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A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin

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Abstract

We have studied the largest kindred with familial dysalbuminemic hyperthyroxinemia (FDH) thus far reported, comprising thirty-three blood relations in four generations and three of their spouses. Our objective was to complement previous evidence concerning the precise mode of inheritance of FDH and to detect any other features of the disorder that had not yet been noted. Among the thirty three, there were thirteen patients with FDH, eight males and five females, in all of whom the abnormality appeared to be fully expressed. Within the kindred, no affected female has borne a female child, but transmission from female to male, male to male, and male to female has been observed. Among the offspring of individuals with FDH, the overall observed frequency of FDH in three filial generations was 12/22, or 54.5 per cent, yielding a computed penetrance ratio of 1.09. Four of the patients with FDH had been investigated for hyperthyroidism, and two of them had mistakenly been treated. Of particular interest were two women with FDH who were receiving oral contraceptives and whose serum thyroxine-binding globulin (TBG) concentrations were increased. The results of their thyroid function tests differed from those of patients with FDH whose TBG concentrations were normal and mainly suggested the presence of only a high TBG state. The diagnosis of FDH in these two patients was obscured, and probably would not have been made were it not for the present investigation, which led to the electrophoretic demonstration of increased binding of T4 by serum albumin. From these data we conclude that: (1) FDH should always be considered in the differential diagnosis of hyperthyroxinemia; (2) the coexistence of FDH with an acquired high TBG or significant thyroid malfunction may confound the diagnosis of the former; and (3) as others have indicated, FDH is transmitted by autosomal dominant inheritance, and at least in this family, with complete penetrance.

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Abbreviations

T4 :

thyroxine

T3 :

3,5,3′-triiodothyronine

rT3 :

3,3′5′-triiodothyronine

RT3U:

serum T3 uptake test

FT4 :

free T4 concentration FT4I, free T4 index

FT3I:

free T3 index

TBG:

thyroxine-binding globulin

TBPA:

thyroxine-binding prealbumin

References

  1. Stockigt 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: 353, 1981.

    Article  PubMed  CAS  Google Scholar 

  2. Docter R., Bos G., Krenning E.P., Fekkes D., Visser T.J., Hennemann G. Inherited T4 excess: a serum abnormality due to an increased affinity for modified albumin. Clin. Endocrinol. (Oxf.) 15: 363, 1981.

    Article  CAS  Google Scholar 

  3. Ruiz M., Rajatanavin R., Young R.A., Taylor C., Brown R., Braverman L.E., Ingbar S.H. Familial dysalbuminemic hyperthyroxinemia: a syndrome that can be confused with thyrotoxicosis. N. Engl. J. Med. 306: 635, 1982.

    Article  PubMed  CAS  Google Scholar 

  4. Barlow J.W., Csicsmann J.M., White El., Funder J.W., Stockigt J.R. Familial euthyroid thyroxine excess: characterization of abnormal intermediate affinity thyroxine binding to albumin. J. Clin. Endocrinol. Metab. 55: 244, 1982.

    Article  PubMed  CAS  Google Scholar 

  5. Borst G.C., Premachandra B.N., Burman K.D., Osburne R., Georges L.P., Johnsonbaugh R.E. Euthyroid familial hyperthyroxinemia due to abnormal thyroid hormone-binding protein. Am. J. Med. 73: 283, 1982.

    Article  PubMed  CAS  Google Scholar 

  6. Silverberg J.D.H., Premachandra B.N. Familial hyperthyroxinemia due to abnormal thyroid hormone binding. Ann. Intern. Med. 96: 183, 1982.

    Article  PubMed  CAS  Google Scholar 

  7. De Nayer P., Malvaux P. Hyperthyroxinemia associated with high thyroxine binding to albumin in euthyroid subjects. J. Endocrinol. Invest. 5: 383, 1982.

    Article  PubMed  Google Scholar 

  8. Lalloz M.R.A., Byfield P.G.H., Himsworth R.L. Hyperthyroxinemia: abnormal binding of T4 by an inherited albumin variant. Clin. Endocrinol. (Oxf.) 18: 11, 1983.

    Article  CAS  Google Scholar 

  9. Yabu Y., Amir S., Braverman L.E., Ingbar S.H. Heterogeneity of T4-binding serum albumins in normals and patients with familial dysalbuminemic hyperthyroxinemia (FDH). J. Clin. Endocrinol. Metab. 60: 451, 1985.

    Article  PubMed  CAS  Google Scholar 

  10. Mendel C.M., Cavalieri R.R. Thyroxine distribution and metabolism in familial dysalbuminemic hyperthyroxinemia. J. Clin. Endocrinol. Metab. 59: 499, 1984.

    Article  PubMed  CAS  Google Scholar 

  11. Rajatanavin R., Young R.A., Braverman L.E. Effect of chloride on serum thyroxine binding in familial dysalbuminemic hyperthyroxinemia. J. Clin. Endocrinol. Metab. 58: 388, 1984.

    Article  PubMed  CAS  Google Scholar 

  12. Rajatanavin R., Fournier L., DeCosimo D., Abreau C., Braverman L.E. Elevated serum free thyroxine by thyroxine analog radioimmunoassays in euthyroid patients with familial dysalbuminemic hyperthyroxinemia. Ann. Intern. Med. 97: 685, 1982.

    Article  Google Scholar 

  13. Brown B.W. Jr., Hollander M. Statistics. A Biomedical Introduction. John Wiley and Sons, New York, 1977.

    Google Scholar 

  14. Borst G.C., Eil C., Burman K.D. Euthyroid hyperthyroxinemia. Ann. Intern. Med. 98: 366, 1983.

    Article  PubMed  CAS  Google Scholar 

  15. Rajatanavin R., Braverman L.E. Euthyroid hyperthyroxinemia. J. Endocrinol. Invest. 6: 493, 1983.

    Article  PubMed  CAS  Google Scholar 

  16. Moses A.C., Lawlor J., Haddow J., Jackson I.M.D. Familial euthyroid hyperthyroxinemia resulting from increased thyroxine binding to thyroxine-binding prealbumin. N. Engl. J. Med. 306: 966, 1982.

    Article  PubMed  CAS  Google Scholar 

  17. Lalloz M.R.A., Byfield P.G.H., Himsworth R.L. A prealbumin variant with an increased affinity for T4 and reverse-T3. Clin. Endocrinol. (Oxf.) 21: 331, 1984.

    Article  CAS  Google Scholar 

  18. Jacobsson B., Pettersson T., Sandstedt B., Carlstrom A. Prealbumin in the islets of Langerhans. I.R.C.S. Med. Sci. 7: 590, 1979.

    CAS  Google Scholar 

  19. Rajatanavin R., Liberman C., Lawrence G.D., D’Arcangues C.M., Young R.A., Emerson C.H. Prealbumin excess in islet cell carcinoma. J. Clin. Endocrinol. Metab. 61: 17, 1985.

    Article  PubMed  CAS  Google Scholar 

  20. Lalloz M.R.A., Byfield P.G.H., Himsworth R.L. A new and distinctive albumin variant with increased affinities for both triiodothyronines and causing hyperthyroxinemia. Clin. Endocrinol. (Oxf.) 22: 521, 1985.

    Article  CAS  Google Scholar 

  21. Croxson M.S., Palmer B.N., Holdaway I.M., Frengley P.A., Evans M.C. Detection of familial dysalbuminaemic hyperthyroxinemia. Br. Med. J. 290: 1099, 1985.

    Article  CAS  Google Scholar 

  22. Young R., Stoffer S., Braverman L.E. Familial dysalbuminemic hyperthyroxinemia (FDH) associated with primary thyroid disease. Am. J. Med. (in press).

  23. Stockigt J.R., Dyer S.A., Mohr V.S., White E.L., Barlow J.W. Specific methods to identify plasma binding abnormalities in euthyroid hyperthyroxinemia. J. Clin. Endocrinol. Metab. 62: 230, 1986.

    Article  PubMed  CAS  Google Scholar 

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Supported in part by research grants AM-18416, AM-18919, AM-27196, and AM-07302 from the NIADDKD, National Institutes of Health, Bethesda, MD.

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Yeo, P.P.B., Yabu, Y., Etzkorn, J.R. et al. A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin. J Endocrinol Invest 10, 33–38 (1987). https://doi.org/10.1007/BF03347147

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