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Figure 1.
Flow of participants through the study.

Flow of participants through the study.

Figure 2.
Cumulative incidence of hip fractures in the risedronate sodium and ergocalciferol with calcium supplementation (risedronate) group and the placebo and ergocalciferol with calcium supplementation (control) group. During 18 months, 19 subjects in the control group and 5 in the risedronate group had a hip fracture (log-rank, P<.001).

Cumulative incidence of hip fractures in the risedronate sodium and ergocalciferol with calcium supplementation (risedronate) group and the placebo and ergocalciferol with calcium supplementation (control) group. During 18 months, 19 subjects in the control group and 5 in the risedronate group had a hip fracture (log-rank, P<.001).

Figure 3.
Percentage changes from baseline in metacarpal bone mineral density (BMD) after 6, 12, and 18 months in the 2 groups of patients. During the 18 months, the differences in the percentage changes in the BMD among the 2 groups were statistically significant (based on Wilcoxon rank sum test; P<.001). Numbers in parentheses are the numbers of the subjects followed.

Percentage changes from baseline in metacarpal bone mineral density (BMD) after 6, 12, and 18 months in the 2 groups of patients. During the 18 months, the differences in the percentage changes in the BMD among the 2 groups were statistically significant (based on Wilcoxon rank sum test; P<.001). Numbers in parentheses are the numbers of the subjects followed.

Table 1. 
Demographic and Baseline Clinical Characteristics of the Female Patients With Alzheimer Disease at Study Entry*
Demographic and Baseline Clinical Characteristics of the Female Patients With Alzheimer Disease at Study Entry*
Table 2. 
Falls and Biochemical Tests in the Risedronate and Control Groups at Baseline and After 6, 12, 18 Months of Follow-up*
Falls and Biochemical Tests in the Risedronate and Control Groups at Baseline and After 6, 12, 18 Months of Follow-up*
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Melton  LJ  III, Beard  CM, Kokmen  E, Atkinson  EJ, O'Fallon  WM.  Fracture risk in patients with Alzheimer's disease. J Am Geriatr Soc. 1994;42:614-619.
PubMedArticle
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van Staa  TP, Leufkens  HG, Cooper  C.  Utility of medical and drug history in fracture risk prediction among men and women. Bone. 2002;31:508-514.
PubMedArticle
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Buchner  DM, Larson  EB.  Falls and fractures in patients with Alzheimer-type dementia. JAMA. 1987;257:1492-1495.
PubMedArticle
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Nurmi  I, Narinen  A, Luthje  P, Tanninen  S.  Cost analysis of hip fracture treatment among the elderly for the public health services: a 1-year prospective study in 106 consecutive patients. Arch Orthop Trauma Surg. 2003;123:551-554.
PubMedArticle
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Holmes  J, House  A.  Psychiatric illness predicts poor outcome after surgery for hip fracture: a prospective cohort study. Psychol Med. 2000;30:921-929.
PubMedArticle
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Matsueda  M, Ishii  Y.  The relationship between dementia score and ambulatory level after hip fracture in the elderly. Am J Orthop. 2000;29:691-693.
PubMed
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Morrison  RS, Siu  AL.  Mortality from pneumonia and hip fractures in patients with advanced dementia. JAMA. 2000;284:2447-2448.
PubMedArticle
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Nightingale  S, Holmes  J, Mason  J, House  A.  Psychiatric illness and mortality after hip fracture. Lancet. 2001;357:1264-1265.
PubMedArticle
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Sato  Y, Asoh  T, Oizumi  K.  High prevalence of vitamin D deficiency and reduced bone mass in elderly women with Alzheimer's disease. Bone. 1998;23:555-557.
PubMedArticle
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Sato  Y, Kanoko  T, Satoh  K, Iwamoto  J.  Risk factors for hip fracture among elderly patients with Alzheimer’s disease. J Neurol Sci. 2004;223:107-112.
PubMedArticle
12.
Kipen  E, Helme  RD, Wark  JD, Flicker  L.  Bone density, vitamin D nutrition, and parathyroid hormone levels in women with dementia. J Am Geriatr Soc. 1995;43:1088-1091.
PubMedArticle
13.
van Beek  ER, Cohen  LH, Leroy  IM, Ebetino  FH, Lowik  CW, Papapoulos  SE.  Differentiating the mechanisms of antiresorptive action of nitrogen containing bisphosphonates. Bone. 2003;33:805-811.
PubMedArticle
14.
Reginster  J, Minne  HW, Sorensen  OH,  et al.  Randomized trial of the effects of risedronate on vertebral fractures in women with established postmenopausal osteoporosis. Osteoporos Int. 2000;11:83-91.
PubMedArticle
15.
McClung  MR, Geusens  P, Miller  PD,  et al.  Effect of risedronate on the risk of hip fracture in elderly women. N Engl J Med. 2001;344:333-340.
PubMedArticle
16.
Fukunaga  M, Kushida  K, Kishimoto  H,  et al.  A comparison of the effect of risedronate and etidronate on lumbar bone mineral density in Japanese patients with osteoporosis: a randomized controlled trial. Osteoporos Int. 2002;13:971-979.
PubMedArticle
17.
Cranney  A, Waldegger  L, Zytaruk  N,  et al.  Risedronate for the prevention and treatment of postmenopausal osteoporosis. Cochrane Database Syst Rev. 2003;(4):CD004523.
PubMed
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McKhann  G, Drachman  D, Folstein  M, Katzman  R, Price  D, Standian  EM.  Clinical diagnosis of Alzheimer’s disease: report on the NINCDS-ADRADA work group under the auspices of the Department of Health and Human Services Task Force on Alzheimer’s disease. Neurology. 1984;34:939-944.
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Sato  Y, Asoh  T, Kaji  M, Oizumi  K.  Benefical effect of intermittent cyclical etidronate therapy in hemiplegic patients following an acute stroke. J Bone Miner Res. 2000;15:2487-2494.
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Sato  Y, Kaji  M, Tsuru  T, Oizumi  K.  Risk factors for hip fracture among elderly patients with Parkinson’s disease. J Neurol Sci. 2001;182:89-93.
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PubMedArticle
Original Investigation
August 8, 2005

The Prevention of Hip Fracture With Risedronate and Ergocalciferol Plus Calcium Supplementation in Elderly Women With Alzheimer DiseaseA Randomized Controlled Trial

Author Affiliations

Author Affiliations: Department of Neurology (Dr Sato), Mitate Hospital, Tagawa; Departments of Rehabilitation Medicine (Dr Kanoko) and Vascular Biology (Dr Satoh), Hirosaki University School of Medicine, Hirosaki; and Department of Sports Medicine (Dr Iwamoto), Keio University School of Medicine, Tokyo; Japan.

Arch Intern Med. 2005;165(15):1737-1742. doi:10.1001/archinte.165.15.1737
Abstract

Background  A high incidence of fractures, particularly of the hip, represents an important problem in patients with Alzheimer disease (AD), who are prone to falls and have osteoporosis. We previously found that deficiency of 25-hydroxyvitamin D and compensatory hyperparathyroidism cause reduced bone mineral density in female patients with AD. We address the possibility that treatment with risedronate sodium and ergocalciferol plus calcium supplementation may reduce the incidence of nonvertebral fractures in elderly women with AD.

Methods  A total of 500 elderly women with AD were randomly assigned to daily treatment with 2.5 mg of risedronate sodium or a placebo, combined with 1000 IU of ergocalciferol and 1200 mg of elementary calcium, and followed up for 18 months.

Results  At baseline, patients of both groups showed 25-hydroxyvitamin D deficiency with compensatory hyperparathyroidism. During the study period, bone mineral density in the risedronate group increased by 4.1% and decreased by 0.9% in the control group. Vertebral fractures occurred in 29 patients (24 hip fractures) in the control group and 8 patients (5 hip fractures) in the risedronate group. The relative risk in the risedronate group compared with the control group was 0.28 (95% confidence interval, 0.13-0.59).

Conclusions  Elderly patients with AD hypovitaminosis D are at increased risk for hip fracture. Treatment with risedronate and ergocalciferol may be safe and effective in reducing the risk of a fracture in elderly patients with AD.

Alzheimer disease (AD) is a common neurodegenerative disorder characterized by progressive loss of memory and cognitive function, and far-advanced AD is associated with generalized weakness. A high incidence of fractures, particularly of the hip,13 represents an important problem in patients with AD, who are prone to falls4 and may have osteoporosis. The odds ratio reported for fracture prevalence between elderly persons with and without AD is 6.9.4 Hip fractures are associated with higher medical costs compared with all other osteoporosis-related fractures combined.5 Functional recovery after hip fracture in AD is poor,68 and patients with dementia have increased mortality during the first 6 months after a hip fracture.9

The physical condition of patients with AD has increasingly become one of the critical issues in their treatment. We previously10 demonstrated that deficiency of 25-hydroxyvitamin D (25-OHD) due to sunlight deprivation contributes to the reduced bone mineral density (BMD) in patients with AD in nursing homes. Also, elderly female patients with AD with low BMD and serum 25-OHD concentrations of 5 ng/mL or lower with secondary hyperparathyroidism had a high risk of hip fracture.11 Kipen et al12 examined women with dementia in the community and found that they have normal BMD, hypovitaminosis D, and compensatory hyperparathyroidism.

Thus, vitamin D deficiency with compensatory hyperparathyroidism contributes to reduced BMD in patients with AD. Risedronate sodium, a pyridinyl bisphosphonate, is known to reduce bone resorption through the inhibition of osteoclastic activity.13 Its antiresorptive action is more potent than that of a related compound, etidronate disodium. Risedronate decreases the risk of fractures and increases BMD in postmenopausal women with osteoporosis.1416 According to a recent review,17 the effectiveness of the risedronate in preventing osteoporotic fractures has been clearly demonstrated in many trials. Risedronate therapy would be beneficial particularly in reducing accelerated osteoclastic bone resorption in patients with AD. We therefore conducted an 18-month randomized, double-blind trial to evaluate the efficacy of risedronate and ergocalciferol with calcium supplementation in preventing the progression of osteoporosis and decreasing the risk of vertebral fractures in elderly women with AD. Also, biochemical indexes of bone metabolism were measured to assess the effectiveness of the therapy. The rate of vertebral fractures was not determined in this study because many vertebral fractures are asymptomatic among elderly patients with AD and the interpretation of spinal x-ray films may be complicated by osteoarthritis or scoliosis.

METHODS
STUDY POPULATION

This study compared the incidence of vertebral fractures in the 2 groups of elderly female patients with AD who were administered risedronate or a placebo, combined with ergocalciferol and calcium supplementation. We recruited 500 ambulatory women from consecutive patients in our outpatient clinic who were 70 years or older, living in the community and cared for by their family caregivers, and who met criteria for dementia and probable AD according to the Diagnostic and Statistical Manual of Mental Disorders, Revised Third Edition.18 Patients were recruited from March 2003 to April 2003, and each patient was followed up for 18 months. Patients younger than 70 years were excluded from the study. Patients with impairment of hepatic, renal, cardiac, or thyroid function or those who had known causes of osteoporosis, such as primary hyperparathyroidism, renal osteodystrophy, or familial osteoporosis, were excluded from this study. Also, patients were excluded if they had received any drug known to alter bone metabolism, such as corticosteroids, anticonvulsants, estrogens, calcitonin, bisphosphonate, calcium, or vitamins D and K (all forms), for 3 months or longer during the 12 months preceding the study. The study neurologist (Y.S.), who remained blind to the results of biochemical assays of bone metabolism, diagnosed AD.

Baseline demographic data and duration of illness were obtained (Table 1). At baseline, we determined body mass index, and the Mini-Mental State Examination19 was given to the patients. Activities of daily living were assessed by the Barthel index, in which a functional dependence score of 100 represents independence.20 Patients who fell at least once in the 3 months before recruitment were defined as “fallers.” Daily intake of calcium and vitamin D was calculated, by comparing with the Japanese Standard Food Table, for each participant on the basis of a food-frequency questionnaire filled out by a family member. Patients who consumed less calcium and vitamin D than the Japanese recommended daily allowance (1000 mg and 100 IU, respectively) were defined as low dietary consumers of vitamin D. Sunlight exposure during the preceding year was assessed by the family members and graded as almost none, less than 15 minutes per week, or 15 minutes or longer per week.21

This study was approved by the local ethics committee (Human Investigation Committee of the Mitate Hospital, Tagawa, Japan). All patients and controls were informed of the nature of the study. Consent was obtained from each participant or from family members when patients were unable to understand because of dementia.

STUDY PROTOCOL

The patients were assigned to 1 of the 2 study groups by means of computer-generated random numbering. Random allocation sequence was implemented using numbered containers, and the sequence was concealed until interventions were assigned. The patients and all study personnel were blinded to treatment assignment and biochemical measurements. The randomization code was generated using a permuted block size of 4 (stratified by site) by a consulting statistician not otherwise involved in the trial. No other restrictions were used in the randomization procedure. Physicians who performed the follow-up assessment of the patients’ condition were blinded to randomization and study group. Patients in the risedronate group (n = 250) received a daily dose of 2.5-mg risedronate sodium in a tablet (Actonel; Aventis Pharmaceuticals, Tokyo, Japan) and 1000 IU of ergocalciferol and 1200 mg of elemental calcium after breakfast. The control group received a placebo and 1000 IU of ergocalciferol and 1200 mg of elemental calcium (n = 250). Patients were instructed to take the tablet with a cup of water (180 mL), 30 to 60 minutes before breakfast, and to remain sitting or maintain an upright position for 60 minutes thereafter. Adherence to study medication was assessed by counting the returned tablets. No dose adjustments were made at any time during the study. Patients were prohibited from taking any other drugs that could affect bone metabolism during the study period, except for those for whom it was decided to be necessary for accompanying conditions. Such exceptions included an anti-inflammatory therapy with a corticosteroid in 2 patients (1 each in the 2 groups) for connective tissue diseases. Follow-up assessment of the patients’ condition was performed by a physician (Y.S.) who did not participate in the initial randomization. Both groups were observed for 18 months. General medical evaluation and laboratory values were assessed on entry and after 18 months. The patients’ clinical status was assessed at baseline, and all patients were followed up every 4 weeks in the outpatient clinic, at which times nonvertebral fractures were recorded. Symptomatic nonvertebral fractures confirmed by radiological examinations were considered adverse clinical events, with no attempt to exclude fractures related primarily to trauma. Falls were registered by means of monthly “fall calendars.” The family members of participants were instructed to complete the calendar daily, marking an “X” for each fall on the date when the fall occurred. In addition, the characteristics of each fall were recorded according to the timing, direction, and severity of the fall, and the activity in which the fall occurred and injuries due to the fall were also recorded.

Both groups were observed for 18 months. General medical evaluation, metacarpal BMD measurement, and laboratory values were assessed on entry and after 6, 12, and 18 months later.

Computed x-ray densitometry (CXD; Teijin Diagnostics, Tokyo)22 via an improved microdensitometric method was used to quantify BMD in the left second metacarpals of each patient as described previously.10 The computer algorithm for CXD compares bone radiodensity with the gradations of an aluminum step wedge, calculating bone thickness as an aluminum equivalent (mm Al) showing the same x-ray absorption. The validity and accuracy of this method have been described elsewhere.23

In the morning of the day of bone evaluation, blood and urine samples were obtained from the 500 patients after an overnight fast. Blood samples were analyzed for ionized calcium, intact parathyroid hormone (PTH), and 25-OHD. Ionized calcium concentration was determined in fresh serum processed under anaerobic conditions using an ion-selective electrode and an ionized calcium analyzer (Jokoh, Tokyo). Serum PTH concentration was measured by an immunoradiometric assay (Sumitomo Biomedical, Osaka, Japan). Serum 25-OHD concentration was determined by an radioimmunoassay (DiaSorin, Stillwater, Mich). Urinary deoxypyridinoline (D-Pyr) was measured with a commercially available, specific enzyme immunoassay kit (Metra Biosystems Inc, Calif). Urinary D-Pyr was expressed relative to urinary creatinine concentration. The normal ranges of the BMD and biochemical indexes in elderly women are given in Table 2.24,25

STUDY END POINTS AND STATISTICAL ANALYSIS

The sample size was based on an expected nonvertebral fracture incidence of 10% in the control group over 18 months. Assuming a 10% dropout rate over 18 months, the study had at least 80% power to detect a 70% reduction in fracture risk, with a 2-sided significance level of α = .05. The primary end point was defined as the incidence of a nonvertebral fracture. An intention-to-treat analysis was performed on all randomized participants to determine relative risk (RR), and the difference between the 2 groups was analyzed by the log-rank test. The within-group changes from the baseline values were assessed by the paired t test. Group differences of the categorical data were tested by the Fisher exact test. Spearman rank correlation coefficients were calculated to determine the relationships between BMD and serum 25-OHD or intact PTH. Laboratory values and BMD were expressed as percentage change from the baseline, and the 2 groups were compared by the Wilcoxon rank sum test. P<.05 was considered statistically significant.

RESULTS
BASELINE CHARACTERISTICS OF STUDY SUBJECTS

Figure 1 illustrates the flow of participants through the study. Nineteen patients in the risedronate group and 20 in the control group dropped out or withdrew from the study owing to noncompliance, loss to follow-up, intercurrent illness, or death. Thus, a total of 461 patients (231 in the risedronate group and 230 in the control group) completed the trial. We included 250 patients in each treatment group in the final intention-to-treat analysis.

Table 1 lists the baseline characteristics of the participants. There was no significant difference between the 2 groups in duration of illness, Mini-Mental State Examination, Barthel index, body mass index, BMD, and numbers of fallers. Body mass index was low in both groups. Many of the patients in both groups had been exposed to sunlight for less than 15 minutes per week or had almost no sun exposure because of being homebound. Mean daily dietary intake of vitamin D and calcium in both groups were less than the Japanese recommended daily allowance (100 IU and 1000 mg, respectively). The average values of metacarpal BMD in the 2 groups were lower compared with the reference range of the normal Japanese population.24,25

As shown in Table 2, in the 2 groups, the baseline values of serum ionized calcium, 25-OHD concentrations were low, whereas serum PTH and bone Gla-protein (BGP) or urinary D-Pyr were high compared with the reference range of the normal Japanese population.24,25

When both patient groups were analyzed together, the BMD correlated positively with body mass index (r = 0.250; P<.01), and 25-OHD (r = 0.261; P<.01) concentrations, whereas BMD correlated negatively with PTH (r = −0.260; P<.01). There were negative correlations between serum 25-OHD and PTH (r = −0.213; P<.01), suggesting the presence of compensatory hyperparathyroidism.

FRACTURES

Nonvertebral fractures occurred in 8 patients in the treatment group (5 hip fractures and 1 fracture each at the distal forearm, proximal humerus, and ankle) and 27 patients in the control group (19 with hip fractures; 3 fractures at the distal forearm; 2 fractures at the proximal femur; and 1 fracture each at the proximal humerus, ribs, and pelvis).

There were 5 hip fractures in the treatment group and 19 in the control group (Figure 2); this difference was statistically significant (log-rank test, P<.001). The number of hip fractures per 1000 patient-years for the risedronate and control groups was 15 and 57, respectively. The RR in the risedronate group vs control group for hip fractures was 0.26 (95% confidence interval, 0.10-0.69).

There were 8 nonvertebral fractures in the treatment group and 29 in the control group; this difference was statistically significant (log-rank test, P<.001). The RR in the risedronate group vs control group for nonvertebral fractures was 0.28 (95% confidence interval, 0.13-0.59).

Table 2 summarizes time-dependent changes in the number of fallers, who fell at least once in 3 months because of sudden loss balance. The numbers of fallers after 6 months remained similar to those at baseline in the 2 groups; however, the numbers in the 2 groups after 12 and 18 months were significantly smaller compared with the baseline number in each group (P<.01). There was no significant difference between the 2 groups in the mean ± SD number of falls per subject during the 18 months (1.9 ± 0.8 in the control group and 1.9 ± 0.9 in the risedronate group).

BONE CHANGES AND BLOOD BIOCHEMICAL MARKERS

Figure 3 shows the percentage changes from the baseline in metacarpal BMD during the 18 months. The mean ± SD percentage changes in BMD were +4.1 ± 0.2 in the risedronate group and −0.9 ± 0.1 in the placebo group. The difference between the 2 groups was statistically significant (P<.001).

Changes in various parameters during the 18-month study period are summarized in Table 2. In both groups, serum calcium and 25-OHD concentrations increased significantly compared with the baseline values, and serum PTH and BGP or urinary D-Pyr concentrations decreased significantly compared with the baseline values in both groups. A significant decrease of serum ionized calcium, BGP, and urinary D-Pyr concentrations in the risedronate group was observed compared with those in control group.

ADVERSE EFFECTS

Serious adverse events including death, overdose, and any other event that was life threatening or permanently disabling or that required intervention to prevent permanent impairment were not observed in either group. In the risedronate group, 2 patients experienced leukopenia, 1 patient had esophagitis, and 3 patients experienced abdominal pain, which eventually disappeared with appropriate therapy without discontinuation of the treatment. Three patients in the control group experienced gastrointestinal symptoms such as epigastric discomfort and nausea, but they subsided within a week without discontinuing ergocalciferol.

COMMENT

Prevention of fractures is one of the important issues in the treatment of elderly women with AD. The high incidence of hip fractures in elderly patients with AD may be attributed to frequent falls4 and osteoporosis due to 25-OHD deficiency with compensatory hyperparathyroidism as suggested in the present study. Serum levels of 25-OHD and PTH and body mass index were found to correlate with BMD in patients with AD. In the present study, the number of falls during the follow-up period was similar and reduced compared with baseline values in the 2 groups, indicating that ergocalciferol may have prevented falls in both groups. A recent study suggested that vitamin D supplementation reduces the risk of falls among ambulatory or institutionalized older individuals.26 This implies that the frequency of fractures due to falls in patients with AD is related to hypovitaminosis D. Despite the reduced incidence of falls and normalization of 25-OHD, incidence of nonvertebral fractures was higher in the control group. Indeed, RRs for hip and nonvertebral fractures were low in the risedronate group compared with the control group. Also, the RR of the risedronate group in the present study (0.26) was low compared with that reported in a recent meta-analysis of 7 trials (0.73) on the effect of risedronate for osteoporotic fractures.17 This difference may be explained by a larger increase in BMD in the present study: the average values of BMD increased by 4.1% in the risedronate group over 18 months. This may reflect a synergistic effect of risedronate and ergocalciferol.

The hip fracture rate in the control group was calculated as 57 per 1000 patient-years. The rate of hip fracture in an elderly reference population between ages 70 and 79 years was reported to be 6.6 per 1000 patient-years.27 Although the mean age of our AD subjects (77.7 years) was within this range, the fracture rate in the present series was far higher than that reported in the reference population.27 In addition to sunlight deprivation, 25-OHD deficiency in these patients was considered to reflect generally poor nutrition, as also evidenced by lower body mass index. It has been reported that patients with dementia had malnutrition and decreased body weight.28 In the present study, 25-OHD deficiency with compensatory hyperparathyroidism resulted in high serum BGP and urinary excretion of D-Pyr, which was corrected by ergocalciferol in both groups. Thus, normalization of 25-OHD, ionized calcium, and bone turnover variables was observed in both groups. The decrease in bone turnover variables was more pronounced in the risedronate group, indicating that greater inhibition of bone resorption may have brought about significant improvement of BMD in the risedronate group.

The patients with deficient 25-OHD levels in the risedronate group benefited from the therapy in terms of increased BMD and prevention of nonvertebral fractures. This implies that treatment with risedronate may be particularly effective in patients with vitamin D deficiency.

We conclude that female patients with AD with low serum vitamin D levels and high bone remodeling due to compensatory hyperparathyroidism are at an increased risk for nonvertebral fractures, particularly in the hip. Combined treatment with risedronate, ergocalciferol, and calcium supplementation may be safe and effective in increasing bone mass and reducing the risk of fractures in elderly women with AD.

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Article Information

Financial Disclosure: None.

Correspondence: Yoshihiro Sato, MD, Department of Neurology, Mitate Hospital, 3237 Yugeta, Tagawa 826-0041, Japan (y-sato@ktarn.or.jp).

Accepted for Publication: April 10, 2005.

References
1.
Johansson  C, Skoog  I.  A population-based study on the association between dementia and hip fractures in 85-year olds. Aging (Milano). 1996;8:189-196.
PubMed
2.
Melton  LJ  III, Beard  CM, Kokmen  E, Atkinson  EJ, O'Fallon  WM.  Fracture risk in patients with Alzheimer's disease. J Am Geriatr Soc. 1994;42:614-619.
PubMedArticle
3.
van Staa  TP, Leufkens  HG, Cooper  C.  Utility of medical and drug history in fracture risk prediction among men and women. Bone. 2002;31:508-514.
PubMedArticle
4.
Buchner  DM, Larson  EB.  Falls and fractures in patients with Alzheimer-type dementia. JAMA. 1987;257:1492-1495.
PubMedArticle
5.
Nurmi  I, Narinen  A, Luthje  P, Tanninen  S.  Cost analysis of hip fracture treatment among the elderly for the public health services: a 1-year prospective study in 106 consecutive patients. Arch Orthop Trauma Surg. 2003;123:551-554.
PubMedArticle
6.
Holmes  J, House  A.  Psychiatric illness predicts poor outcome after surgery for hip fracture: a prospective cohort study. Psychol Med. 2000;30:921-929.
PubMedArticle
7.
Matsueda  M, Ishii  Y.  The relationship between dementia score and ambulatory level after hip fracture in the elderly. Am J Orthop. 2000;29:691-693.
PubMed
8.
Morrison  RS, Siu  AL.  Mortality from pneumonia and hip fractures in patients with advanced dementia. JAMA. 2000;284:2447-2448.
PubMedArticle
9.
Nightingale  S, Holmes  J, Mason  J, House  A.  Psychiatric illness and mortality after hip fracture. Lancet. 2001;357:1264-1265.
PubMedArticle
10.
Sato  Y, Asoh  T, Oizumi  K.  High prevalence of vitamin D deficiency and reduced bone mass in elderly women with Alzheimer's disease. Bone. 1998;23:555-557.
PubMedArticle
11.
Sato  Y, Kanoko  T, Satoh  K, Iwamoto  J.  Risk factors for hip fracture among elderly patients with Alzheimer’s disease. J Neurol Sci. 2004;223:107-112.
PubMedArticle
12.
Kipen  E, Helme  RD, Wark  JD, Flicker  L.  Bone density, vitamin D nutrition, and parathyroid hormone levels in women with dementia. J Am Geriatr Soc. 1995;43:1088-1091.
PubMedArticle
13.
van Beek  ER, Cohen  LH, Leroy  IM, Ebetino  FH, Lowik  CW, Papapoulos  SE.  Differentiating the mechanisms of antiresorptive action of nitrogen containing bisphosphonates. Bone. 2003;33:805-811.
PubMedArticle
14.
Reginster  J, Minne  HW, Sorensen  OH,  et al.  Randomized trial of the effects of risedronate on vertebral fractures in women with established postmenopausal osteoporosis. Osteoporos Int. 2000;11:83-91.
PubMedArticle
15.
McClung  MR, Geusens  P, Miller  PD,  et al.  Effect of risedronate on the risk of hip fracture in elderly women. N Engl J Med. 2001;344:333-340.
PubMedArticle
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