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Pilot study to evaluate the efficacy of polynucleotide sodium compared to sodium hyaluronate and crosslinked sodium hyaluronate in patients with knee osteoarthritis

  • Ji Yeong Kim
  • , Yoo Na Kim
  • , Yu Jung Lee
  • , Sung Eun Sim
  • , Yu Ri Ko
  • , Jin Woo Shim
  • , Ku Sang Lee
  • , Mina Joo
  • , Hue Jung Park
  • Catholic Univ. of Korea Coll. Med.
  • Mapo Hapjung Bone Orthopedics
  • Seoul Bone Pain Clinic

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Degenerative arthritis of the knee joint has become a major social problem worldwide due to population aging. There are several treatment options for knee osteoarthritis, and the intraar-ticular injection of sodium hyaluronate is commonly selected by many clinicians as a nonsurgical treatment. However, the efficacy of the treatment is controversial. In this pilot study, we aimed to compare polynucleotide sodium (Conjuran® ) with sodium hyaluronate (Hyruan Plus® ) and 1,4-butanediol diglycidyl ether-crosslinked sodium hyaluronate (Synovian® ) in terms of analgesic efficacy after intraarticular injection in patients with knee osteoarthritis. One of the three intraarticu-lar agents was selected according to what agents were available for outpatients when each patient was enrolled in the study. The 15 enrolled patients were subdivided into 3 groups of 5 patients each. Three injections were performed under ultrasound guidance at a 1-week intervals over a total of 3 weeks. The visual analog scale (VAS) score, the Korean version of the Western Ontario and McMaster Universities Arthritis Index (K-WOMAC), the EuroQol five-dimension scale (EQ-5D) score, and the Korean version of the painDETECT Questionnaire (K-PDQ) score were evaluated before injection and at 1, 2, and 6 weeks after the start of the treatment protocol. The primary endpoint was the change in weight-bearing pain at 4 weeks after the last injection. Secondary endpoints included pain at rest and during walking and the K-WOMAC, EQ-5D, and K-PDQ scores. Weight-bearing pain decreased significantly more from pretreatment to 6 weeks after the start of the treatment protocol in the polynucleotide sodium-treated patients than in the patients who were treated with other agents (p = 0.006, one-way ANOVA). There were no significant between-group differences in the other secondary endpoints. No adverse events occurred. In conclusion, polynucleotide sodium could effectively reduce weight-bearing pain in the patients with knee osteoarthritis compared to standard hyaluronic acid viscosupplementation.

Original languageEnglish
Article number1138
Pages (from-to)1-9
Number of pages9
JournalJournal of Clinical Medicine
Volume10
Issue number5
DOIs
StatePublished - 1 Mar 2021

Bibliographical note

Publisher Copyright:
Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Keywords

  • Crosslinked sodium hyaluronate
  • Intra-articular injection
  • Knee osteoarthritis
  • Polynucleotide sodium
  • Sodium hyaluronate

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