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SA Orthopaedic Journal

versão On-line ISSN 2309-8309
versão impressa ISSN 1681-150X

SA orthop. j. vol.18 no.1 Centurion Fev./Mar. 2019

http://dx.doi.org/10.17159/2309-8309/2019/v18n1a6 

GENERAL

 

Pharmaceutical management of bone catabolism: the bisphosphonates

 

 

Raubenheimer EJI; Noffke CEEII; Lemmer LBIII; Slavik TIV; van Heerden WFPV; Miniggio HDVI

IMChD, PhD, DSc; Ampath Histopathology Laboratory, Pretoria, Department of Oral Pathology and Oral Biology, University of Pretoria, South Africa, OMFS IMPATH, Katholieke Universiteit Leuven, Belgium
IIMSc; OMFS IMPATH, Katholieke Universiteit Leuven, Belgium
IIIMBChB, M Prax Med, M Med (Path), FCFP (SA); Ampath Histopathology Laboratory, Pretoria, South Africa
IVMBChB, MMed(Anat Path); Ampath Histopathology Laboratory, Pretoria, South Africa
VMChD, PhD, DSc; Department of Oral Pathology and Oral Biology, University of Pretoria, Pretoria, South Africa
VIBDS, MScMed (Bioethics and Health Law); Faculty of Health Sciences, Sefako Makgatho Health Sciences University, Pretoria, South Africa

Correspondence

 

 


ABSTRACT

BACKGROUND: Conditions associated with catabolism of bone are common and progress sub-clinically with devastating skeletal consequences. Over the past two decades, bisphosphonates have become increasingly popular for the preventative management of the skeleton in these conditions
METHODS: Recent literature pertaining to the mechanisms of action, clinical indications and complications of bisphosphonate therapy
was retrieved using Google Scholar and Pubmed.
AIMS OF STUDY: To provide an overview of the mechanisms of action, indications, contraindications and complications of the bisphosphonates available for clinical use in South Africa.
RESULTS: Despite the availability of alternative management regimens, bisphosphonates remain the pharmaceuticals of choice for the management of hypercalcaemia and generalised catabolic skeletal disorders such as osteoporosis, skeletal metastatic disease, Paget's disease of bone, glucocorticoid bone disease and osteogenesis imperfecta. Although adverse complications such as tachycardia, bowel and oesophageal irritation, pain, jawbone necrosis and atypical femur fractures are well documented, information remains limited on the long-term effects of bisphosphonate therapy on skeletal health. This manuscript provides an update on the mechanisms of action, principles applied to the selection of the most appropriate management regimen, monitoring of the response and complications of the bisphosphonates marketed in South Africa
Level of evidence: Level 5

Key words: bisphosphonates, osteoporosis, bone metastases, Paget's disease of bone, glucocorticoid bone disease, osteogenesis imperfecta, jaw bone necrosis


 

 

Introduction

Despite the development of innovative pharmaceuticals and autoantibodies for the manipulation of skeletal metabolism (reviewed elsewhere1), bisphosphonates (BPs) remain the first-line choice for the management of hypercalcaemia and several systemic catabolic skeletal disease states. BPs are derived from natural occurring pyrophosphates, which due to their calcium-binding properties, have been used for more than a century to soften water. Research performed by Procter and Gamble in the early 1960s on the prevention of dental caries and calculus deposits on teeth,2,3 exposed their affinity for bone and subsequent incorporation in the skeleton. It has subsequently been shown that approximately one-third of BPs absorbed are incorporated in the skeleton where they may persist lifelong. The remainder are cleared by the kidney without being further metabolised.4 During bone resorption, the incorporated BPs are released where they exert a profound local influence on the cellular components of the bone metabolic unit (BMU) and in particular the osteoclasts (readers are referred to Raubenheimer et al.5for more information on bone remodelling). These discoveries prompted pharmaceutical companies to manipulate the basic pyrophosphate structure of BP, and several patented drugs with different pharmacokinetics and clinical applications became available in a potentially lucrative market.

The purpose of this review is to highlight the mechanisms of action, clinical applications and complications of the BPs available in South Africa.6

 

Mechanisms of action

First generation BPs

The early non-nitrogen-containing BPs, also referred to as the first generation BPs (Table I), promote osteoclast apoptosis through incorporation in adenosine triphosphate (ATP). The non-hydrolysable state of the modified ATP results in neutralisation of several enzymatic processes of the osteoclast which ultimately culminate in osteoclast apoptosis, thereby effectively reducing resorptive activity.2,7 The calcium-binding capacity of the first generation BPs, which retard mineralisation activity, is an outstanding characteristic which is enhanced by their resistance to neutralisation by alkaline phosphatase. This unique property is the reason for their specific clinical application.

 

 

Clinical applications of first generation BPs

Due to the retardation of mineralising activity and binding of calcium, first generation BPs are not suited for the treatment of osteoporosis.2,3 Indications for their use are restricted to the management of hypercalcaemia which is commonly associated with disseminated skeletal malignancies and as an adjunct to the management of osteolysis resulting from bone metastases of malignant tumours.

During administration (either through the oral or intravenous route) the patient should be monitored for hypocalcaemia and secondary hyperparathyroidism as the drug tends to chelate blood calcium (the reason for its efficiency in correcting hypercalcaemia of malignancy). Furthermore, due to the chelating property, ingestion with milk or if the intravenous (IV) route is followed, with calcium-containing solutions like Ringer's, is contraindicated. Similar to the second and third generation BPs, it should be used with caution in patients with impairment of renal functions, and regular renal function tests are advised before and during the course of therapy. Most of the other precautions and complications of BP therapy, which are discussed later, also apply to the first generation BPs. For more detail on the schedule of administration, drug interactions, complications and contraindications readers are referred to the manufacturers' recommendations.

Second and third generation BPs

The second and third generation BPs, also known as the nitrogen-containing BPs, were developed by adding a nitrogen side chain to the pyrophosphate molecule. This addition increases the efficiency of osteoclast inhibition significantly. Various other modifications to the nitrogen-containing backbone contributed to the development of several commercially available BPs with differing potencies (Table II). Their method of action differs from first generation BPs. Nitrogen-containing BPs bind to a key enzyme in the pathway critical for cytoplasmic stress fibre assembly and membrane ruffling9 and, due to the subsequent osteoclast inhibition, apoptosis is induced.10 The effects are not restricted to osteoclasts only. Although their actions on other cells are less clear, they are known to exert a strong anti-apoptotic influence on the osteoblast lineage and therefore play a role in preserving the vitality of bone-forming cells.11,12 Unlike first generation BPs, these characteristics make second and third generation BPs most appropriate for the preservation of bone in catabolic skeletal disease.

 

 

Clinical applications of second and third generation BPs

 

Osteoporosis

Pharmaceutical intervention in osteoporosis must always be complemented by lifestyle and dietary measures which include weight-bearing exercise, cholecalciferol administration to patients with low vitamin D concentrations, and calcium supplementation. The latter is mandatory if the daily calcium intake is below 700 mg.7,13 Alendronic acid and risedronate are the BPs of choice in the majority of men and women with osteoporosis. In cases with poor drug compliance or intolerance to oral BPs, the IV route or the use of non-BP regimens such as denosumab, raloxifene or hormone replacement therapy could be considered. Several authors reported on the administration of BPs in conjunction with other pharmacological agents (for a synopsis see Drake et al.7). The combination of initial PTH treatment (teriparatide) with maintenance BP therapy seems to provide the strongest anabolic effect on the skeleton.14,15

Due to their hydrophilic nature, BPs are poorly absorbed from the gastrointestinal tract.16 This is the reason why BPs administered intravenously are significantly more effective than those administered via the oral route. Although the recent availability of BPs allowing once weekly (alendronic acid and risedronate) and even once monthly (risedronate and ibandronate) administration has overcome the disadvantage of poor patient compliance associated with daily regimens, the IV route eliminates the gastrointestinal adverse effects experienced by some patients on oral BPs. IV preparations (zoledronic acid, ibandronate, pamidronate) require even less frequent administration but suffer the disadvantage of potentially inducing an acute phase reaction, kidney damage and a higher frequency of osteonecrosis of the jaw than reported with the oral route (see later). The significance of patient compliance should not be underestimated as current evidence suggests that observance of the therapeutic regimen rather than the type of BP used, is of prime importance in minimising fracture risk.17

Although there are no recommendations on the monitoring of therapy beyond ten years, treatment review should be performed regularly (at least after three years with IV BPs and Ave years with oral BPs).13 In treated individuals, reassessment of fracture risk can be performed using FRAX with femoral head bone mineral density (BMD).18 Short-term non-invasive monitoring of response to therapy is the ideal, and the use of molecular markers for bone metabolism are subsequently gaining momentum. The release of 3-hydroxypyridinium cross links of collagen pyridinoline and deoxypyridinoline during bone resorption can be quantified in blood and urine by high-performance liquid chromatography (HPLC). Provided a baseline is established on a patient, a decrease can be interpreted as response to therapy. The two components show a high specificity for bone, are not taken up from food, and although variables resulting from volume distribution and metabolic clearance are as yet exploratory, their concentrations are currently viewed as the most appropriate indicators of bone resorption.19

Discontinuation of administration is advised in high-risk fracture patients who have been treated with alendronate, risedronate and zoledronic acid for longer than Ave years. In low-risk fracture patients a 'drug holiday' is recommended after one to two years for risedronate, three to Ave years for alendronate and three to six years for zoledronic acid.20

Duration of the skeletal-protective action of BPs is related to the potency of the BP used, dosage of administration, metabolism and clearance of the drug. Although the determination of the effective half-life is hampered by technical challenges, it has been suggested that after one IV administration, alendronate has a half-life of more than ten years.21

 

Malignancies affecting the skeleton

The skeletal morbidity of myeloma is related to osteoclast-induced bone resorption with associated pain and hypercalcaemia. In a consensus statement of the Mayo Clinic Myeloma Group, IV pamidronate is recommended as the drug of choice for the management of these morbidities as pamidronate effectively suspends bone resorption, alleviates bone pain and corrects hypercalcaemia. Pamidronate is perceived to have a lower risk for inducing jaw osteonecrosis than the alternative, zoledronic acid.22 Upon remission, treatment is discontinued after two years. If remission is not achieved, pamidronate administration should be considered every three months at a reduced dosage.

In a recent update of 18 trials reporting on 4 843 men with advanced prostate cancer, BP therapy was shown to decrease the number of skeletal events and reduce disease progression.23 Although non-opioid and opioid analgesics are employed to manage metastatic bone pain, BPs can offer added pain reduction.24 A joint review drafted by an expert panel of Cancer Care Ontario and the American Society of Clinical Oncology suggests that BP administration reduces bone recurrence and improves survival of postmenopausal patients with non-metastatic breast cancer.25 In separate studies, a substantial relief of the skeletal complications and pain have been demonstrated in patients with breast cancer receiving IV BPs.26,27 Of the oral BPs, only daily administration of ibandronate has been shown to be beneficial. The skeletal protecting action of BPs is advantageous particularly to women receiving oestrogen ablation therapy for hormone-sensitive breast cancer.28

Other clinical applications

Paget's disease of bone is characterised by an increase of bone resorption followed by defective bone formation. These processes result in a weak skeleton, deformities, skull enlargement and pain. BPs suppress bone resorption with subsequent normalisation of serum alkaline phosphatase concentrations and are therefore recommended for the management of the active and symptomatic phase of the condition.7 A recent practice guideline confirms that oral risedronate, pamidronate and IV zoledronic acid are effective in this regard. BP therapy however does not eradicate the radiological changes, nor does it improve the deformities or reduce pain resulting from the associated osteoarthritis.29

With present data available, BP therapy holds potential for the improvement of the quality of life of children with osteogenesis imperfecta. IV administration of pamidronate results in a significant increase in cortical bone thickness and trabecular bone volume.30 Success has also been reported with oral alendronate in the management of the consequences of this devastating genetic disease.31 Although the mechanism of action is not clear, it appears that the inhibition of osteoclast- induced resorption augments the defective process of bone formation. Although the use of BPs in children is cautioned against,7 the net clinical benefit of BP administration to children suffering osteogenesis imperfecta may outweigh its potential disadvantages.

Glucocorticoid therapy is the most important cause for pharmaceutically induced osteoporosis. Glucocorticoids induce skeletal catabolism which is the result of induction of apoptosis of cells of the osteoblast lineage and activation of bone resorption through prolonging the lifespan of osteoclasts.32 Patients taking 2.5 mg or more prednisone per day for three months or longer and with a high risk for fractures can benefit from BP administration which should start at the onset of glucocorticoid therapy. Risedronate and alendronic acid are first choices and where these drugs are contraindicated, second line agents such as denosumab or teriparatide could be considered.33 Because of limited information on the advantages BP intervention in patients taking glucocorticoids, the American College of Rheumatology advises vitamin D and calcium supplementation without BP administration in patients with a low fracture risk.34

Pamidronate and alendronic acid have been shown to reduce the markers of bone resorption during skeletal immobilisation and their protective influence on the skeleton, and reduction of hypercalcaemia and nephrolithiasis is promising.35,36 Management of the skeletal morbidity of paediatric conditions such as anorexia, juvenile rheumatoid arthritis and cystic fibrosis is awaiting data of long-term studies on whether the net benefit outweighs the potential complications. The embedding of modifications of BPs on implants creating bioactive surfaces which facilitate bio-integration and reduce implant failure will certainly gain momentum in the future.

Adverse effects

Despite considerable attention given to BP-related osteonecrosis of the jaw (ONJ), this complication is rare in patients receiving oral BPs: ONJ occurs in between 0.1% of myeloma patients and 5% of advanced prostate cancer patients on BPs.37,38 The majority of cases with ONJ were described in patients receiving high doses of IV BPs for myeloma and breast cancer (for a summary see Drake, et al.7). The occurrence of ONJ is also related to the anti-angiogenic properties of the BP administered,39,40 host factors which include the presence of dormant jawbone infections and the efficiency of the immune response.41 A variety of infective agents are implicated, including Act/nomyces-like organisms and fungi. It is important to clear all foci of potential jaw bone sepsis before commencement of BP therapy and delay invasive dental surgery in patients receiving the medication. Patients with chronic ear infections may likewise develop osteonecrosis of the external auditory canal.42 Thigh, hip or groin pain should alert clinicians to another rare and not yet fully understood complication, namely atypical femur fracture.43

An acute phase reaction is experienced by nearly a quarter of patients receiving the first IV dose of nitrogen-containing BP and the incidence thereafter decreases progressively with each administration.44 This reaction is characterised by pyrexia with concomitant headache, arthralgia, myalgia and influenza-like symptoms, and pre-treatment with histamine receptor antagonists, antipyretics or corticosteroids may provide relief.1 An increase in serious atrial fibrillation (requiring hospitalisation) was reported in patients receiving IV zoledronic acid.44 Although verifiable data is not yet available for the other BPs, the risk appears to be smaller, if not negligible.7 This complication is an indication for considering one of the non-BP skeletal cytokine modulators or auto-antibodies in the management regimen (summarised elsewhere1).

Oesophageal irritation and erosions are common in patients on oral BPs. Patients should be advised to swallow the BP with a full glass of water and remain in an upright position for one hour after ingestion. Avoid taking anti-acid drugs containing aluminium or magnesium due to the danger of chelating and neutralising the BP. Gastro-oesophageal irritation has not been reported with the IV route which is recommended in patients with uncontrollable oesophageal discomfort.

Renal function can rapidly deteriorate in patients on IV BPs particularly if the creatinine clearance and glomerular filtration rates are below 30 ml/min32,33 and 35 ml/min. respectively.13,45,46 The oral route of administration may be appropriate in patients with mild renal impairment7 or alternatively a cytokine modulator or auto-antibody could be considered as second line regimen. Concomitant use of non-steroidal anti-inflammatory drugs increases the potential for peptic ulcers47 and renal dysfunction46 and is contraindicated.

Severe incapacitating musculoskeletal pain, distinct from the acute phase symptoms, has been reported in a small number of patients receiving alendronate and risedronate.48 The risk factors for this complication are unknown. IV administration may precipitate hypocalcaemia particularly in patients with a substantial skeletal tumour burden, Paget's disease, hypoparathyroidism, compromised renal function and hypovitaminosis D.49-51 In order to minimise the risk of hypocalcaemia, albumin-corrected serum calcium concentrations should be determined and corrected before commencing with IV infusion of BPs.7 If unresponsive, consider an alternate management regimen.1 Conjunctivitis, uveitis, episcleritis and scleritis are rare complications of both oral and IV BPs. The incidence is less than 0.1%, appears to be limited to patients receiving risedronate, and resolves within weeks of discontinuation of therapy.48 Administration of BPs is contraindicated during pregnancy, lactation and in patients manifesting with allergic-type reactions against the drug.

 

Conclusion

The therapeutic roll-out of BPs for the management of generalised skeletal anabolism gained momentum over the past decade. Although the benefits of BP therapy outweigh the risks in several progressive skeletal anabolic states, the lack of long-term studies on large patient samples is hampering the generation of accurate data on the advantages and complication of BP therapy in some of the less common conditions. The long-term effects on the skeleton in particular will be interesting as the repair of micro-fractures, which contribute to skeletal strength, is impaired.

Ethics statement

The authors upheld the principles of non-maleficence and an accurate reflection of the literature during the preparation of the synopsis.

Declaration

The authors declare authorship of this article and that they have followed sound scientific research practice during the preparation thereof. This research is original and does not transgress plagiarism policies.

Acknowledgements

Gratitude is expressed towards the Ampath Histopathology Laboratory, the Catholic University of Leuven and the University of Pretoria for providing support in the preparation of the manuscript.

Author contributions

All the authors were involved in the collection of relevant information from the literature. REJ compiled the manuscript from the data received and all authors contributed to the revision of the manuscript and the final preparation of the submitted copy.

ORCID

Raubenheimer EJ https://orcid.org/000-003-0554-2398

van Heerden WFP http://orcid.org/0000-0003-2494-667X

 

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Correspondence:
Prof EJ Raubenheimer
Ampath Histopathology Laboratory
Pretoria, South Africa
tel: +27 870870176; cell: +27 829082788
email:ejraub@fox5.co.za and raubenheimere@ampath.co.za

Received: June 2018
Accepted: August 2018
Published: March 2019

 

 

Funding: The authors received no funding from any agency in the public or commercial domain before or during the preparation of the manuscript.
Conflict of interest: The authors have no direct or indirect association with any of the companies manufacturing any of the pharmaceuticals or products reflected in the manuscript.

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