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The Role of the Thyroxine Loading Test in Diagnosing Defects of Thyroid Hormonobiogenesis

Year 1981, Volume: 34 Issue: 4, 621 - 638, 31.12.1981

Abstract

Tiroid hormonlarının sentez, dönüşüm ve etkisindeki defektler, son yıllarda önem kazanmıştır. Bu defektler, tiroid patolojisinin genelinde nadir görülse de tiroidolojide büyük önem taşır. Mevcut tanı testlerinin sınırlılıkları, tiroid hormonbiyojenezine dair bozuklukların saptanmasında güçlük yaratmaktadır. Bu çalışmada, radyoaktif işaretli hormonların yerine, ağız yoluyla verilen işaretsiz tiroksin ile yapılan yükleme testi değerlendirilmiştir. A.Ü. Tıp Fakültesi Endokrinoloji Kürsüsünde sekiz dishormonojenez vakasında uygulanan test, T4'ün T3'e periferik dönüşüm defektlerini saptamada faydalı sonuçlar sağlamıştır. Bulgular, T4-toksikoz olgularında bu defektlerin olası rolüne işaret etmektedir faydalı sonuçlar sağlamıştır. Bulgular, T4-toksikoz olgularında bu defektlerin olası rolüne işaret etmektedir.

References

  • 1 - Charlesanslar
  • 1 - Charles, P., DeGroot, L.J. : Dyshormonogen, P., DeGroot, L.J. : Dyshormonogenetic goitre. Clinics in Endocrinologyetic goitre. Clinics in Endocrinology and Metabolism. and Metabolism. Vol. 8, No. 1, Vol. 8, No. 1, 145–165, 1979.
  • 145–165, 1979.
  • 2 - DeGroot, L.J2 - DeGroot, L.J., Stanbury, J.B., Stanbury, J.B. : Hereditary defects. : Hereditary defects in hormone synthesis in hormone synthesis, transport, or action, transport, or action. In: The Thyroid. In: The Thyroid and its Diseases, Wiley, New York and its Diseases, 1975.
  • 3 - Fraser, Wiley, New York, 1975.
  • 3 - Fraser, G.R. : The genetics of thyroid disease, G.R. : The genetics of thyroid disease. In: Progress in Medical Genetics. In: Progress in Medical Genetics, Vol. 6, Grune Strat, Vol. 6, Grune Stratton, New York, 1969.
  • 4 - Koloğluton, New York, 196, S. : Tiro-metabolik status indeksi (TMSI) ve radio9.
  • 4 - Koloğlu, S. : Tiro-metabolik status indeksi (TMSI) ve radioimmunoassay ile tiroid fonksiyon testimmunoassay ile tiroid fonksiyon testlerinin önemi. Alerinin önemi. A.Ü. Tıp Fakültes.Ü. Tıp Fakültesi Yayını, Ankara, 1977.
  • 5 - Kusakabe, T., Miyatei Yayını, Ankara, 1977.
  • 5 - Kusakabe, T., Miyate, T. : Defective deiodination of, T. : Defective deiodination of 131I-labeled L-diidotyrosine. J Clin 131I-labeled L-diidotyrosine. J Clin Endocrinol Metab Endocrinol Metab, 23:1132, 1963., 23:1132, 1963.
  • 6 - Morgans,
  • 6 - Morgans, M.E., Trotter, W.R. : Defective organic M.E., Trotter, W.R. : Defective organic binding of iodine binding of iodine in Hashimoto's thyroid in Hashimoto's thyroiditis. Lancet, 1:553, 1957.
  • 7 - Murray, I.P.C., McGirree, M. : Radioitis. Lancet, 1:553, 1957.
  • 7 - Murray, I.P.C., McGirree, M. : Radioactive iodine studiesactive iodine studies in Hashimoto’s thyroid in Hashimoto’s thyroiditis. BMJ, 1:838, 1960.
  • 8 - Niall, H.D., Wellitis. BMJ, 1:838, 1960.
  • 8 - Niall, H.D., Wellby, M.L. et al. :by, M.L. et al. : Familial goitre Familial goitre with iodotyrosine deiodinase defect with iodotyrosine deiodinase defect. Aust Ann Med, . Aust Ann Med, 17:89, 1968.
  • 17:89, 1968.
  • 9 - Niepomniszcze9 - Niepomniszcze, H., DeGrossi, O, H., DeGrossi, O.J. et al. : Famil.J. et al. : Familial goiter with perial goiter with peroxidase defect. Thyoxidase defect. Thyroid Research, 470, 1976.
  • 10 - Querroid Research, 470, 1976.
  • 10 - Querido, A., Stanburyido, A., Stanbury, J.B. et al. : Met, J.B. et al. : Metabolism of iodotyabolism of iodotyrosines III. J Clinrosines III. J Clin Endocrinol Metab Endocrinol Metab, 16:1096, 1966., 16:1096, 1966.
  • 11 - Rimoin,
  • 11 - Rimoin, D.L., Schimke, R.N. : Familial go D.L., Schimke, R.N. : Familial goiter due to thyroxine biosynthesisiter due to thyrox defect. In: Geneticine biosynthesis defect. In: Genetic Disorders of the Disorders of the Endocrine Glands Endocrine Glands. Mosby, St. Louis. Mosby, St. Louis, 1971.
  • 12 - Stan, 1971.
  • 12 - Stanbury, J.B., Aiginer, P., Harbison, Mbury, J.B., Aiginer, P., Harbison, M.D. : Familial goiter and related.D. : Familial goiter and related disorders. In: End disorders. In: Endocrinology (Ed: Deocrinology (Ed: DeGroot, L.J.), GrGroot, L.J.), Grune Stration, New York, 1978.
  • 13 - Stanbury, J.B., Ohela, K., Pitt-Rivers, R. : Metabolism of iodine in goitrous cretins. J Clin Endune Stration, New York, 1978.
  • 13 - Stanbury, J.B., Ohela, K., Pitt-Rivers, R. : Metabolism of iodine in goitrous cretins. J Clin Endocrinol Metab, 15ocrinol Metab, 15:54, 1955.
  • 14 - Stanbury, J.B:54, 1955.
  • 14 - Stanbury, J.B., Meijer, J.W. et al. : Metabolism., Meijer, J.W. et al. : Metabolism of iodotyrosines II. J Clin Endocr of iodotyrosines II. J Clin Endocrinol Metab, 16:848inol Metab, 16:848, 1966.
  • 15 - Stanbury, J.B., Wynga, 1966.
  • 15 - Stanbury, J.B., Wyngaarden, J.B., Fredricksn, D.S. : Familial goiter. In: The Metabolic Basis of Medicine. McGraw-Hill, New York, 1966.
  • 16 - Stewart, R.D.H., Murray, I.P.C. : Evaluation of the perchlorate discharge test. J Clin Endocrinol Metab, 26:1050, 1966.

Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri

Year 1981, Volume: 34 Issue: 4, 621 - 638, 31.12.1981

Abstract

Defects in thyroid hormone synthesis, conversion, and action have gained increasing attention in recent years. Although rare in general thyroid pathology, they provide critical insight into thyroid physiology. Diagnostic challenges arise due to limitations in available tests. To address this, a non-radioactive thyroxine loading test was developed and assessed in eight cases of dishormonogenesis. Following oral administration of 3 mg thyroxine, serial hormone measurements were taken. The study demonstrated that this simple method could help identify peripheral conversion defects of T4 to T3. Observations also support a role for these defects in T4-toxicosis cases.

References

  • 1 - Charlesanslar
  • 1 - Charles, P., DeGroot, L.J. : Dyshormonogen, P., DeGroot, L.J. : Dyshormonogenetic goitre. Clinics in Endocrinologyetic goitre. Clinics in Endocrinology and Metabolism. and Metabolism. Vol. 8, No. 1, Vol. 8, No. 1, 145–165, 1979.
  • 145–165, 1979.
  • 2 - DeGroot, L.J2 - DeGroot, L.J., Stanbury, J.B., Stanbury, J.B. : Hereditary defects. : Hereditary defects in hormone synthesis in hormone synthesis, transport, or action, transport, or action. In: The Thyroid. In: The Thyroid and its Diseases, Wiley, New York and its Diseases, 1975.
  • 3 - Fraser, Wiley, New York, 1975.
  • 3 - Fraser, G.R. : The genetics of thyroid disease, G.R. : The genetics of thyroid disease. In: Progress in Medical Genetics. In: Progress in Medical Genetics, Vol. 6, Grune Strat, Vol. 6, Grune Stratton, New York, 1969.
  • 4 - Koloğluton, New York, 196, S. : Tiro-metabolik status indeksi (TMSI) ve radio9.
  • 4 - Koloğlu, S. : Tiro-metabolik status indeksi (TMSI) ve radioimmunoassay ile tiroid fonksiyon testimmunoassay ile tiroid fonksiyon testlerinin önemi. Alerinin önemi. A.Ü. Tıp Fakültes.Ü. Tıp Fakültesi Yayını, Ankara, 1977.
  • 5 - Kusakabe, T., Miyatei Yayını, Ankara, 1977.
  • 5 - Kusakabe, T., Miyate, T. : Defective deiodination of, T. : Defective deiodination of 131I-labeled L-diidotyrosine. J Clin 131I-labeled L-diidotyrosine. J Clin Endocrinol Metab Endocrinol Metab, 23:1132, 1963., 23:1132, 1963.
  • 6 - Morgans,
  • 6 - Morgans, M.E., Trotter, W.R. : Defective organic M.E., Trotter, W.R. : Defective organic binding of iodine binding of iodine in Hashimoto's thyroid in Hashimoto's thyroiditis. Lancet, 1:553, 1957.
  • 7 - Murray, I.P.C., McGirree, M. : Radioitis. Lancet, 1:553, 1957.
  • 7 - Murray, I.P.C., McGirree, M. : Radioactive iodine studiesactive iodine studies in Hashimoto’s thyroid in Hashimoto’s thyroiditis. BMJ, 1:838, 1960.
  • 8 - Niall, H.D., Wellitis. BMJ, 1:838, 1960.
  • 8 - Niall, H.D., Wellby, M.L. et al. :by, M.L. et al. : Familial goitre Familial goitre with iodotyrosine deiodinase defect with iodotyrosine deiodinase defect. Aust Ann Med, . Aust Ann Med, 17:89, 1968.
  • 17:89, 1968.
  • 9 - Niepomniszcze9 - Niepomniszcze, H., DeGrossi, O, H., DeGrossi, O.J. et al. : Famil.J. et al. : Familial goiter with perial goiter with peroxidase defect. Thyoxidase defect. Thyroid Research, 470, 1976.
  • 10 - Querroid Research, 470, 1976.
  • 10 - Querido, A., Stanburyido, A., Stanbury, J.B. et al. : Met, J.B. et al. : Metabolism of iodotyabolism of iodotyrosines III. J Clinrosines III. J Clin Endocrinol Metab Endocrinol Metab, 16:1096, 1966., 16:1096, 1966.
  • 11 - Rimoin,
  • 11 - Rimoin, D.L., Schimke, R.N. : Familial go D.L., Schimke, R.N. : Familial goiter due to thyroxine biosynthesisiter due to thyrox defect. In: Geneticine biosynthesis defect. In: Genetic Disorders of the Disorders of the Endocrine Glands Endocrine Glands. Mosby, St. Louis. Mosby, St. Louis, 1971.
  • 12 - Stan, 1971.
  • 12 - Stanbury, J.B., Aiginer, P., Harbison, Mbury, J.B., Aiginer, P., Harbison, M.D. : Familial goiter and related.D. : Familial goiter and related disorders. In: End disorders. In: Endocrinology (Ed: Deocrinology (Ed: DeGroot, L.J.), GrGroot, L.J.), Grune Stration, New York, 1978.
  • 13 - Stanbury, J.B., Ohela, K., Pitt-Rivers, R. : Metabolism of iodine in goitrous cretins. J Clin Endune Stration, New York, 1978.
  • 13 - Stanbury, J.B., Ohela, K., Pitt-Rivers, R. : Metabolism of iodine in goitrous cretins. J Clin Endocrinol Metab, 15ocrinol Metab, 15:54, 1955.
  • 14 - Stanbury, J.B:54, 1955.
  • 14 - Stanbury, J.B., Meijer, J.W. et al. : Metabolism., Meijer, J.W. et al. : Metabolism of iodotyrosines II. J Clin Endocr of iodotyrosines II. J Clin Endocrinol Metab, 16:848inol Metab, 16:848, 1966.
  • 15 - Stanbury, J.B., Wynga, 1966.
  • 15 - Stanbury, J.B., Wyngaarden, J.B., Fredricksn, D.S. : Familial goiter. In: The Metabolic Basis of Medicine. McGraw-Hill, New York, 1966.
  • 16 - Stewart, R.D.H., Murray, I.P.C. : Evaluation of the perchlorate discharge test. J Clin Endocrinol Metab, 26:1050, 1966.
There are 31 citations in total.

Details

Primary Language English
Subjects Endocrinology
Journal Section Research Article
Authors

Selahaddin Koloğlu This is me

Publication Date December 31, 1981
Published in Issue Year 1981 Volume: 34 Issue: 4

Cite

APA Koloğlu, S. (1981). Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri. Ankara Üniversitesi Tıp Fakültesi Mecmuası, 34(4), 621-638. https://izlik.org/JA39KW25EL
AMA 1.Koloğlu S. Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri. Ankara Üniversitesi Tıp Fakültesi Mecmuası. 1981;34(4):621-638. https://izlik.org/JA39KW25EL
Chicago Koloğlu, Selahaddin. 1981. “Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri”. Ankara Üniversitesi Tıp Fakültesi Mecmuası 34 (4): 621-38. https://izlik.org/JA39KW25EL.
EndNote Koloğlu S (December 1, 1981) Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri. Ankara Üniversitesi Tıp Fakültesi Mecmuası 34 4 621–638.
IEEE [1]S. Koloğlu, “Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri”, Ankara Üniversitesi Tıp Fakültesi Mecmuası, vol. 34, no. 4, pp. 621–638, Dec. 1981, [Online]. Available: https://izlik.org/JA39KW25EL
ISNAD Koloğlu, Selahaddin. “Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri”. Ankara Üniversitesi Tıp Fakültesi Mecmuası 34/4 (December 1, 1981): 621-638. https://izlik.org/JA39KW25EL.
JAMA 1.Koloğlu S. Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri. Ankara Üniversitesi Tıp Fakültesi Mecmuası. 1981;34:621–638.
MLA Koloğlu, Selahaddin. “Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri”. Ankara Üniversitesi Tıp Fakültesi Mecmuası, vol. 34, no. 4, Dec. 1981, pp. 621-38, https://izlik.org/JA39KW25EL.
Vancouver 1.Koloğlu S. Tiroid Hormonobiyojenez Defektlerinin Tanısında Tiroksin Yükleme Testinin Yeri. Ankara Üniversitesi Tıp Fakültesi Mecmuası [Internet]. 1981 Dec. 1;34(4):621-38. Available from: https://izlik.org/JA39KW25EL