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Volumn 124, Issue 3, 2000, Pages 161-172

Familial dysalbuminemic hyperthyroxinemia may result in altered warfarin pharmacokinetics

Author keywords

Familial dysalbuminemic hyperthyroxinemia; Human serum albumin; Pharmacokinetics; Warfarin

Indexed keywords

HUMAN SERUM ALBUMIN; RECOMBINANT PROTEIN; THYROXINE; WARFARIN; ARGININE; HISTIDINE; SERUM ALBUMIN;

EID: 0033625049     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-2797(99)00143-X     Document Type: Article
Times cited : (35)

References (26)
  • 1
    • 0028338869 scopus 로고
    • A point mutation in the human serum albumin gene results in familial dysalbuminemic hyperthyroxinemia
    • Petersen C.E., Scottolini A.G., Cody L.R., Mande M., Riemer N., Bhagavan N.V. A point mutation in the human serum albumin gene results in familial dysalbuminemic hyperthyroxinemia. J. Med. Genet. 31:1994;355-359.
    • (1994) J. Med. Genet. , vol.31 , pp. 355-359
    • Petersen, C.E.1    Scottolini, A.G.2    Cody, L.R.3    Mande, M.4    Riemer, N.5    Bhagavan, N.V.6
  • 2
    • 0028024140 scopus 로고
    • An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families
    • Sunthornthepvarakul T., Angekeow P., Weis R.E., Hayashi Y., Refetoff S. An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families. Biochem. Biophys. Res. Commun. 202:1994;781-787.
    • (1994) Biochem. Biophys. Res. Commun. , vol.202 , pp. 781-787
    • Sunthornthepvarakul, T.1    Angekeow, P.2    Weis, R.E.3    Hayashi, Y.4    Refetoff, S.5
  • 3
    • 0030920437 scopus 로고    scopus 로고
    • A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of the familial dysalbuminemic hyperthyroxinemia in a Japanese kindred
    • Wada N., Chiba H., Shimizu C., Kijima H., Kubo M., Koike T. A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of the familial dysalbuminemic hyperthyroxinemia in a Japanese kindred. J. Clin. Endocrinol. Metab. 82:1997;246-250.
    • (1997) J. Clin. Endocrinol. Metab. , vol.82 , pp. 246-250
    • Wada, N.1    Chiba, H.2    Shimizu, C.3    Kijima, H.4    Kubo, M.5    Koike, T.6
  • 4
    • 0026664548 scopus 로고
    • Atomic structure and chemistry of human serum albumin
    • He X.M., Carter D.C. Atomic structure and chemistry of human serum albumin. Nature. 358:1992;208-215.
    • (1992) Nature , vol.358 , pp. 208-215
    • He, X.M.1    Carter, D.C.2
  • 5
    • 0016695949 scopus 로고
    • Spectroscopic techniques in the study of protein binding: A fluorescence technique for the evaluation of albumin binding and displacement of warfarin and warfarin-alchohol
    • Sudlow G., Birkett D.J., Wade D.N. Spectroscopic techniques in the study of protein binding: A fluorescence technique for the evaluation of albumin binding and displacement of warfarin and warfarin-alchohol. Clin. Exp. Pharmacol. Physiol. 2:1975;129-140.
    • (1975) Clin. Exp. Pharmacol. Physiol. , vol.2 , pp. 129-140
    • Sudlow, G.1    Birkett, D.J.2    Wade, D.N.3
  • 6
    • 0017174391 scopus 로고
    • Further characterization of specific drug binding sites on human serum albumin
    • Sudlow G., Birkett D.J., Wade D.N. Further characterization of specific drug binding sites on human serum albumin. Mol. Pharmacol. 12:1976;1052-1061.
    • (1976) Mol. Pharmacol. , vol.12 , pp. 1052-1061
    • Sudlow, G.1    Birkett, D.J.2    Wade, D.N.3
  • 7
    • 0032878898 scopus 로고    scopus 로고
    • Investigations of two unique genotypes that result in familial dysalbuminemic hyperthyroxinemia
    • Petersen C.E., Ha C.-E., Harohalli K., Park D.S., Feix J., Isozaki O., Bhagavan N.V. Investigations of two unique genotypes that result in familial dysalbuminemic hyperthyroxinemia. Clin. Chem. 45(8):1999;1248-1255.
    • (1999) Clin. Chem. , vol.45 , Issue.8 , pp. 1248-1255
    • Petersen, C.E.1    Ha, C.-E.2    Harohalli, K.3    Park, D.S.4    Feix, J.5    Isozaki, O.6    Bhagavan, N.V.7
  • 8
    • 0021738399 scopus 로고
    • Familial dysalbuminemic hyperthyroxinemia: A study of four probands and a kindred of three
    • Scottolini A.G., Bhagavan N.V., Oshiro T., Powers L. Familial dysalbuminemic hyperthyroxinemia: a study of four probands and a kindred of three. Clin. Chem. 30:1984;1179-1181.
    • (1984) Clin. Chem. , vol.30 , pp. 1179-1181
    • Scottolini, A.G.1    Bhagavan, N.V.2    Oshiro, T.3    Powers, L.4
  • 9
    • 0018286658 scopus 로고
    • Inherited abnormal thyroid hormone-binding protein causing selective increase of total serum thyroxine
    • Lee W.N.P., Golden M.P., Van Herlem A.J., Lippe B.M., Kaplan S.A. Inherited abnormal thyroid hormone-binding protein causing selective increase of total serum thyroxine. J. Clin. Endocrinol. Metab. 49:1979;292-299.
    • (1979) J. Clin. Endocrinol. Metab. , vol.49 , pp. 292-299
    • Lee, W.N.P.1    Golden, M.P.2    Van Herlem, A.J.3    Lippe, B.M.4    Kaplan, S.A.5
  • 10
    • 0019748753 scopus 로고
    • Familial euthyroid thyroxine excess: An appropriate response to abnormal thyroxine binding associated with albumin
    • Stockight J.R., Topliss D.J., Barlow J.W., White E.L., Hurley D.M., Taft P. Familial euthyroid thyroxine excess: an appropriate response to abnormal thyroxine binding associated with albumin. J. Clin. Endocrinol. Metab. 53:1981;353-359.
    • (1981) J. Clin. Endocrinol. Metab. , vol.53 , pp. 353-359
    • Stockight, J.R.1    Topliss, D.J.2    Barlow, J.W.3    White, E.L.4    Hurley, D.M.5    Taft, P.6
  • 11
    • 0019426433 scopus 로고
    • Inherited thyroxine excess: A serum abnormality due to an increased affinity for modified albumin
    • Docter R., Bos G., Krenning E.P., Fekkes D., Visser T.J., Hennemann G. Inherited thyroxine excess: a serum abnormality due to an increased affinity for modified albumin. Clin. Endocrinol. 15:1981;363-371.
    • (1981) Clin. Endocrinol. , vol.15 , pp. 363-371
    • Docter, R.1    Bos, G.2    Krenning, E.P.3    Fekkes, D.4    Visser, T.J.5    Hennemann, G.6
  • 13
    • 0030945733 scopus 로고    scopus 로고
    • Mutagenesis studies of thyroxine binding to human serum albumin define an important structural characteristic of subdomain 2A
    • Petersen C.E., Ha C.-E., Harohalli K., Park D.S., Bhagavan N.V. Mutagenesis studies of thyroxine binding to human serum albumin define an important structural characteristic of subdomain 2A. Biochemistry. 36:1997;7012-7017.
    • (1997) Biochemistry , vol.36 , pp. 7012-7017
    • Petersen, C.E.1    Ha, C.-E.2    Harohalli, K.3    Park, D.S.4    Bhagavan, N.V.5
  • 14
    • 0029783551 scopus 로고    scopus 로고
    • Mutations in a specific human serum albumin thyroxine binding site define the structural basis of familial dysalbuminemic hyperthyroxinemia
    • Petersen C.E., Ha C.-E., Jameson D.M., Nadhipuram N.V. Mutations in a specific human serum albumin thyroxine binding site define the structural basis of familial dysalbuminemic hyperthyroxinemia. J. Biol. Chem. 271:1996;19110-19117.
    • (1996) J. Biol. Chem. , vol.271 , pp. 19110-19117
    • Petersen, C.E.1    Ha, C.-E.2    Jameson, D.M.3    Nadhipuram, N.V.4
  • 15
    • 0020400574 scopus 로고
    • Familial euthyroid thyroxine excess: Characterization of abnormal intermediate affinity thyroxine binding to albumin
    • Barlow J.W., Crissmann J.M., White E.L., Funder J.W., Stockigt J.R. Familial euthyroid thyroxine excess: characterization of abnormal intermediate affinity thyroxine binding to albumin. J. Clin. Endocrinol. Metab. 55:1982;244-250.
    • (1982) J. Clin. Endocrinol. Metab. , vol.55 , pp. 244-250
    • Barlow, J.W.1    Crissmann, J.M.2    White, E.L.3    Funder, J.W.4    Stockigt, J.R.5
  • 17
    • 0025998502 scopus 로고
    • Prevalence of familial dysalbuminemic hyperthyroxinemia in serum samples received for thyroid testing
    • Arevalo G. Prevalence of familial dysalbuminemic hyperthyroxinemia in serum samples received for thyroid testing. Clin. Chem. 37:1991;1430-1431.
    • (1991) Clin. Chem. , vol.37 , pp. 1430-1431
    • Arevalo, G.1
  • 18
    • 0017188327 scopus 로고
    • Serum protein binding as a determinant of warfarin body clearance and anticoagulant effect
    • Yacobi A., Udall J.A., Levy G. Serum protein binding as a determinant of warfarin body clearance and anticoagulant effect. Clin. Pharmacol. Ther. 19:1976;552-558.
    • (1976) Clin. Pharmacol. Ther. , vol.19 , pp. 552-558
    • Yacobi, A.1    Udall, J.A.2    Levy, G.3
  • 19
    • 0019784833 scopus 로고
    • Antipyrine and warfarin disposition in a patient with idiopathic hypoalbuminemia
    • Piroli R.J., Passananti G.T., Shively C.A., Vesell E.S. Antipyrine and warfarin disposition in a patient with idiopathic hypoalbuminemia. Clin. Pharmacol. Ther. 30:1981;810-816.
    • (1981) Clin. Pharmacol. Ther. , vol.30 , pp. 810-816
    • Piroli, R.J.1    Passananti, G.T.2    Shively, C.A.3    Vesell, E.S.4
  • 21
    • 0021091394 scopus 로고
    • Removal of fatty acids from serum albumin by Lipidex 1000 chromatography
    • Glatz J.F.C., Veerkamp J.H. Removal of fatty acids from serum albumin by Lipidex 1000 chromatography. J. Biophys. Methods. 8:1983;57-61.
    • (1983) J. Biophys. Methods , vol.8 , pp. 57-61
    • Glatz, J.F.C.1    Veerkamp, J.H.2
  • 22
    • 0023262038 scopus 로고
    • Influence of the N-B transition of human serum albumin on the structure of the warfarin binding site
    • Sadako K.-M., Horie T., Awazu S. Influence of the N-B transition of human serum albumin on the structure of the warfarin binding site. Biochim. Biophys. Acta. 915:1987;277-283.
    • (1987) Biochim. Biophys. Acta , vol.915 , pp. 277-283
    • Sadako, K.-M.1    Horie, T.2    Awazu, S.3
  • 23
    • 0017352224 scopus 로고
    • Optical studies on the mechanism of the interaction of the enantiomers of the anticoagulant drugs phenprocoumon and warfarin with human serum albumin
    • Brown N.A., Jahnchen E., Muller W.E., Wollert U. Optical studies on the mechanism of the interaction of the enantiomers of the anticoagulant drugs phenprocoumon and warfarin with human serum albumin. Mol. Pharmacol. 13:1977;70-79.
    • (1977) Mol. Pharmacol. , vol.13 , pp. 70-79
    • Brown, N.A.1    Jahnchen, E.2    Muller, W.E.3    Wollert, U.4
  • 24
    • 0025157284 scopus 로고
    • Binding of warfarin, salicyclate, and diazepam to genetic variants of human serum albumin with known mutations
    • Kragh-Hansen U., Brennan S.O., Galliano M., Sugita O. Binding of warfarin, salicyclate, and diazepam to genetic variants of human serum albumin with known mutations. Mol. Pharmacol. 37:1989;238-242.
    • (1989) Mol. Pharmacol. , vol.37 , pp. 238-242
    • Kragh-Hansen, U.1    Brennan, S.O.2    Galliano, M.3    Sugita, O.4
  • 25
    • 0019423702 scopus 로고
    • Cooperative interaction of warfarin and phenylbutazone with human serum albumin
    • Madsen B.W., Ellis G.M. Cooperative interaction of warfarin and phenylbutazone with human serum albumin. Biochem. Pharmacol. 30:1981;1169-1173.
    • (1981) Biochem. Pharmacol. , vol.30 , pp. 1169-1173
    • Madsen, B.W.1    Ellis, G.M.2
  • 26
    • 0029835505 scopus 로고    scopus 로고
    • Warfarin resistance: Diagnosis and therapeutic alternatives
    • Hulse M.L. Warfarin resistance: diagnosis and therapeutic alternatives. Pharmacotherapy. 16:1996;1009-1017.
    • (1996) Pharmacotherapy , vol.16 , pp. 1009-1017
    • Hulse, M.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.