1.Telecarers improve osteoporosis treatment and compliance rates in secondary osteoporosis prevention for elderly hip fracture patients.
Linsey Utami GANI ; Francine Chiu Lan TAN ; Thomas Federick James KING
Singapore medical journal 2023;64(4):244-248
INTRODUCTION:
A significant treatment gap has been observed in patients with osteoporosis. Our previous audit found a 31.5% rate of anti-osteoporosis medication initiation after fragility fractures at one year. We piloted the use of telecarers to monitor osteoporosis treatment and compliance.
METHODS:
From January 2017 to January 2018, all hip fracture patients at Changi General Hospital, Singapore, were automatically enrolled into the Health Management Unit valued care hip fracture programme. Telecarer calls were scheduled at discharge, 3, 6 and 12 months. We assessed the acceptability, completion and treatment rates of patients enrolled in this programme.
RESULTS:
A total of 537 patients with a hip fracture were enrolled in the telecarer programme over one year. Their average age was 79.8 ± 8.23 years, and 63.1% of them were female. A total of 341 patients completed 12 months of follow-up, of which 251 (73.6%) patients were on treatment at 12 months. The most common cause of lack of initiation of secondary osteoporosis treatment was patient or family rejection (34.4%), followed by physician failure to prescribe (24.4%) and renal impairment (24.4%). 16.7% of patients were deemed to have advanced dementia with a life-limiting illness and were, thus, deemed unsuitable for treatment.
CONCLUSION
Telecarers may be a useful adjunct in the monitoring of osteoporosis treatment after hip fractures in an elderly population. The main limitations are patient or family rejection and physician inertia. Further studies should focus on a combination of interventions for both patients and physicians to increase awareness of secondary fracture prevention.
Humans
;
Female
;
Aged
;
Aged, 80 and over
;
Male
;
Osteoporotic Fractures/drug therapy*
;
Bone Density Conservation Agents/therapeutic use*
;
Osteoporosis/drug therapy*
;
Hip Fractures/etiology*
;
Secondary Prevention
2.Experimental study on the regulation of subchondral bone plate osteoprotegerin/receptor activator of nuclear factor kappa-B ligand system by berberine to retard the development of osteoarthritis in rabbits.
Jian-Fang ZHANG ; Kai HUANG ; Hai-Li CAI ; Peng-Li ZHANG ; Jian WANG
China Journal of Orthopaedics and Traumatology 2022;35(5):464-469
OBJECTIVE:
To investigate the effect of intra-articular berberine injection on the structural remodeling of subchondral bone plate and osteoprotegerin/receptor activator of nuclear factor kappa-B ligand(OPG/RANKL) system expression in rabbits with osteoarthritis(OA).
METHODS:
Forty 12-month-old male rabbits with an average of(2.73±0.18) kg of body weight, underwent left anterior cruciate ligament transection(ACLT), and were divided into berberine group and placebo groups after operation, 20 rabbits in each group. The berberine group received intra-articular injection of 100 μmol/L berberine 0.3 ml every week for 6 weeks. In placebo group, the same dose of 0.9% sodium chloride injection was injected into the left knee joint cavity every week for 6 weeks. Another 20 12-month-old male rabbits, weighing (2.68±0.18) kg, underwent sham operation on the left knee joint without intra-articular injection intervention (sham operation group). On the last day of the sixth week after operation, three groups of animals were sacrificed to obtain knee joint specimens. The femoral medial condyle samples were obtained for histological evaluation of cartilage and subchondral bone, Mankin scoring system was used to evaluate articular cartilage structure. Image-Pro Plus(IPP) software was used to evaluate subchondral bone plate bone volume(BV), bone volume/total volume(BV/TV), trabecular circumference(TC), mean trabecular thickness (Tb.Th). Real-time quantitative reverse transcription polymerization Enzyme chain reaction(reverse transcription-polymerase chain reaction, RT-PCR) was used to detect the mRNA expression levels of OPG and RANKL in subchondral bone tissue at 6 weeks after operation.
RESULTS:
The cartilage structure evaluation showed that the surface of cartilage tissue in the sham operation group was smooth and flat, and the safranin coloration was full in the full thickness of the cartilage;the cartilage tissue in the berberine group showed uneven surface layer, and the staining of safranin O was mildly decreased;the surface layer fibrosis was seen in placebo group, Safranin O faded significantly. The Mankin score in the berberine group was lower than that in placebo group(P<0.01), but higher than that in sham operation group(P<0.01). The structural evaluation of subchondral bone plate showed that the trabecular bone in sham-operated group was densely arranged;after berberine intervention, the trabeculae were closely arranged;the subchondral bone trabeculae in placebo group were relatively sparse, and the distance between trabeculae was wider. Subchondral bone plate IPP software evaluation showed that BV, BV/TV, TC, Tb.Th in berberine group were higher than those in placebo group(P<0.01), BV, BV/TV, TC, Tb.Th in berberine group were higher than those in placebo group(P<0.01), while lower than the sham operation group (P<0.01). PCR test results showed that the expression of OPG mRNA in the berberine group was significantly higher than that in placebo group(P<0.01), and OPG mRNA in the berberine group was lower than that in sham operation group (P<0.01). There was no significant difference in mRNA expression of RANKL among three groups(P>0.05);the ratio of OPG/RANKL in berberine group was higher than that in placebo group(P<0.01), but lower than that in sham operation group(P<0.01).
CONCLUSION
Intra-articular injection of berberine can effectively inhibit the resorption of subchondral bone in the early stage of OA and delay the development of the disease. The specific mechanism may be that berberine maintains the balance of OPG/RANKL system by up-regulating the expression of OPG gene in subchondral bone.
Animals
;
Berberine/therapeutic use*
;
Bone Density Conservation Agents/therapeutic use*
;
Bone Plates
;
Cartilage, Articular
;
Humans
;
Ligands
;
Male
;
NF-kappa B/metabolism*
;
Osteoarthritis/metabolism*
;
Osteoprotegerin/metabolism*
;
RNA, Messenger/therapeutic use*
;
Rabbits
3.Establishment and assessment of rodent models of medication-related osteonecrosis of the jaw (MRONJ).
Ran YAN ; Ruixue JIANG ; Longwei HU ; Yuwei DENG ; Jin WEN ; Xinquan JIANG
International Journal of Oral Science 2022;14(1):41-41
Medication-related osteonecrosis of the jaw (MRONJ) is primarily associated with administering antiresorptive or antiangiogenic drugs. Despite significant research on MRONJ, its pathogenesis and effective treatments are still not fully understood. Animal models can be used to simulate the pathophysiological features of MRONJ, serving as standardized in vivo experimental platforms to explore the pathogenesis and therapies of MRONJ. Rodent models exhibit excellent effectiveness and high reproducibility in mimicking human MRONJ, but classical methods cannot achieve a complete replica of the pathogenesis of MRONJ. Modified rodent models have been reported with improvements for better mimicking of MRONJ onset in clinic. This review summarizes representative classical and modified rodent models of MRONJ created through various combinations of systemic drug induction and local stimulation and discusses their effectiveness and efficiency. Currently, there is a lack of a unified assessment system for MRONJ models, which hinders a standard definition of MRONJ-like lesions in rodents. Therefore, this review comprehensively summarizes assessment systems based on published peer-review articles, including new approaches in gross observation, histological assessments, radiographic assessments, and serological assessments. This review can serve as a reference for model establishment and evaluation in future preclinical studies on MRONJ.
Animals
;
Bisphosphonate-Associated Osteonecrosis of the Jaw/drug therapy*
;
Bone Density Conservation Agents/adverse effects*
;
Diphosphonates/therapeutic use*
;
Humans
;
Reproducibility of Results
;
Rodentia
4.Comparison of the clinical effects between Dihuang Decoction and alendronate sodium in the treatment of primary osteoporosis.
Jun-Ming WAN ; Jian-Fang ZHANG ; Kai HUANG ; Peng-Li ZHANG ; Shao-Yu ZHU
China Journal of Orthopaedics and Traumatology 2019;32(6):535-538
OBJECTIVE:
To study and compare the clinical effects of Rehmannia Decoction and alendronate sodium for the treatment of primary osteoporosis.
METHODS:
From January 2016 to December 2017, 72 patients with primary osteoporosis who took Dihuang Decoction(DHD) orally and alendronate regularly for more than one year were randomly divided into 2 groups:experimental group and control group. The experimental group consisted of 14 males and 22 females, with an average age of(63.97±3.70) years old. The patients in the experimental group took Chinese medicine DHD, one dose each time, one time in the morning and one time in the evening, twice a week. The control group consisted of 16 males and 20 females with an average age of(63.36±3.07) years old. Patients in the control group were given alendronate 70 mg orally once a week. The basic treatment for osteoporosis remained unchanged in both groups(600 mg of calcium carbonate D3 and 0.5 μg of calcitriol capsules were taken daily). Bone mineral density (BMD) of femoral neck and lumbar vertebrae was measured by dual energy X-ray absorptiometry before and after treatment for one year. The levels of serum collagen type I C-terminal peptide (beta-CTX) and serum osteoclast (SOST) were measured before and after treatment for two groups.
RESULTS:
The age, bone mineral density, SOST and beta-CTX baseline values between the two groups before and after anti-osteoporosis treatment were compared. The difference was not statistically significant(>0.05). Compared with the two groups, the BMD of femoral neck and lumbar vertebrae were increased after 1 year of anti-osteoporosis treatment. The differences were statistically significant (<0.001). The value of serum beta-CTX was significantly lower than before. The values were 52.002 and 50.071 respectively. The value of serum SOST was increased than that before treatment. The values were -29.242 and -30.807 respectively. The differences were statistically significant (<0.001). BMD of the femoral neck and lumbar spine was compared between the two groups after treatment. The P values were 0.294 and 0.478 respectively. The difference was not statistically significant (>0.05). The serum beta-CTX values were compared between the two groups after treatment. The value was 0.908. The serum SOST values were compared between the two groups after treatment. The value was 0.888. The difference was not statistically significant (>0.05).
CONCLUSIONS
In this study, traditional Chinese medicine DHD is used to treat osteoporosis. It is found that DHD and alendronate have a good effect. The DHD can be used as a choice of Chinese medicine in the treatment of primary osteoporosis.
Absorptiometry, Photon
;
Aged
;
Alendronate
;
therapeutic use
;
Bone Density
;
Bone Density Conservation Agents
;
therapeutic use
;
Female
;
Humans
;
Male
;
Middle Aged
;
Osteoporosis
;
drug therapy
5.Progress on medication-related osteonecrosis of the jaw.
Qi-Zhang WANG ; Ji-Yuan LIU ; Jian PAN
West China Journal of Stomatology 2018;36(5):568-572
Medication-related osteonecrosis of the jaw (MRONJ) is a severe complication of bisphosphonates (BPs) or other targeted agent therapies. MRONJ appears as exposed bone, pus, and swelling in the oral and maxillofacial regions. However, neither surgery nor conservative therapy can eliminate symptoms thoroughly. In addition to BPs, several antiresorptive and antiangiogenic agents, such as denosumab and bevacizumab, as well as targeted agents, such as sunitinib and temsirolimus, can cause osteonecrosis of the jaw according to the literature. This review aims to summarize the research progress on these new drugs.
Angiogenesis Inhibitors
;
therapeutic use
;
Bisphosphonate-Associated Osteonecrosis of the Jaw
;
drug therapy
;
Bone Density Conservation Agents
;
adverse effects
;
Denosumab
;
therapeutic use
;
Diphosphonates
;
Humans
6.Effective Treatment of Paget's Disease of the Bone in a Chinese Woman.
Annals of the Academy of Medicine, Singapore 2018;47(12):528-530
Alkaline Phosphatase
;
metabolism
;
Asian Continental Ancestry Group
;
Bone Density Conservation Agents
;
therapeutic use
;
China
;
Denosumab
;
therapeutic use
;
Diabetes Mellitus, Type 2
;
complications
;
Female
;
Humans
;
Hyperlipidemias
;
complications
;
Hypertension
;
complications
;
Middle Aged
;
Osteitis Deformans
;
complications
;
diagnostic imaging
;
drug therapy
;
metabolism
;
Pelvic Bones
;
diagnostic imaging
;
Renal Insufficiency, Chronic
;
complications
;
Singapore
;
Tibia
;
diagnostic imaging
;
Treatment Outcome
7.Medication-related osteonecrosis of the jaw in osteoporotic patients: prevention and management.
Boon Hui CHAN ; Ruixiang YEE ; Rukshini PUVANENDRAN ; Seng Bin ANG
Singapore medical journal 2018;59(2):70-75
Osteoporosis is a major, growing healthcare issue. This is especially of concern in an ageing population like that of Singapore. Osteoporotic patients are at risk of fractures, which can result in increased morbidity and mortality. The use of antiresorptive therapy with bisphosphonates or denosumab has been proven to reduce fracture risk. However, the use of these medications has rarely been associated with the development of osteonecrosis of the jaw, a potentially debilitating condition affecting one or both jaws. Appropriate understanding of the patient's antiresorptive therapy regime, as well as early institution of preventive dental measures, can play an important role in preventing medication-related osteonecrosis of the jaw (MRONJ). Regular monitoring and prompt referral to specialist care is warranted for patients with established MRONJ.
Aged
;
Bone Density Conservation Agents
;
adverse effects
;
therapeutic use
;
Denosumab
;
adverse effects
;
therapeutic use
;
Diphosphonates
;
adverse effects
;
therapeutic use
;
Humans
;
Jaw Diseases
;
chemically induced
;
prevention & control
;
Osteonecrosis
;
chemically induced
;
prevention & control
;
Osteoporosis
;
complications
;
drug therapy
;
Osteoporotic Fractures
;
complications
;
drug therapy
;
Risk Factors
;
Singapore
;
Treatment Outcome
8.Bone-targeted therapies to reduce skeletal morbidity in prostate cancer.
Tanya B DORFF ; Neeraj AGARWAL
Asian Journal of Andrology 2018;20(3):215-220
Bone metastases are the main driver of morbidity and mortality in advanced prostate cancer. Targeting the bone microenvironment, a key player in the pathogenesis of bone metastasis, has become one of the mainstays of therapy in men with advanced prostate cancer. This review will evaluate the data supporting the use of bone-targeted therapy, including (1) bisphosphonates such as zoledronic acid, which directly target osteoclasts, (2) denosumab, a receptor activator of nuclear factor-kappa B (RANK) ligand inhibitor, which targets a key component of bone stromal interaction, and (3) radium-223, an alpha-emitting calcium mimetic, which hones to the metabolically active areas of osteoblastic metastasis and induces double-strand breaks in the DNA. Denosumab has shown enhanced delay in skeletal-related events compared to zoledronic acid in patients with metastatic castration-resistant prostate cancer (mCRPC). Data are mixed with regard to pain control as a primary measure of efficacy. New data call into question dosing frequency, with quarterly dosing strategy potentially achieving similar effect compared to monthly dosing for zoledronic acid. In the case of radium-223, there are data for both pain palliation and improved overall survival in mCRPC. Further studies are needed to optimize timing and combination strategies for bone-targeted therapies. Ongoing studies will explore the impact of combining bone-targeted therapy with investigational therapeutic agents such as immunotherapy, for advanced prostate cancer. Future studies should strive to develop biomarkers of response, in order to improve efficacy and cost-effectiveness of these agents.
Bone Density Conservation Agents/therapeutic use*
;
Bone Neoplasms/secondary*
;
Denosumab/therapeutic use*
;
Diphosphonates/therapeutic use*
;
Endothelins/antagonists & inhibitors*
;
Humans
;
Male
;
Prostatic Neoplasms/pathology*
;
Protein Kinase Inhibitors/therapeutic use*
;
Radioisotopes/therapeutic use*
;
Radiopharmaceuticals/therapeutic use*
;
Radium/therapeutic use*
;
Samarium/therapeutic use*
;
Strontium Radioisotopes/therapeutic use*
9.The Adequacy of Diagnosis and Treatment for Osteoporosis in Patients with Proximal Humeral Fractures.
Tae In KIM ; Jun Ha CHOI ; Sae Hoon KIM ; Joo Han OH
Clinics in Orthopedic Surgery 2016;8(3):274-279
BACKGROUND: The purpose of this study was to evaluate whether physicians' practice was adequate for the diagnosis and treatment of osteoporosis in patients with proximal humeral fracture over the age of 50 years, which is one of major osteoporotic fractures. METHODS: A retrospective nation-wide cohort study was performed using data collected in 2010 by the Korean Health Insurance Review Agency. The incidences of fractures around the hip, spine, and proximal humerus in patients more than 50 years of age, the frequencies of diagnostic bone density scan for osteoporosis, and the prescription for the osteoporosis medication were analyzed and compared. RESULTS: A search of database identified 48,351 hip fractures, 141,208 spine fractures, and 11,609 proximal humeral fractures in patients more than 50 years of age in 2010. Among these patients, 12,097 (25.0%) of hip fractures, 41,962 (29.7%) of spine fractures, and 1,458 (12.6%) of proximal humeral fractures underwent diagnostic bone density scan (p < 0.001); 4,773 (9.9%) of hip fractures, 27,261 (19.3%) of spine fractures, and 639 (5.5%) of proximal humeral fractures were managed with at least one medication approved for the treatment of osteoporosis (p < 0.001). Furthermore, 1,217 (2.5%) of hip fractures, 7,271 (5.2%) of spine fractures, and 188 (1.6%) of proximal humeral fractures received diagnostic bone density scans as well as osteoporosis medications (p < 0.001). Younger patients (50–69 years of age) were less likely to be evaluated and managed for osteoporosis relative to older patients (≥ 70 years of age) (p < 0.001); and men were less likely to be evaluated and managed for osteoporosis relative to women (p < 0.001). CONCLUSIONS: Current physicians' practice pattern may be inadequate for the diagnosis and treatment of osteoporosis in patients of proximal humeral fractures over the age of 50 years. Additional study and educational programs are necessary to improve this care gap, beginning with physicians who are responsible for the fracture treatment and shoulder diseases.
Aged
;
Bone Density
;
Bone Density Conservation Agents/therapeutic use
;
Female
;
Humans
;
Male
;
Middle Aged
;
*Osteoporosis/complications/diagnosis/drug therapy/epidemiology
;
Retrospective Studies
;
Shoulder Fractures/*complications/*epidemiology
10.Vitamin D Repletion in Korean Postmenopausal Women with Osteoporosis.
Yoon Sok CHUNG ; Dong Jin CHUNG ; Moo Il KANG ; In Ju KIM ; Jung Min KOH ; Yong Ki MIN ; Han Jin OH ; Il Hyung PARK ; Yil Seob LEE ; Barbara KRAVITZ ; Brian WATERHOUSE ; Lorraine A FITZPATRICK ; Antonio NINO
Yonsei Medical Journal 2016;57(4):923-927
PURPOSE: Up to 71% of South Korean postmenopausal women have vitamin D deficiency {serum 25-hydroxyvitamin D [25(OH) D] level <50 nmol/L}. Data on vitamin D supplementation was collected during the screening phase of an efficacy/safety study of denosumab in Korean postmenopausal women with osteoporosis. This report describes the effect of vitamin D supplementation on repletion to 25(OH)D levels ≥50 nmol/L in Korean postmenopausal women with osteoporosis. MATERIALS AND METHODS: Vitamin D levels of Korean postmenopausal women (60-90 years old) were measured by extracting 25(OH)D2 and 25(OH)D3 from serum samples via protein precipitation and using liquid chromatography with tandem mass spectrometry detection. Calibration curves were constructed from the mass chromatograms to obtain total vitamin D levels. Subjects with serum 25(OH)D levels <50 nmol/L were supplemented with 1000 IU of vitamin D tablets during the 2.5-month-long screening period. Dose, frequency, and duration were determined by the investigator. If repletion was achieved (≥50 nmol/L) on retest, subjects were eligible to be rescreened for study entry. RESULTS: Of 371 subjects screened, 191 (52%) required vitamin D supplementation, and 88% (168 of 191) were successfully repleted. More than half of the subjects (58%) who were successfully repleted received doses of 2000 IU daily. The mean time to successful repletion was 31 days (standard deviation 8.4 days; range 11-48 days). CONCLUSION: Supplementation with daily median doses of 2000 IU vitamin D successfully repleted 88% of Korean postmenopausal women with osteoporosis within 48 days to a serum vitamin D level of 50 nmol/L.
Aged
;
Aged, 80 and over
;
*Asian Continental Ancestry Group
;
Bone Density Conservation Agents/*therapeutic use
;
*Dietary Supplements
;
Double-Blind Method
;
Female
;
Humans
;
Middle Aged
;
Osteoporosis, Postmenopausal/*complications/drug therapy/ethnology
;
Postmenopause/blood
;
Republic of Korea
;
Vitamin D/analogs & derivatives/blood/*therapeutic use
;
Vitamin D Deficiency/diagnosis/*drug therapy/ethnology

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