Introduction

Tuberc Respir Dis (Seoul)

TRD

Tuberculosis and Respiratory Diseases

1738-35362005-6184

The Korean Academy of Tuberculosis and Respiratory Diseases

31172701

6778739

10.4046/trd.2019.0009

Review Article

Interstitial Lung Disease

Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases: Part 5. Connective Tissue Disease Associated Interstitial Lung Disease

https://orcid.org/0000-0003-1504-9387

Koo

So-My

M.D.1*

https://orcid.org/0000-0001-8627-486X

Kim

Song Yee

M.D.Ph.D.2*

https://orcid.org/0000-0002-0742-6085

Choi

Sun Mi

M.D.3

https://orcid.org/0000-0003-1032-0190

Lee

Hyun-Kyung

M.D.Ph.D.4on behalf of Korean Interstitial Lung Diseases Study Group

1Division of Allergy and Respiratory Medicine, Department of Internal Medicine, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, Seoul, Korea.2Division of Pulmonology, Department of Internal Medicine, Severance Hospital, Institute of Chest Diseases, Yonsei University College of Medicine, Seoul, Korea.3Division of Pulmonary and Critical Care Medicine, Department of Internal Meidicine, Seoul National University Hospital, Seoul, Korea.4Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Inje University Busan Paik Hospital, Busan, Korea.

Address for correspondence: Sun Mi Choi, M.D. Division of Pulmonary and Critical Care Medicine, Department of Internal Meidicine, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul 03080, Korea. Phone: 82-2-2072-4915, Fax: 82-2-762-9662, sunmich81@gmail.comAddress for co-correspondence: Hyun-Kyung Lee, M.D., Ph.D. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Inje University Busan Paik Hospital, 75 Bokji-ro, Busanjin-gu, Busan 47392, Korea. Phone: 82-51-890-6847, Fax: 82-51-890-6341, goodoc@gmail.com

^*So-My Koo and Song Yee Kim contributed equally to this work.

102019

3152019

824285297012201908420191042019

2019

The Korean Academy of Tuberculosis and Respiratory Diseases

It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/)

Connective tissue disease (CTD) is a collection of disorders characterized by various signs and symptoms such as circulation of autoantibodies in the entire system causing damage to internal organs. Interstitial lung disease (ILD) which is associated with CTD is referred to as CTD-ILD. Patients diagnosed with ILD should be thoroughly examined for the co-occurrence of CTD, since the treatment procedures and prognosis of CTD-ILD are vary from those of idiopathic interstitial pneumonia. The representative types of CTD which may accompany ILD include rheumatoid arthritis, systemic sclerosis (SSc), Sjögren's syndrome, mixed CTD, idiopathic inflammatory myopathies, and systemic lupus erythematous. Of these, ILD most frequently co-exists with SSc. If an ILD is observed in the chest, high resolution computed tomography and specific diagnostic criteria for any type of CTD are met, then a diagnosis of CTD-ILD is made. It is challenging to conduct a properly designed randomized study on CTD-ILD, due to low incidence. Therefore, CTD-ILD treatment approach is yet to been established in absence of randomized controlled clinical trials, with the exception of SSc-ILD. When a patient is presented with acute CTD-ILD or if symptoms occur due to progression of the disease, steroid and immunosuppressive therapy are generally considered.

Lung Disease, InterstitialConnective Tissue DiseaseAsian Continental Ancestry GroupGuidelines as TopicDiagnosisDisease ManagementLung

Introduction

Connective tissue disease (CTD) is a disorder characterized by diverse symptoms and signs as autoantibodies circulate in the system, causing damage to internal organs. Interstitial lung disease (ILD) associated with CTD is called CTD-ILD.

At an early stage in diagnosing ILD, it is very important to examine the patient with respect to the existence of various causes of ILD. Of the known causes of ILD, CTD is the most crucial. If ILD is diagnosed in a CTD patient and conversely, if CTD is diagnosed in an ILD patient, CTD-ILD is diagnosed. It is very critical to determine the existence of CTD in ILD patients, because there are significant differences between CTD-ILD and idiopathic interstitial pneumonia (IIP) in terms of both treatment approach and prognosis. Some CTD-ILD patients present with ILD prior to the CTD diagnosis. Therefore, even in those not previously diagnosed with CTD, any clinical symptoms suggestive of CTD, autoantibody test, and chest X-ray findings should be thoroughly checked to determine the existence of CTD.

Classification and Clinical Features of CTD-ILD

The incidence and clinical features of CTD-ILD differ depending on the form of the associated CTD. Across various types of ILD, the incidence of systemic sclerosis (SSc) is the highest, followed by idiopathic inflammatory myopathies (IIM), rheumatoid arthritis (RA), systemic lupus erythematous (SLE), and Sjögren's syndrome.

1. RA associated ILD

ILD is the most common among RA-associated lung diseases, but the prevalence varies depending on the patient group or diagnostic method1. A wide range of RA associated ILD (RA-ILD) prevalence rates, 19%–44%, has been reported in prospective studies using chest high resolution computed tomography (HRCT)2345, because each author used different ILD definitions and diagnostic methods. A cross-sectional study in which chest HRCT was performed at an RA clinic regardless of respiratory symptoms reported an ILD prevalence of 19%. In the study, chest HRCT had a higher sensitivity in diagnosing ILD than pulmonary function tests (PFT)6.

Although RA is more common among women, RA-ILD is reported to be more common in men. Some studies reported a male-to-female ratio of 2:178. Typically, it occurs in patients in their 40s and 50s, and age and smoking history are known risk factors of ILD91011. Rheumatoid factor and anti-cyclic citrullinated peptide were also found to be strongly associated with the occurrence of ILD12131415161718. In RA-ILD, the most common pathological finding in surgical lung biopsy is usual interstitial pneumonia (UIP)19.

2. SSc associated ILD

SSc, also called scleroderma, has a lower incidence but a higher level of pulmonary infiltration compared with RA. Pulmonary function abnormalities due to ILD are observed in as high as 70% of SSc patients, and about a third of the patients show clinically significant evidence of ILD1. Chest HRCT is essential for diagnosing SSc associated ILD (SSc-ILD), and the most common chest HRCT finding is non-specific interstitial pneumonia (NSIP)20. In general, ILD is common in patients with diffuse SSc, a condition in which internal organs as well as the skin are involved, and the autoantibody profile was found to correlate with pulmonary infiltration212223. The autoantibody most commonly found in patients with diffuse SSc is anti-topoisomerase I, also known as anti-scl-70. It has been reported that ILD occurred in 85% of anti-scl-70 positive patients and that the antibody concentration level was correlated with the severity and activity of ILD2425.

Fibrotic NSIP is the most common pattern in the pathological findings of SSc-ILD, and cellular NSIP is found in less than 10% of patients. Typical features of idiopathic pulmonary fibrosis, such as severe fibrosis and fibroblastic foci, are observed in less than 30% of cases with UIP262728.

SSc-ILD patients are at greatest risk for ILD progression in the first 3–4 years (45%–55%), and some patients show rapid pulmonary function decline during this time. Accordingly, PFT should be performed on a regular basis. Treatment should be considered in SSc-ILD patients under the following conditions: (1) if at the time of the initial diagnosis of ILD, ILD involvement exceeds 20% in chest HRCT, or forced vital capacity (FVC) is less than 70% of the predicted value in PFT, or (2) if diffusing capacity of the lungs for carbon monoxide (DLCO) is over 15% or FVC over 10% in a follow-up PFT629.

SSc-ILD in conjunction with pulmonary arterial hypertension (PAH) is a major cause of death among SSc patients30. SSc accompanied by ILD and PAH was found to have 5 times higher mortality risk than that of SSc accompanied by PAH alone31.

3. Sjögren's syndrome associated ILD

Studies have reported that pulmonary infiltration occurs in 9%–24% of all patients with Sjögren's syndrome, and that abnormal findings in PFT, bronchoalveolar lavage (BAL), and chest HRCT were observed in 75% of patients with asymptomatic Sjögren's syndrome32333435. Generally, pulmonary infiltration manifests in the end stage of Sjögren's syndrome and rarely occurs as the first manifestation36.

In Sjögren's syndrome, not only interstitial tissues in the lung but the entire respiratory system could be infiltrated, and so the patient could also present with small airway disease such as follicular bronchiolitis, aside from ILD. In whatever form, 10-year mortality increases by more than 4 times in Sjögren's syndrome patients with pulmonary infiltration compared to those without32.

NSIP is the most common pathological finding. Studies have found NSIP in 28%–61% of all patients with the syndrome, and additionally, lymphocytic interstitial pneumonia (LIP) in 17%3738.

4. Mixed connective tissue disease associated ILD

Mixed connective tissue disease (MCTD) was defined in 1972 for the first time, and there is still a controversy around this category. Generally, it refers to an autoimmune disease with positive anti-U1 ribonucleoprotein antibody. Pulmonary infiltration is quite common in MCTD, found in 47%–78% of patients3940. According to the literature, severe ILD occurred in approximately 19% of MCTD patients, and it was associated with anti-Ro-52 antibody but not with disease duration or smoking history4142.

5. IIM associated with ILD

IIM include polymyositis (PM), dermatomyositis (DM), and clinically amyopathic dermatomyositis, in each of which a varying degree of skin, muscle, joint, and lung infiltration is present. IIM associated with ILD (IIM-ILD) shows a variety of disease progression patterns from asymptomatic to rapidly progressive4344. The prevalence of ILD in IIM is also found to vary considerably, between 20%–78%, and comorbidity and mortality rates are reported to generally increase if ILD co-exists45464748. In IIM-ILD versus other CTD types, ILD more frequently occurs as the very first manifestation before it progresses to a systematic disease49505152.

Antisynthetase syndrome (AS) is a specific subset of IIM, with positive antisynthetase antibodies associated with protein synthesis. It is a syndrome characterized by the co-occurrence of ILD and the presence of some of the following manifestations: fever, joint pain, Raynaud's phenomenon, and mechanic's hands. Of various muscle-specific antibodies, anti-Jo-1 antibody is most commonly used in the diagnosis. As can be seen in the inclusion of ILD as an essential element in diagnosing AS, the importance of ILD in assessment of prognosis is also great. Like other types of IIM-ILD, AS-ILD too shows diverse disease progression patterns. It has been reported that approximately 50% of patients develop acute respiratory failure515354.

6. SLE associated with ILD

In SLE, pulmonary infiltration occurs in as high as 33%–50% of patients. But, in most patients, the entire respiratory system (thoracic cavity, lung parenchyma, airway, and pulmonary vessels) is infiltrated, and pulmonary infiltration of the pattern shown in ILD tends to be relatively infrequent (1%–15%) compared to other types of CTD435556. It has been reported that the longer the duration of SLE (over 10 years), the higher the risk of ILD57 and that SLE is strongly associated with ILD in the presence of Raynaud's phenomenon, positive response to anti-U1 RNP antibody, sclerodactyly, nailfold capillary loops, and old age5859.

Diagnosis of CTD-ILD1. Assessment of disease history and the presence of CTD1) Patients already diagnosed with CTD

If ILD co-occurs in patients already diagnosed with CTD based on CTD diagnostic criteria, it is relatively easy to make a diagnosis of CTD-ILD. But the possibility of ILD occurring due to a drug used to treat CTD or infection should be excluded33560616263.

2) Patients never diagnosed with CTD

In some patients, ILD appears as the first manifestation among diverse clinical features of CTD. Such cases are most commonly observed in IIM (approximately 10%–30%), and additionally, the pattern is reported in some RA patients, and also in SSc patients though very rare6465.

If a patient without notable disease history rapidly develops dyspnea over several weeks to several months and eventually experiences respiratory failure while chest HRCT shows a ground glass opacity that is gradually progressing, the possibility of CTD-ILD should be considered. Particularly, if the level of muscle enzymes (e.g., creatinine phosphokinase, and aldolase) increases, IIM should be suspected as the underlying disease65. Even in cases with chronic ILD, CTD could be the underlying disease. Hence, whether or not the patient presents any symptom or other manifestation suggestive of CTD, this possibility should be considered (Table 1)66. For instance, Raynaud's phenomenon, dry eye and mouth, and muscle weakness tend to have low specificity, but the specificity of mechanic's hands (Figure 1A) or Gottron's papules (Figure 1B) is high. Thus, if mechanic's hands or Gottron's papules are present, DM is highly likely to be an underlying disease67. Such systemic symptoms or other manifestations that raise a suspicion of CTD often occur in women under age 5068697071.

2. Radiologic findings (chest HRCT findings)

It is not possible to differentiate IIP and CTD-ILD based on radiologic findings. CTD-ILD often manifests itself in NSIP or organizing pneumonia (OP), or LIP (albeit rare) (Figure 2A–C), and IIP most often manifests itself in UIP (Figure 3). Thus, if a typical UIP is not found in an imaging test, CTD is likely to be the underlying disease60. An exception is that a radiologic finding of UIP is the most common in RA-ILD, and is often found in SSc-ILD, as well. The prognosis of RA-ILD is known to be poor in patients with a UIP pattern compared to those without UIP60.

The radiologic pattern of ILD in CTD-ILD patients differs according to CTD type. In RA, UIP is the most common (50%–60%); in SSc, NSIP is the most common radiologic finding (80%–90%), although UIP is also found in as many as 10%–20%; in MCTD, NSIP is the most common; and, in PM and DM, NSIP, OP, UIP, and diffuse alveolar damage may be found65.

3. Surgical lung biopsy

It is still controversial whether surgical lung biopsy should be performed to confirm the diagnosis when CTD-ILD is suspected. The prognosis may differ depending on the pathological finding (UIP vs. others), and with biopsy, differential diagnoses of other diseases as well as ILD are possible. But, complications may occur following surgical lung biopsy, and thus the decision should be made by considering the pros and cons. In some patients, BAL is an alternative to biopsy, and using this procedure, infection can be excluded and the number of cells is estimated65.

Because a specific pathology does not exist in CTD-ILD, IIP and CTD-ILD cannot be completely differentiated based on pathological findings alone. However, because the proportion of NSIP is high in CTD-ILD, the presence or absence of underlying CTD should be looked for if NSIP is found on pathological analysis2872737475767778.

In addition, among those with CTD-ILD with a UIP pattern there were more germinal centers, lymphoid hyperplasia, plasma cells, and fewer fibroblastic foci and honeycombing, compared with cases of IIP with UIP. If the aforementioned features are found in conjunction with UIP, the presence or absence of CTD should be examined, because the co-occurrence of lymphocytic or follicular bronchiolitis is common (Figure 4)7980818283.

4. Autoantibodies

When a patient is diagnosed with ILD, autoantibody testing should be performed to determine the likelihood of CTD-ILD. As shown in Table 2, cases exist in which an autoantibody is found but the clinical features do not correspond to the diagnosis of CTD or do not meet specific CTD diagnostic criteria. However, since such patients may present clinical features of CTD later, continuous follow-up is required and consultation with a rheumatologist for the symptoms is necessary6465.

Treatment of CTD-ILD1. Acute presentations of CTD-ILD

Acute presentation of CTD-ILD manifests itself in de novo acute interstitial pneumonia or an acute exacerbation of underlying CTD65. The treatment approach for acute exacerbation of CTD-ILD has not yet been established, but conventionally, it is treated using intravenous methylprednisolone (1 g/day intravenously for 3 days) followed by oral prednisolone (1 mg/kg/day). Cyclosporine (500–750 mg/m² intravenously) and cyclophosphamide (CYC) (2–3 mg/kg/day) may additionally be administered (Table 3). Despite immunosuppressive therapy, patients presenting an acute exacerbation often need a ventilator and the mortality rate is high (83.3%)658485.

2. Chronic presentations of ILD

The fundamental treatment of CTD-ILD is to tackle the primary cause of CTD. Evidence regarding treatment effect in CTD-ILD is lacking, because comparison group studies have not been conducted with the exception of SSc-ILD. Consensus has not yet formed regarding treatment initiation for CTD-ILD, but conventionally, a steroid or immunosuppressive drug is administered in patients in whom clinical features are severe, symptoms have recently started to progress, or the duration of systemic disease has been short86. Lung transplantation may be considered if the patient does not respond to drug therapy and ILD worsens.

1) Initial treatment of CTD-ILD

For the initial treatment of CTD-ILD, steroids are commonly used, but the recommendation as to which steroid is appropriate is undecided. The dose, route of administration, treatment duration, and dose tapering vary according to individual patients' clinical picture and the clinician's impression (Table 4)65. As the most common ILD form in IIM-ILD patients is OP, prednisolone 1 mg/kg/day is often used, i.e., the dose at which clinicians are relatively experienced in the treatment of cryptogenic organizing pneumonia (COP). However, treatment response to the therapy is reported to be low in the all forms of IIM-ILD except COP87.

Azathioprine (1–2 mg/kg/day) is often administered as combination therapy with a steroid to treat CTD-ILD, but evidence regarding monotherapy is insufficient88. A retrospective survival analysis conducted on 192 IIM-ILD patients showed lower mortality in the group administered with azathioprine (hazard ratio, 0.35; 95% confidence interval, 0.16–0.74; p=0.0064)47, but there is no evidence of an improvement in the survival rate in other forms of CTD-ILD.

CYC is the only immunosuppressive investigated in a randomized controlled trial. In SSc-ILD, FVC was improved after 1-year treatment in oral CYC (2 mg/kg/day) group compared with the control group89. Evidence on pulmonary function improvement is lacking in other types of CTD-ILD aside from SSc-ILD.

In a study with 125 patient cases with SSc-ILD, IIM-ILD, and RA-ILD, mycophenolate mofetil (MMF; 1.0–1.5 g bid) showed a reduction in the required dose of steroid and an improvement in FVC90. In addition, a recent randomized controlled trial with SSc-ILD patients demonstrated that the effect of MMF was similar to that of CYC91.

A retrospective study in IIM-ILD patients found that compared to the groups administered with CYC or cyclosporine in combination with a steroid, the group in whom tacrolimus was added had more favorable event-free survival92. The typical dose of tacrolimus is 1–3 mg/day65.

Currently, a randomized controlled trial with rapidly progressive CTD-ILD (including SSC-ILD, IIM-ILD, and MCTD-ILD) is under way to compare the effects of CYC and rituximab with FVC improvement as the primary endpoint93.

Table 5 summarizes treatment options for each CTD-ILD.

2) Treatment of SSc-ILD

(1) PICO for treatment of patients with SSc-ILD: In SSc-ILD, is CYC more effective compared with placebo?

(2) Summary of recommendations for the treatment of patients with SSc-ILD: We suggest that the use of CYC may be considered in consultation with an expert, in some SSc-ILD patients experiencing dyspnea and reduced pulmonary function (weak recommendation, level of evidence; low).

FVC, total lung capacity (TLC), dyspnea, and quality of life index improved in the patient group administered with oral CYC over 1 year compared to placebo. A 1-year follow up after treatment termination showed that the improvement in dyspnea was maintained, but other indices returned to the levels prior to drug administration. Thus, evidence for long-term effectiveness of CYC is not sufficient, but it improved dyspnea and had a short-term effect in improving pulmonary function.

The effect of CYC in SSc-ILD patients has been reported in a considerable number of studies, but most of the studies were retrospective. Even the prospective studies tend to lack a comparison group or be observational. The authors conducted a systematic literature review on randomized placebocontrolled studies to investigate whether CYC has a positive effect on various SSc-ILD related indices such as the rate of pulmonary function decline, severity of dyspnea, quality of life, and functional ability. But the authors could not conduct meta-analysis because there was only one randomized placebo-controlled trial on CYC, i.e., Tashkin et al.'s Scleroderma Lung Study (SLS)89 published in N Engl J Med in 2006.

In SLS, 158 symptomatic SSc-ILD patients in whom disease activity was confirmed on either BAL or chest HRCT were randomly assigned to one of two groups, a group treated with CYC (2 mg/kg/day) for a year and a placebo group. During the study period, patients could be treated with prednisolone up to 10 mg/day. If an FVC reduction of 15% versus the baseline continued over 1 month from month 3 after treatment initiation, it was considered as treatment failure and the patient was unblinded and treated with CYC. The primary endpoint of the study was the FVC (expressed as a percentage of the predicted value) at 1 year after adjusting for baseline values and treatment group. Secondary endpoints were TLC, change in DLCO, disability index of health assessment questionnaire (HAQ), SF-36, transitional dyspnea index (TDI), and skin thickness score. Between-group difference in FVC change after 1 year of CYC administration was 2.53% (95% confidence interval, 0.28–4.79; p<0.03), indicating that treatment with CYC significantly slowed down the rate of FVC reduction. Of the secondary endpoints, TLC, HAQ, TDI, and skin thickness score were significantly improved in the CYC group in comparison to the placebo group.

Side effects of CYC that occurred during the study were hematuria (hemorrhagic cystitis), leukopenia, neutropenia, anemia, pneumonia, etc.8994. Therefore, it is recommended to regularly perform blood test and use mesna for the prevention of hemorrhagic cystitis, in patients treated with CYC. Long-term use of the drug is not recommended because of increased risk for bladder cancer and other malignant diseases.

After the completion of this SLS study, the researchers followed up the patients for an additional 1 year without administering a drug in order to investigate the duration of drug effect94. During the additional 1-year follow-up, if treatment failure (an FVC reduction over 15% compared to the baseline) occurred in either group, the patient was treated with CYC or an immunosuppressive according to the clinician's decision. During the 1-year follow-up, between-group differences in FVC and TLC were significant for the first 6 months, that is, the drug effect was maintained for a total of 18 months from the start of the study. But group difference disappeared by month 12 after treatment termination (that is, 24 months after the start of the study). An additional analysis showed a larger drug effect in patients with FVC less than 70%. On the other hand, the improvement of TDI (an index of dyspnea) was maintained up to month 12 after treatment termination94.

In summary, a year-long treatment with CYC administration improved pulmonary function, dyspnea, and quality of life and the effects were maintained up to 6 months after treatment termination. One year after treatment termination, two groups still showed a significant difference in dyspnea but not in FVC or TLC. Based on the improvement of dyspnea that was maintained as long as 1 year after treatment termination and a short-term improvement of pulmonary function, CYC may be useful in some SSc-ILD patients. Thus, in SSc-ILD patients experiencing dyspnea and reduced FVC, a short-term use of CYC may be considered in consultation with an expert.

Regarding drugs other than CYC, first, a study showed that steroid therapy (0.5–1 kg/kg of prednisolone) could be expected to slow down pulmonary function decline95, though the effect of steroid in treatment of SSc-ILD is controversial. High dose steroid is not recommended because renal crisis can rapidly develop if the daily dose of prednisolone is over 10 mg86.

MMF has been known to suppress lymphoproliferation and to have an antifibrotic effect. A recently presented randomized comparison group study, Scleroderma Lung Study II (SLS II), compared a patient group administered with MMF (1,500 mg bid) for 24 months and a patient group administered with CYC (2 mg/kg/day) for 12 months. There was little difference in the speed of FVC reduction between the MMF group and the CYC group, and the counts of leucocytes and platelets in the MMF group did not decrease as much as in the CYC group91. Based on the findings, MMF may be considered as initial and maintenance therapies in the treatment of SSc-ILD.

Lately, hematopoietic stem cell transplantation (HSCT) has been attempted in SSc-ILD patients. A randomized controlled trial that compared the effects of HSCT and CYC reported that HSCT helped improve long-term event-free survival and overall survival, but recurrence rate was higher96. Accordingly, HSCT may be considered in cases in which patients did not respond to immunosuppressive therapy or the disease had progressed.

In an open-label randomized controlled trial that investigated rituximab (a B cell depletion therapy) in SSc-ILD, the drug showed an effect of increasing FVC and DLCO 1 year after commencement of therapy97. However, the study included only 12 patients in the sample, which is very small. So far, there is not enough evidence regarding rituximab, and large-scale randomized comparison group research is needed98. As for now, it is believed that patients not responding to the currently available immunosuppressives may be tested on rituximab in a limited manner.

Lung transplantation is the only treatment available to prolong survival of SSc-ILD patients not responding to drug therapy. To improve the prognosis following lung transplantation, suitable patient selection is important. A recent study has proposed the following as lung transplantation exclusion criteria: uncontrolled active inflammatory myopathies, active digital ulcerations, severe SSc associated gastrointestinal disease, cardiac arrhythmia, unstable renal function over the last 3 months, and high risk of SSc associated renal crisis99. However, standardized criteria have not yet been established and further research is warranted.

3) Treatment of RA-ILD

(1) PICO for treatment of patients with RA-ILD: In RA-ILD, do steroids and immunosuppressants (MMF, rituximab) slow the worsening of FVC compared with placebo?

(2) Summary of recommendations for the treatment of patients with RA-ILD: We suggest that, in clinically severe cases, the use of the steroid, MMF, and rituximab may be considered in consultation with an expert (recommendation; expert opinion, level of evidence; low).

If RA-ILD deteriorates despite administration of disease modifying antirheumatic drugs (DMARDs: RA treatment) and tumor necrosis factor inhibitors, conventionally high-dose prednisolone therapy is administered100. But, the evidence for the effectiveness and safety of drug therapy is weak100 and comparison group studies have never been conducted to evaluate drugs in RA-ILD patients.

The authors attempted a systematic literature review and meta-analysis on the effects of steroid and immunosuppressive therapy (MMF and rituximab) in RA-ILD, but could not perform comparative analysis because no study compared steroid or immunosuppressive therapy to placebo. Below are the findings reported in a few single-group studies that used steroid or immunosuppressive therapy such as MMF and rituximab in RA-ILD patients. In a retrospective cohort consisting of 40 RA-ILD patients, baseline FVC improved when prednisolone (1 mg/kg/day) was administered for 6 weeks and then tapered down to 10 mg/day while a DMARD was administered during a follow-up over 6–8 months101. A retrospective single-group study was conducted with 18 CTD-ILD patients including some with RA-ILD and it was found that pulmonary function stabilized and prednisolone maintenance dose decreased during a median of 2.5-year follow-up after treatment with MMF90. A prospective cohort study102 and two retrospective studies103104 with RA-ILD patients reported that rituximab stabilized pulmonary function. Also, it was reported that when rituximab (1,000 mg at day 1, 15, and again at weeks 24 and 26, with methotrexate) was used concomitantly with methotrexate, FVC was maintained in six out of seven RA-ILD patients after 48 weeks102. Also, some case studies reported that azathioprine105, abatacept106, tocilizumab107, and infliximab108 each stabilized pulmonary function in RA-ILD patients.

There is no clear consensus as to when to initiate treatment with the drugs mentioned above. Since no other drug has so far been demonstrated to be effective in RA-ILD, the use of steroids, MMF, or rituximab may be considered for clinically severe cases, in consultation with a specialist.

Prognosis of CTD-ILD

The prognosis of CTD-ILD patients varies according to the type of causative CTD. RA-ILD comprises 10%–20% of deaths among RA patients109, and 10% of deaths among all ILD patients789. In SSc-ILD, it is reported that 10-year survival following diagnosis lies in the range 29%–69%. and that in 45%–55% of the patients, pulmonary function deteriorates within the first 3 years, and in 16% severe restrictive pulmonary disease develops1. In Sjögren's syndrome the 5-year survival is reported to be 84%110.

If ILD progresses in spite of immunosuppressive therapy, lung transplantation may be considered. The prognosis of CTD-ILD after lung transplantation is reported to be not very different from that of lung transplantation in IIP patients.

Authors' Contributions:

Conceptualization: Choi SM, Lee HK.

Formal analysis: Koo SM, Km SY, Choi SM, Lee HK.

Data curation: Koo SM, Choi SM.

Writing - original draft preparation: Koo SM, Kim SY.

Writing - review and editing: Choi SM, Lee HK.

Approval of final manuscript: all authors.

Conflicts of Interest: No potential conflict of interest relevant to this article was reported.

Funding: No funding to declare.

Steen

Conte

Owens

Medsger

Severe restrictive lung disease in systemic sclerosis

Arthritis Rheum19943712831289

7945490

Fewins

McGowan

Whitehouse

Williams

Mallya

High definition computed tomography in rheumatoid arthritis associated pulmonary disease

Br J Rheumatol199130214216

2049584

Gabbay

Tarala

Will

Carroll

Adler

Cameron

Interstitial lung disease in recent onset rheumatoid arthritis

Am J Respir Crit Care Med19971562 Pt 1528535

9279235

McDonagh

Greaves

Wright

Heycock

Owen

Kelly

High resolution computed tomography of the lungs in patients with rheumatoid arthritis and interstitial lung disease

Br J Rheumatol199433118122

8162474

Cortet

Perez

Roux

Flipo

Duquesnoy

Delcambre

Pulmonary function tests and high resolution computed tomography of the lungs in patients with rheumatoid arthritis

Ann Rheum Dis199756596600

9389220

Winstone

Assayag

Wilcox

Dunne

Hague

Leipsic

Predictors of mortality and progression in scleroderma-associated interstitial lung disease: a systematic review

Chest2014146422436

24576924

Cavagna

Monti

Grosso

Boffini

Scorletti

Crepaldi

The multifaceted aspects of interstitial lung disease in rheumatoid arthritis

Biomed Res Int20132013

759760

24205507

de Lauretis

Veeraraghavan

Renzoni

Review series: aspects of interstitial lung disease: connective tissue disease-associated interstitial lung disease: how does it differ from IPF? How should the clinical approach differ?

Chron Respir Dis201185382

21339375

Bongartz

Nannini

Medina-Velasquez

Achenbach

Crowson

Ryu

Incidence and mortality of interstitial lung disease in rheumatoid arthritis: a population-based study

Arthritis Rheum20106215831591

20155830

Assayag

Lubin

Lee

King

Collard

Ryerson

Predictors of mortality in rheumatoid arthritis-related interstitial lung disease

Respirology201419493500

24372981

Saag

Kolluri

Koehnke

Georgou

Rachow

Hunninghake

Rheumatoid arthritis lung disease: determinants of radiographic and physiologic abnormalities

Arthritis Rheum19963917111719

8843862

Turesson

Extra-articular rheumatoid arthritis

Curr Opin Rheumatol201325360366

23425964

Doyle

Lee

Dellaripa

Lederer

Matteson

Fischer

A roadmap to promote clinical and translational research in rheumatoid arthritis-associated interstitial lung disease

Chest2014145454463

24590021

Kelly

Saravanan

Nisar

Arthanari

Woodhead

Price-Forbes

Rheumatoid arthritis-related interstitial lung disease: associations, prognostic factors and physiological and radiological characteristics: a large multicentre UK study

Rheumatology (Oxford)20145316761682

24758887

Ytterberg

Joshua

Reynisdottir

Tarasova

Rutishauser

Ossipova

Shared immunological targets in the lungs and joints of patients with rheumatoid arthritis: identification and validation

Ann Rheum Dis20157417721777

24817415

Aubart

Crestani

Nicaise-Roland

Tubach

Bollet

Dawidowicz

High levels of anti-cyclic citrullinated peptide autoantibodies are associated with co-occurrence of pulmonary diseases with rheumatoid arthritis

J Rheumatol201138979982

21362759

Luukkainen

Saltyshev

Pakkasela

Nordqvist

Huhtala

Hakala

Relationship of rheumatoid factor to lung diffusion capacity in smoking and non-smoking patients with rheumatoid arthritis

Scand J Rheumatol199524119120

7747143

Tuomi

Heliovaara

Palosuo

Aho

Smoking, lung function, and rheumatoid factors

Ann Rheum Dis199049753756

2241263

Lamblin

Bergoin

Saelens

Wallaert

Interstitial lung diseases in collagen vascular diseases

Eur Respir J Suppl20013269s80s

11816826

Desai

Veeraraghavan

Hansell

Nikolakopolou

Goh

Nicholson

CT features of lung disease in patients with systemic sclerosis: comparison with idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia

Radiology2004232560567

15286324

Walker

Tyndall

Czirjak

Denton

Farge-Bancel

Kowal-Bielecka

Clinical risk assessment of organ manifestations in systemic sclerosis: a report from the EULAR Scleroderma Trials And Research group database

Ann Rheum Dis200766754763

17234652

Zhang

Bonner

Hudson

Baron

Pope

Canadian Scleroderma Research Group

Association of gastroesophageal factors and worsening of forced vital capacity in systemic sclerosis

J Rheumatol201340850858

23547215

Wells

Margaritopoulos

Antoniou

Denton

Interstitial lung disease in systemic sclerosis

Semin Respir Crit Care Med201435213221

24668536

Briggs

Vaughan

Welsh

Myers

duBois

Black

Immunogenetic prediction of pulmonary fibrosis in systemic sclerosis

Lancet1991338661662

1679476

Fertig

Medsger

JrWright

Correlation of serum anti-DNA topoisomerase I antibody levels with disease severity and activity in systemic sclerosis

Arthritis Rheum20034813631373

12746909

Raghu

Collard

Egan

Martinez

Behr

Brown

An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management

Am J Respir Crit Care Med2011183788824

21471066

Solomon

Olson

Fischer

Bull

Brown

Raghu

Scleroderma lung disease

Eur Respir Rev201322619

23457159

Bouros

Wells

Nicholson

Colby

Polychronopoulos

Pantelidis

Histopathologic subsets of fibrosing alveolitis in patients with systemic sclerosis and their relationship to outcome

Am J Respir Crit Care Med200216515811586

12070056

Moore

Goh

Corte

Rouse

Hennessy

Thakkar

Extent of disease on high-resolution computed tomography lung is a predictor of decline and mortality in systemic sclerosis-related interstitial lung disease

Rheumatology (Oxford)201352155160

23065360

Steen

Medsger

Changes in causes of death in systemic sclerosis, 1972–2002

Ann Rheum Dis200766940944

17329309

Dellaripa

Fischer

Flaherty

Pulmonary manifestations of rheumatic disease: a comprehensive guideNew York

Springer

2014

Palm

Garen

Berge Enger

Jensen

Lund

Aalokken

Clinical pulmonary involvement in primary Sjogren's syndrome: prevalence, quality of life and mortality: a retrospective study based on registry data

Rheumatology (Oxford)201352173179

23192906

Ramos-Casals

Solans

Rosas

Camps

Gil

Del Pino-Montes

Primary Sjogren syndrome in Spain: clinical and immunologic expression in 1010 patients

Medicine (Baltimore)200887210219

18626304

Yazisiz

Arslan

Ozbudak

Turker

Erbasan

Avci

Lung involvement in patients with primary Sjogren's syndrome: what are the predictors?

Rheumatol Int20103013171324

19844720

Uffmann

Kiener

Bankier

Baldt

Zontsich

Herold

Lung manifestation in asymptomatic patients with primary Sjogren syndrome: assessment with high resolution CT and pulmonary function tests

J Thorac Imaging200116282289

11685093

Cain

Noble

Matthay

Pulmonary manifestations of Sjogren's syndrome

Clin Chest Med199819687699

9917960

Parambil

Myers

Lindell

Matteson

Ryu

Interstitial lung disease in primary Sjogren syndrome

Chest200613014891495

17099028

Sirianni

Milaninezhad

Chu

Walker

Alteration of fibroblast architecture and loss of Basal lamina apertures in human emphysematous lung

Am J Respir Crit Care Med2006173632638

16415275

Sharp

Irvin

Tan

Gould

Holman

Mixed connective tissue disease: an apparently distinct rheumatic disease syndrome associated with a specific antibody to an extractable nuclear antigen (ENA)

Am J Med197252148159

4621694

Tani

Carli

Vagnani

Talarico

Baldini

Mosca

The diagnosis and classification of mixed connective tissue disease

J Autoimmun201448-494649

24461387

Gunnarsson

Aalokken

Molberg

Lund

Mynarek

Lexberg

Prevalence and severity of interstitial lung disease in mixed connective tissue disease: a nationwide, cross-sectional study

Ann Rheum Dis20127119661972

22550317

Gunnarsson

El-Hage

Aalokken

Reiseter

Lund

Garen

Associations between anti-Ro52 antibodies and lung fibrosis in mixed connective tissue disease

Rheumatology (Oxford)201655103108

26320136

Fathi

Dastmalchi

Rasmussen

Lundberg

Tornling

Interstitial lung disease, a common manifestation of newly diagnosed polymyositis and dermatomyositis

Ann Rheum Dis200463297301

14962966

Lee

Chen

Tzen

Lin

Peng

Idiopathic inflammatory myopathy with diffuse alveolar damage

Clin Rheumatol200221391396

12223988

Chen

Jan Wu

Lin

Fan

Luo

Interstitial lung disease in polymyositis and dermatomyositis

Clin Rheumatol200928639646

19247576

Hayashi

Tanaka

Kobayashi

Nakazono

Satoh

Fukuno

High-resolution computed tomography characterization of interstitial lung diseases in polymyositis/dermatomyositis

J Rheumatol200835260269

18085731

Kuo

See

Shen

Chang

Survival analysis of patients with dermatomyositis and polymyositis: analysis of 192 Chinese cases

Clin Rheumatol20113015951601

21915609

Zeng

Guo

Tan

Tang

Luo

Predictive factors and unfavourable prognostic factors of interstitial lung disease in patients with polymyositis or dermatomyositis: a retrospective study

Chin Med J (Engl)2010123517522

20367973

Matsushita

Hasegawa

Fujimoto

Hamaguchi

Komura

Hirano

Clinical evaluation of anti-aminoacyl tRNA synthetase antibodies in Japanese patients with dermatomyositis

J Rheumatol20073410121018

17309126

Yoshifuji

Fujii

Kobayashi

Imura

Fujita

Kawabata

Anti-aminoacyl-tRNA synthetase antibodies in clinical course prediction of interstitial lung disease complicated with idiopathic inflammatory myopathies

Autoimmunity200639233241

16769657

Tillie-Leblond

Wislez

Valeyre

Crestani

Rabbat

Israel-Biet

Interstitial lung disease and anti-Jo-1 antibodies: difference between acute and gradual onset

Thorax2008635359

17557770

Kono

Nakamura

Enomoto

Hashimoto

Fujisawa

Inui

Usual interstitial pneumonia preceding collagen vascular disease: a retrospective case control study of patients initially diagnosed with idiopathic pulmonary fibrosis

PLoS One20149

e94775

24736601

Solomon

Swigris

Brown

Myositis-related interstitial lung disease and antisynthetase syndrome

J Bras Pneumol201137100109

21390438

Doyle

Dellaripa

Lung manifestations in the rheumatic diseases

Chest201715212831295

28552544

Mittoo

Fell

Pulmonary manifestations of systemic lupus erythematosus

Semin Respir Crit Care Med201435249254

24668539

Chua

Higton

Colebatch

O'Reilly

Grubnic

Vlahos

Idiopathic inflammatory myositis-associated interstitial lung disease: ethnicity differences and lung function trends in a British cohort

Rheumatology (Oxford)20125118701876

22763991

Eisenberg

Dubois

Sherwin

Balchum

Diffuse interstitial lung disease in systemic lupus erythematosus

Ann Intern Med1973793745

4124484

ter Borg

Groen

Horst

Limburg

Wouda

Kallenberg

Clinical associations of antiribonucleoprotein antibodies in patients with systemic lupus erythematosus

Semin Arthritis Rheum199020164173

2287941

Ward

Polisson

A meta-analysis of the clinical manifestations of older-onset systemic lupus erythematosus

Arthritis Rheum19893212261232

2803325

Perez

Farre

Gosset

Wallaert

Duquesnoy

Voisin

Subclinical alveolar inflammation in rheumatoid arthritis: superoxide anion, neutrophil chemotactic activity and fibronectin generation by alveolar macrophages

Eur Respir J19892713

2540025

Doyle

Hunninghake

Rosas

Subclinical interstitial lung disease: why you should care

Am J Respir Crit Care Med201218511471153

22366047

Gochuico

Avila

Chow

Novero

Ren

Progressive preclinical interstitial lung disease in rheumatoid arthritis

Arch Intern Med2008168159166

18227362

Launay

Remy-Jardin

Michon-Pasturel

Mastora

Hachulla

Lambert

High resolution computed tomography in fibrosing alveolitis associated with systemic sclerosis

J Rheumatol20063317891801

16960939

Cottin

Idiopathic interstitial pneumonias with connective tissue diseases features: a review

Respirology201621245258

26212251

Mathai

Danoff

Management of interstitial lung disease associated with connective tissue disease

BMJ2016352

h6819

26912511

Cottin

Significance of connective tissue diseases features in pulmonary fibrosis

Eur Respir Rev201322273280

23997055

Mosca

Tani

Bombardieri

A case of undifferentiated connective tissue disease: is it a distinct clinical entity?

Nat Clin Pract Rheumatol20084328332

18414458

Kinder

Collard

Koth

Daikh

Wolters

Elicker

Idiopathic nonspecific interstitial pneumonia: lung manifestation of undifferentiated connective tissue disease?

Am J Respir Crit Care Med2007176691697

17556720

Corte

Copley

Desai

Zappala

Hansell

Nicholson

Significance of connective tissue disease features in idiopathic interstitial pneumonia

Eur Respir J201239661668

21920896

Nunes

Schubel

Piver

Magois

Feuillet

Uzunhan

Nonspecific interstitial pneumonia: survival is influenced by the underlying cause

Eur Respir J201545746755

25537566

Moua

Zamora Martinez

Baqir

Vassallo

Limper

Ryu

Predictors of diagnosis and survival in idiopathic pulmonary fibrosis and connective tissue disease-related usual interstitial pneumonia

Respir Res201415154

25472884

Park

Kim

Park

Jang

Kitaichi

Nicholson

Prognosis of fibrotic interstitial pneumonia: idiopathic versus collagen vascular disease-related subtypes

Am J Respir Crit Care Med2007175705711

17218621

Kim

Elicker

Maldonado

Webb

Ryu

Van Uden

Usual interstitial pneumonia in rheumatoid arthritis-associated interstitial lung disease

Eur Respir J20103513221328

19996193

Tansey

Wells

Colby

Nikolakoupolou

du Bois

Variations in histological patterns of interstitial pneumonia between connective tissue disorders and their relationship to prognosis

Histopathology200444585596

15186274

Kim

Interstitial lung disease in rheumatoid arthritis: recent advances

Curr Opin Pulm Med200612346353

16926650

Cottin

Thivolet-Bejui

Reynaud-Gaubert

Cadranel

Delaval

Ternamian

Interstitial lung disease in amyopathic dermatomyositis, dermatomyositis and polymyositis

Eur Respir J200322245250

12952255

Douglas

Tazelaar

Hartman

Decker

Schroeder

Polymyositis-dermatomyositis-associated interstitial lung disease

Am J Respir Crit Care Med200116411821185

11673206

Cottin

Pragmatic prognostic approach of rheumatoid arthritis-associated interstitial lung disease

Eur Respir J20103512061208

20513909

Fischer

du Bois

Interstitial lung disease in connective tissue disorders

Lancet2012380689698

22901890

Antin-Ozerkis

Rubinowitz

Evans

Homer

Matthay

Interstitial lung disease in the connective tissue diseases

Clin Chest Med201233123149

22365251

Song

Kim

Jang

Colby

Kim

Pathologic and radiologic differences between idiopathic and collagen vascular disease-related usual interstitial pneumonia

Chest20091362330

19255290

Fischer

West

Swigris

Brown

du Bois

Connective tissue disease-associated interstitial lung disease: a call for clarification

Chest2010138251256

20682528

Devouassoux

Cottin

Liote

Marchand

Frachon

Schuller

Characterisation of severe obliterative bronchiolitis in rheumatoid arthritis

Eur Respir J20093310531061

19129282

Suda

Kaida

Nakamura

Enomoto

Fujisawa

Imokawa

Acute exacerbation of interstitial pneumonia associated with collagen vascular diseases

Respir Med2009103846853

19181509

Bradley

Branley

Egan

Greaves

Hansell

Harrison

Interstitial lung disease guideline: the British Thoracic Society in collaboration with the Thoracic Society of Australia and New Zealand and the Irish Thoracic Society

Thorax200863 Suppl 5v1v58

18757459

Wallace

Vummidi

Khanna

Management of connective tissue diseases associated interstitial lung disease: a review of the published literature

Curr Opin Rheumatol201628236245

27027811

Aggarwal

Oddis

Therapeutic advances in myositis

Curr Opin Rheumatol201224635641

22955021

Hoyles

Ellis

Wellsbury

Lees

Newlands

Goh

A multicenter, prospective, randomized, double-blind, placebo-controlled trial of corticosteroids and intravenous cyclophosphamide followed by oral azathioprine for the treatment of pulmonary fibrosis in scleroderma

Arthritis Rheum20065439623970

17133610

Tashkin

Elashoff

Clements

Goldin

Roth

Furst

Cyclophosphamide versus placebo in scleroderma lung disease

N Engl J Med200635426552666

16790698

Fischer

Brown

Du Bois

Frankel

Cosgrove

Fernandez-Perez

Mycophenolate mofetil improves lung function in connective tissue disease-associated interstitial lung disease

J Rheumatol201340640646

23457378

Tashkin

Roth

Clements

Furst

Khanna

Kleerup

Mycophenolate mofetil versus oral cyclophosphamide in scleroderma-related interstitial lung disease (SLS II): a randomised controlled, double-blind, parallel group trial

Lancet Respir Med20164708719

27469583

Kurita

Yasuda

Amengual

Atsumi

The efficacy of calcineurin inhibitors for the treatment of interstitial lung disease associated with polymyositis/dermatomyositis

Lupus20152439

25297551

Saunders

Tsipouri

Keir

Ashby

Flather

Parfrey

Rituximab versus cyclophosphamide for the treatment of connective tissue disease-associated interstitial lung disease (RECITAL): study protocol for a randomised controlled trial

Trials201718275

28619061

Tashkin

Elashoff

Clements

Roth

Furst

Silver

Effects of 1-year treatment with cyclophosphamide on outcomes at 2 years in scleroderma lung disease

Am J Respir Crit Care Med200717610261034

17717203

Ando

Motojima

Doi

Nagaoka

Kaneko

Aoshima

Effect of glucocorticoid monotherapy on pulmonary function and survival in Japanese patients with scleroderma-related interstitial lung disease

Respir Investig2013516975

Burt

Shah

Dill

Grant

Gheorghiade

Schroeder

Autologous non-myeloablative haemopoietic stem-cell transplantation compared with pulse cyclophosphamide once per month for systemic sclerosis (ASSIST): an open-label, randomised phase 2 trial

Lancet2011378498506

21777972

Daoussis

Liossis

Tsamandas

Kalogeropoulou

Kazantzi

Sirinian

Experience with rituximab in scleroderma: results from a 1-year, proof-of-principle study

Rheumatology (Oxford)201049271280

19447770

Lam

Hummers

Woods

Wigley

Efficacy and safety of etanercept in the treatment of scleroderma-associated joint disease

J Rheumatol20073416361637

17611970

Launay

Savale

Berezne

Le Pavec

Hachulla

Mouthon

Lung and heart-lung transplantation for systemic sclerosis patients: a monocentric experience of 13 patients, review of the literature and position paper of a multidisciplinary Working Group

Presse Med20144310 Pt 2e345e363

25027464

100

Assayag

Lee

King

Rheumatoid arthritis associated interstitial lung disease: a review

Medicina (B Aires)201474158165

24736263

101

Rojas-Serrano

Gonzalez-Velasquez

Mejia

Sanchez-Rodriguez

Carrillo

Interstitial lung disease related to rheumatoid arthritis: evolution after treatment

Reumatol Clin201286871

22341526

102

Matteson

Bongartz

Ryu

Crowson

Hartman

Dellaripa

Open-label, pilot study of the safety and clinical effects of rituximab in patients with rheumatoid arthritis-associated interstitial pneumonia

Open J Rheumatol Autoimmune Dis201225358

103

Keir

Maher

Ming

Abdullah

de Lauretis

Wickremasinghe

Rituximab in severe, treatmentrefractory interstitial lung disease

Respirology201419353359

24286447

104

Chartrand

Swigris

Peykova

Fischer

Rituximab for the treatment of connective tissue disease-associated interstitial lung disease

Sarcoidosis Vasc Diffuse Lung Dis201632296304

26847096

105

Cohen

Miller

Spiera

Interstitial pneumonitis complicating rheumatoid arthritis. Sustained remission with azathioprine therapy

Chest197772521524

908223

106

Mera-Varela

Perez-Pampin

Abatacept therapy in rheumatoid arthritis with interstitial lung disease

J Clin Rheumatol201420445446

25417684

107

Mohr

Jacobi

Interstitial lung disease in rheumatoid arthritis: response to IL-6R blockade

Scand J Rheumatol201140400401

21961704

108

Dellaripa

Fry

Willoughby

Arndt

Angelakis

Campagna

The treatment of interstitial lung disease associated with rheumatoid arthritis with inflixima

Chest2003124109S

109

Marigliano

Soriano

Margiotta

Vadacca

Afeltra

Lung involvement in connective tissue diseases: a comprehensive review and a focus on rheumatoid arthritis

Autoimmun Rev20131210761084

23684699

110

Ito

Nagai

Kitaichi

Nicholson

Johkoh

Noma

Pulmonary manifestations of primary Sjogren's syndrome: a clinical, radiologic, and pathologic study

Am J Respir Crit Care Med2005171632638

15579729

Figure 1(A) Mechanic's hand, cracking and fissuring along the sides of the digits and palm. (B) Gottron's papules, red and scaly papules that erupt on the metacarpophalangeal joints. (C) Sclerodactyly, fixed fingers in a semi-flexed position with tightened and wax like skin. (D) Digital ulceration, an ulceration on the tip of index finger. (E) Telangiectasias, multiple dilated facial small vessels. (F) Heliotrope rash, violaceous erythema on the upper eyelids (The patient provided verbal consent for the picture).Figure 2(A) Radiologic pattern of non-specific interstitial pneumonia in a patient with systemic sclerosis. High resolution computed tomography (HRCT) image shows bilateral subpleural and basal predominant fine reticular pattern and ground-glass opacity. (B) Radiologic pattern of organizing pneumonia in a patient with dermatomyositis. HRCT image shows multiple peripheral patch consolidations. (C) Radiologic pattern of lymphocytic interstitial pneumonia in a patient with Sjögren's syndrome. HRCT image shows multifocal variable-sized, thin-walled, cystic lesions on both lungs.Figure 3Radiologic pattern of usual interstitial pneumonia in a patient with rheumatoid-arthritis. High resolution computed tomography image shows bilateral subpleural honeycombing and reticular opacity with traction bronchiectasis.Figure 4Histopathology of the lung in a patient with interstitial pneumonia with autoimmune features. (A) Usual interstitial with lymphoid follicles (×10). (B) Lymphoid bronchiolitis (×100). (C) lymphoplasmacytoid cell infiltrates (×200). Hematoxylin eosin saffron. Courtesy of Prof. Shim HS, Yonsei University.

Table 1Core manifestations in ILD patients to diagnose underlying CTD<xref rid="B66-trd-82-285" ref-type="bibr">66</xref>

Organ	Manifestations to check
Peripheral circulation	Raynaud phenomenon
Skin	Sclerodactyly (Figure 1C)
	Digital ulcerations or scars
	Telangiectasia (Figure 1D, E)
	Gottron's sign
	Heliotrope rash around the eyes
	Heliotrope rash in the neck, upper chest and shoulder area (Figure 1F)
	Photosensitivity
	Mechanics' hands
Joint	Joint pain, joint swelling
	Morning stiffness (over 60 minutes)
Muscle	Muscle aches, muscle weakness
Mouth and eye	Dry mouth, dry eye (Sicca syndrome)

ILD: interstitial lung disease; CTD: connective tissue disease.

Table 2Types and significance of autoantibodies<xref rid="B65-trd-82-285" ref-type="bibr">65</xref>

Test	Interpretation
Antinuclear antibody	It is nonspecific, but the likelihood of CTD is high if the titer is high
Rheumatoid factor	It may increase in RA, but is nonspecific in other types of CTD
Scl-70	Associated with SSc
RNP	Associated with MCTD
SSA, SSB	Associated with Sjögren's syndrome
Anti-CCP	Associated with RA
ANCA	It may be observed in pure ILD, though rare
Jo-1	Myositis-specific antibody
Tests associated with other types of myositis
Antisynthetase	PL-7, PL-12, EJ, and OJ antibodies → all associated with ILD
MDA-5	Associated with invasive Gottron's papules and severe ILD
PMScl	Associated with polymyostis co-occurring with sclerosis
Ro-52	Associated with severe ILD
CPK, Aldolase	Muscle enzymes. It may increase in myositis, but may be normal in clinically amyopathic dermatomyositis

CTD: connective tissue disease; RA: rheumatoid arthritis; SSc: systemic sclerosis; RNP: ribonucleoprotein; MCTD: mixed connective tissue disease; CCP: cyclic citrullinated peptide; ANCA: antineutrophil cytoplasmic antibody; ILD: interstitial lung disease.

Table 3Summary of acute presentation of CTD-ILD

Causative factor	Infection
	Pulmonary embolism
	Coronary artery disease
	De novo cardiac arrhythmia
	Pulmonary edema
	Pneumothorax
	Surgery, especially lung biopsy
Risk factor	Pulmonary hypertension associated with ILD
Risk factor	Air pollution, especially exposure to ozone and nitrogen dioxide
Treatment	Broad spectrum antibiotics to treat typical and atypical bacterial-infection
	Test and treatment of Pneumocystis jirovecii and other fungal infection based on immunosuppression risk factors
	Discontinue drug treatment if drug toxicity is suspected
	Methylprednisolone pulse therapy (daily infusion of 1 g for 3 days)

CTD-ILD: connective tissue disease associated with interstitial lung disease.

Table 4Initial treatment of CTD-ILD<xref rid="B85-trd-82-285" ref-type="bibr">85</xref>

Classification	Most types of CTD-ILD (with an exception of SSc-ILD)
Dose	Initial dose: prednisolone 0.5–1 mg/kg
	Maintenance dose: tapered to prednisolone 10 mg/day or lower
Steroid tapering guidance	Oral or intravenous cyclophosphamide or concurrent use of oral azathioprine

CTD-ILD: connective tissue disease associated interstitial lung disease (ILD); SSc-ILD: systemic sclerosis associated ILD.

Table 5Summary of treatment of CTD-ILD

	Treatment
SSc-ILD	Cyclophosphamide, MMF
	Rituximab can be used
RA-ILD	Steroid, MMF, and rituximab can be considered
DM/PM-ILD	Steroid, MMF, azathioprine, tacrolimus, and rituximab can be considered
Other CTD-ILD	Steroid
	Cyclophosphamide or azathioprine according to the steroid tapering

CTD-ILD: connective tissue disease associated interstitial disease (ILD); SSc-ILD: systemic sclerosis associated ILD; MMF: mycophenolate mofetil; RA-ILD: rheumatoid arthritis associated ILD; DM/PM-ILD: dermatomyositis/polymyositis associated ILD.