Evidence map›Paper›PMID 32462056›Full record

ArticleBone reports2020

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

Taro Mawatari, Satoshi Ikemura, Gen Matsui, Takahiro Iguchi, Hiroaki Mitsuyasu, Shinya Kawahara, Masayuki Maehara, Ryoichi Muraoka, Yukihide Iwamoto, Yasuharu Nakashima

Open access · goldAbstract read
In one paragraph

Article in Bone reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Taro MawatariDepartment of Orthopedic Surgery, Hamanomachi Hospital, Fukuoka, Japan.
Satoshi IkemuraDepartment of Orthopedic Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Gen MatsuiDepartment of Orthopedic Surgery, Hamanomachi Hospital, Fukuoka, Japan.
Takahiro IguchiDepartment of Orthopedic Surgery, Hamanomachi Hospital, Fukuoka, Japan.
Hiroaki MitsuyasuDepartment of Orthopedic Surgery, Hamanomachi Hospital, Fukuoka, Japan.
Shinya KawaharaDepartment of Orthopedic Surgery, Hamanomachi Hospital, Fukuoka, Japan.
Masayuki MaeharaAlliance Management Department, EA Pharma Co., Ltd., Tokyo, Japan.
Ryoichi MuraokaData Science Group, Clinical Development Department, EA Pharma Co., Ltd., Tokyo, Japan.
Yukihide IwamotoDepartment of Orthopedic Surgery, Kyushu Rosai Hospital, Fukuoka, Japan.
Yasuharu NakashimaDepartment of Orthopedic Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Hamanomachi Hospital · JPKyushu University · JPEA Pharma (Japan) · JPKyushu Rosai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRisedronate 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.

methodsThis 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

resultsBaseline 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/cm

conclusionsWhen 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.

Indexed as

A, anteriorBAP, bone isoforms of alkaline phosphataseBMD, bone mineral densityBone isoforms of alkaline phosphataseBone turnover markersBTMs, bone turnover markersC, centralC-telopeptide of type I collagenCTX, C-telopeptide of type I collagenDPD, deoxypyridinolineLS-BMD, lumbar spine bone mineral densityP1NP, N-propeptide of type I collagenP, posteriorRisedronateSD, standard deviationTartrate-resistant acid phosphatase-5bTRACP-5b, tartrate-resistant acid phosphatase-5bULN, upper limit of the normal range

Identifiers

PMID32462056
PMCPMC7240327
OpenAlexW3017825159

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.