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Decrease in androgen binding and effect of androgen treatment in a case of X-linked bulbospinal neuronopathy

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Abstract

X-linked recessive bulbospinal neuronopathy is a motoneuron disorder to be distinguished from amyotrophic lateral sclerosis. Effective treatment is not known. Patients with X-linked recessive bulbospinal neuronopathy may show gynecomastia and testicular atrophy, and a mutation in the androgen receptor gene has been found associated with the disease. Intermediate steps leading from the androgen receptor abnormality to the clinical syndrome have not yet been elucidated. Therefore, binding of androgen ([3H]dihydrotestosterone) to its specific receptor by genital skin fibroblasts cultured from a patient with X-linked recessive bulbospinal neuronopathy and confirmed androgen receptor mutation was studied. Markedly decreased binding capacity was found. We treated the patient for 6 months with nandrolone-decanoate. No effect on his neuromuscular status was observed during 2 years of follow-up.

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Abbreviations

AR:

androgen receptor

BSN:

X-linked recessive bulbospinal neuronopathy

References

  1. Amato AA, Prior TW, Barohn RJ, Snyder P, Papp A, Mendell JR (1993) Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor gene. Neurology 43:791–794

    Google Scholar 

  2. Arbizu T, Santamaria J, Gomez JM, Quilez A, Serra JP (1983) A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failure. J Neurol Sci 59:371–382

    Google Scholar 

  3. Bals-Pratsch M, Schweikert H-U, Nieschlag E (1990) Androgen receptor disorder in three brothers with bifid prepenile scrotum and hypospadias. Acta Endocrinol 123:271–276

    Google Scholar 

  4. Belsham DD, Yee WC, Greenberg CR, Wrogemann K (1992) Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy. J Neurol Sci 112:133–138

    Google Scholar 

  5. Biancalana V, Serville F, Pommier J, Julien J, Hanauer A, Mandel JL (1992) Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy. Hum Mol Genet 1:255–258

    Google Scholar 

  6. Breiner M, Romalo G, Schweikert H-U (1986) Inhibition of androgen receptor binding by natural and synthetic steroids in cultured human genital skin fibroblasts. Klin Wochenschr 64:732–737

    Google Scholar 

  7. Brown TR, Migeon J (1981) Cultured human fibroblasts, a model for the study of androgen action. Mol Cell Biochem 36:3–22

    Google Scholar 

  8. Brown TR, Rothwell SW, Migeon CJ (1981) Comparison of methyl trienolone and dihydrotestosterone binding and metabolism in human genital skin fibroblasts. J Steroid Biochem 14:1013–1022

    Google Scholar 

  9. Choi WT, Maclean HE, Chu S, Warne GL, Zajac JD (1993) Kennedy's disease: genetic diagnosis of an inherited form of motor neuron disease. Aust NZ J Med 23:187–192

    Google Scholar 

  10. Doyu M, Sobue G, Mukai E, Kachi T, Yasuda T, Mitsuma T, Takahashi A (1992) Severity of X-linked recessive bulbospinal neuronopathy correlates with size of the tandem CAG repeat in androgen receptor gene. Ann Neurol 32:707–710

    Google Scholar 

  11. Doyu M, Sobue G, Mitsuma T, Uchida M, Iwase T, Takahashi A (1993) Very late onset X-linked recessive bulbospinal neuronopathy: mild clinical features and a mild increase in the size of tandem CAG repeat in androgen receptor gene. J Neurol Neurosurg Psychiatry 56:832–833

    Google Scholar 

  12. Edwards A, Hammond HA, Jin L, Caskey CT, Chakraborty R (1992) Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics 12:241–253

    Google Scholar 

  13. Griffin JE (1992) Androgen resistance — the clinical and molecular spectrum. N Engl J Med 326:611–618

    Google Scholar 

  14. Grüner BM, Müller CR (1992) Genkartierung und molekulare Diagnose den X-chromosomal rezessiven bulbospinalen Muskelatrophie (Typ Kennedy). Akt Neurol 19:70–72

    Google Scholar 

  15. Harding AE, Thomas PK, Baraitser M, Bradbury PG, Morgan-Hughes JA, Ponsford JR (1982) X-linked recessive bulbospinal neuronopathy: a report of ten cases. J Neurol Neurosurg Psychiatry 45:1012–1019

    Google Scholar 

  16. Igarashi S, Tanno Y, Onodera O, Yamazaki M, Sato S, Ishikawa A, Miyatani N, Nagashima M, Ishikawa Y, Sahashi K, Ibi T, Miyatake T, Tsuji S (1992) Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy. Neurology 42:2300–2302

    Google Scholar 

  17. Kaneko K, Igarashi S, Miyatake T, Tsuji S (1993) Hypertrophic cardiomyopathy and increased number of CAG repeats in the androgen receptor gene. Am Heart J 126:248–249

    Google Scholar 

  18. Kaneko K, Igarashi S, Miyatake T, Tsuji S (1993) Essential tremor' and CAG repeats in the androgen receptor gene. Neurology 43:1618–1619

    Google Scholar 

  19. Kennedy WR, Alter M, Sung JH (1968) Progressive proximal spinal and bulbar muscular atrophy of late onset. Neurology 18:71–680

    Google Scholar 

  20. Kurz EM, Sengelaub DR, Arnold A (1986) Androgens regulate the dendritic length of mammalian motoneurons in adulthood. Science 232:395–398

    Google Scholar 

  21. La Spada AR, Wilson EM, Lubahn DB, Handing AE, Fischbeck KH (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352:77–79

    Google Scholar 

  22. La Spada AR, Roling DB, Harding AE, Warner CL, Spiegel R, Hausmanowa-Petrusewicz I, Yee W-C, Fischbeck KH (1992) Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. Nature Genet 2:301–304

    Google Scholar 

  23. Leshin M, Griffin JE, Wilson JD (1978) Hereditary male pseudohermaphroditism associated with an unstable form of 5α-reductase. J Clin Invest 62:685–691

    Google Scholar 

  24. Lowry OH, Rosebrough ND, Randall RH, Farr AL (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193:265–275

    Google Scholar 

  25. Mann K, Siddle K (1988) Evidence for free β-subunit secretion in so-called human chorionic gonadotropin-positive seminoma. Cancer 62:2378–2382

    Google Scholar 

  26. Matsuura T, Demura T, Aimoto Y, Mizuno T, Moriwaka F, Tashiro K (1992) Androgen receptor abnormality in X-linked spinal and bulbar muscular atrophy. Neurology 42:1724–1726

    Google Scholar 

  27. Matsuura T, Ogata A, Demura T, Moriwaka F, Tashiro K, Koyanagi T, Nagashima K (1993) Identification of androgen receptor in the rat spinal motoneurons. Immunohistochemical and immunoblotting analyses with monoclonal antibody. Neurosci Lett 158:5–8

    Google Scholar 

  28. McPhaul MJ, Marcelli M, Tilley WD, Griffin JE, Isidro-Gutierrez RF, Wilson JD (1991) Molecular basis of androgen resistance in a family with a qualitative abnormality of the androgen receptor and responsive to high-dose therapy. J Clin Invest 87:1413–1421

    Google Scholar 

  29. Mhatre AN, Trifiro MA, Kaufman M, Kazemi-Esfarjani P, Figlewicz D, Rouleau G, Pinsky L (1993) Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy. Nature Genet 5:184–188

    Google Scholar 

  30. Nakamura M, Mita S, Murakami T, Uchino M, Watanabe S, Tokunaga M, Kumamoto T, Ando M (1994) Exonic trinucleotide repeats and expression of androgen receptor gene in spinal cord from X-linked spinal and bulbar muscular atrophy. J Neurol Sci 122:74–79

    Google Scholar 

  31. Norris FH, Calanchini PR, Fallat RJ, Panchari S, Jewett B (1974) The administration of guanidine in amyotrophic lateral sclerosis. Neurology 24:721–728

    Google Scholar 

  32. Price P, Wass JAH, Griffin JE, Leshin M, Savage MO, Large DM, Bu'Lock DE, Anderson DC, Wilson JD, Besser GM (1984) High dose androgen therapy in male pseudohermaphroditism due to 5α-reductase deficiency and disorders of the androgen receptor. J Clin Invest 74:1496–1508

    Google Scholar 

  33. Reiter M, Witt TN (1985) Bulbospinale hereditäre motorische Neuropathie (BSHMN), Falldarstellung unter besonderer Berücksichtigung elektrophysiologischer Befunde. Verh Dtsch Ges Neurol 3:828–832

    Google Scholar 

  34. Sar M, Stumpf WE (1977) Androgen concentration in motor neurons of cranial nerves and spinal cord. Science 197:77–80

    Google Scholar 

  35. Scatchard G (1949) The attraction of proteins for small molecules and ions. Ann NY Acad Sci 5:660–672

    Google Scholar 

  36. Schweikert H-U (1979) Conversion of androstenedione to estrione in human fibroblasts cultured from prostate, genital and nongenital skin. Horm Metab Res 11:635–640

    Google Scholar 

  37. Schweikert H-U, Milewich L, Wilson JD (1976) Aromatization of androstenedione by cultured human fibroblasts. J Clin Endocrinol Metab 43:785–795

    Google Scholar 

  38. Schweikert H-U, Schlüter M, Romalo G (1989) Intracellular and nuclear binding of [3H]dihydrotestosterone in cultured genital skin fibroblasts of patients with severe hypospadias. J Clin Invest 83:662–668

    Google Scholar 

  39. Sobue G, Hashizume Y, Mukai E, Hirayama M, Mitsuma T, Takahashi A (1989) X-linked recessive bulbospinal neuronopathy. Brain 112:209–232

    Google Scholar 

  40. Sobue G, Doyu M, Kachi T, Yasuda T, Mukai E, Kumagai T, Mitsuma T (1993) Subclinical phenotypic expressions in heterozygous females of X-linked recessive bulbospinal neuronopathy. J Neurol Sci 117:74–78

    Google Scholar 

  41. Thornton CA, Johnson K, Moxley RT (1994) Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes. Ann Neurol 35:104–107

    Google Scholar 

  42. Trapman J, Brinkmann AO (1993) Mutations in the androgen receptor. Ann NY Acad Sci 684:85–93

    Google Scholar 

  43. Warner CL, Griffin JE, Wilson JD, Jacobs LD, Murray KR, Fischbeck KH, Dickoff D, Griggs RC (1992) X-linked spinomuscular atrophy: a kindred with associated abnormal androgen receptor binding. Neurology 42:2181–2184

    Google Scholar 

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Danek, A., Witt, T.N., Mann, K. et al. Decrease in androgen binding and effect of androgen treatment in a case of X-linked bulbospinal neuronopathy. Clin Investig 72, 892–897 (1994). https://doi.org/10.1007/BF00190748

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