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"apellidos" => "Rello" "referencia" => array:3 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] ] ] "afiliaciones" => array:4 [ 0 => array:3 [ "entidad" => "Vall d’Hebron Institute of Research, Universitat Autónoma de Barcelona, Barcelona, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Centro de Investigaciones Biomédicas en Red (CIBERES), Mallorca, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Servicio de Medicina Intensiva, Hospital Universitario Vall d’Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Servicio de Neumología, Hospital Universitario Vall d’Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain" "etiqueta" => "d" "identificador" => "aff0020" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Papel de los biomarcadores en el diagnóstico diferencial de la insuficiencia respiratoria aguda en el postoperatorio inmediato del trasplante pulmonar" ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">In the last 20 years, lung transplantation has become an established practise for prolonging survival among patients with advanced-stage lung disease. According to the registry of the International Society for Heart and Lung Transplantation,<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> a total of 3272 transplants were carried out in the year 2009, and during the first month mortality was fundamentally attributable to primary graft dysfunction (PGD) (27.1%), followed by infections (20.1%). In turn, almost 4% suffered acute rejection.</p><p id="par0010" class="elsevierStylePara elsevierViewall">Thus, lung transplant recipients are at a high risk of developing many complications during the immediate postoperative period, including PGD, acute graft rejection of the development of infections, as commented above. The most frequent manifestation in all these clinical conditions is acute respiratory failure (ARF). For this reason, the differential diagnosis of these conditions can be very difficult to establish, and may have important consequences, since the treatment required in each case differs in certain aspects. Thus, in the presence of acute rejection, we need to increase the level of immunosuppression; in the case of PGD, immunosuppression must be lowered; and in patients with infections we must prescribe antibiotic treatment. In this context, although the diagnosis of PGD is fundamentally clinical, distinction between rejection and infection often requires histological evaluation of the samples obtained by fibrobronchoscopy with transbronchial biopsy. The use of this technique is limited, however, since it is invasive and has potential complications that can prove serious – particularly in patients with severe ARF.</p><p id="par0015" class="elsevierStylePara elsevierViewall">Despite the existence of preventive measures against PGD,<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> such as the optimization of lung preservation, the minimization of ischemia time, and the avoidance of barotrauma during lung donor maintenance, once the damage has been established, the treatment is similar to that applied in patients with respiratory distress syndrome. In any case, a survival rate of 80% in the first year after transplantation, and of 50% after 5 years of follow-up, is considered acceptable.</p><p id="par0020" class="elsevierStylePara elsevierViewall">The fact that the lungs are in direct contact with the exterior, among other factors, contribute to the need for high levels of immunosuppression; despite such immunosuppression, however, the acute rejection rates remain high.<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Different biomarkers have been investigated with the aim of improving and anticipating the diagnosis of these disorders. A biomarker is defined as a parameter or characteristic that can be objectively measured and evaluated as an indicator of normal biological processes, pathological conditions, or responses to drug treatment.<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> An ideal biomarker is a parameter that can be recorded quickly from a sample obtained in a minimally invasive manner, and which is simple to preserve and handle. In addition, an ideal biomarker should be sensitive, reproducible, predictive and cost-effective. The lack of biological markers capable of predicting the early onset, progression and severity of disease has had a negative impact upon the identification and development of effective drug treatments for improving morbidity and mortality among critical patients.</p><p id="par0030" class="elsevierStylePara elsevierViewall">Many biomarkers potentially useful for the differential diagnosis of post-transplantation ARF have been studied. However, their use in daily clinical practise is very limited, since the available supporting evidence is scarce. The present study offers a clinical review of the available evidence referred to the usefulness of the different biomarkers in application to the differential diagnosis of ARF in the immediate postoperative period of lung transplantation.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Primary graft dysfunction</span><p id="par0035" class="elsevierStylePara elsevierViewall">Primary graft dysfunction (PGD) is a form of acute lung injury occurring in the immediate post-transplantation period, and which has been defined by the consensus document of the International Society for Heart and Lung Transplantation as hypoxemia manifesting in the first 72<span class="elsevierStyleHsp" style=""></span>h after lung transplantation, with pulmonary infiltrates evidenced on the chest X-rays.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> The prevalence of PGD ranges widely from 10–40%,<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6,7</span></a> and its appearance has prognostic implications, since it is associated with increased morbidity-mortality in the Intensive Care Unit (ICU).<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6,8,9</span></a> At clinical level, PGD has been almost exclusively associated with ischemic damage occurring during lung preservation and posterior reperfusion–though factors related to donor maintenance may also play an important role.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> The physiopathology of PGD is characterized by an increase in the concentration of inflammatory and endothelial and epithelial dysfunction biomarkers.<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">11,12</span></a> For this reason, an analysis has been made of the usefulness of different biomarkers in the diagnosis of primary graft dysfunction, taking into account the degree of PGD (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Cytokines</span><p id="par0040" class="elsevierStylePara elsevierViewall">Cytokines are low molecular weight proteins secreted by different immune cells. They play a key role in inflammation and in regulation of the immune response. Different studies have examined the usefulness of cytokine determination in the diagnosis of PGD. In this sense, it has been shown that elevated interleukin 8 (IL-8) levels in the immediate post-transplantation period are significantly correlated to the subsequent development of PGD.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a> On the other hand, studies of changes in the expression of different cytokines and chemokines during the immediate post-transplantation period<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a> have revealed an increase in the plasma levels of monocyte chemotactic protein-1 (MCP-1) and IP-10, a protein induced by gamma-interferon (IFN-γ), implicated in the recruitment of monocytes and lymphocytes, in those patients that develop PGD. These results suggest that macrophage activation induced by IFN-γ, and the attraction of monocytes and effector T cells, could play an important role in the pathogenesis of PGD. In fact, there are data indicating that IP-10 could be an important factor in cardiac and renal post-transplantation injury.<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15–19</span></a> On the other hand, the concentration of interleukin 6 (IL-6), in both bronchoalveolar lavage (BAL) and in plasma, measured in the first hours after transplantation, is directly related to the development of PGD.<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">20</span></a> Likewise, elevated IL-8 concentrations in donor BAL favor the development of PGD and imply a prolongation of mechanical ventilation in the transplant recipient.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Receptor for advanced glycation end products</span><p id="par0045" class="elsevierStylePara elsevierViewall">Studies have also been made of the usefulness of receptor for advanced glycation end products (RAGE) in the diagnosis of PGD after lung transplantation. RAGE is a marker of type I alveolar cell damage,<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">21</span></a> and is a receptor of the immunoglobulin family.<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">22</span></a> RAGE is present in different tissues, and is expressed at low concentrations under normal conditions. Over-regulation of this marker has been associated to different disorders ranging from atherosclerosis to Alzheimer's disease.<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">23</span></a> Although its function at lung level has not been clarified, RAGE is regarded as a marker of the severity of acute lung injury.<a class="elsevierStyleCrossRefs" href="#bib0120"><span class="elsevierStyleSup">24–26</span></a> In lung transplant patients, a positive correlation has been reported between RAGE in donor BAL and the subsequent development of PGD in the recipient.<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> Likewise, an association has been observed between increased plasma concentrations of the marker 6 and 24<span class="elsevierStyleHsp" style=""></span>h after lung transplantation and the development of PGD.<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> On the other hand, it has been reported that the plasma concentration of RAGE four hours after graft perfusion may be of prognostic significance–high plasma RAGE being correlated to a prolongation of mechanical ventilation and stay in the ICU after transplantation.<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">P-selectin</span><p id="par0050" class="elsevierStylePara elsevierViewall">Another of the proposed biomarkers for predicting PGD is P-selectin, a platelet activation marker.<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">30–33</span></a> Previous studies have shown neutrophil adhesion to the pulmonary vascular endothelium, diapedesis, and infiltration of the vessel wall to be a key event in the development of PGD.<a class="elsevierStyleCrossRefs" href="#bib0170"><span class="elsevierStyleSup">34,35</span></a> In this sense, the platelets are involved in neutrophil sequestration, activation and mobilization toward the interstitial and alveolar space. In lung transplant patients with PGD, the plasma P-selectin levels have been correlated to the appearance of grade III PGD.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a></p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Clara cell secretory protein</span><p id="par0055" class="elsevierStylePara elsevierViewall">Another proposed biomarker is Clara cell secretory protein, which appears to participate in the repair and protection of the respiratory epithelium, in toxin detoxification, and in the production of surfactant.<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> A positive correlation has been observed between plasma Clara cell secretory protein levels in the immediate post-transplantation period and the development of PGD.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a> These results support the importance of epithelial damage in the origin of PGD.</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Protein C and plasminogen activator inhibitor</span><p id="par0060" class="elsevierStylePara elsevierViewall">Protein C and plasminogen activator inhibitor (PAI-1) have also been proposed as biomarkers of PGD, and have been the subject of a multicenter study comprising 6 centers and 128 patients.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> The results showed a decrease in protein C and an increase in PAI-1 before transplantation and 6, 24, 48 and 72<span class="elsevierStyleHsp" style=""></span>h after transplantation to be associated with the development of grade III PGD–thus evidencing the importance of coagulation markers in the development of PGD.</p></span></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Acute rejection</span><p id="par0065" class="elsevierStylePara elsevierViewall">Acute rejection is also a frequent complication in the immediate postoperative period of lung transplantation. Its estimated incidence is 36% in the first year after transplantation, and compared with other organs, the lungs appear to be at an increased risk of rejection.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a> On the other hand, the appearance of acute rejection can have important consequences for patient prognosis, since immunosuppressive treatment of acute rejection episodes increases the risk of infections.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a> As has been commented above, the clinical characteristics of the disease are very similar to those of other complications that manifest during the same period, and this complicates the diagnosis. To date, bronchoscopy with the obtainment of a transbronchial biopsy has been the technique of choice for diagnosing acute rejection. Very few biomarkers have been investigated in application to the diagnosis of acute graft rejection (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>).</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Thioredoxin</span><p id="par0070" class="elsevierStylePara elsevierViewall">Some studies have analyzed the usefulness of thioredoxin, a protein that regulates oxidative metabolism<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a> and which exerts antiinflammatory effects in different tissues.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> Results of initial studies in experimental models revealed an association between the appearance of acute graft rejection and high levels of this protein.<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a> More recently, studies have been made of the levels of thioredoxin in BAL and in transbronchial biopsy samples from transplant patients.<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">43</span></a> The results show an increase in the concentration of thioredoxin in BAL of patients with histological criteria of acute graft rejection.</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Pepsin</span><p id="par0075" class="elsevierStylePara elsevierViewall">Pepsin is an enzyme that hydrolyzes proteins in the stomach. Consequently, when found in respiratory samples, pepsin indicates the aspiration of gastric contents. Studies of the concentration of pepsin in BAL samples of lung transplant patients have revealed higher pepsin concentrations in patients presenting acute rejection.<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">44</span></a> These results suggest that acute rejection is conditioned not only by immunological factors but also by direct aggression upon the grafted organ, such as that resulting from the microaspiration of gastric contents.</p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Cytokines</span><p id="par0080" class="elsevierStylePara elsevierViewall">Interleukin 16 (IL-16) is a CD4 receptor ligand that participates in antigen presentation. It is known that CD4+ lymphocytes are implicated in the development of acute rejection, and that IL-16 can inhibit the activity of this complex.<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">45</span></a> Its concentration has been shown to decrease in episodes of acute rejection,<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">45</span></a> in the same way as the levels of TGF-β in CD4+ and CD8+ blood cells. In contrast, the levels of gamma-interferon and tumor necrosis factor-alpha (TNF-α) have been seen to increase in these same cells in BAL samples,<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a> thus suggesting synergic action of both molecules, with activation of the development of acute rejection through the activation of epithelial cells, and demonstrating that acute rejection episodes are associated to a decrease in the levels of Th3 type cytokines (TGF-β) and an increase in the levels of type Th1 cytokines (IFN-γ and TNF-α).</p></span></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Infection</span><p id="par0085" class="elsevierStylePara elsevierViewall">Despite the experience gained in the field of lung transplantation, supported by advances in the form of new surgical techniques and the introduction of new immunosuppressor drugs, the infections which transplant recipients may develop in the postoperative period are an important cause of morbidity and mortality. This problem is particularly manifest in the immediate postoperative period, since it is in this period when the risk of acute rejection is greater and higher levels of immune suppression are therefore needed.<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">47</span></a> Moreover, the patient is in the hospital setting, with an increased risk of nosocomial infections. <a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a> shows the main biomarkers related to the development of the different infectious processes.</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Cytokines</span><p id="par0090" class="elsevierStylePara elsevierViewall">Studies have been made of the usefulness of the determination of IL-6 and interleukin 10 (IL-10) concentrations in the diagnosis of cytomegalovirus (CMV) infection.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">48</span></a> The results revealed an increase in the concentration of IL-6 in plasma and in BAL samples from patients colonized by CMV. However, the great variability observed in the concentration of IL-6 between different patients made it difficult to establish its usefulness in predicting the appearance of CMV infection. In contrast, no correlation to the levels of IL-10 was observed.</p></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Galactomannan antigen</span><p id="par0095" class="elsevierStylePara elsevierViewall">Another pathogen that can colonize the graft in this same time period is <span class="elsevierStyleItalic">Aspergillus</span> spp. Approximately 6–16% of all patients may be colonized by <span class="elsevierStyleItalic">Aspergillus</span>, and some studies have shown 9% of all post-transplantation deaths to be attributable to invasive aspergillosis.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">49</span></a> In recent years, the detection of galactomannan antigen in hematological patients has been found to be reliable in establishing an early diagnosis of <span class="elsevierStyleItalic">Aspergillus</span> infection.<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">50</span></a> Such detection can be made in BAL or serum samples, though serum assaying yields a larger number of false-positive results.<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">50</span></a> In a study involving 60 post-transplantation BAL samples, 8 of which were diagnosed with invasive aspergillosis according to the criteria of the European Organization for Research and Treatment of Cancer/Mycoses study group in the diagnosis of invasive fungal diseases and radiological criteria, an optical density of 1.5 in the results was established as the best cutoff point for the diagnosis of this condition, with a sensitivity of 100% and a specificity of 90%.<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">50</span></a> However, the authors pointed out that the lack of a standard for the bronchoscopic technique poses an important limitation that must be taken into account when interpreting these results.</p></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Procalcitonin</span><p id="par0100" class="elsevierStylePara elsevierViewall">Procalcitonin (PCT) is a 116-amino acid peptide produced and secreted under normal conditions by the thyroid gland as a precursor of calcitonin. The basic inducer of OCT is bacterial wall lipopolysaccharide. In contrast, the secretion of PCT is not stimulated, or is very weakly stimulated, by viral infections and autoimmune processes. Moreover, PCT concentration appears to be closely related to the severity of respiratory infection of bacterial origin.<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">51</span></a></p><p id="par0105" class="elsevierStylePara elsevierViewall">Studies have been made of the plasma concentrations of PCT in the context of infections caused by <span class="elsevierStyleItalic">Pseudomonas aeruginosa</span> and <span class="elsevierStyleItalic">Pneumocystis jirovecii</span> in lung transplant patients. In this regard, the concentration of PCT was seen to increase with the presence of both infections,<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">52</span></a> thus suggesting that determination of the concentration of the peptide might be useful for differentiating between acute rejection and infection.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a></p><p id="par0110" class="elsevierStylePara elsevierViewall">In addition, it has recently been demonstrated<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a> that serial PCT determinations are correlated to the presence of infectious complications.</p></span></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Limitations of the studies</span><p id="par0115" class="elsevierStylePara elsevierViewall">The studies carried out to date have a series of limitations that complicate interpretation of the results obtained. A first problem is the limited number of patients included in the different studies. Secondly, the included patients are very heterogeneous–a fact that makes it difficult to extrapolate the results obtained. Lastly, there are also differences in sample collection and processing, thus indicating the need to standardize such techniques. It is therefore important to emphasize that no ideal biomarker of help in the differential diagnosis of post-transplantation ARF has been defined to date.</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Future lines of research</span><p id="par0120" class="elsevierStylePara elsevierViewall">New faster and more sensitive diagnostic techniques would allow us to establish a more effective diagnosis, based on the precise quantification of a concrete biomarker. In this sense, metabolomics allows the total assessment of metabolites in an organism, and represents a global evaluation of the biochemical and physiological condition of the patient. The detection of these markers can be made in different samples (fluids, cell types and tissues). Critically ill patients might benefit from these techniques, since they frequently suffer metabolic deregulations.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a></p><p id="par0125" class="elsevierStylePara elsevierViewall">Another aspect that may be of interest is research based on microRNA (miRNA), which has been shown to have many applications, such as for example in the early detection of lung cancer or rheumatoid arthritis.<a class="elsevierStyleCrossRefs" href="#bib0280"><span class="elsevierStyleSup">56–58</span></a> MicroRNA consists of small, non-coding molecules which nevertheless are important for the regulation of genic expression. These molecules are implicated in regulation of the development of the immune system and cell proliferation. For these reasons, research has recently focused on the relationship between the appearance of kidney and liver graft rejection and different types of microRNA. The results have revealed an association between certain types of microRNA and acute rejection.<a class="elsevierStyleCrossRef" href="#bib0295"><span class="elsevierStyleSup">59</span></a> However, to date the studies in the field of transplantation include very few patients and have fundamentally focused on these kinds of transplantations.<a class="elsevierStyleCrossRefs" href="#bib0300"><span class="elsevierStyleSup">60,61</span></a></p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Conclusions</span><p id="par0130" class="elsevierStylePara elsevierViewall">The success of lung transplantation is largely dependent upon its management in the immediate postoperative phase. Close monitoring of the evolution of the graft is therefore necessary from the immediate post-transplantation phase, in order to anticipate any problems capable of affecting the outcome. In this context, the analysis of the different biomarkers capable of contributing to the differential diagnosis of post-transplantation ARF is very important. Although some studies offer encouraging results, no ideal biomarker has yet been described capable of substantially improving the management and prognosis of these patients. The use of new techniques, such as the analysis of microRNA, could lead to further advances in this respect.</p></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Conflicts of interest</span><p id="par0135" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:13 [ 0 => array:2 [ "identificador" => "xres288115" "titulo" => "Abstract" ] 1 => array:2 [ "identificador" => "xpalclavsec271588" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xres288114" "titulo" => "Resumen" ] 3 => array:2 [ "identificador" => "xpalclavsec271587" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:3 [ "identificador" => "sec0010" "titulo" => "Primary graft dysfunction" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "sec0015" "titulo" => "Cytokines" ] 1 => array:2 [ "identificador" => "sec0020" "titulo" => "Receptor for advanced glycation end products" ] 2 => array:2 [ "identificador" => "sec0025" "titulo" => "P-selectin" ] 3 => array:2 [ "identificador" => "sec0030" "titulo" => "Clara cell secretory protein" ] 4 => array:2 [ "identificador" => "sec0035" "titulo" => "Protein C and plasminogen activator inhibitor" ] ] ] 6 => array:3 [ "identificador" => "sec0040" "titulo" => "Acute rejection" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0045" "titulo" => "Thioredoxin" ] 1 => array:2 [ "identificador" => "sec0050" "titulo" => "Pepsin" ] 2 => array:2 [ "identificador" => "sec0055" "titulo" => "Cytokines" ] ] ] 7 => array:3 [ "identificador" => "sec0060" "titulo" => "Infection" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0065" "titulo" => "Cytokines" ] 1 => array:2 [ "identificador" => "sec0070" "titulo" => "Galactomannan antigen" ] 2 => array:2 [ "identificador" => "sec0075" "titulo" => "Procalcitonin" ] ] ] 8 => array:2 [ "identificador" => "sec0080" "titulo" => "Limitations of the studies" ] 9 => array:2 [ "identificador" => "sec0085" "titulo" => "Future lines of research" ] 10 => array:2 [ "identificador" => "sec0090" "titulo" => "Conclusions" ] 11 => array:2 [ "identificador" => "sec0095" "titulo" => "Conflicts of interest" ] 12 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2012-11-06" "fechaAceptado" => "2013-01-06" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec271588" "palabras" => array:3 [ 0 => "Biomarkers" 1 => "Lung trasplant" 2 => "Acute respiratory failure" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec271587" "palabras" => array:3 [ 0 => "Biomarcadores" 1 => "Trasplante pulmonar" 2 => "Insuficiencia respiratoria aguda" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Lung transplant recipients are at high risk of suffering many complications during the immediate postoperative period, such as primary graft dysfunction, acute graft rejection or infection. The most common symptom is the presence of acute respiratory failure, and the use of biomarkers could be useful for establishing an early diagnosis of these conditions.</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Different biomarkers have been studied, but none have proven to be the gold standard in the differential diagnosis of acute respiratory failure.</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">This paper offers a review of the different biomarkers that have been studied in this field.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Los receptores de un trasplante pulmonar tienen un alto riesgo de presentar numerosas complicaciones durante el postoperatorio inmediato, como la disfunción primaria del injerto, el rechazo agudo del injerto o las infecciones. El síntoma más común será la presencia de insuficiencia respiratoria aguda, y el uso de biomarcadores podría ser de gran utilidad para establecer un diagnóstico precoz de estas entidades.</p><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Hasta la fecha, se han estudiado diferentes biomarcadores, pero ninguno ha demostrado ser el gold estándar en el diagnóstico diferencial de la insuficiencia respiratoria aguda.</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">En este artículo se expone una revisión de los diversos biomarcadores que han sido estudiados en este campo.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Ruano L, et al. Papel de los biomarcadores en el diagnóstico diferencial de la insuficiencia respiratoria aguda en el postoperatorio inmediato del trasplante pulmonar. Med Intensiva. 2013;37:416–422.</p>" ] ] "multimedia" => array:3 [ 0 => array:7 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">PGD: primary graft dysfunction; IL-6: interleukin 6; IL-8: interleukin 8; IP-10: interferon induced protein; BAL: bronchoalveolar lavage; MCP1: monocyte chemotactic protein-1; PAI-1: plasminogen activator inhibitor; RAGE: receptor for advanced glycation end products; ICU: Intensive Care Unit.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Reference \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Year \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Biomarker \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">No. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Sample type \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Results \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Hoffman et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2009 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " rowspan="3" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cytokines</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">25 (receptors<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>25 controls) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increased MCP1 and IP-10 in cases of PGD \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Moreno <span class="elsevierStyleSmallCaps">I</span> et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2007 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">31 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increased IL-6 in BAL and plasma in PGD \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Almenar et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2009 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">20 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">BAL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IL-8 in donor BAL and correlation to PGD \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Christie et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2009 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " rowspan="3" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">RAGE</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">317 (7 centers) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increased concentrations at 6 and 24<span class="elsevierStyleHsp" style=""></span>h post-transplantation in PGD \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Pelaez et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2010 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">59 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">BAL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increased concentrations in donor condition development of PGD in recipient \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Calfee et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2007 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">20 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Prognostic indicator of duration of mechanical ventilation and stay in ICU \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Kawut et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2009 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">P-selectin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">81 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increased concentrations 72<span class="elsevierStyleHsp" style=""></span>h after transplant in PGD \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Diamond et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2011 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Clara cell secretory protein \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">104 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Clara cells \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increased concentrations 6<span class="elsevierStyleHsp" style=""></span>h after transplant in PGD \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Christie et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2007 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Protein C and PAI-1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">128 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Reduced concentrations of protein C and increased levels of PAI-1 after transplant in association to PGD \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab420306.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Principal biomarkers studied in relation to primary graft dysfunction.</p>" ] ] 1 => array:7 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">IFN-γ: gamma-interferon; IL-16: interleukin 16; TGF-β: transforming growth factor-beta; TNF- α: tumor necrosis factor-alpha; BAL: bronchoalveolar lavage.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Reference \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Year \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Biomarker \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">No. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Sample type \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Results \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Patel et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2008 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Thioredoxin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">18 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">BAL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increase in presence of acute rejection \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Stovold et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2007 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Pepsin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">36 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">BAL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increase in presence of acute rejection and inflammation \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Laan et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2003 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " rowspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cytokines</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">14 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">BAL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Decrease in IL-16 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Hodge et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2007 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">10 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma and BAL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Decrease in TGF-βIncrease in IFN-γ and TNF-α \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab420307.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Principal biomarkers studied in relation to acute graft rejection.</p>" ] ] 2 => array:7 [ "identificador" => "tbl0015" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">IA: invasive aspergillosis; CMV: cytomegalovirus; IL-6: interleukin 6.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Reference \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Year \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Biomarker \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">No. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Sample type \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Results \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Zedtwitz-Liebenstein et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2009 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IL-6 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">111 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IL-6 increases in presence of CMV \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Pasqualotto et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2010 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Galactomannan antigen \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">60 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Bronchoalveolar lavage \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cutoff point established as 1.5 to discriminate presence of IA \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Zeglen et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2009 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Procalcitonin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">15 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Correlation to the presence of <span class="elsevierStyleItalic">Pseudomonas aeruginosa</span> and <span class="elsevierStyleItalic">Pneumocystis jirovecii</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Suberviola et al. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2012 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Procalcitonin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">25 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Plasma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Usefulness of procalcitonin as a diagnostic marker in the presence of infection \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab420308.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Principal 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Year/Month | Html | Total | |
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2024 November | 14 | 11 | 25 |
2024 October | 51 | 32 | 83 |
2024 September | 44 | 30 | 74 |
2024 August | 59 | 44 | 103 |
2024 July | 31 | 22 | 53 |
2024 June | 42 | 35 | 77 |
2024 May | 45 | 38 | 83 |
2024 April | 50 | 41 | 91 |
2024 March | 47 | 31 | 78 |
2024 February | 34 | 41 | 75 |
2024 January | 39 | 38 | 77 |
2023 December | 70 | 35 | 105 |
2023 November | 56 | 36 | 92 |
2023 October | 55 | 36 | 91 |
2023 September | 40 | 36 | 76 |
2023 August | 39 | 23 | 62 |
2023 July | 29 | 26 | 55 |
2023 June | 30 | 24 | 54 |
2023 May | 65 | 35 | 100 |
2023 April | 45 | 23 | 68 |
2023 March | 92 | 30 | 122 |
2023 February | 66 | 36 | 102 |
2023 January | 32 | 16 | 48 |
2022 December | 58 | 51 | 109 |
2022 November | 66 | 42 | 108 |
2022 October | 75 | 28 | 103 |
2022 September | 65 | 43 | 108 |
2022 August | 58 | 32 | 90 |
2022 July | 29 | 28 | 57 |
2022 June | 82 | 31 | 113 |
2022 May | 46 | 37 | 83 |
2022 April | 42 | 45 | 87 |
2022 March | 43 | 48 | 91 |
2022 February | 32 | 30 | 62 |
2022 January | 45 | 31 | 76 |
2021 December | 45 | 49 | 94 |
2021 November | 48 | 35 | 83 |
2021 October | 52 | 64 | 116 |
2021 September | 39 | 40 | 79 |
2021 August | 34 | 35 | 69 |
2021 July | 55 | 54 | 109 |
2021 June | 45 | 36 | 81 |
2021 May | 57 | 39 | 96 |
2021 April | 89 | 58 | 147 |
2021 March | 45 | 18 | 63 |
2021 February | 39 | 22 | 61 |
2021 January | 59 | 32 | 91 |
2020 December | 25 | 30 | 55 |
2020 November | 37 | 17 | 54 |
2020 October | 41 | 35 | 76 |
2020 September | 30 | 19 | 49 |
2020 August | 36 | 14 | 50 |
2020 July | 31 | 18 | 49 |
2020 June | 33 | 17 | 50 |
2020 May | 32 | 14 | 46 |
2020 April | 45 | 17 | 62 |
2020 March | 27 | 13 | 40 |
2020 February | 84 | 28 | 112 |
2020 January | 36 | 22 | 58 |
2019 December | 37 | 16 | 53 |
2019 November | 21 | 19 | 40 |
2019 October | 53 | 13 | 66 |
2019 September | 36 | 24 | 60 |
2019 August | 23 | 26 | 49 |
2019 July | 31 | 17 | 48 |
2019 June | 20 | 14 | 34 |
2019 May | 50 | 23 | 73 |
2019 April | 38 | 8 | 46 |
2019 March | 46 | 21 | 67 |
2019 February | 37 | 31 | 68 |
2019 January | 47 | 26 | 73 |
2018 December | 46 | 40 | 86 |
2018 November | 142 | 67 | 209 |
2018 October | 133 | 18 | 151 |
2018 September | 30 | 13 | 43 |
2018 August | 23 | 8 | 31 |
2018 July | 29 | 14 | 43 |
2018 June | 37 | 17 | 54 |
2018 May | 17 | 8 | 25 |
2018 April | 36 | 9 | 45 |
2018 March | 29 | 7 | 36 |
2018 February | 25 | 9 | 34 |
2018 January | 46 | 14 | 60 |
2017 December | 31 | 9 | 40 |
2017 November | 28 | 11 | 39 |
2017 October | 27 | 10 | 37 |
2017 September | 29 | 14 | 43 |
2017 August | 23 | 12 | 35 |
2017 July | 22 | 9 | 31 |
2017 June | 38 | 17 | 55 |
2017 May | 37 | 15 | 52 |
2017 April | 29 | 18 | 47 |
2017 March | 23 | 27 | 50 |
2017 February | 17 | 10 | 27 |
2017 January | 12 | 5 | 17 |
2016 December | 44 | 7 | 51 |
2016 November | 41 | 17 | 58 |
2016 October | 51 | 14 | 65 |
2016 September | 47 | 5 | 52 |
2016 August | 52 | 7 | 59 |
2016 July | 32 | 0 | 32 |
2015 December | 2 | 0 | 2 |