TY - JOUR
T1 - Efficacy of chondroitin sulfate for painful knee osteoarthritis
T2 - A one-year, randomized, double-blind, multicenter clinical study in Japan
AU - Morita, Mitsuhiro
AU - Yamada, Kotaro
AU - Date, Hideki
AU - Hayakawa, Kazue
AU - Sakurai, Hidetomo
AU - Yamada, Harumoto
N1 - Funding Information:
Acknowledgments We appreciated the clinical support received from Dr. Naoyuki Shizu, Dr. Kanae Shizu, Dr. Yuki Washimi, Dr. Shuntaro Hanamura, Dr. Arihiko Kanaji, Dr. Kazuyuki Maehara, Dr. Hirofusa Ichinose. We also appreciated the technical support received from Mrs. Kaori Tajima. We are grateful to Zeria Pharmaceutical Co., Ltd. for the gift of active and placebo tablets and for funding support.
PY - 2018
Y1 - 2018
N2 - We explored the effects of chondroitin sulfate on knee osteoarthritis in a one-year, randomized, doubleblind, dose-comparison study. Patients with painful, Kellgren-Lawrence grade 2-3, osteoarthritis of the knee were treated with oral chondroitin sulfate at a dose of either 260 mg/d (low-dose group, control group) or 1560 mg/d (high-dose group). Symptoms were evaluated by the Lequesne's index and visual analog scale for pain. We made subgroup analyses according to background symptom severity (Lequesne's index ≥8 or <8) in 73 patients. Serum level of cartilage oligomeric matrix protein and hyaluronic acid were also determined. In the subgroup with severe symptoms (Lequesne's index ≥8), the chondroitin sulfate dose of 1560 mg/d improved pain faster after 6 and 9 months' therapy. However, no dose-related effects were found on cartilage oligomeric matrix protein or hyaluronic acid levels. Chondroitin sulfate also had good tolerability. We conclude that chondroitin sulfate is useful for pain control in knee osteoarthritis.
AB - We explored the effects of chondroitin sulfate on knee osteoarthritis in a one-year, randomized, doubleblind, dose-comparison study. Patients with painful, Kellgren-Lawrence grade 2-3, osteoarthritis of the knee were treated with oral chondroitin sulfate at a dose of either 260 mg/d (low-dose group, control group) or 1560 mg/d (high-dose group). Symptoms were evaluated by the Lequesne's index and visual analog scale for pain. We made subgroup analyses according to background symptom severity (Lequesne's index ≥8 or <8) in 73 patients. Serum level of cartilage oligomeric matrix protein and hyaluronic acid were also determined. In the subgroup with severe symptoms (Lequesne's index ≥8), the chondroitin sulfate dose of 1560 mg/d improved pain faster after 6 and 9 months' therapy. However, no dose-related effects were found on cartilage oligomeric matrix protein or hyaluronic acid levels. Chondroitin sulfate also had good tolerability. We conclude that chondroitin sulfate is useful for pain control in knee osteoarthritis.
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U2 - 10.1248/bpb.b17-00556
DO - 10.1248/bpb.b17-00556
M3 - Article
C2 - 29176264
AN - SCOPUS:85041488920
SN - 0918-6158
VL - 41
SP - 163
EP - 171
JO - Biological and Pharmaceutical Bulletin
JF - Biological and Pharmaceutical Bulletin
IS - 2
ER -