Der Urologe, Ausgabe A

, Volume 42, Issue 10, pp 1345–1350 | Cite as

Erektile Dysfunktion—Wertigkeit neurophysiologischer Diagnoseverfahren

Zusammenfassung

An der Entstehung der erektilen Dysfunktion sind neurogene, insbesondere autonome Störungen, entscheidend beteiligt. Eine Erektion wird parasympathisch und sympathisch, vornehmlich über nichtcholinerge, nichtadrenerge Neurotransmitter und schließlich mit Hilfe der Aktivierung von zyklischen Monophosphaten induziert. Durch die resultierende Erschlaffung der glatten Gefäß- und Schwellkörpermuskulatur kommt es zur Tumeszenz und Rigidität und damit zur Erektion.

Die Diagnostik neurologischer Ursachen der erektilen Dysfunktion sollte eine ausführliche Anamneseerhebung und neurologische Untersuchung beinhalten. Klassische neurophysiologische Untersuchungen, wie etwa die Nadelmyographie des M. sphincter ani externus, Latenzbestimmungen des N. pudendus oder die Messung des Bulbokavernosusreflexes, reflektieren die Funktion der schnellleitenden, dick bemarkten Nervenfasern und sind oft nicht aussagekräftig, da sie nicht die kleinkalibrigen Nervenfasern beurteilen. Die Untersuchung dieser für die Erektion wesentlichen kleinkalibrigen Nervenfasern, z. B. mit Hilfe einer psychophysischen quantitativen Thermotestung, kann die Diagnostik der neurogenen erektilen Dysfunktion bereichern. Daneben kann die Beurteilung der Herzfrequenzvariabilität in Ruhe, während metronomischer Atmung (6/min), Valsalva-Manöver, sowie nach aktivem Aufstehen, hilfreich sein, eine autonome Neuropathie als Ursache einer erektilen Dysfunktion zu erfassen.

Schlüsselwörter

Erektile Dysfunktion Neurophysiologische Testung Autonome Neuropathie Small fiber neuropathy Thermotest Herzfrequenzvariabilität 

Abstract

Neurogenic, particularly autonomic disorders, frequently contribute to the etiology and pathophysiology of erectile dysfunction. Parasympathetic and sympathetic outflow mediates erection. Noncholinergic, nonadrenergic neurotransmitters induce activation of cyclic monophosphates, leading to relaxation of smooth muscles of the corpora cavernosa and by this to tumescence and rigidity, i.e. erection. The diagnosis of neurologic causes of erectile dysfunction requires a detailed history and neurologic examination. Conventional neurophysiological procedures evaluate the function of rapidly conducting, thickly myelinated nerve fibers only. Therefore, techniques such as sphincter ani externus electromyography, latency measurements of the pudendal nerve or bulbocavernosus reflex studies frequently do not contribute to the diagnostic process. The evaluation of small nerve fibers that are essential for erection, for example by means of psychophysical quantitative thermotesting, might improve the diagnosis of neurogenic causes of erectile dysfunction. In addition, the assessment of heart rate variability at rest, during metronomic breathing, Valsalva maneuver, and active standing might be helpful to identify an autonomic neuropathy as the cause of erectile dysfunction.

Keywords

Erectile dysfunction Neurophysiological testing Autonomic neuropathy Small fiber neuropathy Thermotest Heart rate variability 

Literatur

  1. 1.
    Abramowicz M (1992) Drugs that cause sexual dysfunction: An update. Med Lett Drugs Ther 34: 73–78PubMedGoogle Scholar
  2. 2.
    Andersson KE, Wagner G (1995) Physiology of penile erection. Physiol Rev 75: 191–236PubMedGoogle Scholar
  3. 3.
    Aoki H, Matsuzaka J, Yeh KH et al. (1994) Involvement of vasoactive intestinal polypeptide (VIP) as a humoral mediator of penile erection function in the dog. J Androl 15: 174–182Google Scholar
  4. 4.
    Boller F, Frank E (1982) Sexual dysfunction in neurological disorders. Raven Press, New YorkGoogle Scholar
  5. 5.
    Brindley GS (1991) Neurophysiology. In: Kirby RS, Carson CC, Webster GD (eds) Impotence: Diagnosis and management of male erectile dysfunction. Butterworth-Heinemann, Oxford, pp 27–31Google Scholar
  6. 6.
    Daitch JA, Lakin MM, Montague DK (1997) Nocturnal penile tumescence monitoring. In: Mulcahy JJ (ed) Diagnosis and management of male sexual dysfunction. Igaku-Shoin, New York, pp 55–73Google Scholar
  7. 7.
    Derouet H, Jost WH (1997) Neurophysiologische Untersuchungen. In: Stief CG, Hartmann U, Höfner K, Jonas U (Hrsg) Erektile Dysfunktion, Diagnostik und Therapie. Springer, Berlin Heidelberg New York Tokio, S 160–169Google Scholar
  8. 8.
    Ding YQ, Takada M, Kaneko T, Mizuno N (1995) Colocalization of vasoactive intestinal peptide and nitric oxide in penis-innervating neurones in the major pelvic ganglia of the rat. Neurosci Res 22: 129–131Google Scholar
  9. 9.
    Ellenberg M (1971) Impotence in diabetes: the neurologic factor. Ann Intern Med 75: 213–219Google Scholar
  10. 10.
    Feldman HA, Goldstein I, Hatzichristou DG, Krane RJ, McKinlay JB (1994) Impotence and its medical and psychosocial correlates: Results of the Massachusetts Male Aging Study. J Urol 151: 54–61PubMedGoogle Scholar
  11. 11.
    Fowler CJ (1992) Electrophysiologic evaluation of sexual dysfunction. In: Low PA (ed) Clinical autonomic disorders. Little, Brown and Company, Boston, pp 279–285Google Scholar
  12. 12.
    Gerstenberg TC, Nordling J, Halt P, Wagner G (1989) Standardized evaluation of erectile dysfunction in 95 consecutive patients. J Urol 141: 857–862Google Scholar
  13. 13.
    Ghezzi A, Callea L, Zaffaroni M, Montanini R, Tessera G (1991) Motor potentials of bulbo-cavernosus muscle after transcranial and lumbar magnetic stimulation: comparative study with bulbocavernosus reflex and pudendal evoked potentials. J Neurol Neurosurg Psychiatry 54: 524–526.Google Scholar
  14. 14.
    Hilz MJ (2002) Erektile Dysfunktion. MMW Fortschr Med 144: 41–44Google Scholar
  15. 15.
    Hilz MJ, Hecht M, Kölsch C (2000) Erektile Dysfunktion. Akt Neurologie 27: 1–12Google Scholar
  16. 16.
    Jevtich MJ, Kass M, Khavand M (1985) Changes in the corpora cavernosa of impotent diabetics. Comparing histological with clinical findings. J Urol (Paris) 91: 281Google Scholar
  17. 17.
    Jost WH, Schimrigk K (1994) A new method to determine pudendal nerve motor latency and central motor conduction time to the external anal sphincter. Electroenc Clin Neurophysiol 93: 237–239CrossRefGoogle Scholar
  18. 18.
    Kiff ES, Swash M (1984) Normal proximal and delayed distal conduction in the pudendal nerves of patients with idiopathic (neurogenic) faecal incontinence. J Neurol Neurosurg Psychiatry 47: 820–823PubMedGoogle Scholar
  19. 19.
    Kirby RS, Eardley I (1991) Initial assessment of patients with erectile dysfunction. In: Kirby RS, Carson CC, Webster GD (eds) Impotence: diagnosis and management of male erectile dysfunction. Butterworth-Heinemann, Oxford, pp 57–61Google Scholar
  20. 20.
    Kirkeby HJ, Jorgenson JC, Ottensen B (1991) Neuropeptid Y (NPY) in human penile corpus cavernosum tissue and circum flex veins: Occurence and in vitro effects. J Urol 145: 605–609Google Scholar
  21. 21.
    Kulzer B (1997) Verhaltenstherapie bei Diabetes Mellitus. In: Stief CG, Hartmann U, Hoefner K, Jonas U (Hrsg) Erektile Dysfunktion, Diagnostik und Therapie. Springer, Berlin Heidelberg New York Tokio, S 300–312Google Scholar
  22. 22.
    Lilius HG, Valtonen EJ, Wikstrom J (1976) Sexual problems in patients suffering from multiple sclerosis. Scand J Soc Med 4: 41–44PubMedGoogle Scholar
  23. 23.
    Pedersen E (1978) Electromyography of the sphincter muscles. Contemp Clin Neurophysiol 34: 405–416Google Scholar
  24. 24.
    Popken G, Wetterauer U (1997) Pathophysiologie von Erektionsstörungen. In: Stief CG, Hartmann U, Höfner K, Jonas U (Hrsg) Erektile Dysfunktion, Diagnostik und Therapie. Springer, Berlin Heidelberg New York Tokio, S 205–217Google Scholar
  25. 25.
    Sakuta M, Nakanishi T, Toyokura Y (1978) Anal muscle electromyograms differ in amyotrophic lateral sclerosis and Shy-Drager-Syndrome. Neurology 28: 1289–1293Google Scholar
  26. 26.
    Robinson BW, Mishkin M (1968) Penile erection evoked from forebrain structures in Macaca mulatta. Arch Neurol 19: 184–198Google Scholar
  27. 27.
    Sanders DB (1995) Lambert-Eaton myasthenic syndrome: clinical diagnosis, immune-mediated mechanisms, and update on therapies. Ann Neurol 37: 63–73PubMedGoogle Scholar
  28. 28.
    Singer C, Weiner WJ (1996) Male sexual dysfunction. Neurologist 2: 119–129Google Scholar
  29. 29.
    Stief CG, Djamilian M, Schaebsdau F et al. (1990) Single potential analysis of cavernosous activity—a possible diagnosis of autonomic impotence? World J Urol 8: 75–79Google Scholar
  30. 30.
    Stief CG, Thon WF, Djamilian M, Allhoff EP, Jonas U (1992) Transcutaneous registration of cavernous smooth muscle electric activity. Noninvasive diagnosis of neurogenic autonomic impotence. J Urol 147: 47–50Google Scholar
  31. 31.
    Ückert S (1997) Intrazelluläre Mechanismen der Tonusregulation. In: Stief CG, Hartmann U, Höfner K, Jonas U (Hrsg) Erektile Dysfunktion, Diagnostik und Therapie. Springer, Berlin Heidelberg New York Tokio, S 197–205Google Scholar
  32. 32.
    Valleroy ML, Kraft GH (1984) Sexual dysfunction in multiple sclerosis. Arch Phys Med Rehabil 65: 125–128PubMedGoogle Scholar
  33. 33.
    Vodusek DB, Janko M, Lokar J (1983) Direct and reflex responses in perineal muscles on electrical stimulation. J Neurol Neurosurg Psychiatry 46: 67–71PubMedGoogle Scholar
  34. 34.
    Wagner G, Gerstenberg TC, Levin RJ (1989) Electrical activity of corpus cavernosum during flaccidity and erection of the human penis: a new diagnostic method? J Urol 42: 723–725Google Scholar
  35. 35.
    Wein AJ, van Arsdalen KN (1988) Drug-induced male sexual dysfunction. Urol Clin North Am 15: 23–31Google Scholar
  36. 36.
    Wenning GK, Ben Shlomo Y, Magalhaes M, Daniel SE, Quinn NP (1994) Clinical features and natural history of multiple system atrophy. An analysis of 100 cases. Brain 117: 835–845PubMedGoogle Scholar
  37. 37.
    Whitelaw GT, Smithwick RH (1951) Some secondary effcts of sympathectomy. N Engl J Med 245: 121–128Google Scholar

Copyright information

© Springer-Verlag 2003

Authors and Affiliations

  1. 1.Neurologische Klinik der Universität Erlangen-Nürnberg
  2. 2.New York University School of Medicine, Dept. of NeurologyNew York
  3. 3.Neurologische Klinik der Universität Erlangen-NürnbergKopfklinikErlangen

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