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Spondyloarthritis (SpA) includes axial and peripheral SpA, according to the Assessment of SpondyloArthritis international Society classification criteria.1 2 An increasing number of research has focused on the comorbidities and risk factors in SpA. The first and latest international cross-sectional ASAS-COMOSPA study, published in the Annals of the Rheumatic Diseases, has proposed some comorbidities such as cardiovascular diseases, osteoporosis, cancers, infections and gastrointestinal diseases. This research has also proposed the risk factors for cardiovascular diseases, cancers and osteoporosis.3 Other studies have also focused on the cardiovascular diseases among patients with SpA.4–6 However, as for heart comorbidities, valvular heart disease was not mentioned in the ASAS-COMOSPA study, while it has been reported to be associated with SpA in a number of recent studies, based both on epidemiology and pathology.7–9 As for risk factors for cardiovascular diseases, hyperuricaemia was not included as well, while uric acid has also been proven to be related to cardiovascular disease in the recent years.10–13 Since there are still some comorbidities and risk factors to be evaluated, we proposed a research to include valvular heart disease as a comorbidity of SpA and hyperuricaemia as a risk factor of cardiovascular disease among patients with SpA.
From 2016 to 2018, we conducted a cross-sectional study of 202 SpA diagnosed by rheumatologists in the Chinese Shenzhen Second People’s Hospital. We extracted data from the hospital’s information systems by searching medical files at the Department of Rheumatology and Immunology, the Department of Ophthalmology, and the Department of Gastroenterology. All the medical files were examined to see if the diagnosis of axial or peripheral SpA could be confirmed.
Once the diagnosis of axial and peripheral SpA was confirmed, the following categories of data were collected: demographics and disease characteristics, extra-articular manifestations, comorbidities, risk factors for comorbidities, and sacroiliac joint image. The Bath Ankylosing Spondylitis Disease Activity Index,14 the Ankylosing Spondylitis Disease Activity Score calculated with CRP,15 16 and the Bath Ankylosing Spondylitis Functional Index were collected.17 Medications including non-steroidal anti-inflammatory drug (NSAID), corticosteroids, conventional synthetic disease-modifying antirheumatic drugs (DMARDs) and tumour necrosis factor inhibitor (TNFi) were also collected. Extra-articular manifestations included uveitis, psoriasis and inflammatory bowel disease (IBD) (Crohn’s/ulcerative colitis). Comorbidities included cardiovascular disease, diabetes, valvular heart disease and gout. Risk factors for comorbidities of cardiovascular disease included smoking, hypertension, hyperuricaemia and hyperlipidaemia. Hypertension was defined as a history of hypertension or antihypertensive therapy or blood pressure (BP) >140/90 mm Hg, or BP >130/80 mm Hg in the case of history of diabetes or renal insufficiency. Hyperuricaemia was defined as uric acid >416 µmol/L in men and >357 µmol/L in women.18–20 Hyperlipidaemia included factors of triglycerides, low-density lipoprotein (LDL) cholesterol and total cholesterol.3 12 Sacroiliac joint image was evaluated as radiographic SpA or non-radiographic SpA. Radiographic SpA was defined as grade II bilaterally or grade III–IV unilaterally, according to the Modification of the New York Criteria for radiography.21 It can also be defined as an erosion score and/or joint space score of 2 or higher in any of the 24 regions of both joints for CT.22 Non-radiographic SpA was defined as sacroiliac joint image without structural sacroiliitis described above.23 Data were analysed with the use of the statistical packages R (The R Foundation; http://www.r-project.org; version 3.4.3) and EmpowerStats (www.empowerstats.com; X&Y Solutions Inc).
Between 1 January 2016 and 31 December 2018, 202 individuals were included in this study. Individuals who were not examined for renal function (n=111) and those who were not examined for sacroiliac joint imaging (n=21) were not included. The study profile of screening patients for analysis is presented in figure 1.
The demographics and disease characteristics are listed in table 1. More patients presented axial involvement (89.6%), and fewer patients presented only peripheral involvement (12.4%). More patients ever accepted NSAIDs (53.0%), and fewer accepted TNFi (10.4%) compared with conventional synthetic DMARDs (24.3%). However, more and more patients began to accept TNFi (31.2%) as an optimal therapy, instead of conventional synthetic DMARDs (26.2%).
The most common extra-articular manifestation was uveitis (17.3%), while the least common was IBD (2.0%). Diarrhoea was relatively frequent, which was 10.4% of the study population.
The prevalence of comorbidities is presented in figure 2. The prevalence of cardiovascular disease in the study population was 1.0%, while that of diabetes was 3.0%. Of the patients 6.9% ever suffered gout. Cardiac ultrasonography evaluation was performed on 124 of the 202 patients, and the prevalence of valvular heart disease in this population was 24.2%. When evaluated by human leucocyte antigen B27 (HLA-B27)-positive and HLA-B27-negative subgroups, respectively, HLA-B27-positive subgroup presented more patients suffering from valvular heart disease (27.4%), which had statistical significance (p=0.014). This is presented in figure 3.
The prevalence of detected risk factors for comorbidities is presented in figure 4. Conventional risk factors for cardiovascular disease (ie, BP, LDL cholesterol) were detected in this study. Of the patients in this study, 19.3% ever smoked, 20.3% reported to have ever suffered from hypertension, 36.6% had hyperuricaemia, and 30.8% had hyperlipidaemia (hyperlipidaemia detection was conducted in a scope of 133 patients).
Uric acid, a specific risk factor, was evaluated in this study with a mean±SD of 380.2±107.7 umol/L. Uric acid was evaluated by radiographic SpA and non-radiographic SpA, with the radiographic subgroup (n=141, 69.8%) presenting a mean±SD of 397.7±106.6 umol/L and the non-radiographic subgroup (n=61, 30.2%) presenting a mean±SD of 339.8±99.8 umol/L, which had statistical significance (p<0.001). The prevalence of hyperuricaemia in the radiographic SpA subgroup was 40.4%, while in the non-radiographic SpA subgroup was 27.9%; these are all presented in figure 5.
Our study represents the characteristics of Chinese SpA population and reports some unnoticed and specific aspects, as a supplement to ASAS-COMOSPA study.
Although there were a lot of common demographics and disease characteristics of SpA presenting in this study as the ASAS-COMOSPA study, there were noteworthy aspects in extra-articular manifestation, comorbidities, risk factors for comorbidities and sacroiliac joint image.
IBD was less common in Chinese population compared with the worldwide population shown in the ASAS-COMOSPA study. Diarrhoea was a frequent symptom of IBD. In this study of Chinese population 10.4% had diarrhoea, while diarrhoea was not mentioned in the ASAS-COMOSPA study. IBD was diagnosed using endoscopic and histological measures. As for reports about IBD, endoscopic manifestations were not consistent with symptoms such as diarrhoea and stool frequency. Endoscopically inactive disease was not associated with complete normalisation of diarrhoea.24 Diarrhoea, reflecting gut inflammation,25 was a noteworthy symptom of IBD among patients with SpA.
Valvular heart disease, which is also a common heart comorbidity of SpA, was relatively higher (24.2%) in this study, compared with what has been reported in the heart failure population,26 which was also neglected by the ASAS-COMOSPA study. The prevalence of valvular heart disease in HLA-B27-positive subgroup is different from that in the HLA-B27-negative subgroup. We are going to discuss the association between valvular heart disease and HLA-B27 in a subsequent article. The prevalence of gout was higher in our study than the general population of most countries in the world.27
Uric acid, which had been proven to be a new cardiovascular risk factor,28 29 turned out to be relatively higher than the general population,30 and was different between the radiographic and non-radiographic subgroups. We will later discuss the association between uric acid and sacroiliac radiographic image in another article.
Further studies confirming the impact of comorbidities and risk factors in patients with SpA are required. If confirmed, these studies would lead to standardised assessments of patients with SpA.
We are very grateful to the engineers of the medical information system.
YL and YZ contributed equally.
Contributors YL and CX designed the research protocol. SM, JM and TN extracted data from the medical files in the information system and interpreted the data. YZ extracted data from the laboratory system. YL and JX extracted data from the image system and evaluated the sacroiliac CT images. YL, YZ and ZL performed the statistical analysis. YL, YZ and JX wrote the manuscript. YL, YZ, JX and CX approved the version submitted.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient and public involvement The study was a retrospective research that extracted data from a hospital’s information system and did not involve patients in the design, recruitment and conduct of the study. The results of the study will be disseminated to all patients with SpA for better therapy after publication.
Patient consent for publication Not required.
Ethics approval The study was approved by the Ethics Committee of Shenzhen Second People’s Hospital, with approval ID 20200224001.
Provenance and peer review Not commissioned; internally peer reviewed.
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