Pretreatment levels of bone turnover and the antifracture efficacy of alendronate: The fracture intervention trial

被引:129
作者
Bauer, DC
Garnero, P
Hochberg, MC
Santora, A
Delmas, P
Ewing, SK
Black, DM
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94107 USA
[2] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94107 USA
[3] Mol Markers Synarc, Lyon, France
[4] INSERM, Res Unit 403, F-69008 Lyon, France
[5] Univ Lyon 1, F-69365 Lyon, France
[6] Univ Maryland, Div Rheumatol, Baltimore, MD 21201 USA
[7] Merck Res Labs, Rahway, NJ USA
关键词
alendronate; bone turnover; treatment efficacy; fracture;
D O I
10.1359/JBMR.051018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Previous trials have shown that high bone turnover is associated with greater increases in BMD among bisphosphonate-treated women. The influence of pretreatment bone turnover levels on antifracture efficacy has not been well studied. Materials and Methods: We randomized women 55-80 years of age with femoral neck BMD T scores <= -1.6 to alendronate (ALN), 5-10 mg/day (n = 3105), or placebo (PBO; n = 3081). At baseline, 3495 women were osteoporotic (femoral neck BMD T score <= -2.5 or prevalent vertebral fracture), and 2689 were not osteoporotic (BMD T score > -2.5 and no prevalent vertebral fracture). Pretreatment levels of bone-specific alkaline phosphatase (BSALP), N-terminal propeptide of type I collagen (PINP), and C-terminal cross-linked telopeptide of type 1 collagen (sCTx) were measured in all participants using archived serum (20% fasting). The risk of incident spine and nonspine fracture was compared in ALN- and PBO-treated subjects stratified into tertiles of baseline bone marker level. Results and Conclusions: During a mean follow-up of 3.2 years, 492 nonspine and 294 morphometric vertebral fractures were documented. Compared with placebo, the reduction in nonspine fractures with ALN treatment differed significantly among those with low, intermediate, and high pretreatment levels of PINP levels (p = 0.03 for trend). For example, among osteoporotic women in the lowest tertile of pretreatment PINP (< 41.6 ng/ml), the ALN versus PBO relative hazard for nonspine fracture was 0.88 (95% CI: 0.65, 1.21) compared with a relative hazard of 0.54 (95% CI: 0.39, 0.74) among those in the highest tertile of PINP (> 56.8 ng/ml). Results were similar among women without osteoporosis at baseline. Although they did not reach statistical significance, similar trends were observed with baseline levels of BSALP. Conversely, spine fracture treatment efficacy among osteoporotic women did not differ significantly according to pretreatment marker levels. Spine fracture treatment efficacy among nonosteoporotic women was related to baseline BSALP (P = 0.05 for trend). In summary, alendronate nonspine fracture efficacy is greater among both osteoporotic and nonosteoporotic women with high pretreatment,,PINP. If confirmed in other studies, these findings suggest that bisphosphonate treatment may be most effective in women with elevated bone turnover.
引用
收藏
页码:292 / 299
页数:8
相关论文
共 33 条
  • [1] Change in bone turnover and hip, non-spine, and vertebral fracture in alendronate-treated women: The Fracture Intervention Trial
    Bauer, DC
    Black, DM
    Garnero, P
    Hochberg, M
    Ott, S
    Orloff, J
    Thompson, DE
    Ewing, SK
    Delmas, PD
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 (08) : 1250 - 1258
  • [2] Biochemical markers of bone turnover and prediction of hip bone loss in older women: The study of osteoporotic fractures
    Bauer, DC
    Sklarin, PM
    Stone, KL
    Black, DM
    Nevitt, MC
    Ensrud, KE
    Arnaud, CD
    Genant, HK
    Garnero, P
    Delmas, PD
    Lawaetz, H
    Cummings, SR
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (08) : 1404 - 1410
  • [3] Screening for osteoporosis in postmenopausal women: Recommendations and rationale
    Berg, AO
    Allan, JD
    Frame, PS
    Homer, CJ
    Johnson, MS
    Klein, JD
    Lieu, TA
    Mulrow, CD
    Orleans, CT
    Peipert, JF
    Pender, NJ
    Siu, AL
    Teutsch, SM
    Westhoff, C
    Woolf, SH
    [J]. ANNALS OF INTERNAL MEDICINE, 2002, 137 (06) : 526 - 528
  • [4] Fracture risk reduction with alendronate in women with osteoporosis: The Fracture Intervention Trial
    Black, DM
    Thompson, DE
    Bauer, DC
    Ensrud, K
    Musliner, T
    Hochberg, MC
    Nevitt, MC
    Suryawanshi, S
    Cummings, SR
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (11) : 4118 - 4124
  • [5] Randomised trial of effect of alendronate on risk of fracture in women with existing vertebral fractures
    Black, DM
    Cummings, SR
    Karpf, DB
    Cauley, JA
    Thompson, DE
    Nevitt, MC
    Bauer, DC
    Genant, HK
    Haskell, WL
    Marcus, R
    Ott, SM
    Torner, JC
    Quandt, SA
    Reiss, TF
    Ensrud, KE
    [J]. LANCET, 1996, 348 (9041) : 1535 - 1541
  • [6] BLACK DM, 1993, OSTEOPOROSIS INT, V3, P29
  • [7] Serum type I collagen breakdown product (serum CTX) predicts hip fracture risk in elderly women:: The EPIDOS study
    Chapurlat, RD
    Garnero, P
    Bréart, G
    Meunier, PJ
    Delmas, PD
    [J]. BONE, 2000, 27 (02) : 283 - 286
  • [8] Hormone replacement therapy in postmenopausal women: Urinary N-telopeptide of type I collagen monitors therapeutic effect and predicts response of bone mineral density
    Chesnut, CH
    Bell, NH
    Clark, GS
    Drinkwater, BL
    English, SC
    Johnston, CC
    Notelovitz, M
    Rosen, C
    Cain, DF
    Flessland, KA
    Mallinak, NJS
    [J]. AMERICAN JOURNAL OF MEDICINE, 1997, 102 (01) : 29 - 37
  • [9] Prevention of osteoporosis and osteoporotic fractures in postmenopausal women: recommendation statement from the Canadian Task Force on Preventive Health Care
    Cheung, AM
    Feig, DS
    Kapral, M
    Diaz-Granados, N
    Dodin, S
    [J]. CANADIAN MEDICAL ASSOCIATION JOURNAL, 2004, 170 (11) : 1665 - 1667
  • [10] BONE TURNOVER IN POSTMENOPAUSAL OSTEOPOROSIS - EFFECT OF CALCITONIN TREATMENT
    CIVITELLI, R
    GONNELLI, S
    ZACCHEI, F
    BIGAZZI, S
    VATTIMO, A
    AVIOLI, LV
    GENNARI, C
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (04) : 1268 - 1274