Assessment of baseline bone turnover marker levels and response to risedronate treatment: Data from a Japanese phase III trial

Autor: Shinya Kawahara, Satoshi Ikemura, Ryoichi Muraoka, Taro Mawatari, Yukihide Iwamoto, Hiroaki Mitsuyasu, Gen Matsui, Masayuki Maehara, Yasuharu Nakashima, Takahiro Iguchi
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0301 basic medicine
medicine.medical_specialty
lcsh:Diseases of the musculoskeletal system
Endocrinology
Diabetes and Metabolism

BMD
bone mineral density

Osteoporosis
Urology
030209 endocrinology & metabolism
Article
Bone remodeling
Tartrate-resistant acid phosphatase-5b
03 medical and health sciences
0302 clinical medicine
medicine
BTMs
bone turnover markers

Orthopedics and Sports Medicine
P1NP
N-propeptide of type I collagen

TRACP-5b
tartrate-resistant acid phosphatase-5b

LS-BMD
lumbar spine bone mineral density

Baseline (configuration management)
Bone mineral
Bone isoforms of alkaline phosphatase
Risedronate
C-telopeptide of type I collagen
C
central

business.industry
BAP
bone isoforms of alkaline phosphatase

Incidence (epidemiology)
Therapeutic effect
medicine.disease
P
posterior

A
anterior

CTX
C-telopeptide of type I collagen

DPD
deoxypyridinoline

Exact test
ULN
upper limit of the normal range

030101 anatomy & morphology
Analysis of variance
lcsh:RC925-935
SD
standard deviation

business
Bone turnover markers
Zdroj: Bone Reports, Vol 12, Iss, Pp 100275-(2020)
Bone Reports
ISSN: 2352-1872
Popis: Background Risedronate increases bone mineral density (BMD) and reduces fracture risk, but treatment response may depend on the baseline state of bone turnover. Data regarding the selection of therapeutic drugs or the prediction of therapeutic effects with baseline levels of bone turnover markers (BTMs) as a reference are insufficient. We hypothesized that when the baseline levels of BTMs are higher, baseline BMD might be lower, changes in BMD at 12 months after risedronate treatment might be higher, and the reduction of fracture incidence might be greater. This study aimed to analyze the data of a phase III clinical trial of risedronate from Japan to investigate the relationships between baseline BTM levels and (1) baseline BMD, (2) changes in BMD at 12 months after the start of treatment, and (3) the incidence of new vertebral fractures. Methods This post-hoc analysis included 788 postmenopausal women with osteoporosis whose baseline BTM levels as well as baseline and endpoint BMDs were measured. Relationships between baseline BTM levels and BMD at baseline and 12 months after risedronate treatment and new vertebral fractures were examined. One-way analysis of variance, two-tailed Student's t-test, and Fisher's exact test were used to analyze the data. Results Baseline BMD showed a significant upward trend when baseline BTM levels were lower in the analysis by tertiles. New vertebral fractures tended to occur in patients with prevalent vertebral fractures, but the relationship between new fractures and BTM levels was not statistically significant. Regardless of BTM types, BMD percentage increments (%) and increments (g/cm2) with the 12-month treatment were high when pretreatment BTM levels were high (P 5.0% increase in BMD was observed even if baseline BTM levels were within the normal range. A new vertebral fracture occurred in only six patients (0.77%), and there was not enough statistical power to clarify the relationship between baseline BTM levels and fracture risk reduction. Conclusions When pretreatment BTM levels increased, baseline BMD tended to be lower and the increase in BMD with 12-month risedronate treatment was higher. However, BMD could still be increased even if the baseline BTM levels are within the normal range. Combined with available evidence, baseline BTMs may not have an important role in deciding the optimal therapy. To elucidate the relationship between baseline BTM levels and long-term fracture risk, it will be necessary to conduct more large-scale studies with a longer follow-up period in severe osteoporotic patients with a high fracture risk. Mini abstract We evaluated the significance of baseline bone turnover markers in the response to risedronate treatment. The increase in the bone mineral density (BMD) with the 12-month treatment may be higher when the state of bone turnover at baseline is higher, and BMD could still be increased even if the baseline bone turnover is within the normal range.
Highlights • Baseline bone turnover markers in response to risedronate treatment are unknown. • Higher BMD may be achieved when the state of bone turnover at baseline is higher. • Further increase in BMD is possible even if the baseline bone turnover is normal.
Databáze: OpenAIRE