- Open Access
Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials
SpringerPlus volume 5, Article number: 1704 (2016)
High-turnover type bone metabolism derangement has been considered to be one of the major causes of osteoarthritis (OA). Bisphosphonates can attach to hydroxyapatite binding sites on bony surfaces, particularly those which are undergoing active bone resorption. To evaluate the effectiveness of bisphosphonates in OA treatment, literature databases were searched from inception to February 28, 2016 for clinical studies of bisphosphonates for OA treatment. All randomized controlled trials in which bisphosphonates therapy was compared with a placebo or a conventional medication, were selected. 15/1145 studies were eligible for analysis, which included 3566 participants. Bisphosphonates therapy improved pain, stiffness and function significantly in OA assessed by the Western Ontario and McMaster Universities Arthritis Index scale (MD = 4.59; 95 % CI 2.83–6.34; P < 0.00001; MD = 1.43; 95 % CI 0.83–2.23; P = 0.0005; MD = 2.01; 95 % CI 1.27–2.75; P < 0.00001). Bisphosphonates also reduced osteophyte score significantly (MD = −0.51; 95 % CI −0.84 to −0.19; P = 0.002). However, no significant differences were found in subjective improvement, osteoarthritis progression, the number of required acetaminophen treatment or joint replacement. In conclusion, bisphosphonates therapy is effective in relieving pain,stiffness and accelerating functional recovery in OA. Limitations of the studies we analysed included the differences in duration of bisphosphonates use, the doses and types of bisphosphonates and the lack of long-term data on OA joint structure modification after bisphosphonates therapy. More targeted studies are required to evaluate on the effectiveness of bisphosphonates for OA treatment.
Osteoarthritis (OA) is the most common form of arthritis. It is a major cause of disability among the ageing population. The affected joint is undergoing a complex combination of degradative and reparative processes (Collins et al. 2016a; Palazzo et al. 2016), the mechanism of which is still unclear. There are currently no treatments that delay or halt OA progression.
The main clinical manifestations include pain, swelling and disability caused by topical cartilage loss, subchondral bony changes, osteophyte formation and synovitis (Liu et al. 2016). OA has long been believed as a cartilage disease, but more recent evidence suggests that periarticular bone abnormality is also involved in the disease initiation and progression (Kalunian 2016). Decreased bone mineral content and trabecular numbers in subchondral bone structure in the early OA have been observed by magnetic resonance imaging (Madry et al. 2016). High-turnover type bone metabolism derangement has been considered as a main cause of OA (Collins et al. 2016b).
Previous experimental studies on bone anti-resorptive agents for OA have shown promising results (Fenty et al. 2012). The Duncan-Hartley guinea pig model is a widely used spontaneous model of OA progression, which is characterized by subchondral bony changes (Sun et al. 2015). In rat anterior cruciate ligament transection (ACLT) models of KOA, alendronate could protect cartilage from degeneration and inhibit subchondral bone remodeling (Strassle et al. 2010).
Bisphosphonates can inhibit bone resorption and therefore they are the mainstream medications for osteoporosis. But for OA treatment, there is no official statement or guideline for bisphosphonates therapy. Recently, more and more evidence have shown bisphosphonates are effective in OA treatment. Bisphosphonates can suppress local bone turnover or inhibit the level of local pro-inflammatory cytokines. Further studies confirmed that defective subchondral bone metabolism in OA could alter chondrocytes during subchondral bone remodeling. Increased subchondral bone turnover may contribute to pain in OA, which may be relieved by targeting osteoclasts. Although bisphosphonates therapy seems to have positive effects on OA, these effects have not been extensively studied. To our knowledge, only one systematic review and meta-analysis was conducted with a limited number of poor-quality RCTs, which demonstrated limited evidence of bisphosphonates for pain relief in OA (Davis et al. 2013). Moreover, osteoarthritis progression, required acetaminophen treatment and joint replacement were not analyzed.
Therefore, this review aims to summarize the results of these clinical trials and evaluate the clinical effects, which may be useful to clinical practice. This meta-analysis was conducted in accordance with Cochrane guidelines (Higgins and Green 2011).
All searches were conducted from database MEDLINE, PubMed, EMBASE, and the Cochrane Central Register of Controlled Trials (CENTRAL) from inception to February 28, 2016. The MeSH terms we used were (Osteoarthritis) AND (OA) AND (Bisphosphonates). To ensure a more complete meta-analysis, we used a maximally sensitive search for RCTs according to the Cochrane Highly Sensitive Search Strategy. Systematic review and meta-analysis were manually searched as references for included studies.
The inclusion criteria were (1) RCTs comparing bisphosphonates with any control methods, include a placebo or a conventional medication. And published as peer-reviewed indexed papers; (2) patients with established OA administering medication or other control interventions; (3) studies detailing the type and dosage of medications and treatment course; (4) primary outcomes included visual analogue scale (VAS) pain score, WOMAC pain, stiffness, function score and osteophyte score, while secondary outcomes included subjective improvement, osteoarthritis progression and the number of required acetaminophen treatment or joint replacement. Studies reported at least two of the primary outcomes. (5) Literature in English.
The exclusion criteria were (1) non-randomized controlled trials; (2) studies without available data; (3) duplicate publications among authors or centers.
Data extraction and quality assessment
Data from all eligible papers were extracted and independently verified. Data extracted included study characteristics, patient characteristics, primary and secondary outcomes.
Study characteristics included study design, name of first author, sample size and follow-up period. Patient characteristics included the number of patients, gender, affected joint, type of intervention and dosage. If a study reported the outcomes of multiple doses of bisphosphonates, only data of the maximum dose were extracted for analysis. If a study reported the outcomes of multiple time points after treatment, only data of the final follow-up time point was extracted for analysis.
The methodological quality of each included study was evaluated in accordance with the Cochrane Collaboration’s risk of bias tool (Higgins and Green 2011), which used the following items as random sequence generation, allocation concealment, blinding of outcome assessors,patients and other participants, incomplete outcome data, selective reporting of outcomes and other biases. The bias risk of each item was graded as low, high or unclear.
All statistical analyses were conducted with RevMan version 5.3 software (provided by Cochrane Collaboration). Heterogeneity was evaluated with Q tests and I 2, and P < 0.10 was determined as significant. If there was no or low heterogeneity then the fixed-effects model was used. Otherwise, the random-effects model was used. The risk ratio (RR) was calculated for dichotomous data, and weighted mean differences (WMD) or standard mean differences (SMD) were used for continuous variables. Both differences were presented with 95 % CI. For continuous variables, if data were presented with medians and ranges, then the means and SDs were calculated according to Hozo et al. (2005). If the study presented the median and interquartile range, the median was treated as the mean, and the interquartile ranges were calculated using 1.35 SDs, as described in the Cochrane handbook.
The results of the literature search strategy identified a total of 1145 papers. 294 full texts were reviewed and a total of 15 papers were deemed eligible and included in this systematic review (covering a total of 3566 patients, including 1517 in bisphosphonates group and 2049 in control groups) (Fig. 1). (Neogi et al. 2008; Rossini et al. 2015; Laslett et al. 2014; Nishii et al. 2013; Arti and Azemi 2012; Laslett et al. 2012; Saviola et al. 2012; Fujita et al. 2011; Rossini et al. 2009; Fujita et al. 2009; Bingham et al. 2006; Spector et al. 2005; Carbone et al. 2004; Fujita et al. 2001).
Characteristics of included studies
Of the 15 eligible studies, 1517 patients received bisphosphonates therapy, and 2049 patients received control interventions. The baseline characteristics were similar among these trials (Table 1).
Methodological quality of studies
The quality assessment of the trials was performed using the Cochrane Collaboration’s Risk of Bias tool. The results of quality assessment illustrated there were some methodological limitations in these studies, quality of which was moderate (Fig. 2). Random sequence generation was described clearly in 6 studies (40 %) and unclearly in 8 studies (53 %). 3 studies (20 %) had a high risk of bias relating to allocation concealment, and 12 studies (80 %) had an unclear risk of bias relating to allocation concealment. Only 7 studies (46.7 %) blinded outcome assessors and the blindness in 5 studies (33.3 %) were unclear. All RCTs had a low risk of bias relating to incomplete outcome data and selective reporting. Biases relating to other aspects were unclear.
Primary outcome parameters
VAS pain score: the results of 6 studies (627 patients) with combined data indicated that bisphosphonates therapy improved pain nosignificantly assessed by VAS pain scores (MD = 0.80; 95 % CI −1.13 to 2.73; P = 0.42) compared with respective control group (Fig. 3).
WOMAC pain score: the results of 5 studies (1879 patients) with combined data indicated that bisphosphonates therapy improved pain significantly assessed by WOMAC pain score (MD = 4.59; 95 % CI 2.83–6.34; P < 0.00001) compared with respective control group (Fig. 4).
WOMAC stiffness score: the results of 3 studies (1757 patients) with combined data indicated that bisphosphonates therapy improved stiffness in affected joints significantly assessed by WOMAC stiffness score (MD = 1.43; 95 % CI 0.83–2.23; P = 0.0005) compared with respective control group (Fig. 5).
WOMAC function score: the results of 3 studies (1757 patients) with combined data indicated that bisphosphonates therapy improved the function of affected joints significantly assessed by WOMAC function scores (MD = 2.01; 95 % CI 1.27–2.75; P < 0.00001) compared with respective control group (Fig. 6).
Osteophyte score: the results of 4 studies (1125 patients) with combined data indicated that bisphosphonates therapy relieved osteophyte formation in affected joints significantly assessed by osteophyte score (MD = −0.51; 95 % CI −0.84 to −0.19; P = 0.002) compared with respective control intervention (Fig. 7).
There were no significant differences in osteoarthritis progression (3 studies including 2578 patients), required acetaminophen treatment (3 studies including 940 patients) and joint replacement (3 studies including 424 patients) between the application of bisphosphonates therapy and respective control intervention (Figs. 8, 9, 10, 11).
This meta-analysis demonstrated bisphosphonates therapy in OA had better effect on joint pain, stiffness and function, although it had no better effect on osteoarthritis progression, required acetaminophen treatment and joint replacement comparing to other medications. However, there was some heterogeneity across the included studies as for pain, stiffness and function scores, which may result from variation in the types or doses of bisphosphonates in different studies. When a sensitivity analysis was performed, the heterogeneity disappeared.
Current pharmacologic therapies for OA aim majorly to symptom control with analgesics, non-steroidal anti-inflammatory drugs (NSAIDs) and COX-2 inhibitors (Smith et al. 2016). NSAIDs, a most commonly used medication in symptomatic OA management, are found to be associated with gastrointestinal adverse reaction dose-related risks of renal toxicity and cardiovascular diseases (Brown 2013). Glucosamine has been suggested as a potential structure-modifying OA drug, but the data concerned are inconsistent (Krader 2014). Increased evidence suggests that high turnover metabolism derangement plays an important role in the initiation and progression of OA, which has resulted in an increased level of interest in drugs that affecting bone metabolism may slow the progression of OA (McGrory et al. 2016).
Based on 15 RCTs, this meta-analysis indicated that bisphosphonates therapy have better effect in relieving pain and accelerating functional recovery for OA. In our study, there were no significant differences on the number of required acetaminophen treatment and joint replacement between bisphosphonates therapy and other conventional medications. But the causes that patients received NSAID were various, and few researchers provided the details of clinical stage and pathological grade of their patients. Therefore, further studies are needed to provide more solid evidence.
Quality of the evidence
The overall methodological quality was moderate, and most studies had at least one aspect of unclear or high risk of bias. Not all outcome assessors were blinded, which may produce performance or measurement biases. Selection bias may exist since only 3 studies used allocation concealment. As bisphosphonates are only be evaluated as “off label” therapy for OA, there was no corresponding standardized treatment guideline. Although we had performed sensitivity analysis, the effect of bisphosphonates may be underestimated.
This meta-analysis showed that bisphosphonates therapy is effective for patients with OA in relieving pain and accelerating functional recovery. However, the conclusions are limited due to small sample sizes and methodological study quality, the different doses and treatment courses among studies. Further studies are needed to provide more solid evidence.
Arti HR, Azemi ME (2012) Comparing the effect of glucosamine and glucosamine with alendronate in symptomatic relieve of degenerative knee joint disease: a double- blind randomized clinical trial study. Jundishapur J Nat Pharm Prod 7(3):87–92
Bingham CO, Buckland-Wright JC, Garnero P, Cohen SB, Dougados M, Adami S, Clauw DJ, Spector TD, Pelletier JP, Raynauld JP, Strand V, Simon LS, Meyer JM, Cline GA, Beary JF (2006) Risedronate decreases biochemical markers of cartilage degradation but does not decrease symptoms or slow radiographic progression in patients with medial compartment osteoarthritis of the knee: results of the two-year multinational knee osteoarthritis structural arthritis study. Arthritis Rheum 54(11):3494–3507
Brown GA (2013) AAOS clinical practice guideline: treatment of osteoarthritis of the knee: evidence-based guideline, 2nd edition. J Am Acad Orthop Surg 21(9):577–579. doi:10.5435/JAAOS-21-09-577
Buckland-Wright JC, Messent EA, Bingham III CO, Ward RJ, Tonkin C (2007) A 2 yr longitudinal radiographic study examining the effect of a bisphosphonate (risedronate) upon subchondral bone loss in osteoarthritic knee patients. Rheumatology (Oxford) 46:257–264. doi:10.1093/rheumatology/kel213
Carbone LD, Nevitt MC, Wildy K, Barrow KD, Harris F, Felson D, Peterfy C, Visser M, Harris TB, Wang BW, Kritchevsky SB (2004) The relationship of antiresorptive drug use to structural findings and symptoms of knee osteoarthritis. Arthritis Rheum 50(11):3516–3525
Collins NJ, Prinsen CA, Christensen R, Bartels EM, Terwee CB, Roos EM (2016a) Knee Injury and Osteoarthritis Outcome Score (KOOS): systematic review and meta-analysis of measurement properties. Osteoarthr Cartil. doi:10.1016/j.joca.2016.03.010
Collins J, Beutel B, Bosco J, Strauss E, Youm T, Jazrawi L (2016b) Bone marrow edema: chronic bone marrow lesions of the knee and the association with osteoarthritis. Bull Hosp Jt Dis 74(1):24–36
Davis AJ, Smith TO, Hing CB, Sofat N (2013) Are bisphosphonates effective in the treatment of osteoarthritis pain: a meta-analysis and systematic review. PLoS ONE 8(9):e72714. doi:10.1371/journal.pone.0072714
Fenty MC, Dodge GR, Kassey VB, Witschey WR, Borthakur A, Reddy R (2012) Quantitative cartilage degeneration associated with spontaneous osteoarthritis in a guinea pig model. J Magn Reson Imaging 35(4):891–898. doi:10.1002/jmri.22867
Fujita T, Fujii Y, Okada SF, Miyauchi A, Takagi Y (2001) Analgesic effect of etidronate on degenerative joint disease. J Bone Miner Metab 19(4):251–256
Fujita T, Ohue M, Fujii Y, Miyauchi A, Takagi Y (2009) Comparison of the analgesic effects of bisphosphonates: etidronate, alendronate and risedronate by electroalgometry utilizing the fall of skin impedance. J Bone Miner Metab 27(2):234–239. doi:10.1007/s00774-009-0035-0
Fujita T, Ohue M, Nakajima M, Fujii Y, Miyauchi A, Takagi Y (2011) Comparison of the effects of elcatonin and risedronate on back and knee pain by electroalgometry using fall of skin impedance and quality of life assessment using SF-36. J Bone Miner Metab 29(5):588–597. doi:10.1007/s00774-011-0259-7
Higgins J, Green S (2011) Cochrane handbook for systematic reviews of interventions Version 5.1.0. [Updated March 2011]. The Cochrane Collaboration, 2011. www.cochrane-handbook.org
Hozo SP, Djulbegovic B, Hozo I (2005) Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol 5:13. doi:10.1186/1471-2288-5-13
Kalunian KC (2016) Current advances in therapies for osteoarthritis. Curr Opin Rheumatol 28(3):246–250. doi:10.1097/BOR.0000000000000273
Krader CG (2014) Guidance on non-surgical management of knee osteoarthritis. Med Econ 91(9):12
Laslett LL, Doré DA, Quinn SJ, Boon P, Ryan E, Winzenberg TM, Jones G (2012) Zoledronic acid reduces knee pain and bone marrow lesions over 1 year: a randomised controlled trial. Ann Rheum Dis 71(8):1322–1328. doi:10.1136/annrheumdis-2011-200970
Laslett LL, Kingsbury SR, Hensor EM, Bowes MA, Conaghan PG (2014) Effect of bisphosphonate use in patients with symptomatic and radiographic knee osteoarthritis: data from the osteoarthritis initiative. Ann Rheum Dis 73(5):824–830. doi:10.1136/annrheumdis-2012-202989
Liu SH, Driban JB, Eaton CB, McAlindon TE, Harrold LR, Lapane KL (2016) Objectively measured physical activity and symptoms change in knee osteoarthritis. Am J Med. doi:10.1016/j.amjmed.2015.12.029
Madry H, Kon E, Condello V, Peretti GM, Steinwachs M, Seil R, Berruto M, Engebretsen L, Filardo G, Angele P (2016) Early osteoarthritis of the knee. Knee Surg Sports Traumatol Arthrosc
McGrory B, Weber K, Lynott JA et al (2016) The American Academy of Orthopaedic Surgeons evidence-based clinical practice guideline on surgical management of osteoarthritis of the knee. J Bone Joint Surg Am 98(8):688–692. doi:10.2106/JBJS.15.01311
Neogi T, Nevitt MC, Ensrud KE, Bauer D, Felson DT (2008) The effect of alendronate on progression of spinal osteophytes and disc-space narrowing. Ann Rheum Dis 67(10):1427–1430. doi:10.1136/ard.2007.085563
Nishii T, Tamura S, Shiomi T, Yoshikawa H, Sugano N (2013) Alendronate treatment for hip osteoarthritis: prospective randomized 2-year trial. Clin Rheumatol 32(12):1759–1766. doi:10.1007/s10067-013-2338-8
Palazzo C, Nguyen C, Lefevre-Colau MM, Rannou F, Poiraudeau S (2016) Risk factors and burden of osteoarthritis. Ann Phys Rehabil Med. doi:10.1016/j.rehab.2016.01.006
Rossini M, Viapiana O, Ramonda R, Bianchi G, Olivieri I, Lapadula G, Adami S (2009) Intra-articular clodronate for the treatment of knee osteoarthritis: dose ranging study vs hyaluronic acid. Rheumatology (Oxford) 48(7):773–778. doi:10.1093/rheumatology/kep084
Rossini M, Adami S, Fracassi E, Viapiana O, Orsolini G, Povino MR, Idolazzi L, Gatti D (2015) Effects of intra-articular clodronate in the treatment of knee osteoarthritis: results of a double-blind, randomized placebo-controlled trial. Rheumatol Int 35(2):255–263. doi:10.1007/s00296-014-3100-5
Saviola G, Abdi-Ali L, Campostrini L, Sacco S, Baiardi P, Manfredi M, Mannoni A, Benucci M (2012) Clodronate and hydroxychloroquine in erosive osteoarthritis: a 24-month open randomized pilot study. Mod Rheumatol 22(2):256–263. doi:10.1007/s10165-011-0506-8
Smith SR, Deshpande BR, Collins JE, Katz JN, Losina E (2016) Comparative pain reduction of oral non-steroidal anti-inflammatory drugs and opioids for knee osteoarthritis: systematic analytic review. Osteoarthr Cartil. doi:10.1016/j.joca.2016.01.135
Spector TD, Conaghan PG, Buckland-Wright JC, Garnero P, Cline GA, Beary JF, Valent DJ, Meyer JM (2005) Effect of risedronate on joint structure and symptoms of knee osteoarthritis: results of the BRISK randomized, controlled trial [ISRCTN01928173]. Arthritis Res Ther 7(3):R625–R633
Strassle BW, Mark L, Leventhal L, Piesla MJ, Jian Li X, Kennedy JD, Glasson SS, Whiteside GT (2010) Inhibition of osteoclasts prevents cartilage loss and pain in a rat model of degenerative joint disease. Osteoarthr Cartil 18(10):1319–1328. doi:10.1016/j.joca.2010.06.007
Sun Y, Scannell BP, Honeycutt PR, Mauerhan DR, Norton J, Hanley EN (2015) Cartilage Degeneration, subchondral mineral and meniscal mineral densities in Hartley and Strain 13 guinea pigs. Open Rheumatol J 9:65–70. doi:10.2174/1874312901409010065
RLX and PMW had the initial idea. RLX and LRZ collected, analyzed and interpreted the data. RLX and LRZ wrote and revised the manuscript, and PMW approved the final version of the manuscript. All authors read and approved the final manuscript.
We would like to thank Dr. B. Xu and X.C. Li for assistance with planning this meta-analysis.
The authors declare that they have no competing interests.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
About this article
Cite this article
Xing, R.L., Zhao, L.R. & Wang, P.M. Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials. SpringerPlus 5, 1704 (2016). https://doi.org/10.1186/s40064-016-3359-y