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Reduction of Vertebral Fracture Risk in Postmenopausal Women With Osteoporosis Treated With Raloxifene
Results From a 3-Year Randomized Clinical Trial
Bruce Ettinger, MD;
Dennis M. Black, PhD;
Bruce H. Mitlak, MD;
Ronald K. Knickerbocker, PhD;
Thomas Nickelsen, MD;
Harry K. Genant, MD;
Claus Christiansen, MD;
Pierre D. Delmas, MD, PhD;
Jose R. Zanchetta, MD;
Jacob Stakkestad, MD;
Claus C. Glüer, PhD;
Kathryn Krueger, MD;
Fredric J. Cohen, MD;
Stephen Eckert, PhD;
Kristine E. Ensrud, MD, MPH;
Louis V. Avioli, MD;
Paul Lips, MD, PhD;
Steven R. Cummings, MD;
for the Multiple Outcomes of Raloxifene Evaluation (MORE) Investigators
JAMA. 1999;282:637-645.
ABSTRACT
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Context Raloxifene hydrochloride, a selective estrogen receptor modulator, prevents bone loss in postmenopausal women, but whether it reduces fracture risk in these women is not known.
Objective To determine the effect of raloxifene therapy on risk of vertebral and nonvertebral fractures.
Design The Multiple Outcomes of Raloxifene Evaluation (MORE) study, a multicenter, randomized, blinded, placebo-controlled trial.
Setting and Participants A total of 7705 women aged 31 to 80 years in 25 countries who had been postmenopausal for at least 2 years and who met World Health Organization criteria for having osteoporosis. The study began in 1994 and had up to 36 months of follow-up for primary efficacy measurements and nonserious adverse events and up to 40 months of follow-up for serious adverse events.
Interventions Participants were randomized to 60 mg/d or 120 mg/d of raloxifene or to identically appearing placebo pills; in addition, all women received supplemental calcium and cholecalciferol.
Main Outcome Measures Incident vertebral fracture was determined radiographically at baseline and at scheduled 24- and 36-month visits. Nonvertebral fracture was ascertained by interview at 6-month-interim visits. Bone mineral density was determined annually by dual-energy x-ray absorptiometry.
Results At 36 months of the evaluable radiographs in 6828 women, 503 (7.4%) had at least 1 new vertebral fracture, including 10.1% of women receiving placebo, 6.6% of those receiving 60 mg/d of raloxifene, and 5.4% of those receiving 120 mg/d of raloxifene. Risk of vertebral fracture was reduced in both study groups receiving raloxifene (for 60-mg/d group: relative risk [RR], 0.7; 95% confidence interval [CI], 0.5-0.8; for 120-mg/d group: RR, 0.5; 95% CI, 0.4-0.7). Frequency of vertebral fracture was reduced both in women who did and did not have prevalent fracture. Risk of nonvertebral fracture for raloxifene vs placebo did not differ significantly (RR, 0.9; 95% CI, 0.8-1.1 for both raloxifene groups combined). Compared with placebo, raloxifene increased bone mineral density in the femoral neck by 2.1% (60 mg) and 2.4% (120 mg) and in the spine by 2.6% (60 mg) and 2.7% (120 mg) P<0.001 for all comparisons). Women receiving raloxifene had increased risk of venous thromboembolus vs placebo (RR, 3.1; 95% CI, 1.5-6.2). Raloxifene did not cause vaginal bleeding or breast pain and was associated with a lower incidence of breast cancer.
Conclusions In postmenopausal women with osteoporosis, raloxifene increases bone mineral density in the spine and femoral neck and reduces risk of vertebral fracture.
INTRODUCTION
Raloxifene hydrochloride is a nonsteroidal benzothiophene that binds to estrogen receptors and inhibits bone resorption without stimulating the uterine endometrium in postmenopausal women.1 However, the effect of raloxifene on the risk of fracture is not known. Observational studies in postmenopausal women have suggested that long-term estrogen therapy reduces the incidence of fracture,2-3 but the efficacy ofestrogen in reducing fractures has been demonstrated in only 1 small prospective study.4 In addition, in the US Breast Cancer Prevention Trial,5 tamoxifen citrate, another selective estrogen receptor modulator, appeared to have a favorable effect on the incidence of fractures. The Multiple Outcomes of Raloxifene Evaluation (MORE) study was undertaken in 1994 primarily to examine the effect of raloxifene on the skeleton. We report herein the results of measurements of bone mineral density and assessment for fractures from a planned 36-month interim analysis.
METHODS
Subjects
We studied 7705 women who were at least 2 years postmenopausal and had no severe or long-term disabling conditions but who had osteoporosis, defined as low bone mineral density or radiographically apparent vertebral fractures. Subject recruitment and follow-up are summarized in Figure 1. The women were divided into 2 study groups and then were randomized to receive either placebo or 1 of 2 dosage amounts of raloxifene. Study group 1 included those whose femoral neck or lumbar spine bone mineral density t score was below -2.5. Study group 2 included women who had low bone mineral density and 1 or more moderate or severe vertebral fractures or 2 or more mild vertebral fractures or who had at least 2 moderate fractures, regardless of their bone mineral density. A mild vertebral fracture corresponds to a 20% to 25% reduction in height and a moderate vertebral fracture corresponds to a 25% to 40% reduction from expected vertebral height.6-7
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Figure 1. Study Recruitment and Follow-up
Prior to randomization, patients were stratified to 1 of 2 study groups at the time of radiographic screening: 5064 were assigned to study group 1 if they had no vertebral fractures and 2641 were assigned to study group 2 if they had vertebral fractures.
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Women were excluded if they had experienced bone disease other than osteoporosis, substantial postmenopausal symptoms or abnormal uterine bleeding, endometrial carcinoma, a history of or suspected breast carcinoma at any time, or a history of nonskin cancer in the previous 5 years; taken an androgen, calcitonin, or bisphosphonate within the previous 6 months; been taking oral estrogen within the previous 2 months; been receiving fluoride therapy for more than 3 months during the previous 2 years; undergone systemic glucocorticoid therapy for more than 1 month within the past year; taken antiseizure drugs or pharmacologic doses of cholecalciferol; had a history of thromboembolic disorders within the last 10 years (except in association with an injury; experienced endocrine disorders requiring therapy (except for type 2 diabetes or hypothyroidism); had serum creatinine levels above 225 µmol/L (2.5 mg/dL); had active renal lithiasis, abnormal hepatic function, or untreated malabsorption; or consumed more than 4 alcoholic drinks per day. In addition, we excluded women with pathologic fractures, those from whom satisfactory thoracic and lumbar radiographs could not be obtained, and those with fewer than 2 lumbar and 4 thoracic vertebrae that were evaluable. The women were enrolled at 180 centers in 25 countries. Approximately half the study subjects were recruited by a centralized campaign in the United States and Canada that used both print and radio advertisements. Women responding to campaign advertisements were screened by telephone. Qualifying women were referred to study sites for further evaluation. The other half of the study subjects were enrolled at sites that may have used their own institutional or other databases to identify and contact potential subjects. The protocol was approved by the human studies review board at each center, and informed consent was obtained.
Treatment
Within each substudy, women were randomly assigned to treatment groups and were asked to take daily 1 of 3 types of identically appearing pills: placebo or 60 mg or 120 mg of raloxifene. Randomization was performed by the Eli Lilly Clinical Trials Materials Group, Indianapolis, Ind. This clinical trials group was also responsible for packaging the study drug materials but was not involved in either study design or patient monitoring. Study drug assignments were generated randomly. Upon entry into the study, all women received daily supplements of 500 mg of calcium and 400 to 600 IU of cholecalciferol.
Assessment of Vertebral Fracture
Participants underwent vertebral radiography at baseline, 24 months, and 36 months. When symptoms of vertebral fracture occurred, women underwent radiography at interim 6-month visits. When possible, radiographies were performed on women who had terminated from the study early. All vertebral radiographs were assessed at a central site by radiologists blinded to treatment group assignment. To establish eligibility for study group 2, the baseline radiographs were scored using a semiquantitative scale6-7 for each vertebra (T4-L4). The grading scores were set as 0 for none, 1 for mild, 2 for moderate, and 3 for severe fractures. After 36 months, a radiologist blinded to treatment group assignment graded the baseline and end point radiographs using the same semiquantitative scale.6-7 An incident fracture was defined as a grade change of at least 1. If no fractures were detected after the review of baseline and end point radiographs, the analysis stopped for that patient. For fractures observed at baseline or end point, a second radiologist determined whether a fracture was present for each vertebra and also performed quantitative morphometry (with an incident fracture defined as a decrease in anterior, mid, or posterior vertebral height of at least 20% and at least 4 mm). Vertebral fractures were scored when they were confirmed by at least 2 of the 3 types of determinations from 2 independent semiquantitative readings and 1 quantitative assessment. A new vertebral fracture was defined as an incident fracture of a vertebra that was not fractured at baseline. We defined clinical vertebral fractures as incident fractures found at interim 6-month visits through additional unscheduled radiographies performed because of back pain suggestive of fractures. When incident fractures were adjudicated from these nonscheduled radiographs, they were counted as a clinical fracture as well as an incident fracture.
Nonvertebral fractures were determined by direct questioning every 6 months at each clinic visit. Fractures resulting from a traffic collision, a beating, or having been struck by a falling or moving object were considered traumatic and were excluded from the analysis. In addition, pathologic fractures and those involving the fingers, toes, and skull were excluded.
Assessment of Bone Mineral Density
Spine and femoral neck bone mineral density were measured annually by dual-energy x-ray absorptiometry. A central reading facility provided correction factors to adjust for intersite differences and changes in the performance of the densitometers over time.7-8
Participants were required to discontinue the study if at 1 year they had experienced a bone mineral density decrease of at least 7% in their lumbar spine or 10% in their femoral neck; if at 2 years they had experienced a lumbar spine decrease of at least 11% or femoral neck decrease of at least 14%; or if at any time during the study, they had experienced more than 2 incident vertebral fractures.
Assessment of Adverse Events
Mammography was performed at baseline, was optional at 1 year, but was required after 2 and 3 years. Transvaginal ultrasonography was performed at baseline, annually at 17 large clinical centers, and in others if clinically indicated. A total of 1781 women had a baseline and at least 1 postbaseline transvaginal ultrasonography. All women were questioned about the adverse effects of treatment at each visit; all serious adverse effects reported for up to 40 months of follow-up and all nonserious adverse effects reported for up to 36 months of follow-up were analyzed regardless of the investigators' assessments of causality. Adverse events that resulted in death, hospitalization, cancer, permanent disability, or threat to life were classified as serious. The Coding Symbol and Thesaurus for Adverse Reaction Terminology (COSTART)9 dictionary was used to categorize reported adverse events. We report all categories of adverse events for which frequency was different (P<.05) between the placebo and combined raloxifene groups and for which the incidence was at least 2% in any group.
Biochemical Assessment of Physiologic Functions and Bone Turnover
Hematologic, renal, and hepatic function was tested periodically during the study. Markers of bone turnover, including serum osteocalcin (ELSAOSTEO, CIS Biointernational, Gifsur Yvette, France)10 and the urinary type I collagen C-telopeptide excretion, corrected for urinary creatinine excretion (CrossLaps, Osteometer A/S, Herlev, Denmark),11 were measured in 2622 women who were enrolled at some sites in North America, Europe, and South America.
Statistical Analysis
The primary end points in each substudy were the effects of raloxifene on incident vertebral fractures and bone mineral density; a secondary end point was any nonvertebral fracture. The sample size provided a greater than 90% power (2-tailed t test, P<.05 significance level) to detect a 40% reduction in vertebral fractures between pooled raloxifene doses and placebo. Power calculations were based on the assumptions that after 3 years, the cumulative incidence of osteoporotic vertebral fractures among women receiving placebo would be 7.2% for those free of vertebral fracture at baseline and 19.5% for those with 1 or more fractures at baseline. On the basis of observed incidence of vertebral fractures in the placebo group, the study's power was slightly greater than predicted.
We included only women who had incident fractures in vertebrae that were not fractured at baseline. We examined 12 categories of nonvertebral fracture: humerus, wrist, hip, patella, tibia/fibula, ankle, metatarsal, rib/sternum, clavicle, scapula, sacrum, and pelvis. Using log-rank tests, we compared the time to first occurrence of nonvertebral fracture between the raloxifene and placebo groups. Adverse effects were analyzed using  2 tests. All analyses were performed as intention to treat (ie, participants were classified according to their substudy group and treatment assignment regardless of compliance). Missing postbaseline data were imputed by carrying forward the last observation. All comparisons were 2 sided and were performed at a P=.05 level of significance. No adjustments were made for multiple comparisons. The number needed to treat was calculated as the reciprocal of the difference in vertebral fracture incidence between treatment and placebo.
RESULTS
The 7705 women enrolled in the study ranged in age from 31 to 80 years (mean, 67 years). Almost all (95.7%) were white. There were no statistically significant differences in baseline characteristics (Table 1). Compared with the women in study group 1, women in study group 2 (see "Methods" section for study group assignment criteria) were older and had lower bone mineral density at baseline. We found no difference in adherence to treatment among the groups: 92% of the women took more than 80% of the study medication.
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Table 1. Characteristics of 6828 Postmenopausal Women*
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Vertebral Fracture
Baseline and follow-up radiographs were available for 6828 women (89%); the study groups were similar in percentage of women having available radiographs. Of these women, 88% had radiography performed at the 36-month visit; for the others, the last postbaseline radiograph was used. We found no difference in baseline characteristics between these women and the 877 women who discontinued treatment and had had no follow-up radiographs. After 36 months, 503 (7.4%) of the 6828 women had 1 or more new vertebral fractures. Overall and in each study group, women receiving raloxifene had fewer new vertebral fractures (Table 2) regardless of whether the women had existing fractures at the beginning of the study (Figure 2). Overall, we found no difference in the rate of vertebral fracture incidence between the 2 raloxifene-treated groups; however, in study group 2, we saw a lower incidence of fractures in the women given 120 mg of raloxifene compared with women given 60 mg of raloxifene (10.7% vs 14.7%, respectively; P=.02). Twenty-two women in study group 1 and 95 women in study group 2 had 2 or more new vertebral fractures (relative risk [RR], 0.2; 95% confidence interval [CI], 0.1-0.6; and RR, 0.5; 95% CI, 0.3-0.7, respectively, for pooled raloxifene groups vs placebo). The reduction in fracture risk for the subset of 65 women with clinical vertebral fractures was similar to those discovered by routine radiographic assessment (RR, 0.4; 95% CI, 0.3-0.7, for pooled raloxifene groups vs placebo). The reduction in vertebral fracture risk associated with raloxifene treatment was similar in each of the following subgroups: tertiles of age, tertiles of baseline femoral neck or lumbar spine bone mineral density, prior hysterectomy vs not, and prior hormone replacement therapy vs none.
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Table 2. New Vertebral Fracture in 6828 Postmenopausal Women Receiving Placebo or Raloxifene Hydrochloride Therapy for Osteoporosis*
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Figure 2. Reduction in New Vertebral Fractures Among 6828 Women Who Completed the Study
Women did or did not have vertebral fracture at the beginning of study. RR indicates relative risk; CI, confidence interval.
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Nonvertebral Fracture
When assessed at 36 months, 240 women (9.3%) receiving placebo reported at least 1 nonvertebral fracture compared with 437 women (8.5%) in the pooled raloxifene groups (RR, 0.9; 95% CI, 0.8-1.1) (Table 3 and Figure 3). The analyses of individual fracture sites for pooled raloxifene groups and placebo showed 237 wrist, 62 ankle, and 58 hip fractures. Among all 12 categories of nonvertebral fractures, only the ankle fracture risk reduction was statistically significant (Figure 3).
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Table 3. Nonvertebral Fractures in 4536 Women Receiving Raloxifene Hydrochloride Therapy and 2292 Women Receiving Placebo
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Figure 3. Occurrence of First Nonvertebral Fracture Since Start of Study
This represents 2292 women who received placebo and 4536 women who received raloxifene therapy for osteoporosis. For osteoporotic nonvertebral fractures, P=.24; hip fractures, P=.71; wrist fractures, P=.34; and ankle fratures, P < .05. Percentages are calculated from survival distribution using the product limit (Kaplan-Meier) method.
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Bone Mineral Density and Bone Turnover
Compared with bone mineral density in the placebo group, bone mineral density increased after 36 months by 2.1% and 2.6% at the femoral neck and spine in the 60-mg raloxifene group and by 2.4% and 2.7% at the femoral neck and spine in the 120-mg raloxifene group, respectively (P<.001, all comparisons) (Figure 4). In the raloxifene groups, bone density of the hip peaked at 24 months, and spinal density remained constant between 2 and 3 years. A total of 94 women (3.6%) assigned to the placebo group, 28 (1.1%) assigned to the 60 mg of raloxifene group, and 22 (0.9%) assigned to the 120 mg of raloxifene group withdrew from the study for having multiple fractures or for excessive bone mineral density loss, a predefined study end point (P<.001 for each raloxifene dose vs placebo).
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Figure 4. Percentage Change in Bone Mineral Density in Lumbar Spine and Femoral Neck
Data represent 1490 women receiving 60 mg/d of raloxifene, 1512 women receiving 120 mg/d of raloxifene, and 1522 women receiving placebo.
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The median baseline serum osteocalcin concentration was 24.1 µg/L, and urinary excretion of C-telopeptide was 248 µg/mmol of creatinine. After 36 months, the serum osteocalcin concentrations decreased by a median of 8.6%, 26.3%, and 31.1%, and the urinary C-telopeptide excretion decreased by 8.1%, 34.0%, and 31.5% in the placebo, the 60 mg of raloxifene, and the 120 mg of raloxifene groups, respectively (P<.001 for each raloxifene dose vs placebo).
Adverse Effects
After 36 months, 24.2% of the women had serious adverse effects regardless of treatment group. Venous thromboembolic events, including deep vein thrombophlebitis and pulmonary embolism, were the only serious adverse effects believed to be causally related to raloxifene treatment; by 40 months, venous thromboembolic events had been reported by 8 (0.3%), 25 (1.0%), and 24 (1.0%) of all patients in the placebo, the 60 mg of raloxifene, and the 120 mg of raloxifene groups, respectively (RR, 3.1; 95% CI, 1.5-6.2 for both raloxifene groups combined vs placebo).
Breast cancer was less frequent in the women receiving raloxifene. By 40 months, 54 women had a confirmed diagnosis of breast cancer (RR, 0.3; 95% CI, 0.2-0.6 for both raloxifene groups combined vs placebo). Ten women had endometrial cancers: 4 in the placebo group, 4 in the 60 mg of raloxifene group, and 2 in the 120 mg of raloxifene group.
A total of 83 adverse effects occurred in at least 2% of the women in any treatment group. Table 4 lists only those adverse events experienced by at least 2% of the women in each group and those for which the numbers and percentages of women experiencing adverse events in the combined raloxifene groups differed from the placebo group (P<.05). Vaginal bleeding was reported by 62 (3.1%), 67 (3.4%), and 56 (2.8%) of women in the placebo, the 60 mg of raloxifene, and the 120 mg of raloxifene groups, respectively. In addition, the proportion of women reporting breast pain did not differ among groups (data not shown).
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Table 4. Adverse Events With Incidence of at Least 2% and Differing Significantly for Women Receiving Raloxifene Hydrochloride Than for Women Receiving Placebo
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A total of 754 women (9.8%) withdrew from the study due to an adverse event: 527 women (10.3%) in the raloxifene groups and 227 women (8.8%) in the placebo group (P=.04). Hot flashes were the most common nonserious adverse event, prompting withdrawal in 0.1%, 0.7%, and 0.5% of the women in the placebo, the 60 mg of raloxifene, and the 120 mg of raloxifene groups, respectively.
There were no clinically important changes in hemotologic, renal, or hepatic function laboratory, assessments.
COMMENT
The risk for vertebral fractures, detected clinically or by radiography, was decreased by 30% to 50% among women treated with raloxifene for 36 months. The reduction compared with placebo was statistically significant for women both with and without vertebral fractures at baseline. The decreased risk was marginally greater in the women with prevalent vertebral fractures who were in the 120 mg of raloxifene group compared with those who were in the 60 mg of raloxifene group.
These results are comparable with those found in prospective trials of other antiresorptive drugs, including a trial of bisphosphonate alendronate12-14 and a small trial with transdermal estrogen.4 Radiographic deformities, whether clinically apparent or not, have been associated with substantial increases in back pain and back-related disability.15 A recent trial of another selective estrogen receptor modulator, tamoxifen, suggested a decrease in the risk of clinical osteoporotic fractures by 19%.5
Similar to previous studies of raloxifene in early postmenopausal women without osteoporosis,1 we found about a 2% to 3% increase in spine and hip bone mineral density after 2 and 3 years of raloxifene treatment compared with those who were in the placebo group. We found a moderate reduction in biochemical markers of bone turnover and the median levels in the raloxifene groups were similar to the mean levels found in premenopausal women.15-16 Thus, although the effects we saw on bone density and biochemical markers were about half those observed in women treated with alendronate,11 the reduction in vertebral fracture risk was similar. Our study supports previous observations that the effect of fracture reduction is not clearly related to the increase in bone mineral density,16-17 suggesting that other factors also contribute to prevention of fractures. Indeed, lower bone turnover in elderly women is associated with decreased risk of hip fracture independent of bone density.16-17
We did not observe a significant reduction in nonspine fractures after 3 years. However, the cumulative incidence curves for nonvertebral fractures begin to diverge after about 2 years. Although this trend was not significant at 3 years, the MORE study is continuing for another year to assess the effects of 4 years of raloxifene treatment.
Only a few other agents have been tested for their effects on nonvertebral fractures, and few studies have been primarily designed to evaluate the effect of treatment on a specific nonvertebral fracture such as the hip.18-19 A combination of calcium and cholecalciferol has been shown to significantly reduce the risk of nonvertebral fractures in elderly women18 and elderly men.18-19 In the MORE trial, all women received calcium and cholecalciferol supplements, which might have attenuated the risk of fractures in both placebo and raloxifene groups. Among 13,388 women at high risk of breast cancer, a median of 4.5 years of treatment with tamoxifen produced a nonsignificant trend for reduction in risk of hip and wrist fractures.5 In the Heart and Estrogen/Progestin Replacement Study (HERS) of 2705 women with heart disease, those receiving estrogen and progestin for an average of 4 years did not show a reduction in nonvertebral fractures compared with those receiving a placebo.20 The Fracture Intervention Trial12 reported that 2027 women with vertebral fractures who were treated with alendronate had a reduced risk of nonvertebral fractures. However, in a parallel 4-year study of 4272 women who had no vertebral fracture, the reduction in risk of nonvertebral fracture with alendronate was not statistically significant. A subset of women with femoral neck t scores below -2.5 showed a statistically significant reduction (RR, 0.6, 95% CI, 0.5-0.8) in the risk of vertebral and nonvertebral fracture, but the study did not report this subgroup's risk for nonvertebral fracture only.14 Based on the observed rate of fractures in the placebo group, our study had 80%, 38%, and 12% power to detect a 20% reduction in risk (placebo vs pooled raloxifene groups) in total nonspine, wrist, and hip fractures, respectively. However, there was a greater number of women removed from the placebo group because of rapid bone loss or multiple vertebral fractures during the trial. Because these women were at high risk of nonvertebral fractures, their removal may have decreased the ability to detect a statistically significant effect.
The women receiving raloxifene had an increased incidence of venous thromboembolic events compared with the women receiving placebo. Overall, the RR for venous thromboembolic events was approximately 3, which is comparable to that reported for postmenopausal women receiving estrogen therapy in observational studies,21-23 for those in a prospective trial of estrogen therapy,20 and for those receiving tamoxifen for prevention of breast cancer.5 Breast cancer was statistically significantly less frequent in the women receiving raloxifene, an effect similar to that reported for tamoxifen in the Breast Cancer Prevention Trial.5
During surveillance of the uterus by ultrasonography, about 1 in 12 of the women studied were found to have at least trace amounts of fluid in the endometrial cavity. In previous studies, endometrial fluid was detected in 6% to 12% of asymptomatic postmenopausal women in the absence of associated pathology.24-25 Of the women found to have endometrial fluid, 52 (31%) had undergone an endometrial biopsy; none of the women treated with raloxifene were found to have endometrial hyperplasia or endometrial carcinoma. Thus, raloxifene-associated endometrial fluid accumulation appears to be clinically unimportant. The study was not designed or powered to examine effects of raloxifene on endometrial cancer. The adverse events of leg cramps and peripheral edema were also reported more frequently in the women given raloxifene; these symptoms have also been reported in women receiving estrogen replacement therapy.26
We conclude that 3 years of raloxifene treatment preserves bone density, reduces bone turnover, and reduces the incidence of vertebral fractures in postmenopausal women with osteoporosis.
AUTHOR INFORMATION
Financial Disclosures: Dr Ettinger received research funding from Berlex Laboratories, Montville, NJ, and Solvay Pharmaceuticals, Marietta, Ga. Dr Genant received research funding from or honoraria for speaking for or has served on the scientific advisory board of Parke-Davis, Morris Plains, NJ, Shanghai Aloka Medical Equipment Co Ltd, Tsuen Wan, Hong Kong, Stratec, Medizintechnik Pforzheim, Germany, and Sunlight Ultrasound Technology Ltd, Rehovot, Israel. Drs Genant, Glüer, and Krueger received research funding from or honoraria for speaking for, served as paid consultants for, or own stock in Hologic Inc, Waltham, Mass. Dr Christiansen received research funding from, honoraria for speaking for, served as a paid consultant or on the scientific advisory board for Besins Iscovesco, Paris, France; Cortecs, Deeside, England; Schering-Plough Corp, Kenilworth, NJ; and Rotta Pharmaceuticals, Milano, Italy. Drs Delmas and Stakkestad received research funding from or honoraria for speaking for or have served as consultants for or on the scientific advisory board of Boehringer Mannheim Pharmaceuticals, Gaithersburg, Md, and Rhone-Poulenc Rorer, Collegeville, Pa. Dr Zancetta served as principal investigator for and along with Dr Glüer received research funding from Hoeschst Marion Roussel Pharmaceuticals Inc, Kansas City, Mo. Drs Genant and Glüer received research funding from or honoraria for speaking for or served as paid consultants for or on the scientific advisory board for Metra Biosystem, Mountain View, Calif; IGEA, Carpi, Italy; and Lunar Corp, Madison, Wis. Drs Mitlak, Knickerbocker, Nickelsen, Krueger, Cohen, and Eckert are employees and own stock in and Drs Black, Genant, Christiansen, Delmas, Zanchetta, Stakkestad, Glüer, Ensrud, Avioli, Lips, and Cummings received research funding from or honoraria for speaking for, served as paid consultants for or on the scientific advisory board of, or own stock in Eli Lilly and Co, Indianapolis, Ind. Drs Genant, Delmas, Stakkestad, and Glüer received research funding from or received honoraria for speaking for or served as paid consultants for or on the scientific advisory board for Diagnostic Medical Systems, Perols, France. Dr Zanchetta served as a principal investigator for and along with Drs Ettinger, Black, Genant, Ensrud, Lips, and Cummings received research funding from or honoraria for speaking for, served as paid consultants for or on the scientific advisory board of Merck and Co, West Point, Pa. Drs Ettinger, Genant, Christiansen, Delmas, and Glüer received research funding from or honoraria for speaking for or served as paid consultants for or on the scientific advisory board of Novartis Pharmaceuticals Corp, East Hanover, NJ. Drs Christiansen, Delmas, and Stakkestad received research funding from or honoraria for speaking for or served as paid consultants for or on the scientific advisory board of Novo Nordisk Pharmaceuticals, Princeton, NJ. Dr Delmas have received research funding or honoraria for speaking for or served on the scientific advisory board of Organon, West Orange, NJ. Drs Glüer and Christiansen received research funding or honoraria for speaking for or served as paid consultants for or on the scientific advisory board of, or own stock in Osteometer Biotech. Dr Christiansen owns several patents for Osteometer Biotech, Herlev, Denmark. Dr Avioli declines to list other clinical trials in phase 2 or 3 studies with other pharmaceutical companies involved in developing drugs for the prevention or treatment of osteoporosis. Dr Zanchetta served as a principal investigator for clinical trials and along with Drs Genant and Delmas received research funding from or honoraria for speaking for or served as paid consultants for or on the scientific advisory board of Pfizer Inc, New York, NY. Drs Black, Genant, Christiansen, Delmas, Glüer, and Ensrud have received research funding or honoraria for speaking for or served as paid consultants for or served on the scientific advisory board of Procter & Gamble Pharmaceuticals, Cincinnati, Ohio. Drs Christiansen, Delmas, Stakkestad, Glüer, and Ensrud received research funding or honoraria for speaking for or served as paid consultants for or on the scientific advisory board of Hoffmann Roche Laboratories, Nutley, NJ. Dr Stakkestad received research funding from Sanofi Winthrop Pharmaceuticals, New York, NY. Drs Christiansen and Delmas received research funding from or honoraria for speaking for or served as paid consultants or on the scientific advisory board of Servier Laboratories, Durenes, France. Drs Genant, Delmas, and Cummings received research funding from or honoraria for speaking for or served as paid consultants for or served on the scientific advisory board of SmithKline Beecham, Philadelphia, Pa. Drs Genant and Christiansen received research funding from or honoraria for speaking for, served as paid consultants for or on the scientific advisory board of, or own stock in Synarc, San Francisco, Calif. Dr Black received research funding from Wyeth-Ayerst, Philadelphia, Pa.
Investigators for the Multiple Outcomes of Raloxifene Evaluation (MORE) trial: Argentina: Carlos Mautalen, MD, Centro De Osteopatias Medicas, and Jose R. Zanchetta, MD, Instituto de Investigaciones Metabolicas and USAL University School of Medicine, Buenos Aires. Australia: Michael J. Hooper, MB, BS, FRACP, University of Sydney and Concord Repatriation General Hospital, Sydney; Geoffrey Nicholson, MBBS, PhD, MRCP, FRACP, The Geelong Hospital, Geelong, Kong; Wah Ng, FRACP, MD, and Ego Seeman, BSc, MBBS, FRACP, MD, Austin & Repatriation Medical Centre, University of Melbourne, Melbourne, Victoria; Richard L. Prince, MD, FRACP, University of Western Australia, Nedlands, Western Australia; and Sir Charles Gairdner Hospital; Anthony P. Roberts, MD, Ashford Specialist Centre, Ashford Hospital, Ashford; Margaret M. Williamson, MBChB, MRCP, FRACP, Princess Alexandra Hospital, Brisbane, Queensland. Austria: Ewald Boschitsch, MD, Ambulatorium Klimax; and Georg Leb, MD, Graz–Universitatskliniken. Belgium: Thierry Appelboom, MD, Hopital Universitaire Erasme; Jean J. Body, MD, Institut Jules Bordet, Anne Peretz, MD, Hopital Universitaire Brugmann; and Jean P. Devogelaer, MD, Cliniques Universitairies Saint Luc, Brussels; Jan Dequeker, MD, Universitaire Ziekenhuis Pellenberg Lubbeek; Piet Geusens, MD, Limburgs Universitaires Diepenbeek; Jean-Marc Kaufman, MD, Universitairi Ziekenhuis, Gent; and Jean-Yves Reginster, MD, Polycliniques Universitaires L. Brull, Liege. Canada: David A. Hanley, MD, FRCP, University of Calgary, Endocrinology & Metabolism Health Sciences Center, Alberta; John P. Wade, MD, The Arthritis Centre, Vancouver, British Columbia; William Leslie, MD, MSc, FRCPC, St Boniface General Hospital, University of Manitoba, Winnipeg; Carol A. Joyce, MD, Memorial University of Newfoundland, St John's; Roger S. Rittmaster, MD, Centre for Clinical Research, and Jack R. Wall, MD, PhD, Dalhousie University, Halifax, Nova Scotia; Angela M. Cheung, MD, PhD, FRCP, University Health Network and Mount Sinai Hospital, University of Toronto, Gillian A. Hawker, MD, FRCPC, Womens College Hospital, and William C. Sturtridge, MD, Toronto Hospital General Division; Anthony B. Hodsman, MD, University of Western Ontario, London; and Theodore C. Monchesky, MD, Oshawa General Hospital, Oshawa, Jonathan R. Adachi, MD, Charlton Medical Centre, Charlton, and William G. Bensen, MD, FRCPC, St Joseph's Hospital, Alfred A. Cividino, BASc, MD, FRCP, McMaster University, Hamilton, Ontario; Jacques P. Brown, MD, FRCPC, Centre Hospitalier Universitaire De Quebec–Pavillon Chul; and Alan Tenenhouse, MD, Clinical Research Consultant Group, Quebec; and Wojciech P. Olszynski, MD, PhD, FRCP, University of Saskatchewan, Saskatoon, and Kerry G. Siminoski, MD, Endocrine Centre of Edmonton and Medical Imaging Consultants, Edmonton, Saskatchewan. Czech Republic: Jan J. Stepan, MD, DSc, Vfn A 1, Lf Univerzity Karlovy. Denmark: Claus Christiansen, MD, and Henrik Lawaetz, MD, Center for Clinical and Basic Research, Ballerup; Erik F. Eriksen, MD, Aarhus Amtssygehus; Lars Hydstrup, MD, Hvidovre Hospital; and Ole H. Sørensen, MD, Kommunehospitalet I Koebenhavn, Copenhagen. Finland: Esko Alhava, MD, Kuopion Yliopistollinen Keskussairaalal; Martti Kormano, MD, PhD, Laakariasema Vagus, Turku; Pasi Salmela, MD, Oulun Yliopistollinen Sairaala; Jorma Salmi, MD, PhD, Koskiklinikka, Tampere; and Matti Valimaki, MD, PhD, Helsinki University Central Hospital. France: Christian Alexandre, MD, Chu De St Etienne Hopital Bellevue; Maurice Audran, MD, Chu D'Angers; Daniel Briancon, MD, Hopital Reine Hortense; Pierre Delmas, MD, PhD, INSERM, Lyon; Marie C. DeVeine Joul, MD, Hopital Lariboisiere, Paris; Patrice Fardellone, MD, Chu D'Amiens Hopital Sud; D. Kuntz, Jacques LeClere, MD, CHU De Nancy Hopital D'Adultes De Brabois; and Claude Ribot, MD, Chu De Toulouse Hopital De Rangueil. Germany: J. Beyer, H. Franck, Claus C. Glüer, MD, Department of Diagnostic Radiology, Christian-Albrechts-Universität, Kiel; Elmar Keck, MD, Landesarztekammer Hessen, Wiesbaden; Peter Maier, MD, Staedt. Kurbetriebe Bad Waldsee; Gerhard Scholz, MD, Universitat Leipzig; and J. Semler and Christian Wuester, MD, Universitat Heidelberg. Hungary: Geza Balint, MD, Orszagos Reumatologiai Es Fizioterapias Intezet, and Janos Szuecs, MD, Semmelweis Medical University, Budapest; Adam Balogh, MD, Debreceni Orvostudomanyi Egyetem, Debrecen; and Jonas Julesz, MD, PhD, Szent-Gyorgyi Albert Orvostudomanyi Egyetem. Israel: Avraham Karasik, MD, and Iris Vered, MD, Sheba Medical Center, Tel-Hashomer; Uri Liberman, MD, PhD, Rabin Medical Center, Petah Tiqva. Italy: Maria Luisa Brandi, MD, PhD, Department of Clinical Physiopathology, University of Florence; Antonio Del Puente, MD, and Pasquale Oriente, MD, Universita "Federico II," Napoli; Carmelo Fiore, MD, Universita Di Catania; Andrea R. Genazzani, MD, Ospedale Santa Chiara Di Pisa; Carlo Gennari, MD, Institute of Internal Medicine, University of Siena; Giancarlo Isaia, MD, University of Torino; Gianfranco Mazzuoli, MD, Universita La Sapienza, Roma; Gian B. Melis, MD, Universita Di Cagliari; Torquato Nencioni, MD, Istituto Mangiagalli, Milano; Mario Passeri, MD, Universita Di Parma; and Leonardo Sartori, MD, PhD, Universita Di Padova. Mexico: Ricardo Correa-Rotter, MD, Instituto Nacional De La Nutricion, and Alfonso Murillo-Uribe, MD, Instituto Nacional De Perinatologia, Mexico City. The Netherlands: Paul Lips, MD, PhD, Academic Hospital Vrije Universiteit, Amsterdam; Henk Mulder, MD, Medisch Onderzoekscentrum Gcp, and Huibert A. Pols, MD, PhD, Erasmus University Medical Center, Rotterdam; New Zealand: Nigel Gilchrist, MD, Canterbury Geriatric Medical Research Trust, The Princess Margaret Hospital, Christchurch. Norway: Johan Halse, MD, PhD, Betanien Med Lab, Oslo; Rolf Jorde, MD, Regionsykehuset I Tromsoe; and Jacob A. Stakkestad, MD, PhD, CECOR AS, Center for Clinical Osteoporosis, Haugesund. Poland: Janusz Badurski, MD, Center of Osteoporosis and Osteoarticular Diseases, Bialystok; Krzysztof Hoszowski, MD, Szpital Kolejowy, Warszawa; and Jaroslaw Ogonowski, MD, Pomorska Akademia Medyczna, Szczecin. Singapore: Kamal Bose, MBBS, MS, National University Hospital. Slovak Republic: Rastislav Dzurik, MD, PhD, DSc, Institute of Preventive and Clinical Medicine, Bratislava. Slovenia: Andreja Kocijancic, MD, University Clinical Center, Ljubljana. Spain: Juan J. Garcia Borras, MD, PhD, Hospital Universitario La Fe, Valencia; Jorge B. Cannata, MD, PhD, Hospital General De Asturias, Oviedo; Fernando Escobar, MD, PhD, and Manuel Muñoz, MD, Endocrine Unit Hospital Universitatio S. Cecilio, Granada; Jardi Farrerons, MD, PhD, Hospital De La Santa Creu I Sant Pau, and Adolfo Diez-Perez, MD, PhD, Hospital Del Mar, Barcelona; and Federico Hawkins, MD, PhD, Hospital 12 De Octubre, Madrid. Sweden: Sverker Ljunghall, MD, and Karin Larsson, MD, Academic Hospital Uppsala; Dan Mellstrøm, MD, PhD, Uppsala University, Goteborg; Britt-Marie Nyhäll-Wåhlin, MD, and Mats Palmér, MD, Uppsala University, Orebro; Goran Toss, MD, Uppsala University, Linkoping. United Kingdom: Richard Eastell, BSc, MB, ChB, The Osteoporosis Centre, University of Sheffield; Ignac Fogelman, BSc, MD, Guy's Hospital, London; Robert Landray, MCCHB, Synexus Ltd; David W. Purdie, MB, ChB, MD, The University of Hull, Centre for Metabolic Bone Disease; David M. Reid, MB, ChB, MD, University of Aberdeen; Ian Smith, BMS, MB, ChB, NHS Trust Royal Preston Hospital, Lancashire; Michael D. Stone, BA, MB, BS, Llandough Hospital, South Glamorgan. United States: Cora Lewis, MD, MSPH, University of Alabama, Birmingham, and William J. Shergy, MD, Clinical Research Rheumatology Associates, Ala; Robert C. Biesbroeck, MD, Valley Endocrine Associates, PC, Mesa, and Michael J. Maricic, MD, University of Arizona Health Sciences Center, Tucson, Ariz; Thomas T. Aoki, MD, Aoki Diabetes Research Institute, Sacramento, Claude D. Arnaud, MD, and Steven T. Harris, MD, University of California, San Francisco, Elizabeth Barrett-Connor, MD, University of California, San Diego, David J. Baylink, MD, Musculoskeletal Disease Center, Loma Linda University and Pettis Veterans Affairs Medical Center, Loma Linda, Bruce Ettinger, MD, Division of Research, Kaiser Permanente, Oakland, Richard O. Kamrath, MD, John Muir Health Network/The Osteoporosis Center, Robert Marcus, MD, Department of Veterans Affairs Medical Center, Palo Alto, Sidney Rosenblatt, MD, The Irvine Clinical Research Center, Irvine, Charles F. Sharp, Jr, MD, Huntington Memorial Hospital, Stuart L. Silverman, MD, University of California, Los Angeles, West Los Angeles-Veterans Affairs Medical Center, Osteoporosis Medical Center; Frederick Singer, MD, John Wayne Cancer Institute at St John's Health Center, Santa Monica, and Stuart R. Weiss, MD, San Diego Endocrine and Medical Clinic, San Diego, Calif; David A. Podlecki, MD, Longmont Clinic, Longmont, Colo; Robert Lang, MD, Osteoporosis Evaluation Center, Hamden, Conn; Mark P. Ettinger, MD, Clinical Research Center of South Florida, Marvin A. Heuer, MD, Florida Medical and Research Institute, and Silvina Levis, MD, University of Miami; Nelson B. Watts, MD, Emory University, Atlanta, Ga; Richard D. Wasnich, MD, Hawaii Osteoporosis Center, Honolulu; Sheldon Berger, MD, Chicago Center for Clinical Research, and Murray J. Favus, MD, University of Chicago Medical Center, Chicago, and Robert G. Trapp, MD, The Arthritis Center, Springfield, Ill; M. Rashid Khairi, MD, Physicians Research Group, Indianapolis, and Randall R. Stoltz, MD, GFI Research Center, Ind; Barbara P. Lukert, MD, University of Kansas, Kansas City; Christine L. Cook, MD, University of Louisville, Ky; Alan Burshell, MD, Alton Ochsner Clinic, New Orleans, La; Clifford J. Rosen, MD, Maine Center for Osteoporosis Research and Education, St Joseph's Hospital, Bangor, Me; Michael A. Bolognese, MD, Osteoporosis Analysis Center, Norman S. Koval, MD, Center for Rheumatology and Bone Research, Philip Levin, MD, Greater Baltimore Medical Center, Baltimore, and Nathan Wei, MD, Arthritis & Osteoporosis Center of Maryland, Frederick, Md; Robert M. Neer, MD, Massachusetts General Hospital, Boston; Kristine E. Ensrud, MD, Veterans Affairs Medical Center, University of Minnesota, Minneapolis; Louis V. Avioli, MD, Washington University School of Medicine, St Louis, Mo; Robert R. Recker, MD, Creighton University, Omaha, Neb; Keith S. Usiskin, MD, Morristown Memorial Hospital, Morristown, NJ; Arnold M. Moses, MD, State University of New York Health Science Center, Louis L. Shane, MD, Physician's Clinical Research Service, White Plains, Ethel Siris, MD, Irvine Center to Clinical Research, Irvine, and Stuart Weinerman, MD, North Shore University Hospital, NY; Michelle Hooper, MD, University Hospitals of Cleveland, James H. Liu, MD, University of Cincinnati, David Bacha, MD, Crystal Arthritis Center, Akron, Ohio; William C. Orr, PhD, Lynn Health Science Institute, Oklahoma City, Okla; Jane A. Cauley, MD, DrPH, University of Pittsburgh, Solomon Epstein, MD, Allegheny University of the Health Sciences, Allegheny, and Susan B. Ward, MD, Jefferson Osteoporosis Center, Jefferson, Pa; Joseph Tucci, MD, Roger Williams Medical Center, Providence, RI; Norman H. Bell, MD, Medical University of South Carolina, Charleston, SC; William Applegate, MD, and Suzanne Satterfield, MD, DrPH, University of Tennessee, Memphis; M. Cedars and Stanley B. Cohen, MD, Metroplex Clinical Research Center, Dallas, Tex; Clark McKeever, MD, Research for Health/Health Advance, Veronica K. Piziak, MD, PhD, Scott & White Clinic, Julio Rosenstock, MD, Dallas Diabetes Endocrine Center, Dallas, and Sherwyn L. Schwartz, MD, Diabetes & Glandular Disease Clinic, Tex; C. Deal and Robert Downs, MD, Virginia Commonwealth University, Richmond; Barbara Drinkwater, PhD, Pacific Medical Center, Seattle, Wash; and Noel Binkley, MD, University of Wisconsin Hospital & Clinics, Madison.
Contributions: Erin Walls, ELS, assisted in preparation of the manuscript; the Medical Editing Department, Kaiser Foundation Research Institute, also provided editorial assistance.
Funding/Support: The research was supported by a grant from Eli Lilly and Company.
Disclaimer: Data were analyzed at Lilly Research Laboratories, Eli Lilly and Co.
Acknowledgment: We thank Ty McClure, PhD, for statistical programming and Leo Plouffe, MD, for review and advice on the manuscript.
Corresponding Author and Reprints: Bruce Ettinger, MD, Division of Research, Kaiser Permanente Medical Care Program, 3505 Broadway, 13th Floor, Oakland, CA 94611-5400 (e-mail: bxe{at}dor.kaiser.org).
Author Affiliations: Division of Research, Kaiser Permanente, Oakland, Calif (Dr Ettinger) and Departments of Epidemiology and Biostatistics (Drs Black and Cummings), Radiology (Dr Genant), and Medicine (Dr Cummings), University of California, San Francisco; Eli Lilly and Co, Indianapolis, Ind (Drs Mitlak, Knickerbocker, Nickelsen, Krueger, Cohen, and Eckert); Center for Clinical and Basic Research, Ballerup, Denmark (Dr Christiansen); INSERM, Lyon, France (Dr Delmas); Instituto de Investigaciones Metabólicas, Buenos Aires, Argentina (Dr Zanchetta); Center for Clinical Osteoporosis Research CECOR AS, Haugesund, Norway (Dr Stakkestad); Department of Diagnostic Radiology, Cristian-Albrechts–Universität Kiel, Germany (Dr Glüer); Veterans Affairs Medical Center, Minneapolis, Minn (Dr Ensrud); Washington University, St Louis, Mo (Dr Avioli); and Vrije Universiteit, Amsterdam, the Netherlands (Dr Lips).
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Multidisciplinary patient education in groups increases knowledge on osteoporosis: A randomized controlled trial
Nielsen et al.
Scand J Public Health 2008;36:346-352.
ABSTRACT
Osteoporosis: Management and Treatment Strategies for Orthopaedic Surgeons
Gehrig et al.
JBJS 2008;90:1362-1374.
FULL TEXT
Randomized Trial of Once-Weekly Parathyroid Hormone (1-84) on Bone Mineral Density and Remodeling
Black et al.
J. Clin. Endocrinol. Metab. 2008;93:2166-2172.
ABSTRACT
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Gut, inflammation and osteoporosis: basic and clinical concepts
Tilg et al.
Gut 2008;57:684-694.
ABSTRACT
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Improving Evaluation and Treatment for Osteoporosis Following Distal Radial Fractures. A Prospective Randomized Intervention
Rozental et al.
JBJS 2008;90:953-961.
ABSTRACT
| FULL TEXT
Persistent Hot Flushes in Older Postmenopausal Women
Huang et al.
Arch Intern Med 2008;168:840-846.
ABSTRACT
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ASHP Therapeutic Position Statement on the Prevention and Treatment of Osteoporosis in Adults
MacLaughlin and Raehl
Am J Health Syst Pharm 2008;65:343-357.
FULL TEXT
Differential Regulation of Native Estrogen Receptor-Regulatory Elements by Estradiol, Tamoxifen, and Raloxifene
Levy et al.
Mol. Endocrinol. 2008;22:287-303.
ABSTRACT
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Drugs for pre-osteoporosis: prevention or disease mongering?
Alonso-Coello et al.
BMJ 2008;336:126-129.
FULL TEXT
Long-term Risk of Incident Vertebral Fractures
Cauley et al.
JAMA 2007;298:2761-2767.
ABSTRACT
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Relationship between Bone Mineral Density Changes and Fracture Risk Reduction in Patients Treated with Strontium Ranelate
Bruyere et al.
J. Clin. Endocrinol. Metab. 2007;92:3076-3081.
ABSTRACT
| FULL TEXT
Bone Density in Breast Cancer: When to Intervene?
Gralow
JCO 2007;25:3194-3197.
FULL TEXT
Raloxifene Enhances Material-Level Mechanical Properties of Femoral Cortical and Trabecular Bone
Allen et al.
Endocrinology 2007;148:3908-3913.
ABSTRACT
| FULL TEXT
The role of DXA bone density scans in the diagnosis and treatment of osteoporosis
Blake and Fogelman
Postgrad. Med. J. 2007;83:509-517.
ABSTRACT
| FULL TEXT
Assessment of non-vertebral fracture risk in postmenopausal women
Roux et al.
Ann Rheum Dis 2007;66:931-935.
ABSTRACT
| FULL TEXT
Patient Assessment in the Diagnosis, Prevention, and Treatment of Osteoporosis
Lata and Elliott
Nutr Clin Pract 2007;22:261-275.
ABSTRACT
| FULL TEXT
Review of Postmenopausal Osteoporosis Pharmacotherapy
Mayes
Nutr Clin Pract 2007;22:276-285.
ABSTRACT
| FULL TEXT
Altered Ovarian Function Affects Skeletal Homeostasis Independent of the Action of Follicle-Stimulating Hormone
Gao et al.
Endocrinology 2007;148:2613-2621.
ABSTRACT
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Use of Alendronate After 5 Years of Treatment
Ott
JAMA 2007;297:1979-1979.
FULL TEXT
Once-Yearly Zoledronic Acid for Treatment of Postmenopausal Osteoporosis
Black et al.
NEJM 2007;356:1809-1822.
ABSTRACT
| FULL TEXT
SERMs: Meeting the Promise of Multifunctional Medicines
Jordan
JNCI J Natl Cancer Inst 2007;99:350-356.
ABSTRACT
| FULL TEXT
Twenty-Year Follow-up of the Royal Marsden Randomized, Double-Blinded Tamoxifen Breast Cancer Prevention Trial
Powles et al.
JNCI J Natl Cancer Inst 2007;99:283-290.
ABSTRACT
| FULL TEXT
Selective Activation of Estrogen Receptor-{beta} Transcriptional Pathways by an Herbal Extract
Cvoro et al.
Endocrinology 2007;148:538-547.
ABSTRACT
| FULL TEXT
Osteoporosis and its management
Poole and Compston
BMJ 2006;333:1251-1256.
FULL TEXT
A 55-Year-Old Woman With Osteopenia
Cummings
JAMA 2006;296:2601-2610.
ABSTRACT
| FULL TEXT
Effect of raloxifene on salivary sex steroid concentrations in premenopausal women
Chatterton et al.
J Endocrinol 2006;191:599-604.
ABSTRACT
| FULL TEXT
Osteoporosis Redux
Lentle and Worsley
JNM 2006;47:1945-1959.
FULL TEXT
Commentary on Mobley and Others: Importance of Assumptions About VTE Mortality in Modeling the Cost-effectiveness of Osteoporosis Therapies
Meadows et al.
Med Decis Making 2006;26:633-635.
Clinical Applications of Vertebral Fracture Assessment by Dual-Energy X-Ray Absorptiometry
Lewiecki and Laster
J. Clin. Endocrinol. Metab. 2006;91:4215-4222.
ABSTRACT
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Skeletal complications of breast cancer therapies.
Hirbe et al.
Clin. Cancer Res. 2006;12:6309s-6314s.
ABSTRACT
| FULL TEXT
Treatment-related osteoporosis in men with prostate cancer.
Smith
Clin. Cancer Res. 2006;12:6315s-6319s.
ABSTRACT
| FULL TEXT
Effect of Raloxifene on the Incidence of Invasive Breast Cancer in Postmenopausal Women with Osteoporosis Categorized by Breast Cancer Risk
Lippman et al.
Clin. Cancer Res. 2006;12:5242-5247.
ABSTRACT
| FULL TEXT
Hemodynamic effects of acute and repeated exposure to raloxifene in ovariectomized sheep
Zoma et al.
Am. J. Physiol. Heart Circ. Physiol. 2006;291:H1216-H1225.
ABSTRACT
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Does Vertebroplasty Cause Incident Vertebral Fractures? A Review of Available Data
Trout and Kallmes
Am. J. Neuroradiol. 2006;27:1397-1403.
ABSTRACT
| FULL TEXT
Characterization of patients with an inadequate clinical outcome from osteoporosis therapy: the Observational Study of Severe Osteoporosis (OSSO)
Jakob et al.
QJM 2006;99:531-543.
ABSTRACT
| FULL TEXT
Preventing fragility hip fracture in high risk groups: an opportunity missed.
Peng et al.
Postgrad. Med. J. 2006;82:528-531.
ABSTRACT
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Effects of raloxifene on cardiovascular events and breast cancer in postmenopausal women.
Barrett-Connor et al.
NEJM 2006;355:125-137.
ABSTRACT
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Risk-benefit profiles of raloxifene for women.
Stefanick
NEJM 2006;355:190-192.
FULL TEXT
Effects of Tamoxifen vs Raloxifene on the Risk of Developing Invasive Breast Cancer and Other Disease Outcomes: The NSABP Study of Tamoxifen and Raloxifene (STAR) P-2 Trial
Vogel et al.
JAMA 2006;295:2727-2741.
ABSTRACT
| FULL TEXT
Patient-Reported Symptoms and Quality of Life During Treatment With Tamoxifen or Raloxifene for Breast Cancer Prevention: The NSABP Study of Tamoxifen and Raloxifene (STAR) P-2 Trial
Land et al.
JAMA 2006;295:2742-2751.
ABSTRACT
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Progress in Chemoprevention Drug Development: The Promise of Molecular Biomarkers for Prevention of Intraepithelial Neoplasia and Cancer--A Plan to Move Forward
Kelloff et al.
Clin. Cancer Res. 2006;12:3661-3697.
ABSTRACT
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The Cost-effectiveness of Therapy With Teriparatide and Alendronate in Women With Severe Osteoporosis.
Liu et al.
Arch Intern Med 2006;166:1209-1217.
ABSTRACT
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Meta-analysis: accuracy of quantitative ultrasound for identifying patients with osteoporosis.
Nayak et al.
ANN INTERN MED 2006;144:832-841.
ABSTRACT
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Linking Ligand-Induced Alterations in Androgen Receptor Structure to Differential Gene Expression: A First Step in the Rational Design of Selective Androgen Receptor Modulators
Kazmin et al.
Mol. Endocrinol. 2006;20:1201-1217.
ABSTRACT
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Diagnosis, Screening, Prevention, and Treatment of Osteoporosis
Mauck and Clarke
Mayo Clin Proc. 2006;81:662-672.
ABSTRACT
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Venous thrombosis and conjugated equine estrogen in women without a uterus.
Curb et al.
Arch Intern Med 2006;166:772-780.
ABSTRACT
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Cancer-treatment-induced bone loss, part 2
Michaud and Goodin
Am J Health Syst Pharm 2006;63:534-546.
ABSTRACT
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Cost-Effectiveness of Osteoporosis Screening and Treatment with Hormone Replacement Therapy, Raloxifene, or Alendronate
Mobley et al.
Med Decis Making 2006;26:194-206.
ABSTRACT
The Effect of Raloxifene after Discontinuation of Long-Term Alendronate Treatment of Postmenopausal Osteoporosis
Michalska et al.
J. Clin. Endocrinol. Metab. 2006;91:870-877.
ABSTRACT
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Glucocorticoid-Induced Bone Loss in Dermatologic Patients: An Update
Summey and Yosipovitch
Arch Dermatol 2006;142:82-90.
ABSTRACT
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Intervertebral disc height in treated and untreated overweight post-menopausal women
Baron et al.
Hum Reprod 2005;20:3566-3570.
ABSTRACT
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Tamoxifen for the Prevention of Myocardial Infarction in Humans: Preclinical and Early Clinical Evidence
Grainger and Schofield
Circulation 2005;112:3018-3024.
FULL TEXT
Expression Profiling of Rat Femur Revealed Suppression of Bone Formation Genes by Treatment with Alendronate and Estrogen but Not Raloxifene
Helvering et al.
Mol. Pharmacol. 2005;68:1225-1238.
ABSTRACT
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Analysis off Estrogen Agonism and Antagonism of Tamoxifen, Raloxifene, and ICI182780 in Endometrial Cancer Cells: A Putative Role for the Epidermal Growth Factor Receptor Ligand Amphiregulin
Gielen et al.
Reproductive Sciences 2005;12:e55-e66.
ABSTRACT
The prevention of osteoporotic fractures
Karlsson et al.
J Bone Joint Surg Br 2005;87-B:1320-1327.
FULL TEXT
The mechanisms and managements of hormone-therapy resistance in breast and prostate cancers
Rau et al.
Endocr Relat Cancer 2005;12:511-532.
ABSTRACT
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Bazedoxifene Acetate: A Selective Estrogen Receptor Modulator with Improved Selectivity
Komm et al.
Endocrinology 2005;146:3999-4008.
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