Serum catestatin levels in patients with rheumatoid arthritis

Catestatin (CST) is an important peptide that influences various inflammatory diseases. Our goal was to investigate CST concentrations in patients with RA compared to healthy subjects. This cross-sectional observational study included 80 patients with RA and 80 healthy control subjects. Demographic characteristics and laboratory parameters were recorded. Serum CST levels were determined by an enzyme-linked immunosorbent assay (ELISA). Serum CST levels were significantly higher in RA patients than in the control group (10.53 ± 3.90 vs 5.24 ± 2.37 ng/mL, p < 0.001). In RA patients, there was a statistically significant correlation between CST and patient age (r = 0.418, p < 0.001) and both DAS28 (r = 0.469, p < 0.001) and HAQ scores (r = 0.483, p < 0.001). There was a statistically significant correlation between serum CST levels and RA duration (r = 0.583, p < 0.001). Multiple linear regression analysis showed that serum CST levels retained a significant association with RA duration (β ± SE, 0.13 ± 0.04, p = 0.002) and DAS28 score (0.94 ± 0.45, p = 0.039) after model adjustment for age, body mass index (BMI) and HAQ score, with serum CST levels as a dependent variable. These findings imply that CST is possibly associated with RA complex pathophysiology and disease activity. However, future larger multicentric longitudinal studies are necessary to define the role of CST in RA.


Scientific Reports
| (2022) 12:3812 | https://doi.org/10.1038/s41598-022-07735-x www.nature.com/scientificreports/ (CVDs), IBD, chronic kidney disease and RA 14,18,19,25,26 . As already mentioned, several recent studies have shown that CTS attenuates the inflammatory response through the downregulation of macrophage differentiation toward the production of proinflammatory cytokines (TNF-α, IL-1, IL-6) 12,27,28 . Therefore, all of the aforementioned evidence points to a possible link between RA and CST through either an immunomodulatory or atherogenic role. To the best of our knowledge, until this point, there have been no published studies that explored the association of serum CST levels with RA. The aim of this study was to determine serum CST levels in RA patients in comparison with healthy controls and to assess the relationship between CST levels and chronic inflammation, duration and activity of RA, as well as other clinical, biochemical and anthropometric parameters.

Methods
Study design. This cross-sectional observational study was conducted at the Department of Internal Medicine, Division of Clinical Immunology and Rheumatology, University Hospital of Split over a period from October 2020 to June 2021.
Ethics approval. The  Subjects. This study included 80 patients with RA and 80 healthy control subjects matched by age and sex.
One hundred RA patients were screened for inclusion in the study, and 85 patients were eligible for inclusion in the study. Among the participants mentioned, three were excluded due to refusal of further procedures, and two were excluded due to sudden disease worsening. A total of 120 healthy control subjects were screened at the beginning of the study. Among them, twenty participants were excluded due to inability to schedule an appointment and remaining others due to refusal of further procedures. RA diagnosis was made in accordance with the latest 2010 American College of Rheumatology/European League Against Rheumatism Classification Criteria for RA 29 . All participants were above 18 years of age and underwent the full study protocol, except measurement of disease activity [using Disease Activity Score-28 (DAS28) and functional disability [using The Stanford Health Assessment Questionnaire (HAQ)], which were measured only in the patient group [30][31][32] . Patients with RA were recruited from the outpatient clinic of the Department of Clinical Immunology and Rheumatology, University Hospital of Split, while control subjects were recruited from healthy blood donors, medical staff and healthy volunteers from the local primary health care center.
The exclusion criteria were: chronic inflammatory disorders other than RA; diabetes mellitus; pregnancy; breastfeeding; renal impairment [eGFR (estimated glomerular filtration rate) ≤ 60 mL/min/1.73 m 2 ]; history of heart failure; respiratory disease; liver disease; active malignant disease; clinically significant drug abuse and consumption of alcohol more than 40 g/day, and long-term exposure to oral glucocorticoid therapy ≥ 10 mg/day. All control subjects were screened for the presence of systemic autoimmune diseases, as well as any other symptoms suggestive of inflammation of the musculoskeletal system. Furthermore, all potential control group subjects underwent detailed physical examination along with laboratory analysis [the complete blood count, differential blood count and levels of C-reactive protein (CRP)]. We excluded all participants who showed any sign of inflammation in any of these steps.
Clinical assessment and anthropometric measurements. All participants had a detailed medical history, a physical examination and anthropometric data assessment. Anthropometric measurements included body height, weight and body mass index (BMI). A calibrated medical scale with built-in heights (Seca, Birmingham, UK) was used to measure body mass and height, and BMI was calculated according to the formula = [body weight (kg)]/[height per square (m 2 )]. Arterial blood pressure was measured using a standard mercury sphygmomanometer Riester Big Ben Aneroid [Rudolf Riester GmbH, Jungingen, Germany] with a suitable arm, and values were obtained after a minimum of two measurements. The subjects were seated and relaxed for 10 min before the measurements, with the upper arm at heart level. The mean values of arterial blood pressure was determined after those two measurements. Data on smoking, coffee and alcohol consumption were taken from all study participants. Finally, we checked the medical records of all patients and extracted clinical data relevant for this study.
Biochemical analysis. Blood samples were collected from all participants after 12 h of overnight fasting from the cubital vein via a polyethylene catheter. Serum samples were centrifuged, and routine laboratory tests were performed the same day. Sample aliquots for CST analyses were stored at − 80 °C for further analysis. All analyses were performed according to standard laboratory protocols by the same experienced biochemist who was blinded to the participants' group affiliation. Serum CST levels were determined by enzyme-linked immunosorbent assay (ELISA), using a commercially-available diagnostic kit (EK-053-27CE, EIA kit, Phoenix Pharmaceuticals Inc., Burlingame, CA, USA). According to the manufacturer's instruction, the reported sen- www.nature.com/scientificreports/ sitivity of the assay kit for CST was 0.05 ng/mL with a linear range of 0.05-0.92 ng/mL. Cross-reactivity with endogenous human CST peptide for this assay kit was 100% (manufacturer declared intra-assay and inter-assay coefficients of variation were < 10% and < 15%, respectively). CRP and rheumatoid factor (RF) were determined by the immunoturbidimetric method (Roche ® Diagnostics GmbH, Mannheim, Germany). Anti-citrullinated protein antibodies (ACPA) were determined by chemiluminescence microparticle immunoassay on an Architect analyzer (Abbott, Abbott Park, IL, USA). Other biochemical analyses were conducted using standard laboratory procedures.
Assessment of disease activity. DAS score in RA patients was performed by two experienced rheumatology specialists independently and score was estimated using the online Dawn ® visual DAS28 calculator 30 , using number of tender and swollen joints, levels of an acute phase reactant [either ESR (mm/h) or CRP (mg/L)] plus measure of general health [GH; patient assessment of disease activity using a 100 mm visual analogue scale (VAS) with 0 = best, 100 = worst]. Disease activity was graded according to the following thresholds: DAS-28 score < 2.6 indicates remission; score from 2.6 to 3.2 indicates low disease activity; score from 3.2 to 5.1 indicates moderate disease activity and; DAS-28 score above 5.1 is considered high disease activity 31 .
Measurement of functional disability. The HAQ was used to examine the extent of functional ability in daily living and activities in patients with RA. The HAQ score ranges from 0 to 3 and is a good predictor of future disability. HAQ was performed by an experienced rheumatology specialist. The HAQ evaluates the patient's level of functional ability through 20 questions in eight categories, which include the patient's disturbance of movements and activities that involve both upper and lower extremities. In accordance with previous findings, a score below 0.5 is considered normal, whereas a score above 1.5 indicates severe disability 32 .

Statistical analysis.
The data for the present study were analyzed using SPSS Statistics for Windows ® (version 25.0, IBM, Armonk, NY, USA) and MedCalc (MedCalc Software, Ostend, Belgium, version 19.1.2). Continuous data are presented as the mean ± standard deviation or median (interquartile range) based on the variable distribution normality, whereas categorical data are expressed as numbers (N) with percentages (%). Normality of distribution for continuous variables was assessed using the Kolmogorov-Smirnov test. For differences between the groups, an independent samples t-test was used for continuous variables with normal distribution, whereas the Mann-Whitney U test was employed for the analysis of continuous variables with non-normal distribution. The chi-squared (χ 2 ) test was used to determine differences between groups in terms of categorical variables. To investigate the correlation between CST and various clinical parameters, we used either Pearson's correlation coefficient or Spearman's rank correlation coefficient based on the variable distribution normality. Comparison of serum CST levels between RA duration tertiles was performed using one-way analysis of variance (ANOVA) with a post hoc Tukey test. Finally, a multiple linear regression analysis with a forward algorithm was applied to determine significant and independent correlates of the CST serum levels, which was defined as a dependent continuous variable. The level of statistical significance was set at a p-value < 0.05.
Sample size analysis. Sample size analysis was conducted using the data from a pilot study on 10 subjects from the RA population and 10 matched control subjects. The value of serum CST, which was the main result of the study, was used for the calculation. The mean serum CST levels were 9.40 ± 2.75 ng/mL in the RA group and 3.71 ± 2.55 ng/mL in the control group. With a type I error of 0.05 and a power of 90%, the required sample size was 29 participants per group.

Results
Baseline characteristics and laboratory parameters. There were no statistically significant differences in anthropometric measurements between the RA patients and the healthy control group. The demographic and anthropometric characteristics of the RA patients and the healthy control group are shown in Table 1. The median duration of RA was 15.0 (10.0-20.0) years, while 51 (63.7%) patients had a positive RF and 56 (70%) had a positive ACPA (Table 1).

Catestatin correlations with laboratory and anthropometric parameters in the RA group.
In patients with RA, there was a statistically significant correlation between CST levels and age (r = 0.418, p < 0.001). There were no other statistically significant correlations between catestatin levels and laboratory or anthropometric parameters (Table 3).
CST and RA duration. The RA group was divided into tertiles depending on the disease duration. The 1st tertile was 2-11 years; the 2nd was 12-17 years, and the 3rd was > 17 years of duration.

Multiple linear regression analysis.
Multiple linear regression analysis showed that serum CST levels retained a significant association with RA duration (β ± SE, 0.13 ± 0.04, p = 0.002) and DAS28 (0.94 ± 0.45, p = 0.039) after model adjustment for age, BMI and HAQ score, with serum CST levels as a dependent variable (Table 4). Table 1. Baseline characteristics of the RA group and the control group. Data are presented as the whole number (percentage), mean ± standard deviation or median (IQR). SBP systolic blood pressure, DBP diastolic blood pressure, DAS28 Disease Activity Score 28, HAQ Health Assessment Questionnaire, csDMARD conventional synthetic disease-modifying antirheumatic drug, tsDMARD targeted synthetic disease-modifying antirheumatic drug, bDMARD biologic disease-modifying antirheumatic drug. *Chi-square test. **t-test for independent samples. † Time period since the initial diagnosis.

Discussion
This study showed that patients with RA who were treated with either bDMARDs or tsDMARDs had significantly higher levels of serum CST than healthy control subjects. Furthermore, CST had a significant positive correlation with both DAS28 and HAQ scores, as well as with RA duration. To the best of our knowledge, this is the first clinical study that evaluates the serum concentration of CST in patients with RA and its correlation with specific disease characteristics. As already mentioned, CST participates in the regulation of hypertension and cardiac functions and in promoting angiogenesis 13,33 . The data from several experimental models and in vivo studies indicated that high plasma concentrations of CgA in RA patients could be involved in persistent vascular inflammation, endothelial barrier dysfunction and systemic sympathetic hyperactivity 26,34,35 . Moreover, it was proposed that noticeable increase in CgA levels in RA, potentially could induce the attenuation of its anti-angiogenic impact 36 . Accordingly, plasma CgA could be used as both a diagnostic and prognostic marker in various inflammatory conditions,   27,34 . Based on these findings, elevated levels of the CgA degradation product CST in RA patients could be expected, which was confirmed by this study. Our results imply that CST plays a role in the pathophysiology of RA, which is consistent with its well-established systemic anti-inflammatory effects 13,27,[37][38][39] .
In addition to higher CST levels in our group of RA patients than in healthy subjects, we found that CST is an independent predictor of disease activity and functional disability. Based on the existing literature, a possible explanation for these findings is that CST participates in a cascade of signal transduction pathways between immune and noimmune cells, particularly altering the balance between pro-and anti-inflammatory cytokines 39 . Furthermore, these results would presume that a more active disease triggers regulatory mechanisms that lead to compensatory secretion of CST to protect the host from the chronic inflammatory process. Experimental animal studies in colitis and atherosclerosis mouse models have shown that administration of CST reduces the prevalence of macrophages and monocytes in inflamed tissues 13,40 . There is an abundance of macrophages in the inflamed synovial membrane that strongly promote overexpression of proinflammatory cytokines 41,42 . CST could attenuate the intensity of inflammation in RA through modification of the differentiation of monocytes to macrophages. Although the mechanisms by which CST affects monocyte and macrophage migration are still unclear, there are several assumptions about this effect. One possible pathophysiological mechanism includes the reductive effect of CST on the expression of vascular cell adhesion molecule-1 (VCAM-1) and consequent changes in the inflammatory environment 13 . VCAM-1 is a glycoprotein expressed by endothelial cells that mediates leukocyte-endothelial cell adhesion during inflammation 41 . Several studies reported significantly higher serum VCAM-1 levels in patients with RA [42][43][44] . In addition, serum VCAM-1 levels correlate with endothelial dysfunction and the initiation and progression of RA 42,43,45 . The expression of VCAM-1 in synovial tissue is upregulated by proinflammatory cytokines (TNF-α and IL-6) 45 . By lowering the production of proinflammatory cytokines, CST could decrease the expression of adhesion molecules in the endothelium. Moreover, an in vitro study showed that anti-VCAM-1 monoclonal antibody injection into a collagen-induced RA mouse model did not alter the incidence, but decreased the severity of arthritic joints compared with the control mice 46 . Another possible mechanism by which CST regulates macrophages refers to the polarization of RA synovial www.nature.com/scientificreports/ tissue "activated macrophages" towards two different phenotypes depending on the disease activity: M1 (classically activated) and M2 (alternatively activated) 47 . The M1 phenotype releases high levels of proinflammatory cytokines and consequently prevails in patients with highly active RA alongside the increased presence of proinflammatory macrophage receptor with collagenous domain (MARCO) 48 . Based on the results of in vivo and in vitro studies, CST treatment decreases proinflammatory cytokine (IL-6, IL-1β, TNF-α) and macrophage levels 13,17,40 . Additionally, the production of CST by macrophages could result in reduction of the inflammation by feedback inhibition mode 15 . Considering that the RA population investigated in this study was treated with biological agents, a synergistic effect of those drugs and CST in RA is possible. Although this could, to some extent, explain the association between CST and RA, further studies are necessary to confirm the precise role of CST in the complex pathophysiology of RA.
Limited data indicate that high CST levels could reflect advanced CV disease burden, a burden that is significantly increased in RA 49 . Moreover, CVDs are still the leading cause of mortality in patients with RA (30-40% of deaths) 4,5,50,51 . Additionally, it has been established that both traditional CV risk factors and intrinsic RA features contribute to excess CV-related morbidity and mortality 22 . The most significant intrinsic RA features are the disease duration, the presence of ACPAs, RF, elevated proinflammatory cytokines and hsCRP serum levels [52][53][54][55][56][57] . Premature atherosclerosis is the hallmark of CVD development in RA 3 . According to this point, the precise effects of CST on atherosclerosis have not yet been clarified. A recent animal study conducted on apolipoprotein-deficient mice that were fed a high cholesterol diet showed that administration of CST to the same mice significantly reduced aortic atherosclerotic lesions and attenuated macrophages. Furthermore, by in vitro analysis, the authors determined that CST could suppress atherogenesis by inhibiting inflammatory responses in endothelial cells and macrophages 13 . In addition, the administration of CST to the mouse hindlimb ischemia model resulted in improvement of blood flow and reduction of necrosis 38 . Given these considerations,  www.nature.com/scientificreports/ we hypothesize that the effects of CST on the inflammatory process in patients with RA could interfere with the process of atherogenesis and CV risks themselves. However, all of these findings should be interpreted with caution and need to be explored in further, large-scale studies. This study has several limitations. First, our study was designed as a cross-sectional study, thereby preventing the establishment of causal relationships. Second, it had single-centre patient inclusion with a relatively small sample size. Additionally, due to technical restrictions, we were not able to measure all inflammatory parameters, which could potentially have an impact on some of the results.
In conclusion, this study showed that patients with RA have higher serum CST levels than healthy controls. Furthermore, CST was positively correlated with HAQ and DAS28 scores and disease duration. These findings imply that CST possibly plays a role in RA complex pathophysiology, especially in the severity of inflammation and atherogenesis. However, future larger multicentre longitudinal studies are necessary to explain the association between CST and RA.

Data availability
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/.