Luteal serum BDNF and HSP70 levels in women with premenstrual dysphoric disorder


ORAL E. A., ÖZCAN H., Kirkan T. S., AŞKIN S., Gulec M., AYDIN N.

EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, cilt.263, sa.8, ss.685-693, 2013 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 263 Sayı: 8
  • Basım Tarihi: 2013
  • Doi Numarası: 10.1007/s00406-013-0398-z
  • Dergi Adı: EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.685-693
  • Anahtar Kelimeler: Brain-derived neurotrophic factor, Heat-shock protein-70, Premenstrual dysphoric disorder, Premenstrual syndrome, HEAT-SHOCK PROTEINS, PITUITARY-ADRENAL RESPONSES, NEUROTROPHIC FACTOR LEVELS, MOLECULAR CHAPERONES, STRESS RESPONSES, RECEPTOR COMPLEX, RAT HIPPOCAMPUS, MESSENGER-RNAS, SHORT-TERM, BRAIN
  • Atatürk Üniversitesi Adresli: Evet

Özet

Premenstrual dysphoric disorder (PMDD) is a severe form of premenstrual syndrome characterized by psychological and somatic symptoms commencing in the luteal phase of the menstrual cycle and concludes with menstrual bleeding. PMDD affects 3-8 % of premenopausal women and represents a significant public health problem especially in young women. Decreased brain-derived neurotrophic factor (BDNF) levels are associated with several mental disorders. Heat-shock protein-70 (HSP70) is an important member of the molecular chaperone system, which provides a molecular defense against proteotoxic stress. We hypothesized that there would be changed levels of BDNF and HSP70 in women with PMDD compared with non-symptomatic women, reflecting impaired and/or activated stress-related responses involved in the underlying pathogenesis of PMDD. Female medical students were screened, and 24 women without premenstrual symptoms and 25 women with PMDD were enrolled in the study. Psychiatric evaluation and the Daily Record of Severity of Problems-Short Form were used for two consecutive menstrual cycles to diagnose PMDD. Serum BDNF and HSP70 levels were assessed in the third luteal phase. Participants with PMDD had significantly higher serum BDNF and HSP70 levels compared with controls, and there was a significant positive correlation between serum BDNF and HSP70 levels. Increased HSP70 levels may reflect cellular distress in PMDD. Increased serum BDNF levels in the luteal phase in subjects with PMDD may reflect a compensation process, which results in subsequent improvement of PMDD-associated depressive symptoms in the follicular phase. Thus, increased serum BDNF levels may be indicative of a compensating capacity in PMDD.