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https://doi.org/10.33004/reumatizam-66-2-8

ULTRASOUND EVALUATION OF THE ANKLE JOINTS AND TENDONS IN SYSTEMIC LUPUS ERYTHEMATOSUS

Ljiljana Smiljanić Tomičević ; Division of Clinical Immunology and Rheumatology, Department of Internal Medicine, University of Zagreb, School of Medicine, University Hospital Center Zagreb, Croatia / Zavod za kliničku imunologiju i reumatologiju, Klinika za unutarnje bolesti, Klinički bolnički centar Zagreb, Medicinski fakultet Sveučilišta u Zagrebu, Zagreb, Hrvatska
Darija Čubelić ; Division of Clinical Immunology and Rheumatology, Department of Internal Medicine, University of Zagreb, School of Medicine, University Hospital Center Zagreb, Croatia / Zavod za kliničku imunologiju i reumatologiju, Klinika za unutarnje bolesti, Klinički bolnički centar Zagreb, Medicinski fakultet Sveučilišta u Zagrebu, Zagreb, Hrvatska
Miroslav Mayer ; Division of Clinical Immunology and Rheumatology, Department of Internal Medicine, University of Zagreb, School of Medicine, University Hospital Center Zagreb, Croatia / Zavod za kliničku imunologiju i reumatologiju, Klinika za unutarnje bolesti, Klinički bolnički centar Zagreb, Medicinski fakultet Sveučilišta u Zagrebu, Zagreb, Hrvatska
Branimir Anić ; Division of Clinical Immunology and Rheumatology, Department of Internal Medicine, University of Zagreb, School of Medicine, University Hospital Center Zagreb, Croatia / Zavod za kliničku imunologiju i reumatologiju, Klinika za unutarnje bolesti, Klinički bolnički centar Zagreb, Medicinski fakultet Sveučilišta u Zagrebu, Zagreb, Hrvatska


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Sažetak

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with musculoskeletal involvement as one of the most common clinical manifestations. High-resolution ultrasound (US) has been proven to be a useful diagnostic tool for the evaluation of joints and tendons in the majority of inflammatory rheumatic diseases. The aim of this study is to assess the frequency of ankle joint and tendon involvement in SLE patients with the use of US, and correlate the findings with the physical examination, laboratory tests, and disease activity scores. Here we will show preliminary results of the survey in the first 10 out of 60 included patients. Ten consecutive SLE patients were enrolled in the study and underwent clinical evaluation, laboratory tests, and bilateral high-resolution US on the same day. Gray-scale and power Doppler (PD) US were performed for imaging of the talocrural (TC) and subtalar joints (ST), ankle tendons, second and third metacarpophalangeal (MCP) joints, second and third proximal interphalangeal (PIP) joints, second and third metatarsophalangeal (MTP) joints, and wrists. A total of 180 joints and 200 tendons were examined. Preliminary results showed US-detected inflammatory joint abnormalities in 7/10 (70%) patients and tendon involvement in 1/10 (10%). Both the MTP and TC joints were affected in 60% of the patients, MCP joints in 50%, ST in 40%, wrists in 30%, and PIP joints in 10% of the patients. The most prevalent pathological US finding was joint effusion, less frequently synovial hypertrophy, while a positive PD signal was rarely detected. Effusion in the TC joints was present in 60% of the patients, synovial hypertrophy in 40%, and a positive PD in 10%. As many as 62.5% of the patients without inflammatory joint symptoms had pathological US findings in the ankle joints. The results showed a high prevalence of US-verified inflammatory joint changes in SLE patients. Surprisingly, the MTP and ankle joints were most commonly affected. Additionally, a great number of asymptomatic patients also had pathological US findings in the ankle joints.

Ključne riječi

Lupus erythematosus, systemic – complications; Ankle joint – diagnostic imaging; Joint diseases – diagnostic imaging, etiology; Synovitis – diagnostic imaging, etiology; Tenosynovitis – diagnostic imaging, etiology; Metacarpophalangeal joint – diagnostic imaging; Metatarsophalangeal joint – diagnostic imaging; Ultrasonography

Hrčak ID:

247780

URI

https://hrcak.srce.hr/247780

Datum izdavanja:

17.12.2020.

Posjeta: 723 *




INTRODUCTION

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease of complex pathogenesis with a wide range of clinical manifestations (1). It is characterized by multi-system inflammation with the production of autoantibodies and the formation of immune complexes and their deposition into tissues. Affection of the musculoskeletal system is one of the most common and earliest manifestations of the disease, occurring in 95% of patients (1,2). The joint involvement may range from mild arthralgia and arthritis to a rare non-erosive deforming arthropathy (Jaccoud arthropathy) (1), and almost all joints can be affected. In older studies, the most commonly affected joints were the small joints of the hands, the wrist, and the knee, while recent studies point to the frequent involvement of the joints of the feet (3,4). Periarticular structures may also be affected by inflammation. Tendonitis, tenosynovitis, and changes or ruptures of the tendons have also been described in SLE patients, sometimes being the only cause of pain and instability in these patients. Affection of the ankle often occurs in patients with inflammatory rheumatic diseases. Clinical examination of the ankle may underestimate the type and distribution of the pathological changes due to the complexity of the anatomical structures of that area. Conventional radiological examination of the ankle provides bone structure data while providing very little information about the surrounding soft tissue. Magnetic resonance imaging (MRI) is a high-resolution imaging that can show both bone and soft tissue structures. It is very sensitive to changes in joints, but it is expensive and often unavailable in routine clinical practice.

High resolution Power Doppler (PD) and musculoskeletal ultrasound (MSUS) has been proven to be a useful and non-invasive diagnostic technique for assessing and tracking pathological changes in joints, tendons, and entheses (5). There is extensive literature on the benefits of MSUS in various inflammatory rheumatic diseases, mostly in rheumatoid arthritis, psoriatic arthritis, and other spondyloarthropathies (6,7). However, so far few ultrasound studies have been conducted that evaluate the joints in SLE patients (4,8,9).

PATIENTS AND METHODS

The pilot study included 10 consecutive SLE patients diagnosed according to the 1997 revised ACR criteria, who were treated at the Division of Clinical Immunology and Rheumatology at the University Hospital Center Zagreb (10). The study protocol included an ultrasound and physical examination performed the same day as the regular rheumatologist follow-up and laboratory reevaluation. The MSUS examination was performed in all patients, regardless of the presence or absence of pain and swelling in the joints and tendons. The study was conducted according to the guidelines of good clinical practice as well as the Helsinki Declaration. All patients signed an informed consent form.

Clinical and demographical data (date of diagnosis, disease duration, system involvement, current and previous therapy, previous presence of pain and swelling of the ankle) were collected from each study patient. All patients were subjected to a standardized physical examination that evaluated the presence of painful and swollen joints and deformities (44 joints), with the evaluation of tendons and joints of the feet and ankles. To assess the disease activity, the SLEDAI-2K (Systemic Lupus Erythematosus Disease Activity Index 2000) and ECLAM (European Consensus Lupus Activity Measurement) were used (11,12). For the purposes of the study, data on patients with SLE included in the hospital register were used as well. A single rheumatologist, who was blinded to the clinical and laboratory data, performed the MSUS examination and scored the static images. The images were also scored by another independent rheumatologist expert in MSUS.

A high-resolution US equipped with a multifrequency linear array transducer (4–15 MHz) with PD was used. Multiplanar examination techniques were performed in accordance with the International Guidelines for MSUS in Rheumatology for imaging of the TC and ST joints, ankle tendons, second and third MCP joints, second and third PIP joints, second and third MTP joints, and wrists (13). A total of 18 joints and 20 tendons were examined in each patient and the inflammatory US score and global inflammatory US score were calculated. The joints for global inflammatory US scoring were selected according to the shown frequency of the joint involvement in recent studies. The presence of joint effusion, synovial hypertrophy, bone erosion, tenosynovitis, and enthesitis was defined according to the OMERACT definitions (13). US-detected elementary lesions were evaluated with a dichotomous score (absence/presence). A semi-quantitative scale (0–3) was used for scoring joint effusion, synovial proliferation, and PD.

RESULTS

Ten consecutive patients, all females, were enrolled in the study. The mean age was 45.3 years and the mean disease duration 164 months. Half of the enrolled subjects did not have musculoskeletal symptoms at the time of examination. The demographic, clinical, and serologic data are reported inTable 1. For the majority of patients, treatment was based on corticosteroids alone or combined with various different disease-modifying anti-rheumatic drugs.

Table 1 Demographic, clinical, and serologic data of enrolled patients according to musculoskeletal disease status
Feature / ObilježjeAll patients / Svi bolesnici
n = 10
Patients with MSK symptoms / Bolesnici s MSK simptomima
n = 5
No MSK symptom / Bez MSK simptoma
n =5
Age, years, mean (range) / Dob, godine, srednja vrijednost (raspon)45.3 (24–67)44.845.8
Disease duration, months, mean (S.D.) / Trajanje bolesti, mjeseci, srednja vrijednost (S. D.)164 (121.01)133.2 (116.5)194.8 (130.4)
Joint involvement, n (%) / Zahvaćenost zglobova, n (%)5 (50)5 (100)0(0)
CRP, mg/L, mean value (range) / CRP, mg/L, srednja vrijednost (raspon)8.36 (0.9–57)1.2615.46
ESR mm/h, mean value (range) / SE, mm/h, srednja vrijednost (raspon)34 (8–80)34.233.8
ANA, n (%)9 (90)4 (80)5 (100)
Anti-dsDNA, n (%) / AntidsDNK, n (%)4 (40)2 (40)2 (40)
C3, mg/L, mean value (range) / C3, mg/L, srednja vrijednost (raspon)1.168 (0.88–1.5)1.1561.186
C4, mg/L, mean value (range) / C4, mg/L, srednja vrijednost (raspon)0.176 (0.05–0.35)0.1340.218
Glucocorticoids, n (%) / Glukokortikoidi, n (%)9 (90)4 (80)5 (100)
Glucocorticoids, mean daily dosage, mg / Glukokortikoidi, prosječna dnevna doza, mg13.2517.512.5
Hydroxychloroquine and chloroquine, n (%) / Hidroksiklorokin i klorokin, n (%)8 (80)4(50)4 (50)
MTX, AZA, MMF, CyA, CyC, n (%)4 (40)2(40)2(40)
SLEDAI-2K, mean value (range) / SLEDAI-2K, srednja vrijednost (raspon)3.6 (0–10)5.61.6
ECLAM, mean value (range) / ECLAM, srednja vrijednost (raspon)2.05 (0–5.5)31.1
Number of tender joints, mean value (range) / Broj bolnih zglobova, srednja vrijednost (raspon)2 (0–10)4
Number of swollen joints, mean value (range) / Broj otečenih zglobova, srednja vrijednost (raspon)1.3 (0–3)2.6

Ultrasonographic findings

A total of 180 joints and 200 tendons were examined. Preliminary results in 10 patients showed US-detected inflammatory joint abnormalities in 7/10 (70%) patients and tendon involvement in 1/10 (10%). Both the MTP and TC joints were affected in 60% of the patients, MCP joints in 50%, ST in 40%, wrists in 30%, and PIP joints in 10% of the patients. According to these findings, the TC and MTP were the most frequently involved joints. The most severely affected joints were the TC and MCP, with clinical and ultrasound synovitis at the time of evaluation. The most prevalent pathological US findings in all examined joints were joint effusion and synovial hypertrophy (present in 80% of the patients), while a positive PD signal was rarely detected (30%). Only one patient had bone erosion verified. Furthermore, the most prevalent pathological US finding in the ankles was also joint effusion (60%), less frequently synovial hypertrophy (40%), while a positive PD signal was present in 10% of the patients. As many as 62.5% of the patients without inflammatory joint symptoms had pathological US findings in the ankle joints. The mean value of the global US inflammatory score was 5.6, while the mean value of the ankle US inflammatory score amounted to 2.9.

DISCUSSION

Existing studies indicate a high prevalence of joint and tendon inflammatory changes in SLE patients and it is apparent that ultrasound changes of the hand and wrist joints are common in those patients, depending on the type of arthropathy (4,8,9,14,15). Furthermore, most studies have shown that there is significant subclinical joint involvement in SLE patients (4,14,15). This leads to the conclusion that reliance on the physical examination of the joints can underestimate the presence of active joint inflammation. In the systematic review by Lins and Santiago from 2015, which included a literature overview from 1950 to 2015, the high frequency of subclinical joint and tendon US pathology was also shown (14). Most articles in this review demonstrated hand and wrist joint changes (14). In the research by Iagnocco et al. in 2014, ultrasonographic changes of the joints were described in a large proportion of patients (87%), while only 40% of them presented with clinical involvement of the joints. That study unexpectedly showed that the MTP joints were more commonly affected (72% of the patients) compared with the wrist (53%), MCP (46%), and PIP joints (19%) (4). In addition, the MTP joints were affected by more severe inflammatory changes compared with other examined joint levels. There are very few other studies that have evaluated the MTP joint region (4,15). The high prevalence of MTP joint ultrasound pathology was also demonstrated in a pilot study by Mukherjee in 2016 (15). This study also showed a high frequency of US-detected forefoot bursal prevalence and bursal PD (100% of patients). Significant associations between bursal prevalence and MTP joint PD were noted (15).

Studies conducted in other rheumatic diseases have found US with PD a useful tool for the assessment of pathologies in ankle joint and tendons, as well as the differentiation of inflammatory and degenerative changes (16). To the best of our knowledge, this is the first US study aimed at an analysis of inflammatory changes in the ankle joints and tendons in SLE patients. In our study we found that the most commonly affected joints were the TC and MTP joints (60% of the patients). That correlates with the research of Iagnocco et al., although it has to be noted that ankle joints were not analyzed in that study. Gabba et al., in a study that was conducted in 108 SLE patients with musculoskeletal symptoms, found that patients with active musculoskeletal disease had more US pathology in the joints, while asymptomatic subjects had more pathological findings in the tendons (9). Our findings showed that the most common changes in joints were joint effusion followed by synovial hypertrophy, while a positive PD signal was rarely observed, which correlates with other studies (4,5). It is important to emphasize that joint effusion was also present in 40% of asymptomatic patients in our study.

Data on the correlation between ultrasound findings and the inflammatory activity index SLEDAI-2k are contradictory. In our study both the SLEDAI-2k and ECLAM indexes were higher in the group of patients with pathological ultrasound findings in the ankle joints than in the group of patients without US changes. SLEDAI was 4.66/2 and ECLAM 2.5/1.375.

CONCLUSION

Results of the preliminary study show a high prevalence of US-verified inflammatory joint changes in SLE patients. Surprisingly, the foot and ankle joints were most commonly affected and a great number of asymptomatic patients also had pathological US findings in the ankle joints.

Notes

[1] Conflicts of interest Conflict of interest statement: Authors declare no conflict of interest.

REFERENCES / LITERATURA

1 

Pipili C, Sfritzeri A, Cholongitas E. Deforming arthropathy in systemic lupus erythematosus. Eur J Intern Med. 2008;19(7):482–7. https://doi.org/10.1016/j.ejim.2008.01.017 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/19013374

2 

Cerovec M, Anić B, Padjen I, Cikes N. Prevalence of the American College of Rheumatology classification criteria in a group of 162 systemic lupus erythematosus patients from Croatia. Croat Med J. 2012;53(2):149–54. https://doi.org/10.3325/cmj.2012.53.149 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/22522993

3 

Grossman JM. Lupus arthritis. Best Pract Res Clin Rheumatol. 2009;23(4):495–506. https://doi.org/10.1016/j.berh.2009.04.003 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/19591780

4 

Iagnocco A, Ceccarelli F, Rizzo C. Truglia S i sur. Ultrasound evaluation of hand, wrist and foot joint synovitis in systemic lupus erythematosus. Rheumatology. 2014;53(3):465–72. https://doi.org/10.1093/rheumatology/ket376 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/24231444

5 

Joshua F, Lassere M, Bruyn GA. Szkudlarek M i sur. Summary findings of a systematic review of the ultrasound assessment of synovitis. J Rheumatol. 2007;34(4):839–47. PubMed: http://www.ncbi.nlm.nih.gov/pubmed/17407235

6 

Hoving JL, Buchbinder R, Hall S. Lawler G i sur. A comparison of magnetic resonance imaging, sonography, and radiography of the hand in patients with early rheumatoid arthritis. J Rheumatol. 2004;31(4):663–75. PubMed: http://www.ncbi.nlm.nih.gov/pubmed/15088290

7 

Riente L, Delle Sedie A, Filippucci E. Iagnocco A i sur. Ultrasound imaging for the rheumatologist IX. Ultrasound imaging in spondyloarthritis. Clin Exp Rheumatol. 2007;25(3):349–53. PubMed: http://www.ncbi.nlm.nih.gov/pubmed/17631728

8 

Iagnocco A, Ossandon A, Giulio C. Fabrizio C i sur. Wrist joint involvement in systemic lupus erythematosus. An ultrasonographic study. Clin Exp Rheumatol. 2004;22(5):621–4. PubMed: http://www.ncbi.nlm.nih.gov/pubmed/15485017

9 

Gabba A, Piga M, Vacca A. Porru G i sur. Joint and tendon involvement in systemic lupus erythematosus: an ultrasound study of hands and wrists in 108 patients. Rheumatology. 2012;51(12):2278–85. https://doi.org/10.1093/rheumatology/kes226 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/22956550

10 

Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum. 1997;40(9):1725. https://doi.org/10.1002/art.1780400928 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/9324032

11 

Gladman DD, Ibañez D, Urowitz MB. Systemic lupus erythematosus disease activity index 2000. J Rheumatol. 2002;29(2):288–91. PubMed: http://www.ncbi.nlm.nih.gov/pubmed/11838846

12 

Mosca M, Bencivelli W, Vitali C. Carrai P i sur. The validity of the ECLAM index for the retrospective evaluation of disease activity in systemic lupus erythematosus. Lupus. 2000;9(6):445–50. https://doi.org/10.1191/096120300678828640 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/10981649

13 

Wakefield RJ, Balint PV, Szkudlarek M. Filippucci E i sur. Musculoskeletal ultrasound including definitions for ultrasonographic pathology. J Rheumatol. 2005;32(12):2485–7. PubMed: http://www.ncbi.nlm.nih.gov/pubmed/16331793

14 

Lins CF, Santiago MB. Ultrasound evaluation of joints in systemic lupus erythematosus: a systematic review. Eur Radiol. 2015;25(9):2688–92. https://doi.org/10.1007/s00330-015-3670-y PubMed: http://www.ncbi.nlm.nih.gov/pubmed/25716942

15 

Mukherjee S, Cherry L. Zarroug J i sur. A pilot investigation of the prevalence of US-detectable forefoot joint pathology and reported foot-related disability in participants with systemic lupus erythematosus. J Foot Ankle Res. 2016;9:27. https://doi.org/10.1186/s13047-016-0158-1 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/27486482

16 

Suzuki T. Power Doppler ultrasonographic assessment of the ankle in patients with inflammatory rheumatic diseases. World J Orthop. 2014;5(5):574–84. https://doi.org/10.5312/wjo.v5.i5.574 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/25405085


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