Micronized Palmitoylethanolamide-Polydatin Reduces the Painful Symptomatology in Patients with Interstitial Cystitis/Bladder Pain Syndrome

Biomed Res Int. 2019 Nov 11:2019:9828397. doi: 10.1155/2019/9828397. eCollection 2019.

Abstract

Aims: To assess the efficacy of a micronized-palmitoylethanolamide-polydatin (m-PEA-Pol) based product on chronic pelvic pain and severity of other symptoms in interstitial cystitis/bladder pain syndrome (IC/BPS) patients refractory to conventional therapies.

Methods: A pilot, open-label bicentric study was carried out involving 32 IC/BPS patients. Chronic, oral m-PEA-Pol treatment lasted 6 months. Bladder pain was evaluated using the visual analog scale, while changes from baseline in other urinary symptoms were evaluated by means of the O'Leary-Sant Interstitial Cystitis Symptom and Problem Index and the Pelvic Pain and Urgency/Frequency (PUF) symptom scale questionnaires. The generalized linear mixed model was used to evaluate significant mean changes across time.

Results: A significant and progressive reduction of pain intensity was observed during m-PEA-Pol treatment (p < 0.0001 for reduction over time). The effect was associated with a reduction in severity of patients' symptoms evaluated with the O'Leary-Sant questionnaire (p=0.0110 and p=0.0014 for cystitis symptoms and problem mean scores, respectively) and the PUF scale (p=0.0163 and p=0.0005 for symptom and bother mean scores, respectively). m-PEA-Pol therapy elicited a significant reduction over time in the urinary frequency evaluated with voiding diary (p=0.0005) and a small but not significant improvement of bladder capacity.

Conclusions: These data highlight the potential benefit of m-PEA-Pol in patients with rare pathology such as IC/BPS and confirm the good safety profile of micronized PEA-based products.

Publication types

  • Clinical Study
  • Multicenter Study

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Amides
  • Chronic Pain / drug therapy
  • Chronic Pain / pathology
  • Cystitis, Interstitial / drug therapy*
  • Cystitis, Interstitial / pathology
  • Ethanolamines / administration & dosage*
  • Female
  • Glucosides / administration & dosage*
  • Humans
  • Male
  • Middle Aged
  • Pain Measurement / methods
  • Palmitic Acids / administration & dosage*
  • Pelvic Pain / drug therapy*
  • Pelvic Pain / pathology
  • Pilot Projects
  • Stilbenes / administration & dosage*
  • Urination / drug effects

Substances

  • Amides
  • Ethanolamines
  • Glucosides
  • Palmitic Acids
  • Stilbenes
  • palmidrol
  • polydatin