Introduction

Osteoporosis is a disease characterised by progressive bone loss and deterioration of the microarchitecture leading to an increased fracture risk. Osteoporosis can have distinctive causes including lack of sex hormones, long-term use of glucocorticoids or disuse. Current standard therapy consists of reducing further bone loss using bisphosphonates [1]. The use of bisphosphonates is accompanied by potential side effects such as gastrointestinal complaints, osteonecrosis of the jaw and atypical femoral fractures [2]. As an alternative treatment biophysical stimuli have long been proposed. These might be cheaper and induce fewer side effects. Pulsed electromagnetic fields (PEMF) might be one such treatment and indeed there is some evidence that these positively influence bone mass.

The finding that electrical currents are induced during mechanical loading of bone has led to the development of PEMF [3, 4]. Much research has been done on the effects of PEMF on bone. In vitro studies do show that a variety of growth factors that are important in bone metabolism are affected, including bone morphogenetic protein 2 (BMP-2), transforming growth factor beta (TGF-β) and insulin-like growth factor II (IGF-II) [511]. Furthermore, PEMF result in the activation of extracellular signal-regulated kinase (ERK), mitogen-activated protein kinase (MAPK) and prostaglandin synthesis, which might also lead to stimulatory effects on bone [1214]. Clinically PEMF are widely used for the treatment of non-unions, although they have never been proven to be effective in a prospective randomised controlled trial [1522].

PEMF as treatment for osteoporosis have been studied before. In a clinical study it was shown that PEMF treatment of the wrist induced an increase in bone mineral density (BMD) in the distal radius of osteoporosis-prone women [23]. Re-examination 12 years later did show that these effects had lapsed [24]. Only a few animal studies have been published on the subject. In one study complete preventive effects of PEMF on trabecular bone loss in an ovariectomised rat model were demonstrated [12]. PEMF consisted of a single pulse wave form with a maximum of 8 G and were applied eight hours per day. In another study it was shown that PEMF led to trabecular thickening in ovariectomised rats when treated with pulse bursts with a maximum of 9.6 G for six hours per day [25]. In a third study electromagnetic fields (EMF) induced pronounced cortical bone formation [26]. EMF consisted of a sinusoid wave form with a maximum electromagnetic field of 10 G and were applied for four hours per day. One study using osteoporotic rats did not demonstrate a beneficial effect on bone mass when treated with PEMF with 15 G for 24 hours per day [27]. Furthermore, PEMF have also been shown to influence bone mass in disuse osteoporosis both clinically and experimentally [2830].

Because treatment of osteoporosis with PEMF can have important consequences for today’s standard treatment, we examined the effect of whole-body PEMF treatment on the bone microarchitecture in a rat model of osteoporosis. Cancellous and cortical bone changes in the proximal tibia were followed over time using in vivo microCT scanning.

Methods

Twenty female Wistar WU rats were obtained (Charles River, The Netherlands). All animals were housed in pairs in the institute’s animal facility with a 12-hour light/dark regimen and received standard food pellets and water ad libitum. The study protocol was approved by the local Animal Experiments Committee (EUR 415) and was in accordance with Dutch law on animal experimentation.

At an age of 20 weeks a bilateral ovariectomy (OVX) was performed under sterile conditions to simulate osteoporosis. This was done under 3% isoflurane gas anaesthesia (Rhodia Organique Fine Ltd., Bristol, UK). Buprenorphine 0.05 mg/kg per 12 hours (Schering-Plough, Kenilworth, NJ, USA) was given for pain relief for three days post-operatively.

The second day after OVX, PEMF treatment was started for five days/week over a period of six weeks. During treatment the animals were placed in a cage (24 × 30 × 12 cm) in pairs, with food and water ad libitum. The cage was surrounded by two connected coils normally used in the treatment of non-unions of the femur (IMD, Uden, The Netherlands) (Fig. 1). The rats were divided into five groups of four animals/group. The sample size was chosen for logistical reasons and not on the basis of a power analysis. The group sizes were kept relatively small because in vivo microCT analysis can accurately measure small changes over in time. A custom-made generator produced the electromagnetic signals (see details below). The first group served as controls and was placed in a cage covered with non-functioning coils for two hours per day.

Fig. 1
figure 1

Rat receiving systemic PEMF treatment. The cage is surrounded by coils. The custom-made generator can produce different electromagnetic signals

The second group was treated with a commercially available PEMF device that is effective for the treatment of non-unions and is clinically used (Orthopulse®, IMD, Uden, The Netherlands) [31]. The device produces PEMF with a 1-G electromagnetic field, consisting of 5-ms pulse bursts with 5-μs pulses, and the bursts repeat at 15 Hz. Rats were treated for two hours per day.

The treatment protocols of the third and fourth groups were designed to investigate whether a non-continuous PEMF stimulus would be more effective than a continuous stimulus, similar to studies investigating the effects of mechanical vibration on bone mass [3234]. The third group received the same PEMF signal as the second group, but with a five minute on/off regimen; these animals were placed in the coil-covered cage for four hours per day to ensure that the total amount of PEMF time was the same in each animal. The fourth group also received the basic PEMF signal, but a custom-made amplifier added random noise of 50–150 kHz over the basic stimulus. Animals were treated with this latter signal for two hours per day.

A fifth group received a PEMF signal that was not characterised by pulse bursts as in the other treatment groups, but consisted of quasi-rectangular single pulses of 1 G given at 7.5 Hz with a pulse duration of 0.3 ms. These animals were treated for two hours per day.

In vivo microCT scans were made at zero, three and six weeks after OVX. Using isoflurane (3%) rats were anaesthetised and the right hind leg was scanned (voltage of 60 kV, current of 167 μA, 0.5-mm aluminium filter, 196° with a rotation step of 1°) (SkyScan 1076 Microtomograph, Kontich, Belgium). Then 3D reconstructions with an isotropic voxel size of 18 μm were made of the proximal tibia and the mid-diaphysis (Nrecon software version 1.5, SkyScan) (Fig. 2). The proximal metaphysis mainly consists of cancellous bone. A length of 5.4 mm was selected of which the epiphysis was manually deselected. The mid-diaphysis consists of cortical bone and the region of interest was selected 9 mm distal from the epiphysis and continued to 3.6 mm more distally. Using a local threshold, bone was separated from non-osseous structures, which resulted in binary data sets [35]. After automatic separation between trabecular and cortical bone using in-house software bone parameters were determined (3D-calculator, SkyScan) [36]. On the metaphyseal region of interest, volume fraction (BV/TV), connectivity density (Conn/TV), structure model index (SMI), in which an index of 3 indicates the presence of rods and an index of 0 indicates the presence of plates, and 3D trabecular thickness (TbTh) were determined. On the diaphyseal region of interest, cortical volume (CtV) and cortical thickness (CtTh) were determined.

Fig. 2
figure 2

Three-dimensional reconstruction of a microCT scan of the proximal tibia. The regions of interest in the metaphysis and diaphysis are indicated

Differences between means of the different treatment groups were statistically analysed using one-way analysis of variance (ANOVA) with a Tukey’s multiple comparison test for each time point separately (GraphPad Software, San Diego, CA, USA).

Results

All surgical procedures were performed without complications. At the start of the study the average body weight of the rats was 224.6 g (SD 5.3). No period of weight loss was observed during the experimental period. The average weight gain was 57.6 g (SD 8.7) and there was no difference in weight gain between controls and any of the PEMF-treated groups.

In non-treated control animals BV/TV decreased from 31.7% (SD 4.8) at week zero to 24.2% (SD 4.1) and 19.7% (SD 3.5) at weeks three and six, respectively, as a consequence of OVX (Table 1). Morphometric parameters changed concomitantly, especially between weeks zero and three, with a decrease in mean TbTh, a decrease in Conn/TV and a structural change of trabeculae towards more rod-like structures, as apparent from an increase in SMI (Table 1). CtV increased from 12.3 (SD 0.23) mm3 at week zero to 12.9 (SD 0.23) mm3 and 13.3 (SD 0.43) mm3 at weeks three and six, respectively. Mean CtTh also increased during this period.

Table 1 Bone changes in the proximal tibia of ovariectomised non-treated control animals. Mean values with standard deviations are given (n = 4)

None of the PEMF-treated groups showed a significant difference in BV/TV or CtV compared with the control group at any time point (Fig. 3). The morphometric parameters also showed no significant differences compared with control animals. There were no indications to speculate the presence of any non-significant trend in the follow-up outcome variables.

Fig. 3
figure 3

Trabecular volume fraction and cortical volume in the tibia of ovariectomised rats that received PEMF treatment (n = 4) or received no treatment (controls, n = 4). Data are mean values and standard deviations

Discussion

In this study we examined the effects of PEMF on bone changes in the cancellous and cortical bone during a six-week follow-up period. Although we used in vivo microCT scanning, which is a very sensitive analysis method, we were unable to reproduce the strong beneficial effects of PEMF on osteoporosis in ovariectomised rats as shown by others [12, 25, 26].

In this study four treatment protocols were used. Three of these protocols were based on a commercially available PEMF generator used for the treatment of non-unions. The fourth signal was developed as a single burst in order to be more comparable with the study of Chang and Chang [12]. In the study of Chang and Chang it was shown that PEMF prevented the trabecular bone loss induced by ovariectomy. Although one of the groups received PEMF with characteristics based on their signal, some differences in the experimental set-up still remain. Our signal had an electromagnetic current of 1 G instead of 4–8 G in the signal of Chang and Chang. Furthermore, they treated the rats for eight hours per day instead of two hours as used in our study. To examine whether longer exposure to PEMF would prevent further bone loss in our experimental set-up, we extended the experiment for an additional six weeks and treated the same animals for eight hours per day. However, trabecular bone loss was comparable to non-treated controls and no preventive effects of longer treatment could be found.

In a more recent article PEMF, consisting of pulse bursts with an electromagnetic current of 9.6 G, were applied to ovariectomised rats during day time or night time [25]. In both groups PEMF treatment resulted in an increase in BMD and increased trabecular bone mass compared to ovariectomised controls. It was shown that treatment during daytime was more efficient than an overnight treatment. No effect on cortical bone was found. In another study in which ovariectomised rats were exposed to a 50-Hz sinusoidal waveform of 10 G an increase in cortical volume of 71% compared to non-treated controls was found [26]. One study has been published in which a negative finding is described. In that study 24 hours per day of systemic PEMF with a maximum magnetic field of 15 G did not result in an increased bone mineral content after eight months of treatment [27].

Apart from differences in the characteristics of PEMF treatment used in each study, the ages of the animals also vary. In the studies that did find a positive effect of PEMF, eight to 13-week-old rats were used [12, 25, 26]. In our study 20-week-old rats were used and in the study of Takayama et al. five-month-old rats were used [27]. Rats younger than 20 weeks of age undergo extensive longitudinal growth, which probably affects the outcomes. For osteoporotic research it might be preferable to use skeletally mature animals, so that the results are easier to interpret in relation to the clinical situation.

Use of in vivo microCT scanning allows one to detect very small changes, because longitudinal data are collected. In the control group we observed an absolute decline in BV/TV of 7.5% (SD 1.63) at three weeks (Table 1). At a power of 0.8, an α of 0.05 and with four animals per group, this gives a detectable alternative of 2.5% when comparing means of two groups. Thus, we would have been able to detect an effect of PEMF if the treatment had decreased trabecular bone loss to 5% or less compared to controls. Similar calculations for changes in CtV show that we would have been able to detect an effect of PEMF when cortical thickening was prevented by 0.25 mm3 or less given that control animals gain 0.6 (SD 0.17) mm3 of cortical bone in three weeks. In our opinion this is sufficient power because effects smaller than this would most likely not be of clinical significance. With this power we were also able to detect differences when bone changes at the magnitude of other studies were found.

In a clinical trial it was shown that by treating the proximal forearm of osteoporosis-prone women, an increase in BMD was induced at the distal radius of the treated side and also at the contralateral side, which suggests PEMF induced a systemic effect [23]. It is peculiar that this research and the strong beneficial effects in earlier animal experiments have not led to a range of clinical trials in which the effect of this safe and non-invasive intervention on bone mass is further examined. For many years attempts have been made to perform a prospective randomised controlled trial to determine the effect of PEMF on non-unions, but due to a lack of sufficient numbers for adequate statistical power this has never been achieved [17, 20, 37, 38]. Obtaining sufficient numbers would not be a problem in a clinical trial examining the effects of PEMF on bone mass in healthy or osteoporotic individuals. Because PEMF does not induce any side effects and the exact experimental set-up is important for the outcome, it would be more logical and favourable to perform future studies on the effect of PEMF on bone in humans and not in animals. With the use of non-invasive techniques such as dual-energy X-ray absorptiometry (DXA) scanning and peripheral microCT scanning the role of PEMF in osteoporosis could be determined with certainty.

In this study we could not demonstrate a positive effect of PEMF on the bone architecture in a ovariectomised rat model of osteoporosis. This is in accordance with earlier published work. However, because there are studies that did find strong effects, it might be that PEMF are very effective under the right circumstances. It might therefore be more practicable to examine the effects of PEMF on bone mass directly in humans such that translation from small animal experiments is not an issue. However, the results obtained in our study do not substantiate a potential role for the use of PEMF in post-menopausal osteoporosis.