|Ahead of print publication
The clinicoserological spectrum of inflammatory myopathy in the context of systemic sclerosis and systemic lupus erythematosus
John D Pauling1, Sarah Skeoch1, Julie J Paik2
1 Royal National Hospital for Rheumatic Diseases (Part of the Royal United Hospitals NHS Foundation Trust); Department of Pharmacy and Pharmacology, University of Bath, Bath, USA
2 Johns Hopkins Myositis Center, 4500 Baltimore, MD, USA
|Date of Submission||28-May-2020|
|Date of Acceptance||13-Jul-2020|
John D Pauling,
Department of Pharmacy and Pharmacology, University of Bath, Bath; Royal National Hospital for Rheumatic Diseases (Part of the Royal United Hospitals NHS Foundation Trust), Bath
Source of Support: None, Conflict of Interest: None
Autoimmune rheumatic diseases (ARDs) are characterized by a pathological triad composed of autoimmunity/inflammation, microangiopathy, and aberrant tissue remodeling. Disease terms such as idiopathic inflammatory myopathy (IIM), scleroderma/systemic sclerosis (SSc), and systemic lupus erythematosus (SLE) are helpful clinically but disguise the considerable overlap that exists within these “distinct” disorders. This is perhaps best demonstrated by inflammatory myopathy, which can be present in SSc or SLE, but can itself be absent in clinically amyopathic IIM. Archetypal clinical manifestations of ARD (such as Raynaud's phenomenon) are frequently present, albeit with varying prominence, within each of these diseases. This is certainly the case for inflammatory myositis, which has long been recognized as an important clinical feature of both SSc and SLE. Progress in elucidating the clinicoserological spectrum of ARDs has identified autoantibody specificities that are strongly associated with “overlap” disease and the presence of inflammatory myositis in SSc and SLE. In this review, we shall describe the prevalence, burden, prognostic value, and management considerations of IIM in the context of both SSc and SLE. A major emphasis on the value of autoantibodies shall highlight the value of these tools in predicting the future occurrence of inflammatory myositis in both SSc and SLE. Where applicable, unmet research needs shall be highlighted. The review emphasizes the importance of myopathy as a common feature across all the ARDs and highlights specific antibody specificities that are strongly associated with myopathy in the context of SLE and SSc.
Keywords: Classification, clinical phenotype, dermatomyositis, overlap syndromes, polymyositis, systemic lupus erythematosus, systemic sclerosis
|How to cite this URL:|
Pauling JD, Skeoch S, Paik JJ. The clinicoserological spectrum of inflammatory myopathy in the context of systemic sclerosis and systemic lupus erythematosus. Indian J Rheumatol [Epub ahead of print] [cited 2020 Oct 29]. Available from: https://www.indianjrheumatol.com/preprintarticle.asp?id=297398
| Introduction|| |
Autoimmune rheumatic diseases (ARDs) are characterized by a pathological triad composed of autoimmunity/inflammation, microangiopathy, and aberrant tissue remodeling. Disease entities such as idiopathic inflammatory myopathy (IIM), scleroderma/systemic sclerosis (SSc), and systemic lupus erythematosus (SLE) are helpful clinically but disguise the considerable overlap that exists within these “distinct” disorders. The archetypal clinical manifestations of ARD, such as Raynaud's phenomenon (RP), occur across each of these diseases, albeit varying in prevalence. The prominence of specific clinical features helps to determine both the clinical diagnosis and disease classification for the purposes of clinical research. This is certainly the case for inflammatory myositis, which is the pathological hallmark of IIM (although not an essential feature for diagnosis) and has long been recognized as an important clinical feature of SSc and SLE. In this review, we shall describe the prevalence, burden, prognostic value, and management considerations of inflammatory myopathy in the context of SLE and SSc. Progress in elucidating the clinicoserological spectrum of ARDs has revealed antibody specificities that are strongly associated with “overlap” disease. The role of autoantibodies in predicting the future occurrence of inflammatory myositis in SSc and SLE shall be discussed. Where applicable, unmet research needs shall be highlighted.
Search strategy and selection criteria
References for the present review were identified through a search in PubMed (April 18, 2020) using the following search terms: ([myositis OR Myopathy]) AND ([lupus] OR [scleroderma] OR [systemic sclerosis]). No language or date restrictions were placed on the search. Of the 3897 studies identified, the titles and abstracts were reviewed for inclusion in the review on the basis of their relevance and originality. Additional cited manuscripts were identified through searches of the authors' own files.
| Systemic Sclerosis|| |
Clinical and pathological overlap between idiopathic inflammatory myopathy and systemic sclerosis-spectrum disorders
The most common clinical manifestations of SSc relate more to dysregulated fibrosis (in the skin (scleroderma and other organs) and vasculopathy (manifesting as RP, ischemic digital ulceration, pulmonary arterial hypertension, and scleroderma renal crisis), than overt inflammation. Nonetheless, inflammation in the muscles (and joints) is not an uncommon feature of SSc. Similarly, vascular injury (a pathological hallmark of SSc) is a cardinal feature of IIM, leading to an early proposal for the term “angiomyositis” to describe IIM at the turn of the 20th century. The etiopathogenesis of SSc and tissue injury in the skin and muscle of IIM shares many key features that include endothelial injury, perivascular inflammatory cell infiltrate, reduction in capillary density, and peri-fascicular ischemia.,,, Clinical features such as RP occur in ~50% of patients with IIM, and morphological abnormalities of the nailfold capillaries (NC) are common. In contrast to the progressive microangiopathy of SSc, which is generally associated with poorer clinical outcomes, there can be resolution of NC abnormalities in IIM (particularly dermatomyositis [DM]), which can be associated with favorable clinical outcomes.,,, Putative important molecular pathways, such as those relating to vascular endothelial growth factor (a factor strongly implicated in the pathogenesis of SSc-related vasculopathy), are also overexpressed in IIM (and may be associated with the direct production of aminoacyl-tRNA synthetases in IIM)., Myositis-specific antibodies (particularly anti-synthetase antibodies) are not infrequently identified in IIM patients with a strong SSc phenotype (or even SSc patients without features of IIM), highlighting the strong clinical and pathological associations between these conditions., Impaired blood flow in microcirculation of the skeletal muscles may also be a contributing factor to the pathophysiology of muscle disease in SSc as was demonstrated in a novel muscle magnetic resonance imaging (MRI) study. Sometimes, evidence of muscle inflammation is an incidental finding on routine biochemistry [Figure 1], although inquiry about muscle symptoms and muscle strength assessment can be easily overlooked by clinicians whose focus is directed to other organ systems. In other patients, an overt symptomatic inflammatory myopathy is more clinically manifested.
|Figure 1: Asymptomatic low-grade myopathy in overlap syndrome with anti-Ku antibodies. A 67-year-old female developed inflammatory arthritis, Raynaud's phenomenon, and diffuse skin thickening (modified Rodnan Skin Score 18/51) with positive Anti-Ku antibodies. There were no myopathic symptoms/signs, but moderately elevated creatine kinase was identified on routine biochemistry. The arthritis was treated with steroids (a) with mycophenolate mofetil added as a steroid-sparing agent (b), leading to reduction in CpK to normal range. Asymptomatic nonspecific interstitial pneumonia was present on computed tomography thorax|
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Burden of myopathy in systemic sclerosis-spectrum disorders
The prevalence of myopathy in SSc is greatly influenced by the definition (and objective testing) applied. Early attempts to assess muscle disease in SSc struggled to differentiate between a primary myopathy and disuse muscle atrophy secondary to general debility, associated arthropathy, and skin disease. There is a high prevalence of reduced muscle strength and endurance in SSc compared with age-matched controls, not all of which can be attributed to myositis. Generalized fatigue is one associated factor that may contribute to muscle weakness in SSc. The objective evidence of inflammatory myopathy can also be present in the absence of overt patient-reported symptoms of muscle weakness, possibly owing to a more insidious onset compared with that of IIM.
The typical distribution of proximal myopathy can mirror that of IIM, although distal weakness can also accompany skin involvement of the hands and forearms. It was initially thought that the myopathy of SSc was not particularly strongly influenced by disease subset, although subsequent studies have identified a paucity of IIM in the context of anti-centromere antibodies and an association between myopathy and diffuse cutaneous SSc (dcSSc). Large registry analyses have identified objective evidence of muscle weakness in around a quarter of SSc patients in the EUSTAR database, although only a third of these (8% of the total) had an elevated creatine kinase. The Canadian Scleroderma Research Group (CSRG), applying different definitions of myopathy, have reported evidence of myositis in ~13% of SSc patients. The point prevalence of elevated creatinine kinase in SSc patients in the CSRG was 5.6%, with approximately 10% of patients having a history of myositis/myopathy. In the CSRG registry, a raised creatine kinase was associated with being male (~1/4 of patients), younger age, dcSSc, tendon friction rubs, higher skin score, and an Forced Vital Capacity (FVC) <70%. Alongside U1-RNP, patients with a raised creatine kinase were more likely to carry anti-topoisomerase antibodies. Patients reported muscle pain and/or weakness is present in around 1/3rd of patients with dcSSc, but there is objective evidence of muscle weakness and/or a raised creatine kinase is only present in around 10% of patients with dcSSc.,, Muscle involvement is approximately twice as common in dcSSc compared with limited cutaneous SSc (e.g., creatine kinase is elevated in 11.3% of dcSSc vs. 4.4% in lcSSc). Sometimes, evidence of a low-grade myopathy in SSc can be identified on routine serum biochemistry in the absence of any muscle weakness [Figure 1]. In other cases of SSc, the myopathy is more clinically overt, often with a correspondingly significantly elevated muscle enzyme level [Figure 2].
|Figure 2: Systemic sclerosis-associated myopathy with concomitant organizing pneumonia in association with anti-PM-Scl antibodies. A 55-year-old male with Raynaud's phenomenon, sclerodactyly, and antibodies to PmScl-75, Pm-Scl 100, and Ro-52 developed acute proximal myopathy with raised CpK. Initial response to 6 intravenous cyclophosphamide infusions (a) was not maintained with mycophenolate mofetil. Rituximab was started (b) alongside the ongoing mycophenolate mofetil. Computed tomography thorax identified patchy organizing pneumonia. The numbers represent Myositis Muscle Dysfunction Scores (range 0–40, with higher numbers indicative of better strength)|
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The first major study in 1978 to prospectively examine and classify myopathy in SSc included 24 patients with SSc (the majority of whom it seems had a diffuse cutaneous disease). Twenty-three of 24 (95.8%) of this cohort had one or more myopathic features (raised muscle enzymes, objective weakness on muscle testing, abnormal electromyography [EMG], and/or abnormal biopsy when performed). The majority (19/24) were perceived to have a “simple myopathy” which they defined as a myopathy with modest rise in muscle enzymes (creatine kinase ~ 140% of normal) and often not necessitating treatment with corticosteroids. The remaining patients had a “complicated myopathy” which they defined as patients with significant weakness, abnormal EMG, and significantly elevated muscle enzymes (creatine kinase ~ 1700% of normal). While this classification of myopathy dichotomized muscle disease in SSc, it became apparent in a subsequent study in 2009 focused on the histological features of 35 patients with SSc-myopathy that muscle disease was far more heterogeneous than previously thought. Muscle biopsy features ranged from inflammation, atrophy, necrosis, fibrosis, and microangiopathy. Scleroderma-specific associations in this study also identified the diffuse subset in 26 (74%) cases and that myopathy was an early feature of SSc, typically occurring within 5 years from diagnosis [Figure 1] and [Figure 2]. A case–control study comparing SSc patients with and without an associated myopathy (matched for disease subset, age, and gender) identified an increased frequency of reduced FVC, heart involvement, and scleroderma renal crisis in patients versus controls. Sudden cardiac death in the setting of muscle disease in SSc has also been reported, highlighting the importance of early identification of these patients. Associated cardiac disease has been highlighted as a challenge in children with SSc-associated myopathy.
Investigation of myopathy in systemic sclerosis-spectrum disorders
Role of muscle enzymes
SSc patients with a raised creatine kinase or clinical evidence of myopathy have higher Health Assessment Questionnaire Disability Index scores.,,, Myopathy is an independent risk factor for worse outcomes such as disability even after controlling for potential confounders such as age, restrictive lung disease, or gastrointestinal disease. Both assessment of muscle strength and laboratory evidence of muscle inflammation are important modes of investigation in SSc-associated myopathy. An analysis from the Pittsburgh cohort identified proximal muscle weakness as an important determinant of future death on univariate analysis and Cox proportional hazards analysis. Furthermore, in this study, aldolase was suggested as having a stronger association with death than creatinine kinase. A separate French study also demonstrated that elevated muscle enzymes are a useful predictor of future myopathy in SSc (9/137 over 4 years) and plasma aldolase may be superior to creatinine kinase in this regard. Raised creatine kinase and/or those with a past history myopathy has also been associated with higher mortality. Therefore, based on these studies, the assessment of muscle strength, in particular in the proximal distribution and muscle enzymes (both CK and aldolase), can be an easy and important tool to determine the presence of a myopathy.
Because there can be multiple other etiologies for elevated muscle enzymes and proximal muscle weakness, to comprehensively assess for the presence of a myopathy in SSc, patients should ideally include additional studies such as EMG, MRI of the muscles, or muscle biopsy, when available. EMG results supporting a myopathic process are usually identified in patients with SSc-associated myopathy. Similarly, symmetric muscle edema will be classically seen in T2 Short-TI Inversion Recovery (STIR) images typical of myositis.
Histological assessment of myopathy in systemic sclerosis
Muscle biopsy can be a helpful diagnostic and management tool in SSc-associated myopathy, particularly if the diagnosis is unclear. In a study of 42 SSc patients with a myopathy, muscle histopathology was studied to identify whether unique subsets existed in SSc muscle disease. Distinct histopathological categories were identified that included polymyositis (5%, often associated with early disease), acute denervation (7%), and muscle fibrosis (7%, often associated with anti-PM-Scl antibodies). On a follow-up study of this cohort, the histopathological subset that was identified with predominant fibrosis on muscle biopsy, or a fibrosing myopathy, was found to be a distinct clinical phenotype. The presence of fibrosing myopathy on muscle biopsy was associated with diffuse cutaneous disease, African-American race, a lower FVC, and a higher mortality (5/8, 62.5%), when compared to those with an inflammatory myopathy. Interestingly, patients with a fibrosing myopathy also tended to have lower muscle enzymes when compared to those with an inflammatory myopathy, and patients died of cardiac complications (i.e., nonischemic cardiomyopathy). The predominance of fibrosis on muscle biopsy was also reported in another case series of 35 SSc patients when compared to those with an inflammatory myopathy (80% vs. 32%, P < 0.05).
The treatment of SSc-associated myopathy is not well defined. The recently published data classify SSc-associated myopathy based on muscle histopathology, but it is not known if this is predictive of outcomes or should be better utilized to guide specific personalized treatment approaches in SSc-associated myopathy. While it is clear that those with a clear overlap myositis will respond to immunosuppression, it is not clear whether those with significant fibrosis on muscle biopsy will have the same response. In fact, in one case series, a lymphocytic infiltrate on muscle biopsy (identified in 2/3rd of cases) was associated with a more favorable response to corticosteroids (90% vs. 38% response rate). Future studies should examine the value of histological analysis of myopathy in predicting treatment response and outcomes in the context of SSc.
The clinical relevance of autoantibodies in systemic sclerosis-associated myopathy
Autoantibodies have proved reliable prognostic markers for a number of disease manifestations of SSc. This is also true of SSc-associated myopathy. In the aforementioned case–control study, anti-centromere antibodies were protective against SSc-myopathy (odds ratio [OR], 0.11), whereas the presence of antibodies targeting PM-Scl (OR, 5.0) and U1-RNP (OR, 6.9) was strongly associated with SSc-associated myopathy. Despite the aforementioned reported association between myopathy and dcSSc, antibodies targeting RNA polymerase III (4% of patients) and topoisomerase (9%) are not strongly associated with SSc-associated myositis. Unsurprisingly, the antibodies most commonly associated with lcSSc (anti-centromere and anti-Th/To) are also weakly associated with SSc-myositis (1% and 6% of patients, respectively).
It is over 40 years since Wolfe et al. identified antibodies targeting a novel antigen present in a high proportion of patients with myositis (but not other diseases), that they termed anti-PM-1. A subsequent work noted an association between this antibody and a strong SSc clinical phenotype (RP, sclerodactyly, proximal scleroderma, telangiectases, and interstitial lung disease [ILD]) in over half of the patients, resulting in the re-designation of this antibody as anti-PM-Scl. The strong clinical SSc phenotype (particularly RP, ILD and sclerodactyly), in comparison with other IIMs, has been confirmed on subsequent studies [Figure 2]. Overall, antibodies targeting PM-Scl are identified in between 2.5% and 10.6% of cases of SSc, and typically associated with either the lcSSc subtype (88%) and/or overlap syndromes., The 75 kDa subunit is the major antigen target of anti-PM-Scl antibodies, although there is some evidence that patients carrying antibodies targeting the 100 kDa subunit have a higher creatine kinase elevation. Overall, a raised creatine kinase is present in around 35% of patients carrying anti-PM-Scl (compared with 6%–8% of all SSc patients). Muscle weakness is only present in around 1/3rd of patients with anti-PM-Scl at presentation, but over 90% will develop myopathy at some stage during the disease course, typically affecting the upper limbs more often than in other forms of IIM. Antibodies to PM-Scl have the strongest association with myopathy overall (58% prevalence of myopathic features in SSc patients), followed by antibodies to U1-RNP (27%, see later) and U3-RNP (18% with myopathy in a cohort of whom ~1/3rd were African-American).,
Overall, the features of SSc (such as RP) are present in ~40% of patients with a diagnosis of IIM carrying anti-PM-Scl antibodies. This rises to 78%–100% when the clinical features of unselected anti-PM-Scl-positive patients are reported, allowing more of those whose clinical phenotype may be more consistent with SSc to be included., One cohort of IIM patients carrying anti-PM-Scl, noted that 30% of the patients also fulfilled classification criteria for SSc with clinical features such as RP (78%), sclerodactyly (66%), telangiectases (66%), gastro-esophageal reflux disease (61%), puffy hands (39%), and calcinosis cutis (39%), more commonly identified in PM-Scl-positive patients compared with patients with anti-synthetase syndrome, diabetes mellitus, or immune-mediated necrotizing myopathy. It was noted that even when the overt features of IIM or SSc did not allow a diagnosis to be made in patients carrying PM-Scl antibodies, there were often still features of SSc-spectrum disorders such as ILD [Figure 2].
A rarer antibody that occurs in patients with polymyositis–scleroderma overlap are anti-Ku antibodies (targeting DNA-binding proteins). Anti-Ku antibodies are occasionally identified in SLE, rheumatoid arthritis, Sjogren's syndrome, or as part of an undifferentiated connective tissue disease, sometimes in conjunction with other autoantibodies [Figure 1]. They are present in only 1%–2% of patients with isolated clinical features of SSc or SLE, but found in 33%–55% of patients with SLE-SSc-polymyositis overlap syndromes. A recent study that combined several large SSc registries identified anti-Ku antibodies in 1.1% of SSc patients (24/2140), around half of whom (13/24) had no other antibodies. SSc patients with single-specificity anti-Ku antibodies had higher prevalence of ILD (58% vs. 34%) and raised creatine kinase levels (>3 × normal) at both baseline (11% vs. 1%) and during follow-up (10% vs. 2%). Patients with anti-Ku fall within two distinct clusters comprising those with a strong SLE phenotype characterized by raised dsDNA (associated with glomerulonephritis) or those with a stronger SSc/IIM phenotype characterized by a raised creatine kinase (associated with ILD)., Lung disease in patients with Ku autoantibodies has also been reported to have more corticosteroid-resistant disease.
The most recently identified SSc-specific antibody to be associated with myositis in SSc is anti-RUV-BL1/2. Anti-RuvBL1/2
antibodies are identified in ~2% of SSc cases and associated with dcSSc in overlap with myositis. In contrast to anti-PM-Scl and anti-Ku, anti-RuvBL1/2 antibodies are associated with an older age of onset, male sex, and diffuse skin involvement.
Other causes of myopathy in systemic sclerosis-spectrum disorders
While no longer typically included in the modern management of SSc, there have been a number of reports of myositis occurring following D-penicillamine use in rheumatic disease such as SSc., An early report of the clinical experience of D-penicillamine in SSc noted mortality from cardiomyopathy in ~10% of cases, although this was attributed to the disease rather than the intervention. Other forms of myopathy (e.g., neuromuscular disease) should also be considered in the work of SSc patients with myopathic features.
| Systemic Lupus Erythematosus|| |
Burden of myopathy in systemic lupus erythematosus
Musculoskeletal manifestations in SLE have a major impact on health-related quality of life. The most common musculoskeletal manifestations of SLE are inflammatory arthritis and fibromyalgia, each of which could impact on the assessment of myopathy in SLE depending on the definition applied. While myositis is a recognized manifestation of SLE, it is less well studied compared with myositis in other rheumatic diseases such as SSc. The first major assessment of myopathy in SLE examined the records of 228 patients with SLE, identifying prominent muscle involvement in 18 (8%) of the cohort. Consistent with the aforementioned study of SSc, this preliminary work suggested that serum aldolase may be a better marker than creatine kinase for assessing muscle involvement in SLE. This early work also noted that up to 20% of patients carried antibodies to either U1-RNP and/or PM-Scl (then termed PM-1), which may partly account for early observations that that myopathy in SLE seldom occurred in the presence of renal involvement. Indeed, early reports of lupus myositis consistently reported an association with a more favorable disease course. While some of the earliest studies suggested that SLE was associated with a milder myopathy, a prospectively identified cohort study which used the Bohan and Peter criteria found very similarly elevated creatine kinase and objective muscle weakness between IIM and SLE myositis groups. This study also suggested that patients with SLE myositis were more likely to be female and younger at disease onset, than patients with other forms of IIM. A more recent large retrospective study evaluated the prevalence of myositis in 1718 SLE cases (including 451 pediatric patients) identified during a 9-year period. They found an overall prevalence of myopathy in SLE of around 6%, similar to earlier studies. Of the 108 SLE myositis patients in this cohort, myositis was a presenting feature in 64% [as seen in the case described in [Figure 3] and myositis preceded the diagnosis of SLE in 15%. In those where it was not a presenting feature, myositis occurred on an average of 5.25 years after SLE diagnosis. Applying a more stringent definition of myopathy (requiring the presence of objective muscle weakness, raised creatine kinase, and abnormal EMG), another recent cross-sectional study of over 1700 SLE patients identified a point prevalence of myopathy of only 2.6%. The prevalence of myositis may be higher in pediatric populations with one estimate of 31% within a US cohort in Alabama (based on symptoms, objective weakness, raised muscle enzymes, and/or MRI findings).
|Figure 3: Myositis in newly diagnosed systemic lupus erythematosus. A 49-year-old male presented with arthralgia, malaise, and plasma viscosity 2.22 (Normal range < 1.74). He developed fever, myalgia, proximal weakness, synovitis, and neutropenia. The CpK rose from normal (a) to 3400 (b). He had positive ds-DNA (59.9 IU/mL) and low complement. (b) Magnetic resonance imaging revealed symmetrical edema within sartorius3a (s), tensor fascia lata (tfl), and rectus femoris (rf); (c) Treatment with pulsed intravenous methylprednisolone and mycophenolate mofetil resulted in resolution of symptoms and normalization of creatine kinase, ds-DNA, and complements |
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The distribution of myopathy can differ in SLE in comparison with other forms of IIM. Early studies of lupus myopathy noted a predilection for disuse muscle atrophy in proximity to the affected joint inflammation, that was distinct from a true inflammatory myopathy. Orbital myositis is a specific rare manifestation of SLE,, although impaired extraocular muscle movement can also occur secondary to focal tenosynovitis.
Clinical and serological characteristics associated with systemic lupus erythematosus myopathy
The enormous overlap across the ARDs is again highlighted by the observation that almost half of the SLE-associated IIM patients had at least two features of SSc, with 28% of patients fulfilling classification criteria for SSc (many carrying U1-RNP or myositis-associated antibodies), once again emphasizing the futility of considering these disorders truly distinct. An association with Black ethnicity and pediatric-onset SLE has also been noted. A number of studies have also demonstrated an association between myositis and other specific SLE manifestations including arthritis (up to 94% in one study,) leukopenia, thrombocytopenia, hypocomplementemia, and mucocutaneous and pulmonary diseases., A negative association has been observed with the presence of renal disease. High SLE disease activity, as measured by the SLE Disease Activity Index, has also been shown to be independently associated with the presence of myositis, suggesting as seen in case 3 that myositis is often present in conjunction with other manifestations of active SLE.
As with SSc-associated myopathy, serological studies can help predict the likelihood of myopathy in SLE, particularly anti-U1-RNP (found in up to 77% of SLE myositis cases) and raised dsDNA antibodies [Figure 3]. Patients with anti-Ku antibodies with a strong SLE phenotype characterized by raised dsDNA (often associated with glomerulonephritis) appear to be less likely to develop myopathy than patients with stronger SSc clinical phenotype., Interestingly, one study also found the presence of anti-phospholipid antibodies in 71% of SLE myositis patients. However, only 20% of the cohort had clinical antiphospholipid syndrome, which is similar to the prevalence in the SLE population as a whole.
Histological findings in systemic lupus erythematosus
Abnormal muscle histology is common in SLE. Studies examining muscle biopsies in SLE have identified two major histological patterns. A lymphocytic vasculitis is often associated with a raised erythrocyte sedimentation rate, arthritis, and sicca symptoms (often with antibodies to Ro/La), whereas a true inflammatory myositis is typically associated with a raised creatinine kinase, proximal myopathy, and U1-RNP antibodies. Several studies have also described cases of necrotizing myositis on biopsy.,
Other causes of myopathy in systemic lupus erythematosus
High cumulative exposure to corticosteroids was thought to be a common cause of chronic myopathy in SLE, prior to the emergence of effective steroid-sparing treatment strategies., Hydroxychloroquine myopathy is another potential explanation for acute myositis in the context of SLE. Myopathy is thought to occur in around 1%–1.2% of people treated with antimalarial therapy, and the risk is considered to be higher with chloroquine than hydroxychloroquine., Unilateral myositis (typically lower limb), in association with fever and adjacent joint inflammation, should prompt consideration of pyomyositis in SLE, particularly in patients receiving corticosteroids.
| Mixed Connective Tissue Disease|| |
No clinical diagnosis better encapsulates the considerable overlap that exists across the ARDs than the disease entity known as mixed connective tissue disease (MCTD). As the name implies, MCTD is the archetypal overlap syndrome, and the presence of an (often low grade) steroid-responsive inflammatory myopathy in overlap with features of other ARDs represents one of the defining characteristics of patients carrying antibodies targeting U1-RNP. It was the identification of autoantibodies targeting ribonucleoproteins in patients with a clinical phenotype comprising features of SLE, SSc, and polymyositis, that resulted in the term MCTD. Subsequent efforts to identify and characterize the clinical phenotype of patients carrying what was subsequently characterized to be anti-U1RNP antibodies, consistently identified a high prevalence of RP, swollen hands, inflammatory arthralgia, and myopathy. Whereas these antibodies were found to occur in ~ 15% of patients with a clinical diagnosis of SSc (of whom around 27% have an associated myopathy) and a smaller proportion of patients with SLE (10%); they were virtually never found within cohorts of patients with a clinical diagnosis of isolated IIM, highlighting the overlap features with myopathy that characterize the presence of these antibodies., MCTD is particularly strongly associated with the co-existence of myositis with clinical features of SSc such as RP and of SLE such as inflammatory arthralgia and mucocutaneous lesions. The aforementioned early study examining myopathy in SSc, noted the presence of anti-U1RNP antibodies in half of the patients designated as having a “complicated myopathy” with muscle enzyme levels and EMG findings that more closely resembled that of IIM controls. Furthermore, as previously mentioned, Bitencourt et al. found that 77% of SLE patients with myositis has u1-RNP antibodies.
| Conclusions|| |
SSc, SLE, and IIM are each part of a unified clinicoserological spectrum of disease [Figure 4]. Consistent with the considerable overlap of clinical features across the ARDs and shared etiopathogenic pathways, it is unsurprising that features of inflammatory myopathy are common in both SLE and SSc. The exclusion of myopathic features in classification criteria for both SSc and SLE should not dissuade clinicians from making a clinical diagnosis of either SLE or SSc, where the overriding clinical features indicate the presence of one of these disorders.
|Figure 4: The clinicoserological spectrum of overlap connective tissue disease. The square boxes reflect the clinical diagnosis, with the oval shapes representing the common clinical characteristics (and relative frequency) of relevant antibody specificities. For example, anti-Ku antibodies, meanwhile, can be found in systemic sclerosis, systemic lupus erythematosus, overlap systemic lupus erythematosus/myositis, or overlap systemic sclerosis/myositis. The mixed connective tissue disease is frequently diagnosed in all patients with anti-U1 RNP antibodies, although only a minority of patients with this antibody will truly have overlap features of systemic lupus erythematosus, systemic sclerosis, and myositis|
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Similarly, clinicians need to be alert to the possibility of inflammatory myopathy in both SSc and SLE, and it is prudent to routinely inquire about myopathic symptoms and incorporate an assessment of muscle strength during physical examination (and consider assessing muscle enzymes in routine serum biochemistry), particularly early in the disease course and during periods of increased disease activity. Open muscle biopsy should be considered in patients with elevated muscle enzymes and/or objective muscle weakness, particularly if there is doubt as to the cause (e.g., disease-related or iatrogenic) or if myopathy is refractory to immunomodulatory treatments (when alternative genetic or metabolic forms of myopathy may need to be excluded). The identification and characterization of antibodies targeting PM-Scl, U1-RNP, Ku, RuvBL-1/2, and others has provided considerable insight into the clinicoserological relationship between myopathy and ARDs [Table 1], in addition to providing a valuable prognostic marker to alert clinicians to the possibility of future muscle involvement in ARDs.
|Table 1: Summary of clinicoserological spectrum of myopathy in the context of scleroderma/systemic sclerosis and systemic lupus erythematosus with respect to major overlap antibody specificities|
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Financial support and sponsorship
JJP is supported by NIAMS K23 AR073927.
Conflicts of interest
There are no conflicts of interest.
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