Skip to main content
Log in

Geschlechterunterschiede in der neuropsychiatrischen Pharmakotherapie

Gender differences in psychopharmacology

  • Arzneimitteltherapie
  • Published:
Der Internist Aims and scope Submit manuscript

Zusammenfassung

Mindestens die Hälfte aller psychisch kranken Menschen sind Frauen. Bei depressiven Erkrankungen sind Frauen sogar doppelt so häufig betroffen wie Männer. Die geschlechtsspezifischen Aspekte der Psychopharmakotherapie finden jedoch meistens zu geringe Beachtung. Dabei weiß man, dass Frauen besser auf Substanzen mit serotoninmodulierender Wirkung ansprechen als Männer, dass sich dieser Effekt aber postmenopausal umkehrt. Ferner entwickeln Frauen unter bestimmten Psychopharmaka gynäkologische Komplikationen, die den Einsatz dieser Substanzen in Frage stellen. Nebenwirkungen wie Gewichtszunahme, Hyperglykämie, Herzrhythmusstörungen und sexuelle Dysfunktionen treten bei Frauen ebenfalls häufiger auf als bei Männern. Die Schwangerschaft ist ein besonders sensibler Aspekt. Hier muss das Risiko der psychisch kranken Mutter, bei Absetzen eines Psychopharmakons erneut einen Rückfall zu erleiden, gegen das Risiko für das Kind, Fehlbildungen zu erleiden oder pränatale Komplikationen zu entwickeln, abgewogen werden.

Abstract

At least half of all patients with psychiatric disorders are female. Depressive disorders occur twice as often in women than in men. Despite the need for a gender-specific approach in treating psychiatric disorders, little is known about gender issues in psychopharmacology. It has been recognized that women respond better than men to serotonin-modulating substances but that this effect is reversed after menopause. Furthermore, women develop gynecological complications under medication with certain psychopharmacological agents which calls the use of these drugs into question. Side effects such as weight gain, hyperglycemia, cardiac arrhythmias, and sexual dysfunction also occur more frequently in women than in men. Pregnancy is a particularly sensitive aspect. The risk that a mother with a psychiatric disorder could relapse if the drug is discontinued has to be weighed against the risk of the child being born with an anomaly or developing prenatal complications.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Abb. 1

Literatur

  1. Aichhorn W, Whitworth AB, Weiss EM et al. (2007) Differences between men and women in side efffects of second generation antipsychotics. Nervenarzt 78: 45–52

    Article  PubMed  CAS  Google Scholar 

  2. Altshuler LL, Hendrick V, Cohen LS (1989) Course of mood and anxiety disorders during pregnancy and the postpartum period. J Clin Psychiatry 59 (Suppl 2) 29–33

    Google Scholar 

  3. Aström-Lilja C, Odeberg JM, Ekman E, Hägg S (2008) Drug-induced torsades de pointes: a review of the swedish pharmacovigilance database. Pharmacoepidemiol Drug Saf 17: 587–592

    Article  PubMed  Google Scholar 

  4. Bromiker R, Kaplan M (1994) Apparent intrauterine fetal withdrawal from clomipramine Hydrochloride. JAMA 272: 1722–1723

    Article  PubMed  CAS  Google Scholar 

  5. Cohen LS, Friedman JM, Jefferson JW et al. (1994) A reevaluation of risk of utero exposure to lithium. JAMA 271: 146–150

    Article  PubMed  CAS  Google Scholar 

  6. Cohen LS, Heller VL (1990) On the use of anticonvulsants for manic depression during pregnancy. Psychosomatics 31: 462–464

    PubMed  CAS  Google Scholar 

  7. Cohen LS, Heller VL, Rosenbaum JF (1989) Treatment guidelines for psychotropic drug use in pregnancy. Psychosomatics 30: 25–33

    PubMed  CAS  Google Scholar 

  8. Cohen LS, Rosenbaum JF, Heller VL (1988) Prescribing lithium for pregnant women. Am J Psychiatry 159: 772–773

    Google Scholar 

  9. Compton MT, Miller AH (2002) Antipsychotic-induced hyperprolactinemia and sexual dysfunction. Psychopharmacol Bull 36: 143–164

    PubMed  Google Scholar 

  10. Flores PJ, Juarez OH, Flores PC (2003) Effect of menstrual cycle on the pharmacokinetics of ranitidine in healthy volunteers. J Clin Pharmacol 43: 1026

    Google Scholar 

  11. Frank E, Rush AJ, Blehar M et al. (2002) Skating to where the puck is going to be: a plan for clinical trials and translation research in mood disorders. Biol Psychiatry 52: 631–654

    Article  PubMed  Google Scholar 

  12. Genton P, Bauer J, Duncan S et al. (2001) On the association between valproate and polycystic ovary syndrome. Epilepsia 42: 295–304

    Article  PubMed  CAS  Google Scholar 

  13. Gex-Fabry M, Balant-Gorgia AE, Balant LP (2003) Therapeutic drug monitoring of olanzapine the combined effect of age, gender, smoking, and comedication. Ther Drug Monit 25: 46–53

    Article  PubMed  CAS  Google Scholar 

  14. Goodnick PJ, Rodriguez L, Santana O (2002) Antipsychotics: impact on prolactin levels. Expert Opin Pharmacother 3: 1381–1391

    Article  PubMed  CAS  Google Scholar 

  15. Grigoriadis S, Robinson GE (2007) Gender issues in depression. Ann Clin Psychiatry 19: 247–255

    Article  PubMed  Google Scholar 

  16. Grunder G, Wetzel H, Schlosser R (1999) Neuroendocrine response to antipsychotics: effects of drug type and gender. Biol Psychiatry 45: 89–97

    Article  PubMed  CAS  Google Scholar 

  17. Haddad L, Milke P, Zapata L (1998) Effect of the menstrual cycle in ethanol pharmacokinetics. J Appl Toxicol 18: 15–18

    Article  PubMed  CAS  Google Scholar 

  18. Haddad PM, Wieck A (2004) Antipsychotic-induced hyperprolactinaemia: mechanisms, clinical features and management. Drugs 64: 2291–2314

    Article  PubMed  CAS  Google Scholar 

  19. Homel P, Casey D, Allison DB (2002) Changes in body mass index for individuals with and without schizophrenia, 1987-1996. Schizophr Res 55: 277–284

    Article  PubMed  Google Scholar 

  20. Hummer M, Huber J (2004) Hyperprolactinaemia and antipsychotic therapy in schizophrenia. Curr Med Res Opin 20: 189–197

    Article  PubMed  CAS  Google Scholar 

  21. Hummer M, Malik P, Gasser RW (2005) Osteoporosis in patients with schizophrenia. Am J Psychiatry 162: 162–167

    Article  PubMed  Google Scholar 

  22. Kamimori GH, Joubert A, Otterstetter R (1999) The effect of the menstrual cycle on the pharmacokinetics of caffeine in normal, healthy eumenorrheic females. Eur J Clin Pharmacol 55: 445–449

    Article  PubMed  CAS  Google Scholar 

  23. Kasthuba ADM, Nafziger AN (1998) Physiological changes during the menstrual cycle and their effects on the pharmacokinetics and pharmacodynamics of drugs. Clin Pharmacokinet 34: 203–218

    Article  Google Scholar 

  24. Kennedy SH, Eisfeld BS, Dickens SE et al. (2000) Antidepressant-induced sexual dysfunction during treatment with moclobemide, paroxetine, sertraline, and venlafaxine. J Clin Psychiatry 61: 276−281

    PubMed  CAS  Google Scholar 

  25. Khan A, Brodhead AE, Schwarzt KA et al. Sex differences in antidepressant response in recent antidepressant clinical trials. J Clin Psychopharmacol 24: 318–324

  26. Kleiner J, Altshuler L, Hendrick V, Hershman JM (1999) Lithium-induced subclinical hypothyroidism: review of the literature and guidelines for treatment. J Clin Psychiatry 60: 249–255

    PubMed  CAS  Google Scholar 

  27. Kopecek M, Bares M, Svarc J (2004) Hyperprolactinemia after low dose of amisulpride. Neuro Endocrinol Lett 25: 419–422

    PubMed  CAS  Google Scholar 

  28. Kulin NA, Pastuszak A, Sage SR et al. (1998) Pregnancy outcome following maternal use of the new selective serotonin Reuptake inhibitors: a prospective controlled multicenter study. JAMA 279: 609–610

    Article  PubMed  CAS  Google Scholar 

  29. Kulin NA, Rastuszak A, Koren G (1998) Are the new SSRIs safe for pregnant women? Can Fam Physician 44: 2081–2083

    PubMed  CAS  Google Scholar 

  30. Kupfer DJ, Frank E, Perel JM et al. (1992) Five-year outcome for maintenance therapies in recurrent depression. Arch Gen Psychiatry 49: 769–773

    PubMed  CAS  Google Scholar 

  31. Laukaran VH, van den Berg BJ (1980) The relationship of maternal attitude to pregnancy outcomes and obstetric complications. A cohort study of unwanted pregnancy. Am J Obstet Gynecol 136: 374–379

    PubMed  CAS  Google Scholar 

  32. Montgomery J, Winterbottom E, Jessani M (2004) Prevalence of hyperprolactinemia in schizophrenia: association with typical and atypical antipsychotic treatment. J Clin Psychiatry 65: 1491–1498

    Article  PubMed  Google Scholar 

  33. O’Keane V, Meaney AM (2005) Antipsychotic drugs: a new risk factor for osteoporosis in young women with schizophrenia? J Clin Psychopharmacol 25: 26–31

    Article  CAS  Google Scholar 

  34. Russell JM, Mackell JA (2001) Bodyweight again associated with atypical antipsychotics: epidemiology and therapeutic implications. CNS Drugs 15: 537–551

    Article  PubMed  CAS  Google Scholar 

  35. Schimmell MS, Katz EZ, Shaag Y et al. (1991) Toxic neonatal effects following maternal clomipramine therapy. J Toxicol Clin Toicol 29: 479–484

    Article  CAS  Google Scholar 

Download references

Interessenkonflikt

Die korrespondierende Autorin gibt an, dass kein Interessenkonflikt besteht.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to S. Krüger.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Regitz-Zagrosek, V., Schubert, C. & Krüger, S. Geschlechterunterschiede in der neuropsychiatrischen Pharmakotherapie. Internist 49, 1516–1523 (2008). https://doi.org/10.1007/s00108-008-2233-6

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00108-008-2233-6

Schlüsselwörter

Keywords

Navigation