The serum uric acid is longitudinally related to patients global assessment of disease activity in male patients with axial spondyloarthritis

Axial spondyloarthritis (axSpA) is a chronic inflammatory rheumatic disorder, and the clinical manifestations are varied [1]. In general, axSpA mostly affects the spinal column and the sacroiliac joint [2], resulting in inflammatory back pain and progressive bony fusion [3]. Additionally, extraarticular manifestations affect the patient's prognosis and quality of life [4]. The ASAS/EULAR international guidelines recommend that clinicians need to be alert and pay attention to extra-articular manifestations, which can be beneficial in the treatment of axSpA. Common extra-articular manifestations of axSpA such as uveitis, psoriasis and intestinal inflammation have been reported, but there are limited studies related to the effect of SUA levels on axial sclerosis.

Uric acid is an end product of purine metabolism. As purines are among the primary components of DNA and RNA, Uric acid is closely associated with life. Accordingly, as living conditions have improved in China over the past two decades, increasing levels of SUA have been linked to excessive consumption of purine-rich foods (such as red meat and seafood), unhealthy lifestyle habits (such as smoking, excessive alcohol consumption, and sedentary habits), and underlying comorbidities [5, 6]. The study shown that low levels of serum uric acid have a significant negative effect on bone mineral density in axSpA patients [7]. In a cross-sectional study, it was found that patients with hyperuricemia had much lower levels of the condition compared to patients without hyperuricemia in China [8]. The study, however, was based on cross-sectional data analysis, which look at data collected over time, and the results do not offer a complete picture. AxSpA is a chronic inflammatory immune disease with a recurrent inflammatory course [9], so the cross-sectional study cannot reflect the effect of time changes on the disease and SUA levels.

The current studies of SUA in spondyloarthritis are cross-sectional. Despite this, little is known about the relationship between SUA and disease indicators over time. Disease activity measurement in axial SpA included patient global assessment (PtGA), spinal pain , BASDAI, ASDAS-CRP, and Health-related Quality of Life Score (HRQoLs). Our objective was to determine if SUA levels was longitudinally related to disease activity measures over time in patients with axSpA.

In total, 102 patients were included in the study. In the present study, the average age was 35.54 (8.69) years, and the mean duration of disease was 11.25 years. All patients met the inclusion criteria and were followed for more than 2 years. However, 72 patients had SUA results at the second year with a baseline of 6.62 ± 1.52 mg/dl, 33.33% were hyperuricemic, their baseline socio-demographic and clinical characteristics are summarised in table 1. In the baseline clinical data of patients with hyperuric acid and normal uric acid levels, there was no significant difference (Table 2).

In the univariable generalized estimating equations (GEE) model, ,SUA levels as continuous variables, outcomes as the dependent variables, SUA was negatively correlated with PtGA in univariable analysis [P=0.039, β=-1.9981, 95%CI (-3.863, -0.099)] and spinal pain [P=0.04,β=-1.9979, 95%CI (-3.862, -0.094)], On the other hand, ASDAS-CRP, BADAI, BASFI, CRP, and ESR did not show a significant correlation with SUA (Figure 1, Table S1). Based on the univariable analysis that analyzed the relationship between SUA levels and health-related quality of life (HRQoL), it was found that SUA levels had a positive relationship with Physical Functioning (PF) [P=0.006, β=2.039, 95%CI (0.58, 3.499)], General Health (GH) [P=0.035, β=2.577, 95%CI (0.182, 4.972)], and Social Functioning (SF) [P=0.004, β=2.267, 95%CI (0.705, 3.83)]. No significant correlation was seen with other SF-36 indicators (Figure 1, Table S1).

Contextual factors were not effect modifiers of the relationship between the PtGA and SUA (Supplementary Table S3–S6), so we did not perform a stratified analysis. Multivariable generalized estimating equations (GEE) were used to eliminate the influence of confounding factors. The results indicate that SUA level is negatively related to PtGA [P=0.041, β=-2.059,95%CI(-4.032, -0.086)]. This effect was independent of age, symptom duration, hyperuricemia at baseline, and medication use, No relationship was found between spinal pain and SUA in the multivariable analysis, and no relationships were seen with SUA for other indicators of disease activity (Figure 2, Table S2). In multivariable model analysis with SF-36, SUA was still positively correlated with Vitality (VT) [P=0.01, β (95% confidence interval) and Social Functioning (SF) [P=0.002, β=2.968,95%CI (1.067,4.869)], indicating that the quality of life of patients with higher SUA was improved. However there is a significant interaction between SF and Medication use, since the number of cases was small, we did not perform stratified analysis in these cases (Figure 2, Table S2).

To the best of our knowledge, it is the first time to explore the effect of SUA levels on axSpA from longitudinal cohort data. UA is known to function as an important oxidant in the human body [17], Hyperuricosuria is harmful to human health [18]. But is it seems to indeed be the case in axSpA patient? The longitudinal observation of SUAand axSpA disease has not been reported. we used a longitudinal observational cohort study for the first time to study the effect of SUA levels over time in patients with axSpA. In the results of this study, we observed a longitudinal relationship between SUA levels and PtGA and mental health assessment. Exploring the relationship between SUA levels and disease activity in axSpA patients over time suggests that hight SUA levels during treatment has the negative relationship with PtGA in axSpA. We use the univariable GEE analysis in this study, the results suggested that during follow-up, a decrease in PtGA with increasing SUA level, and the same with spinal pain, contextual factors were included in the multivariable analysis model, this relationship was statistically significant.

In our cohort study, the longitudinal relationship between SUA levels and PtGA was independent of medication use. The results can be seen in (Tables S3-S6). Serum creatinine levels, urea nitrogen, and other biochemical indexes in the patient remained stable and no side effects were observed during the follow-up. Therefore, we conjectured that renal dysfunction and drugs were not the cause for higher levels of SUA in our cohort study, which might due to the remision of inflammatory. As a result of the analysis, It was found that the patient had increased SUA levels and decreased PtGA levels.

During clinical observation, the SUA levels of gout patients in the acute phase were within normal value s[19]. Waldron and colleagues demonstrated a significant reduction in SUA when patients without gout during a systemic inflammatory response (SIR) provoked by orthopedic surgery [20]. In recent years, some scholars have proposed decreasing systemic inflammation leads to an increase in serum urate [21]. For example, people found an increased level of SUA that patients after treated with three mouths anti-TNF inhibitors in a study from 201 9[22]. It seems that uric acid elevation is associated with decreased levels of inflammation in axSpA.

Uric acid is the end-product of endogenous and dietary purine metabolism [23]. In addition to renal excretion, elevated uric acid is related to the endogenous purine metabolism. Hence the metabolic rate of endogenous purine metabolism maybe cause more adenosine. Extracellular adenosine exerts immunosuppressive effects on immune cells via the adenosine receptor [24], resulting in the reduced production and release of inflammatory cytokines [24]. In fact, there is a growing body of evidence supporting the concept that regulatory T cells suppress effector T cells mainly via generating adenosine [25, 26]. In preclinical studies, adenosine A2_A receptor agonists have a wide range of anti-inflammatory effects in inflammatory diseases. In the preclinical models of rheumatoid arthritis [27], encephalomyelitis [28] andallergic asthma [29] beneficial effects of A2_A receptor agonists have been observed. Adenosine receptors are associated with the remission of the disease among AS patients [30]. It is suggested that adenosine receptors are involved in reducing inflammation of AS patients [31], the anti-inflammatory effects of disease-modifying antirheumatic drugs approved for the clinical treatment of axSpA is also associated with adenosine receptors. For instance, Adenosine mediates the anti-inflammatory effects of methotrexate [32]. The A2_A receptor is the receptor responsible for the anti-inflammatory effects of sulfasalazine [33]. It is, of course, possible that adenosine receptors and uric acid corporately participate in the regulation of inflammatory responses. In a mouse model of colitis, the efficacy of adenosine receptor agonists in relieving enteritis might be more pronounced with a higher level of uric acid [34]. Therefore, we speculated that the remission of auto-inflammation may account for the enhanced uric acid levels. The potential mechanism may be related to the metabolism of adenosine.

SUA is association with SF36 scores (8 domains) was considered during data analysis, and it was positively and significantly correlated to Social Functioning and Vitality (the scores in the SF-36 can range from 0 to 100), while higher scores indicate better health status. The 8 multi-item scales of the SF-36 were summarized into two components (mental and physical components respectively) [35]. Social Functioning and Vitality belonged to the SF36 mental health domain [35], our data suggested that SUA improved the SF36 mental health domain scores. Maybe improvement in mental health associated with the amelioration of inflammatory. But the effect of uric acids in mental cannot be ruled out. Early observations in manic patients reported an increased excretion of uric acid [36], later studies supported SUA levels are associated with mania and depression [37]. Experimental studies supported that different adenosine concentrations and adenosine receptors had anti-depressant or anti-anxiety effects [38]. So uric acid as a metabolite of adenosine might have an effect on mental. However, the specific mechanism is unclear.

We find that SUA levels is longitudinally related to PtGA and mental health assessment Age, gender and symptom duration do not have an impact on the relationships. during the follow-up period. No significant association with inflammation has been found. In the light of the complexity of the pathogenesis of axSpA, the association of subjective symptoms remission with SUA level maybe is part of the pathogenesis of axSpA. Uric acid is the final product of adenosine metabolism. We suggest adenosine and adenosine receptors may play important roles in the pathogenesis of axSpA. And further studies are warranted to investigate their relationship and the underlying mechanism.

The limitations of this study were summarized. Firstly, the follow-up period was short and the sample size was also limited. The patients enrolled in this study may not be representative of all axSpA patients. Secondly, the patients taking urate-lowering therapy within 3 months before into the group were excluded, and the effect of therapy on hyperuricemia could not be analyzed.