TY - JOUR
T1 - Design of a randomized clinical trial of concurrent treatment with vitamin K2 and risedronate compared to risedronate alone in osteoporotic patients
T2 - Japanese Osteoporosis Intervention Trial-03 (JOINT-03)
AU - Tanaka, Shiro
AU - Miyazaki, Teruhiko
AU - Uemura, Yukari
AU - Kuroda, Tatsuhiko
AU - Miyakawa, Nobuaki
AU - Nakamura, Toshitaka
AU - Fukunaga, Masao
AU - Ohashi, Yasuo
AU - Ohta, Hiroaki
AU - Mori, Satoshi
AU - Hagino, Hiroshi
AU - Hosoi, Takayuki
AU - Sugimoto, Toshitsugu
AU - Itoi, Eiji
AU - Orimo, Hajime
AU - Shiraki, Masataka
N1 - Funding Information:
The authors express thanks to the chairman (Dr. Rikushi Morita) and the members of the ethics committee—Ms. Mamiko Matsumura, Dr. Tetsuro Inoue, Dr. Isao Yoshimura, Dr. Mitsuyoshi Nakajima, Tooru Ebihara, R.Ph., Mr. Shinya Hattori and Mr. Kousaku Uchida. This JOINT study was sponsored by the Public Health Research Foundation. The authors would like to thank those who participated as clinical investigators in JOINT-03. The authors also thank the Japan Arteriosclerosis Prevention Fund, Teijin Pharma Limited, Asahi Kasei Corporation, Takeda Pharmaceutical Company Limited, GE Healthcare Japan, Toyo Medic Co., Ltd., MSD Co., Ltd., and Dainippon Sumitomo Pharma Co., Ltd., for their generous donations.
PY - 2014/5
Y1 - 2014/5
N2 - Concurrent treatments with bisphosphonates and vitamin K are promising given that bisphosphonates possibly interfere with vitamin K activation. This is a prospective, multi-center, open-labeled, randomized trial of the efficacy of concurrent treatment with vitamin K2 and risedronate compared with risedronate alone and to explore subsets of patients for which concurrent treatment is particularly efficacious (trial identification number UMIN000000991). Inclusion criteria are women who meet the criteria for pharmacological therapy for osteoporosis, aged ≥65 years, have any of pre-specified risk factors, can walk unassisted, and are able to answer questionnaires. Exclusion criteria are prior warfarin use, secondary osteoporosis or non-osteoporotic metabolic bone diseases, contraindication for vitamin K2 and risedronate, hyper- or hypoparathyroidism, mental disorders, prevalent vertebral fracture at ≥6 sites, severe degenerative spinal deformation between T4 and L4, serious heart, liver, or kidney disease, or bisphosphonate use within the previous 6 months. Patients were recruited from 123 institutes between January 2008 and February 2010, and allocated to vitamin K2 (45 mg/day) and risedronate (2.5 mg/day or 17.5 mg/week) or risedronate alone (2.5 mg/day or 17.5 mg/week) groups. Primary endpoint is a vertebral or non-vertebral fracture. Secondary endpoints are bone mineral density, height, undercarboxylated osteocalcin, JOQOL, EQ-5D and safety. A sample size of 910 subjects per group and 2-year follow-up will provide 80% power to detect 35% risk reduction for fracture, with a two-sided significance level of 5%. Subgroup analysis stratified to adjustment factors for random allocation, body mass index, 25-hydroxyvitamin D, estimated glomerular filtration rate, grade of vertebral fracture, JOQOL, EQ-5D, and co-morbidity is pre-specified.
AB - Concurrent treatments with bisphosphonates and vitamin K are promising given that bisphosphonates possibly interfere with vitamin K activation. This is a prospective, multi-center, open-labeled, randomized trial of the efficacy of concurrent treatment with vitamin K2 and risedronate compared with risedronate alone and to explore subsets of patients for which concurrent treatment is particularly efficacious (trial identification number UMIN000000991). Inclusion criteria are women who meet the criteria for pharmacological therapy for osteoporosis, aged ≥65 years, have any of pre-specified risk factors, can walk unassisted, and are able to answer questionnaires. Exclusion criteria are prior warfarin use, secondary osteoporosis or non-osteoporotic metabolic bone diseases, contraindication for vitamin K2 and risedronate, hyper- or hypoparathyroidism, mental disorders, prevalent vertebral fracture at ≥6 sites, severe degenerative spinal deformation between T4 and L4, serious heart, liver, or kidney disease, or bisphosphonate use within the previous 6 months. Patients were recruited from 123 institutes between January 2008 and February 2010, and allocated to vitamin K2 (45 mg/day) and risedronate (2.5 mg/day or 17.5 mg/week) or risedronate alone (2.5 mg/day or 17.5 mg/week) groups. Primary endpoint is a vertebral or non-vertebral fracture. Secondary endpoints are bone mineral density, height, undercarboxylated osteocalcin, JOQOL, EQ-5D and safety. A sample size of 910 subjects per group and 2-year follow-up will provide 80% power to detect 35% risk reduction for fracture, with a two-sided significance level of 5%. Subgroup analysis stratified to adjustment factors for random allocation, body mass index, 25-hydroxyvitamin D, estimated glomerular filtration rate, grade of vertebral fracture, JOQOL, EQ-5D, and co-morbidity is pre-specified.
KW - 25-hydroxyvitamin D
KW - Bisphosphonate
KW - Osteoporosis
KW - Quality of life
KW - Undercarboxylated osteocalcin
UR - http://www.scopus.com/inward/record.url?scp=84904664260&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84904664260&partnerID=8YFLogxK
U2 - 10.1007/s00774-013-0491-4
DO - 10.1007/s00774-013-0491-4
M3 - Article
C2 - 23828145
AN - SCOPUS:84904664260
SN - 0914-8779
VL - 32
SP - 298
EP - 304
JO - Journal of Bone and Mineral Metabolism
JF - Journal of Bone and Mineral Metabolism
IS - 3
ER -