Serum levels of leptin and high molecular weight adiponectin are inversely associated with radiographic spinal progression in patients with ankylosing spondylitis: results from the ENRADAS trial

Ankylosing spondylitis (AS) is a chronic inflammatory disease belonging to a family of spondyloarthritides (SpA), which is characterized by inflammation in the pelvis and the spine with subsequent new bone formation that might lead to partial or total ankylosis of the spine. New bone formation in the spine, and particularly development of specific bony bridges between the vertebral bodies, is usually assessed on spinal radiographs and is referred to as radiographic spinal progression. It has been shown in the past that radiographic spinal progression and disease activity are two main determinants of spinal mobility and functional status in AS [1–3]. However, there is substantial individual variation in the radiographic spinal progression rates in AS [4, 5]. It has been shown that baseline syndesmophytes [4, 5], inflammatory activity as assessed by C-reactive protein (CRP), by the Ankylosing Spondylitis Disease Activity Score (ASDAS), or by the presence of inflammatory changes on magnetic resonance imaging (MRI) [6–12], and cigarette smoking [13] are factors associated with more rapid radiographic spinal progression. Further, several biomarkers in the blood were found to be positively associated with new bone formation in the spine: the already mentioned CRP [7], matrix-metalloproteinase-3 [14], vascular endothelial growth factor [15], calprotectin [16], and the adipokine, visfatin [17]. Some biomarkers, such as sclerostin [18] and dickkopf 1 [19], have been associated with radiographic spinal progression, suggesting that these molecules might have a protective effect.

Identification of biomarkers related to the development of structural damage in AS helps not only to predict progression (there are currently no proven therapeutic options to retard progression; however, this might, change in the near future), but it also helps us to better understand disease mechanisms. For instance, until now, the reason why men with AS develop more structural damage in the axial skeleton than women has not been explained [5, 20].

Adipokines are biologically active substances, which are synthesized and released by fat tissue. They have a wide range of regulatory functions not only in energy metabolism, but also in inflammation and osteogenesis [21, 22]. The role of adipokines in the development of inflammation and new bone formation in AS, however, is as yet unclear. The aim of the present study was to investigate the association between adipokine serum levels and radiographic spinal progression in patients with AS.

A total of 29 patients had radiographic progression defined as mSASSS worsening by ≥2 points after 2 years; 25 patients had syndesmophyte formation/progression. The intraclass correlation coefficient (ICC) between the two readers of the X-rays was good: the ICC was 0.96 for baseline and 0.95 for year-2 X-rays; the ICC for change in the mSASSS was 0.50 [23].

HMW-APN serum levels did not differ between the two treatment arms (NSAIDs continuously vs. on demand) at baseline and after 2 years of follow up; there was, however, a difference in the leptin levels at baseline (but not at year 2): 13.6 ± 13.2 ng/mL in the continuous intake group vs. 15.5 ± 12.6 ng/mL in the on-demand group, p = 0.046. Overall, there was an increase in the leptin level after 2 years in both treatment groups (continuous vs. on-demand NSAIDs); this was statistically significant in the continuous treatment group only: increase of 13.6 ± 13.2 ng/ml to 15.6 ± 15.6 ng/mL, p = 0.002. However, in the ANCOVA, there was no statistically significant difference in the change in the leptin serum level: increase of 2.0 ± 4.84 ng/mL in the continuous vs. 1.26 ± 7.43 ng/mL in the on-demand group, p = 0.405, adjusted for baseline leptin. Further, there was no significant association between change in leptin and HMW-APN (or the BMI-corrected values) over 2 years and radiographic spinal progression. Treatment had no effect on the levels of other adipokines.

There was no evidence of association between radiographic spinal progression and BMI in this patient population: BMI at baseline was 26.9 ± 4.1 kg/m² vs. 27.4 ± 5.6 kg/m² in patients with and without mSASSS worsening by ≥2 points, respectively, p = 0.93, and 28.1 ± 6.6 kg/m² vs. 27.1 ± 4.9 kg/m² in patients with and without syndesmophytes formation respectively, p = 0.58.

There was no meaningful correlation between leptin and HMW-APN serum levels, and no correlation with serum CRP. In the ROC analysis, baseline serum leptin, the leptin/BMI ratio, serum HMW-APN, the HMW-APN/BMI ratio, and the HMW-APN/APN ratio were good predictors of no mSASSS progression ≥2 points and of no syndesmophyte formation/progression (Fig. 1). Leptin and the leptin/BMI ratio was generally a slightly better predictor as compared to HMW-APN.

In the current study we investigated the association between serum adipokines and radiographic spinal progression in patients with AS. We report for the first time that baseline leptin and HMW-APN serum levels, and to a further extent the HMW-APN/APN ratio were inversely associated with (i.e., predicted protection against) radiographic spinal progression. Initially, we investigated eight adipokines and only those with evidence suggesting an association with radiographic progression were entered the main analysis. We have chosen the homogeneous population of the ENRADAS trial consisting of patients with advanced AS. The lack of differences in radiographic spinal progression between the study arms justified pooling both groups of patients (treated with NSAIDs continuously or on demand). However, due to some change in the leptin level over 2 years that was especially evident in the continuous treatment group, the parameter estimates in the regression analysis were adjusted for NSAID intake.

In the study population, leptin and HMW-APN levels were higher in female patients with AS compared to male patients, even after adjustment for BMI. At the same time, there was no association between BMI and radiographic spinal progression. There are data on gender-dependent differences in adipokine levels in the general population [29, 30]. In one study, leptin and APN levels were higher in women than in men independent of BMI or waist-to-hip ratio [29], while in another study such an association was shown for leptin, but not for adiponectin [30]. Similarly, differences in adipokine levels between male and female patients have also been described in patients with AS [17, 31]. Such an association between sex and adipokine levels is especially interesting in the context of the current study, since the women in our study also had significantly lower mSASSS scores than men. It has been shown several times that female patients with AS develop new bone formation to a lesser extent than male patients with AS [5, 20]. Therefore, we can speculate that leptin and HMW-APN might be biomarkers (or even pathophysiological factors) linking gender with radiographic spinal progression in patients with AS.

Remarkably, in the analyses stratified by sex, an association between adipokines and radiographic spinal progression was evident in male patients only. On the one hand, the absence of association between serum adipokine and radiographic spinal progression in female patients could be related to the smaller sample size and a small number of progressors in the female group. On the other hand, female patients had generally higher levels of leptin and adiponectin in comparison to male patients, suggesting that in female patients who progressed after 2 years, there could have been other factors playing a part.

In our previous study involving patients from the German Spondyloarthropathy Inception Cohort (GESPIC) cohort, who had early axial SpA, we found a positive association between visfatin and radiographic spinal progression; leptin and HMW-APN were not investigated [17]. In the current study, we found only a trend for such an association for visfatin that might be related to the differences in disease duration in the GESPIC (early disease) and ENRADAS (rather advanced disease) studies or to the test system used.

Until now, serum adipokines and their relationship to clinical or radiographic parameters in AS have only been investigated in a few small trials. In some studies, leptin serum was found to be lower in patients with AS compared to healthy controls [32–34], but in others there were either no differences or even higher leptin serum levels in patients with AS [35–37]. A meta-analysis from Mei et al, which included eight studies that had compared leptin levels in patients with AS with those in healthy controls, came to the conclusion that there are no significant differences in leptin levels in patients with AS vs. controls [38]. Differences in serum APN (including the HMW isoform) have also not been identified at group level in patients with AS and healthy controls [17, 32, 34]. However, in one study serum APN was higher in male patients with AS versus healthy controls, and at the same time there was almost no correlation between leptin or APN and inflammatory activity, and anti-inflammatory treatment (anti-TNF-α) did not have an effect on serum leptin and APN [35].

Data on the association between structural damage in the spine and leptin in AS are very limited. In one study, higher serum leptin was positively associated with the presence of syndesmophytes in a cross-sectional analysis; however, no prospective data were reported [36]. In the aforementioned study of patients with early axial SpA, APN was only numerically higher in non-progressors, but the HMW isoform was not investigated [17].

What are the possible mechanisms linking leptin and adiponectin with radiographic spinal progression in AS? Adipokines are known to be involved in the regulation of immune processes, displaying both pro-inflammatory and anti-inflammatory effects, and in bone metabolism that explains their possible relationship with the pathophysiology of chronic inflammatory conditions such as rheumatoid arthritis or AS [21, 22, 39]. Our current observation of a protective effect of leptin and APN (especially its HMW isoform) against radiographic spinal progression in AS can probably be best explained by the effects of both molecules on the process of osteogenesis, since there is no association between adipokines and inflammatory activity as measured by CRP.

Many studies have previously assessed the part played by leptin in bone metabolism; however, published data show both positive and negative effects of leptin on bone formation [40]. Two main regulatory pathways are currently discussed. One targets the central nervous system, the other one acts through peripheral regulation [41]. The peripheral effect is based on a rather direct interaction of leptin with several bone cell types. For instance, leptin enhances new bone formation through interaction with bone marrow stem cells, which can either differentiate into osteoblasts or into adipocytes. It promotes differentiation and growth of osteoblasts and enhances bone mineralization [42–44]. Furthermore, leptin administered peripherally can inhibit formation of human osteoclasts [44, 45].

In contrast, a central regulatory effect of leptin on bone metabolism is rather anti-osteoproliferative. It has been shown that bone loss could be induced in leptin-deficient mice through an intracerebrovascular infusion of leptin [46], indicating a role of leptin as a hormone which induces pathways of the sympathetic nervous system (SNS) through the ventromedial hypothalamus (VMH), which then results in bone loss. Further studies have confirmed this theory [47, 48]. The available evidence indicates that leptin binds to its receptors on neurons of the VMH, which then activate a signal pathway from the VMH to osteoblasts via β2 adrenergic receptors of the SNS. Through the signals of the SNS two cascades in osteoblasts are activated leading to increased osteoclast formation and decreased osteoblast differentiation [41].

Hamrick et al. proved in 2004 that the effects of leptin on the skeleton differ between skeletal regions. Comparing leptin-deficient obese mice (ob/ob) with lean mice they found that ob/ob mice had significantly reduced femoral bone mineral density (BMD), bone mineral content (BMC), cortical thickness and trabecular bone volume compared to lean mice. On the other hand, they found ob/ob mice to have higher BMC, BMD and trabecular bone volume in the lumbar spine than the lean mice. Hence, their study suggests that leptin regulates bone metabolism differently according to the location within the skeleton [49]. Martin et al. found in 2007 that there could be a bimodal threshold response to serum leptin levels, meaning that slight increases in leptin might initially stimulate bone formation, while higher leptin levels inhibit bone formation [50].

Thus, leptin might have contradictory effects on bone metabolism that also depend on the localization of the bone. We hypothesize that in patients with AS a higher level of leptin has protective properties against radiographic spinal progression mainly via the central pathway with inhibition of excessive new bone formation.

As for APN, different effects on bone metabolism have been discovered as well, yielding similarly conflicting results. APN was found to be expressed in osteoblasts along with its receptors and to stimulate their proliferation and differentiation, for example, through enhancement of the expression of bone morphogenetic protein 2 (BMP-2) [51–53]. Additionally, APN was found to be able to suppress osteoclastogenesis and promote osteoblastogenesis [54]. However, APN is also able to indirectly activate osteoclasts by stimulating receptor activator of nuclear factor kappa-B (NFкB) ligand (RANKL) and inhibiting osteoprotegerin (OPG) production in osteoblasts, which are known to be essential stimulators of osteoclastogenesis [55].

An inverse relationship between APN and BMD was found in vivo in a number of studies [39] indicating that APN might have predominantly catabolic effects on bone. In line with this, the meta-analysis of Biver et al., which included 59 studies of healthy male and female patients who were evaluated for BMD or fracture risk and adipokines, showed that APN seems to be the most important adipokine that is negatively associated with BMD [56].

There are two main circulating isoforms of APN in the blood stream: one low molecular weight (LMW) hexamer and the HMW multimer [28, 57]. Previous data suggest that HMW-APN might be the predominantly active isoform and that the HMW-APN/APN ratio might be an important determinant of the metabolic effects of the hormone [28]. The importance of the HMW-APN/APN ratio was also confirmed in another study, in which the ratio was a better predictor of insulin resistance and metabolic syndrome than total plasma APN [58]. In line with these data, we found that HMW-APN (and to a further extent the HMW-APN/APN ratio) was inversely associated with radiographic spinal progression in AS, and the association between radiographic progression and HMW-APN was better than that between radiographic progression and total APN.

Our study has limitations. First, this was an analysis based on a population of a randomized controlled trial. Although we corrected our analysis for differences in the intervention, we cannot completely exclude bias resulting from treatment. Further, only relatively few women were included in this trial, which made the interpretation of the subgroup analysis results difficult in this population. Also, no fat mass measurement was performed in the ENRADAS trial beyond BMI calculation. Finally, since no biologic agents were allowed in the ENRADAS trial it is currently unclear whether leptin and HMW-APN might also have protective effects against radiographic spinal progression in patients treated with anti-TNF or anti-interleukin-17 drugs. Therefore, an independent validation of our results is highly desirable not only in patients treated with NSAIDs but also in patients undergoing biologic treatment. Despite a significant association with radiographic spinal progression, leptin or HMW-APN alone would not be sufficient for identification of patients at high (or low) risk of radiographic spinal progression. However, these biomarkers seem to be good candidates for inclusion in multi-parameter predictive models for estimation of the risk of radiographic spinal progression in AS.

Serum levels of leptin and HMW-APN are inversely associated with radiographic spinal progression in patients with AS. Current data on the role of adipokines in bone metabolism indicates that leptin and HMW-APN might not only be markers but also true pathophysiological factors influencing new bone formation in AS. Female patients with AS have a higher level of leptin and APN, which might play a natural protective role against radiographic spinal progression in AS, explaining the generally lower prevalence of extended new bone formation in the spine in female patients with AS.