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  1. Berger P., Gruschwitz M., Spoetztl G., Dirnhofer S., Madersbacher S., Gerth R., Mezr W.E., Plas E., Sampson N.:
    “Human chorionic gonadotropin (HCG) in the male reproductive tract“
    Molecular and Cellular Endocrinology, 190-196, (260-262), 2007

    Normal hypothalamic-pituitary testicular and prostatic functions are essential for maintenance of male fertility, whereby glycoprotein hormones (GPH) as well as androgens are major endocrine and local regulators. We have investigated whether the GPH human chorionic gonadotropin (hCG) and the free alpha and beta subunits thereof are produced in the target organs themselves and potentially act as auto/paracrine modulators of fertility. Immunofluorometric assays (IFMAs) based on our panel of highly selective monoclonal antibodies, immunohistochemistry (IHC), confocal laser scanning microscopy (CLSM) and 1- and 2D gel electrophoreses with subsequent western blotting have been utilized for the detection of hCGalpha, hCGbeta and its metabolite hCGbeta core fragment (cf) in human testis, prostate and seminal plasma. Both organs synthesize hCGalpha and hCGbeta, which are subsequently detectable at high concentrations in seminal plasma of healthy probands (n=17): hCGalpha 2630+/-520 ng/mL (mean+/-S.E.M.), hCGbeta 2+/-0.28 ng/mL, hCGbetacf and hCG 0.19+/-0.039 ng/mL. These parameters significantly exceed physiological values, e.g. ten thousand-fold in the case of hCGalpha, in serum of young men (n=20): hCGalpha 0.142+/-0.054 ng/mL (mean+/-S.E.M.), hCGbeta 0.05 ng/mL and hCG 0.004+/-0.003 ng/mL. Levels of these markers were not correlated with sperm counts. Of all body fluids including those of pregnant women seminal plasma is the richest physiological source for genuine free i.e. non-dissociated GPHalpha (M(r,app) 23k) which may even appear as di- or tetramers. Its concentration is similar to that observed in maternal serum (weeks 10-12 of gestation) and in extra-embryonic coelomic fluid. In contrast to those fluids where ratios of free subunits to hCG are in the range of 1:100 highly inverse ratios in the range of 10.000:1.000:1 were observed for hCGalpha:hCGbeta:hCG in seminal plasma. hCGalpha is not derived from heterodimeric GPH suggesting hCG-independent functions of hCGalpha and hCGbeta in male and female fertility.

  2. Daha L., Lazar D., Simak R., Pflüger H.:
    “Is there a relation between urinary interleukin-6 levels and symptoms before and after intra-vesical glycosaminoglycan substitution therapy in patients with bladder pain syndrome/interstitial cystitis?“
    Int. Urogynecol J, 18, (1449-1452), 2007

    Urinary interleukin-6 (IL-6) has been proposed as a sensitive and specific inflammatory marker in bladder pain syndrome/interstitial cystitis (BPS/IC). We therefore investigated the presence of urinary IL-6 in patients with BPS/IC to find a possible correlation with the symptoms before and after glycosaminoglycan substitution therapy. Urinary IL-6 levels of 25 BPS/IC patients were assessed semi-quantitavely (Milenia Quickline) before and after intra-vesical glycosaminoglycan substitution therapy. Patients received therapy twice weekly with 300 mg pentosanpolysulphate for 5 weeks. Responders were treated for another 5 weeks, whilst non-responders received 40 mg hyaluronic acid weekly for another 10 weeks instead. Treatment response was assessed by the visual analogue scale (VAS) for quality of life and O'Leary-Saint Symptom and Problem Index (OSPI) before, during the 5th week of the treatment and 1 week after the treatment. Before treatment, measurable IL-6 was found in urine samples from 9 out of 25 patients. After treatment, urinary IL-6 was detected in two patients only. The average VAS and OSPI scores before the treatment were 7.9 (4-10) and 25.4 (12-37), respectively. After the treatment, the average VAS and OSPI scores dropped to 5.5 (0-10) and 14.7 (1-29), respectively. No statistically significant difference was found between patients with and without urinary IL-6 and the VAS and OSPI scores before and after the treatment. The urinary IL-6 level in BPS/IC patients is neither suited as a diagnostic marker nor as a predictor of responses to therapies. For the future, it would be important to clarify whether there are subsets of patients with diseases of different aetiologies.

  3. Daha L., Lazar D., Engelhardt P.F., Simak R., Pflüger H.:
    “Acupuncture Treatment of Psychogenic Erectile Dysfunction: A Four-Year Follow-Up Study“
    Curr.Uro., 1, (39-41), 2007

    The aim of the study was to assess the longterm effects of acupuncture treatment in patients suffering from psychogenic erectile dysfunction (ED). Patients and Methods: Twenty patients with psychogenic ED who underwent acupuncture treatment between 1999 and 2001 were invited to an after-care interview with the items International Index of Erectile Function (IIEF) 15 Score, influence of acupuncture on quality of life, effect and duration of acupuncture treatment on erectile status and willingness to repeat the treatment. Results: Fifteen patients accepted our invitation. Comparison of the IIEF 15 Score shortly after treatment with the Score in 2005 showed no statistically relevant difference (P = 0.608). Sixty-seven percent (n = 10) of the after-care patients reported an improvement in their quality of life and 53% (n = 8) would repeat this acupuncture treatment. Conclusions: The results are a first indication that long-term effects could be reached through acupuncture treatment.

  4. Plas E., Berger I.:
    “Genital Trauma“
    Buch “Emergencies in Urology”, 2, (260-269), 2007

  5. Plas E.:
    “Androgensubstitution: wer, wann, wie lange”
    CliniCum Urologie, 4, (8-10), 2007

  6. Plas E., Pernkopf D.:
    “Sexualität: Auch im Alter ein wichtiges Thema“
    Geriatrie Praxis Österreich, 2, (18-20), 2007

  7. Daha L., Simak R.:
    “Harnleiter- und Nierenbeckentumore: Diagnostik und Therapie“
    Krebshilfe!, 3, (6-7), 2007

  8. Stancik I., Plas E.:
    “Diagnostik und Therapie des invasiven Blasenkarzinoms“
    Krebshilfe!, 3, (11-12), 2007

  9. Plas E.:
    “Kinderwunsch: Onkologie und Fertilität“
    Urologik, 2, (16-17), 2007

  10. Plas E.:
    “Männlicher Kinderwunsch und Genetik – Was soll der Urologe wissen?“
    J.Urol.Urogynäkol., 5, (2-3), 2007
    PDF-Volltextartikel

  11. Stancik I., Plas E.:
    “Neues zum Harnblasenkarzinom – Diagnostik und Therapie“
    Urologik, 2, (16-17), 2007
    PDF-Volltextartikel

  12. Plas E.:
    “Die Bedeutung der erektilen Dysfunktion“
    MEDahead report, (1-2), 2007

  13. Plas E.:
    “Höheres Risiko für Prostatakarzinom bei Testosteron-Behandlung?“
    Uroscope, Juni, (5-6), 2007

  14. Plas E.:
    “Rauchen begünstigt Erektionsstörungen“
    Ärztekrone, 8, (30-32), 2007

  15. Höltl W., Jeschke K., Jungwirth A., Loidl W., Plas E., Rauchenwald M., Reiter W., Schatzl G., Schratter-Sehn A., Zigeuner R., Reissigl A.:
    “Expertise: PDE-5-Hemmer zur Behandlung nach Prostatektomie“
    Österreichische Ärztezeitung, Supplementum 5, (1-4), 2007

  16. Plas E., Essl A.:
    “Welchen Stellenwert hat Sexualität für einen Urologen und Patienten in Abhängigkeit vom Alter“
    J.Urol.Urogynäkol., Sonderheft 2, 35, 2007

  17. Stancik I., Plas E., Daha K., Juza J., Pflüger H.:
    “IL-6, IgG, IgA und Leukozytenzahl-Bestimmung im Seminalplasma/Ejakulat und Postmasturbationsharn bei Patienten mit einer chronischen Prostatitis“
    J.Urol.Urogynäkol., Sonderheft 2, 39-40, 2007

  18. Loidl W., Hobisch A., Riedl C., Penkoff H., Pflüger H., Jeschke K., Schmeller N., Schmidbauer J., Zaack D.:
    “Konsensus: Leitlinien zur Anwendung der Fluoreszenzzystoskopie mit Hexaminolevulinat beim Harnblasenkarzinom “
    Universimed-Verlag, 1-8, 2007

  19.  Lazar D.:
    “Impact of BPS/IC (Bladder Pain Syndrome / Interstitial Cystitis) on Sexual Functions and Partnerships of Female Patients“
    Poster, ausgezeichnet als beste Posterpräsentation am Europ. Kongress für Sexualmedizin in Lissabon 2007

   
Stand:2009-03-09

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