietsell LA, Fuji Y, Brans YW. Maternal administration of vitamin K does not improve the coagulation profile of preterm infants. Pediatrics 1989; 84: 1045-1050
    PubMedGoogle Scholar
  • 28 Motohara K, Takagi S, Endo F, Kiyota Y, Matsuda I. Oral supplementation of vitamin K for pregnant women effects on levels of plasma vitamin K and PIVKA-II in the neonate. J Pediatr Gastroenterol Nutr 1990; 11: 32-36
    CrossrefPubMedGoogle Scholar
  • 29 Sadowski JA, Bacon DS, Hood S, Davidson KW, Ganter CM, Haroon Y, Shepard DC. The application of methods used for the evaluation of vitamin K nutritional status in human and animal studies. In: Current Advances in Vitamin K Research, Steenbock Symposium. Suttie JW. ed New York, NY: Elsevier Science; 1988. pp 453-463
    Google Scholar
  • 30 Mulhare PE, Tracy PB, Golden EA, Brnada RF, Bovill EG. A case of acquired factor X deficiency with in vivo and in vitro evidence of inhibitor activity directed against factor X. Am J Clin Pathol 1991; 96: 196-200
    CrossrefPubMedGoogle Scholar
  • 31 Lindgren FT, Jensen LC, Hatch FT. The isolation and quantitative analysis of serum lipoproteins. In: Blood Lipids and Lipoproteins: Quantitation, Composition and Metabolism. Nelson GS. ed New York: John Wiley and Sons, Inc; 1972. p 181
    Google Scholar
  • 32 Haroon Y, Bacon DS, Sadowski JA. Liquid-chromatographic determination of vitamin K1 in plasma, with fluorometric detection. Clin Chem 1986; 32: 1925-1929
    PubMedGoogle Scholar
  • 33 Shearer MJ, Barkham P, Webster GR. Absorption and excretion of an oral dose of tritiated vitamin K1 in man. Brit J Haem 1970; 18: 297-308
    CrossrefPubMedGoogle Scholar
  • 34 McNinch AW, Upton C, Samuels M, Shearer MJ, McCarthy P, Tripp JH, Orme RL E. Plasma concentrations after oral or intramuscular vitamin K1 in neonates. Arch Dis Child 1985; 60: 814-818
    CrossrefPubMedGoogle Scholar
  • 35 Shinzawa T, Mura T, Tsune M, Shiraki K. Vitamin K absorption capacity and its association with Vitamin K deficiency. Am J Dia Child 1989; 143: 686-689
    PubMedGoogle Scholar
  • 36 Wittmaack FM, Gafvels ME, Bronner M, Matsuo H, McCrae KR, Tomaszewski JE, Robinson SL, Strickland DK, Strauss JF. Localization and regulation of the human very low density lipoprotein/apolipoprotein-E receptor: Trophoblast expression predicts a role for the receptor in placental lipid transport. Endocrinology 1995; 136: 340-348
    CrossrefPubMedGoogle Scholar
  • 37 Naoum HG, De-Chazal RC, Eaton BM, Contractor SF. Characterization and specificity of lipoprotein binding to term human placental membranes. Biochem Biophys Acta 1987; 902: 193-199
    CrossrefPubMedGoogle Scholar
  • 38 Saupe J, Shearer MJ, Kohlmeier M. Phylloquinone transport and its influence on γ-carboxyglutamate residues of osteocalcin in patients on maintenance hemodialysis. Am J Clin Nutr 1993; 58: 204-208
    CrossrefPubMedGoogle Scholar
  • 39 Israels LG, Friesen E, Jansen AH, Israels ED. Vitamin K1 increases sister chromatid exchange in vitro in human leukocytes and in vivo in fetal sheep cells: a possible role for “vitamin K deficiency” in the fetus. Pediatr Res 1987; 22: 405-408
    CrossrefPubMedGoogle Scholar
  • 40 Freeman BA, Tanswll AK, Cunningham MK. Vitamin K1 stimulates endothelial free radical production. Am Rev Respir Dis 1987; 135: A98 abstr
    PubMedGoogle Scholar
  • 41 Cornelissen M, Smeets D, Merkx G, DeAbreu R, Kollee L, Monnens L. Analysis of chromosome aberrations and sister chromatid exchanges in peripheral blood lymphocytes of newborns after vitamin K prophylaxis at birth. Pediatr Res 1991; 30: 550-553
    CrossrefPubMedGoogle Scholar