Serum CCL18 is predictive for lung disease progression and mortality in systemic sclerosis.
نویسندگان
چکیده
While we accept that there is a group of ILD patients in whom a specific ILD diagnosis is not possible, despite all efforts, we wish to encourage respiratory physicians to pursue an accurate ILD diagnosis, rather than accepting a diagnosis of unclassifiable ILD without full and accurate investigation. Although this is a tempting option, particularly in the absence of ready access to MDD, it is associated with more diagnostic and prognostic uncertainty, and ultimately may delay specific treatment options.
منابع مشابه
Serum CC chemokine ligand-18 predicts lung disease worsening in systemic sclerosis.
Elevated serum CC chemokine ligand (CCL)18 reflects lung fibrosis activity in systemic sclerosis (SSc) and could be an early marker of lung function worsening. Therefore, we sought to evaluate whether serum CCL18 levels at baseline could predict worsening of lung disease in SSc. In this prospective study, 83 SSc patients were analysed longitudinally over a 4-yr observation period for the risk o...
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Interstitial lung disease (ILD) is a major cause of morbidity and mortality in patients with systemic sclerosis (SSc). Although a large proportion of SSc patients have only limited interstitial involvement with an indolent course, in a significant minority ILD is progressive, requiring prompt treatment and careful monitoring. One of the main challenges for the clinician treating this highly var...
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OBJECTIVE In diffuse parenchymal lung diseases, the evolution of pulmonary fibrosis is often devastating and may result in death. In this study the role of CCL18 as a biomarker of disease activity in idiopathic interstitial pneumonias (IIPs) and systemic sclerosis (SSc) with lung involvement was evaluated. METHODS CCL18 was assessed in supernatants of cultured bronchoalveolar lavage (BAL) cel...
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OBJECTIVE To examine the predictive significance of 2 pneumoproteins, surfactant protein D (SP-D) and CC-chemokine ligand 18 (CCL18), for the course of systemic sclerosis (SSc)-related interstitial lung disease. METHODS The pneumoproteins were determined in the baseline plasma samples of 266 patients with early SSc enrolled in the GENISOS observational cohort. They also were measured in 83 fo...
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Background: Systemic sclerosis is an autoimmune disease affecting connective tissues, (including epidermal, subepidermal, microvasculature, etc.), leading to various extent of end-organ damage. The leading cause of mortality among these patients is lung involvement. The cardiovascular events happen more frequently in patients suffering systemic scleroderma, comparing to healthy population. This...
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عنوان ژورنال:
- The European respiratory journal
دوره 43 5 شماره
صفحات -
تاریخ انتشار 2014