Assessing the quality of studies supporting genetic susceptibility and outcomes of ARDS

The acute respiratory distress syndrome (ARDS) is a severe inflammatory disease manifested as a result of pulmonary and systemic responses to several insults. It is now well accepted that genetic variation influences these responses. However, little
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  PERSPECTIVE ARTICLE published: 06 February 2014doi: 10.3389/fgene.2014.00020 Assessing the quality of studies supporting geneticsusceptibility and outcomes of ARDS Marialbert Acosta-Herrera  1,2,3  , Maria Pino-Yanes  1,2,4  , Lina Perez-Mendez  1,2  , Jesús Villar  1,3,5  and Carlos Flores  1,2,6  *  1 CIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain 2  Research Unit, Hospital Universitario N.S. de Candelaria, Santa Cruz de Tenerife, Spain 3  Research Unit, Hospital Universitario Dr. Negrin, Las Palmas de Gran Canaria, Spain 4  Department of Medicine, University of California, San Francisco, CA, USA 5  Keenan Research Center at the Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, ON, Canada  6  Applied Genomics Group (G2A), Genetics Laboratory, Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias, Universidad de La Laguna,Santa Cruz de Tenerife, Spain Edited by:  Jill Barnholtz-Sloan, Case WesternReserve University School of Medicine, USA Reviewed by:  Catherine Stein, Case WesternReserve University, USARobin T. Wilson, The Pennsylvania State University, USA *Correspondence:  Carlos Flores, Unidad de Investigación, Hospital Universitario N.S. de Candelaria, Carretera del Rosario s/n, Santa Cruz de Tenerife 38010, Spaine-mail:  The acute respiratory distress syndrome (ARDS) is a severe inflammatory diseasemanifested as a result of pulmonary and systemic responses to several insults. It is nowwell accepted that genetic variation influences these responses. However, little is knownabout the genes that are responsible for patient susceptibility and outcome of ARDS.Methodological flaws are still abundant among genetic association studies with ARDSand here, we aimed to highlight the quality criteria where the standards have not beenreached, to expose the associated genes to facilitate replication attempts, and to providequick-reference guidance for future studies. We conducted a PubMed search from January2008 to September 2012 for srcinal articles. Studies were considered if a statisticallysignificant association was declared with either susceptibility or outcomes of all-causeARDS.Fourteencriteriawereusedforevaluationandresultswerecomparedtothosefroma previous quality assessment report. Significant improvements affecting study designand statistical analysis were detected. However, major issues such as adjustments for theunderlying population stratification and replication studies remain poorly addressed. Keywords: genetic susceptibility, acute respiratory distress syndrome, outcome, genetic factors, populationstratification INTRODUCTION Acute lung injury (ALI) and its severe form, the acute respiratory distresssyndrome(ARDS),arecharacterizedbyacutediffuselunginflammation and non-cardiogenic pulmonary edema resultingfrom increased capillary-alveolar permeability. While ALI andARDS terms continue to be used in the medical literature, theirdefinition criteria were recently revised, although a consensushas not been reached (Ranieri et al., 2012; Villar et al., 2013). New definitions support the categorization of ARDS based onthe hypoxemia severity under mechanical ventilation, as well ason other physiological and clinical parameters, discouraging theuse of ALI as one of the categories. Hereafter, we will refer tothis constellation of syndromes using the term ARDS, irrespectiveof the classification used by the studies reviewed (Bernard et al.,1994). ARDS shows profound incidence variability across coun-tries (Rubenfeld et al., 2005; Villar et al., 2013), and it is unknownwhether differences also exist among ethnic groups (Martin et al.,2003; Erickson et al., 2009; Linko et al., 2009; Villar et al., 2011)and the extent to which demographic, cultural, economical, andhealth system particularities might underlie such differences.Predisposing genetic factors can interact with the environ-ment to determine the diversity of clinical manifestations, theresponse to treatment and outcomes among ARDS patients(Cobb and O’Keefe, 2004; Villar et al., 2004; Rahim et al., 2008).Exposing those genetic factors might reveal therapeutic targetsand a foundation to predict ARDS susceptibility and outcomes.Association studies have been widely used for detecting common,low-penetrant, genetic variants that are suggested to contribute tothe genetic architecture of complex diseases (Khoury and Yang,1998), including ARDS (Flores et al., 2008). For ARDS, these studies have mostly focused on particular biological candidatesand, only recently, have explored the entire genome (Christieetal.,2012).Wehavepreviouslyassessedthequalityofstatistically significant associations of genetic variants with ARDS from 1996to 2008 based on major recommendations that support study robustness (Flores et al., 2008). We hypothesized that, despitethis previous evaluation and the availability of well-known stan-dardguidelines(Janssensetal.,2011),manyassociationstudiesinthis field continue to be performed without awareness of minimalstandards and that methodological flaws are still abundant. Here,we aimed to identify those quality criteria where the standardshave not been reached, to expose the associated candidate genesto facilitate replication studies, and to create a guidance frame-work for ongoing and future studies. For that, we have critically assessed statistically significant candidate-gene associations withsusceptibility or outcome of all-cause ARDS from 2008 to 2012using14majorqualitycontrolcriteria,andcomparedtheupdatedresults with our previous evaluation (Flores et al., 2008).  February 2014 | Volume 5 | Article 20  |  1  Acosta-Herrera et al. Genetic association studies in ARDS MATERIALSANDMETHODS LITERATURE SEARCH We have previously assessed the quality of genetic associationstudies supporting susceptibility and/or outcome in adult ARDSpatients of the period of 1996–2008 (Flores et al., 2008). We havenowconductedaPubMedsearchfromJanuary2008toSeptember2012 by utilizing the same keyword combinations for querying(“polymorphism” and “acute lung injury,” “polymorphism” and“ARDS,”and“polymorphism”and“acuterespiratorydistresssyn-drome”). Because of the plausibilitythat a fraction of risk variantsfor ARDS susceptibility could be also risk factors for outcomes,both possibilities were jointly analyzed. The retrieved referenceswere then manually reviewed. Excluding meta-analysis, thosereporting statistically significant associations in adults (  p ≤ 0 . 05)for any cause of ALI or ARDS irrespective of the type of geneticvariants associated, and published in English, were reviewed by three of the authors. We are aware that a number of such reportedassociations might be false positives. However, this threshold forsignificance is preferable over a more conservative strategy at thisstage of field development (Thomas and Clayton, 2004). Finally, weconsideredthegeneastheunitofreplication(NealeandSham,2004). STUDY ASSESSMENT For simplicity, we focused on the 14 most relevant criteria, pre-viously utilized by us in Flores et al. (2008), modifying theexhaustive list provided by  Chanock et al. (2007), scoring eachitem as present or absent. Chi-squared tests were performed inSPSS (SPSS Inc., Chicago, IL). GENE COVERAGEINGENOTYPINGARRAYS Gene coverage was calculated with the tagger tool (Barrett et al.,2005) for SNPs with minor allele frequency   > 5% in the generegion captured directly and indirectly by the genome-wide geno-typing array utilized (with a multi-marker  r  2 ≥ 0 . 8). RESULTS The PubMed search on the period 2008–2012 allowed a closerreview of 27 original articles reporting statistically signifi-cant association findings on 31 candidate genes with suscep-tibility and/or outcomes of all-cause ARDS (Table S1), andthe first genome wide association study (GWAS) for thissyndrome (Christie et al., 2012). The latter was excludedfrom the evaluation as its quality control assessment dif-fers substantially from those applied to candidate-gene stud-ies. A complementary search querying for the syndrome namein the HuGeNet Navigator (Yu et al., 2008) gave over-lapping results, showing studies for additional genes albeitall reporting statistically non-significant findings. We, there-fore, continued the quality assessment based on the PubMedsearch.Seventeen studies (63%) provided statistically significant find-ings with a case-control design and ten (37%) with a cohort.These were based on a median sample size of 251 cases[interquartile range ( P  25 – P  75 ): 84–365] and 288 controls ( P  25 – P  75 : 190–724) in case-control studies, whereas for cohort studiesthe median sample size was 145 patients ( P  25 – P  75 : 118–215).In this period, almost all studies (96%) appropriately describeddemographical and clinical data for cases and all had an adequatecharacterization of the control group (47.1% of them utilizedhealthy subjects or population-based controls and 52.9% optedto use at risk patients as controls). However, only 50% of thestudies explored their power to detect statistically significantfindings.While roughly a third of studies (35%) focused on a singlevariant of the gene under study, the majority (65%) analyzed sev-eral polymorphisms attaining appropriate gene coverage of com-mon variation by means of linkage disequilibrium (LD)-basedmethods. In most cases (74%), the studies allowed to unambigu-ously identify the genomic location of the associated variant(s)on public resources. Similarly, most studies declared that Hardy-Weinberg equilibrium expectations were assessed (93%), andthat further genotyping error checks were implemented duringthe study (59%). Almost half of the studies (48%) stated thatgenotyping was performed blind to the disease status of samples.Focusing on the statistical analyses, 65% of the studies thatneeded to control type-I error due to multiple hypothesis testingdid so, and 89% included covariates in the regression analyses.The magnitude of effects was appropriately reported in terms of hazard ratios (HRs) or odds ratios (ORs) in almost all reviewedstudies (96%) (Table S1). The adjustment for population stratifi-cation and replication, in at least an independent study sample,were declared only in 22 and 19% of the studies, respectively,two major issues that has not improved over the years (Floreset al., 2008) ( Figure 1 ). Similarly, almost half of the studies (44%)pursued the functional significance of associated variants.On a side-by-side comparison of the two periods reviewedto date (i.e., 1996–2008 reviewed by  Flores et al., 2008 and thisone from 2008 to 2012), significant improvements in the qual-ity of the published studies were observed in the most recentperiod ( Figure 1 ) affecting study design, study reproducibility,and statistical analysis. These improvements were due to anincrease of studies exploiting the available tools for LD explo-ration to efficiently select the genetic variants (from 24 to 67%,chi-squared  p = 0 . 003); controlling type-I error by incorporat-ing multiple testing adjustments on the analyses (from 10 to 65%,chi-squared  p = 0 . 0003); and accurately identifying the genomiclocation of the associated variant(s) (from 45 to 74%, chi-squared  p = 0 . 033). DISCUSSION We have assessed the evidence obtained during 2008–2012 fromARDS candidate-gene association studies and compared themwith our previous assessment to objectively evaluate the evolu-tion of the field, especially in light of the methodology appliedin genetic susceptibility studies. In total, including the evidenceaccumulated before 2008 (Flores et al., 2008), 56 studies on 41candidate genes reported statistically significant associations withsusceptibility or outcomes of all-cause ARDS ( Figure 2 ).We detected significant improvements affecting the exploita-tion of resources for LD exploration, the inclusion of multipletesting adjustments, and the way studies identified the associatedvariants by established recommendations. This was also extensi-ble to sample sizes for case-control designs, as these have roughly  Frontiers in Genetics  | Applied Genetic Epidemiology  February 2014 | Volume 5 | Article 20  |  2  Acosta-Herrera et al. Genetic association studies in ARDS FIGURE 1 | Histogram comparing quality control scores of associationstudies in ARDS published from 1996 to 2008 (taken from Flores et al.,2008) and from 2008 until present.  Statistically significant improvementsaffected criteria relevant to study design (LD exploration), studyreproducibility (polymorphism identification) and statistical analysis (multipletesting adjustments).  ∗ p  -value ≤ 0.05;  ∗∗ p  -value ≤ 0.001. doubled their median sample by group compared to studies pub-lished before 2008. Despite this improvement, replications inindependent studies are needed to improve the association reli-ability. Worth noting, the diversity of samples has increased overtheyears,sothatacrossallpublishedstudiesafewhavefocusedonAfrican-Americans (6.6%), while the majority continues to useEuropeans (66.7%), East Asians (15%), or multiethnic samples(11.7%). While all these improvements are stimulating, a down-side continues to be recognized on the adjustment for populationstratification and replication attempts, as these were conducted inless than a fifth of all reviewed reports.The identification of genuine gene associations with ARDSrelies on conducting more replication studies, albeit without sac-rificing study robustness, as only a few associated genes have beenreplicated to date ( Figure 2 ). Among those genes,  ACE   was asso-ciated several times and a meta-analysis was recently published(Matsudaetal.,2012).Althoughresultsshouldbetakenwithcau- tion because of power limitations, they revealed variable effectsof an  ACE   polymorphism with ARDS mortality, present in EastAsians but lacking in Europeans. This illustrates the growing evi-dence supporting that genetic risks may be population-specific,either because of gene-gene or gene-environment interactions orbecause of frequency effects (Need and Goldstein, 2009). Given that we are far from having a complete list of ARDS genes, andthat an incomplete overlap of genetic risks between populationsis expected, the study of samples of diverse ancestry should beencouraged in future studies. It must be noted that across allreviewed studies, genetic associations with ARDS susceptibility or outcomes with opposite effects in different ancestry groupswere absent, despite differences by the ARDS triggering insulthave been detected (Christie et al., 2008). One major issue that is determinant of the robustness of association studies with unre-lated individuals is the assessment and adjustment of resultsfor the underlying (sometimes cryptic) population stratification,which is usually based on data from independent genetic poly-morphisms (Price et al., 2006). Still today, more than 80% of the published association studies in ARDS did not apply such anapproach, despite few dozen of very informative genetic variants(termed AIMs) have demonstrated their utility in specific pop-ulations (Pino-Yanes et al., 2011; Galanter et al., 2012). As thestudies that focus on particular genomic regions will continue tobe relevant in the field (Chanock et al., 2007), population strati-fication effects should be minimized in future association studies,irrespective of the study population being assessed. Therefore, itbecomes essential to develop efficient and straightforward meth-ods that: (1) could be applied to different populations and beuniversally used, and (2) could assist researchers to easily selecta reduced set of AIMs to accurately assess ancestry maintain-ing affordable costs. Such tools would be useful to validate study robustness as well as to address the biological differences betweenpopulations, and whether these may trigger disparities in ARDSsusceptibility or outcomes. It must be noted; however, that pop-ulation stratification also introduces non-genetic effects that willnot be addressed by these methods. It is expected that analysesof these effects and interactions will bring new opportunities andchallenges in the field (Rotimi and Jorde, 2010).Establishing the association of genes with ARDS susceptibil-ity is only the beginning of a process that should continue with  February 2014 | Volume 5 | Article 20  |  3  Acosta-Herrera et al. Genetic association studies in ARDS FIGURE 2 | Diagram showing the official gene symbols for the 41candidate genes associated with ARDS susceptibility and outcomes,depicting both chromosome locations and the number of study sampleswith statistically significant associations.  For each chromosome, lowerarrowheads indicate the location of genes with a single sample association,and upper arrowheads indicate the location of genes with statisticallysignificant association findings in at least two study samples. Arrowheadswith asterisk indicate more than one gene in that region. Dots denote thatthe gene was replicated in the only GWAS of ARDS published to date.Underlined gene names indicate that the product has been suggested as abiomarker for ARDS or its progression in at least one study.  ACE  , angiotensinI converting enzyme;  ANGPT2  , angiopoietin 2;  CXCL2  , chemokine (C-X-Cmotif) ligand 2;  DARC  , duffy blood group, chemokine receptor;  DIO2  ,deiodinase, iodothyronine, type II;  EGF  , epidermal growth factor;  F5  ,coagulation factor V (proaccelerin, labile factor);  FAS  , TNF receptorsuperfamily, member 6;  FTL , ferritin, light polypeptide;  GP5  , glycoprotein V(platelet);  HMOX1 , heme oxygenase 1;  HMOX2  , heme oxygenase 2;  IL6  ,interleukin 6;  IL10  , interleukin 10;  IL18  , interleukin 18;  IL32  , interleukin 32; IRAK3  , interleukin-1 receptor-associated kinase 3;  LTA , lymphotoxin alpha; MBL2  , mannose-binding lectin 2;  MIF  , macrophage migration inhibitoryfactor;  MYLK  , myosin light chain kinase;  NAMPT  , nicotinamidephosphoribosyltransferase;  NFE2L2  , nuclear factor (erythroid-derived 2)-like2;  NFKB1 , nuclear factor of kappa light polypeptide gene enhancer in B-cells1;  NFKBIA , nuclear factor of kappa light polypeptide gene enhancer in B-cellsinhibitor alpha;  NQO1 , NAD(P)H dehydrogenase, quinone 1;  PI3  , peptidaseinhibitor 3;  PLAU  , plasminogen activator, urokinase;  PPARGC1A , peroxisomeproliferator-activated receptor gamma, coactivator 1 alpha;  SFTPA1 , surfactantprotein A1;  SERPINE1 , serpin peptidase inhibitor, clade E (nexin, plasminogenactivator inhibitor type 1), member 1;  SFTPA2  , surfactant protein A2;  SFTPB  ,surfactant protein B;  SFTPD  , surfactant protein D;  SOD3  , superoxidedismutase 3;  STAT1 , signal transducer and activator of transcription 1, 91kDa; TIRAP  , toll-interleukin 1 receptor (TIR) domain containing adaptor protein; TLR1 , toll-like receptor 1;  TNF  , tumor necrosis factor;  TRAF6  , TNFreceptor-associated factor 6;  VEGFA , vascular endothelial growth factor A. the discovery of the causal genetic variants. The challenge contin-ues to be the validation of existing and novel ARDS associationsvia robust studies, and future and ongoing studies should amendthe critical issues here recognized. In this effort, new technologiesare allowing a faster field development by means of genome-widestudies, either using genotyping arrays or exome/whole genomesequencing. GWAS are as efficient as candidate-gene studies fordetecting weak effect risks, not requiring a previous hypothe-sis of the biological processes related to the trait. They haveallowed to identify new disease genes never anticipated and ledto new hypothesis and perspectives about disease pathogenesis(Marchini and Howie, 2010). Despite that, GWAS have majorlimitations including high costs, usually impacting on the sam-ple size, the statistical burden and the gene coverage. In addition, Frontiers in Genetics  | Applied Genetic Epidemiology  February 2014 | Volume 5 | Article 20  |  4  Acosta-Herrera et al. Genetic association studies in ARDS mostcommercialplatformsmayofferlesscoverageforthegene(s)of interest compared to that achieved in optimal candidate-gene studies, which can substantially impact study power (Voightet al., 2012). The first GWAS of ARDS was recently published by Christie et al. (2012), revealing  PPFIA1  as a novel susceptibility gene involved in cell adhesion and cell-matrix interactions, andsuggesting many others with putative functional roles. This study also replicated the association of four candidate genes including IL10  ,  MYLK  ,  ANGPT2 , and  FAS . This may suggest that all othercandidate gene associations should be considered false discover-ies. However, one explanation for this inconsistency could be alsothe insufficient GWAS coverage of the non-associated candidategenes (average ≈ 57%; Table S2). Whatever the case, commercialplatforms will only allow studying a fraction of the millions of existing genetic variants (Abecasis et al., 2012), and it is antici-pated that the associations to be revealed will only explain a smallcomponent of the disease (Manolio et al., 2009). Only completere-sequencing of individual genomes will guarantee the analysisof all genetic variation.Here we have shown that the field still faces several method-ological challenges, and in the clinical arena there are key issuesto be improved in order to fully understand the genetic pro-cesses underlying ARDS. Misclassification of phenotypes canlead to significant reduction in statistical power to detect truegenetic associations, therefore it becomes necessary a better andmore homogeneous patient classification. This could be achievedby combining the clinical information with different integra-tive approaches, those based on the determination of the causalmicroorganisms by means of metagenomics (Lysholm et al.,2012) or performing gene expression profiling among patients(Hu et al., 2012), to name a few. As a proof of concept, in a recentstudy by  O’Mahony et al. (2012), only when the samples were restricted to the more severe phenotype, new associations wererevealed and previous findings were replicated. Furthermore,quantitative phenotypes could be utilized for association testing,such as ventilator-free days (Kangelaris et al., 2012) or ideally other traits that are closer to the genotype. This possibility hasbeen explored in the field with striking (Wurfel et al., 2008) andreplicable results (Pino-Yanes et al., 2010). Additionally, the selec-tion of the control samples remains a challenge; it is not an easy taskandnotasingledesignisfreeofbias.Theuseofeitherhealthy subjects or at-risk individuals is common among the reviewedstudies.Analternativesolutioncanbetheutilizationofbothtypesof controls to reduce selection biases and be able to confidentially assess the quality of the genotypic data. This strategy has beenused (Song et al., 2010), and will surely reduce the chances thatrisk variants reported are causally associated with a confounderand not with ARDS.In summary, the methodology for assessing genetic risks incomplex diseases is under development. For ARDS, we concludethat the main challenge continues to be in providing an analyti-cally rigorous methodology (adjusting for population stratifica-tion, relatedness, and technical quality) accompanied by inde-pendent replication and mechanistic explanations for the resultsprovided. Still today, the evidence supporting the genetic associ-ations with ARDS susceptibility or outcomes is at best uncertain,given the limited statistical power of most studies and the effectsexpected for genetic variants involved in complex traits. To guar-antee proper and high quality studies on genetic susceptibility and outcomes, we strongly encourage the use of large and well-defined collection of samples. Consequently, a shift toward theestablishment of international consortia will be necessary. AUTHORCONTRIBUTIONS All authors contributed equally in the assessment design and readand approved the final manuscript. ACKNOWLEDGMENTS This work was supported by grants CB06/06/1088 and PI10/0393from the Health Institute “Carlos III” (ISCIII, Spain) and co-financed by the European Regional Development Funds, “A way of making Europe” from the European Union. Marialbert Acosta-Herrera and Maria Pino-Yanes were supported with fellow-ships from ISCIII (FI11/00074) and Fundación Ramón Areces,respectively. SUPPLEMENTARYMATERIAL The Supplementary Material for this article can be foundonline at: REFERENCES Abecasis, G. R., Auton, A., Brooks, L. D., Depristo, M. A., Durbin, R. M.,Handsaker, R. E., et al. (2012). An integrated map of genetic variation from1,092 human genomes.  Nature  491, 56–65. doi: 10.1038/nature11632Barrett, J. C., Fry, B., Maller, J., and Daly, M. J. (2005). Haploview: analysisand visualization of LD and haplotype maps.  Bioinformatics  21, 263–265. doi:10.1093/bioinformatics/bth457Bernard, G. R., Artigas, A., Brigham, K. L., Carlet, J., Falke, K., Hudson, L., et al.(1994). The american-european consensus conference on ARDS. Definitions,mechanisms, relevant outcomes, and clinical trial coordination.  Am. J. Respir.Crit. Care Med.  149, 818–824. doi: 10.1164/ajrccm.149.3.7509706Chanock, S. 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Racial and ethnic disparities inmortality from acute lung injury.  Crit. Care Med.  37, 1–6. doi:10.1097/CCM.0b013e31819292eaFlores, C., Pino-Yanes Mdel, M., and Villar, J. (2008). A quality assessment of genetic association studies supporting susceptibility and outcome in acute lunginjury.  Crit. Care  12, R130. doi: 10.1186/cc7098Galanter, J. M., Fernandez-Lopez, J. C., Gignoux, C. R., Barnholtz-Sloan, J.,Fernandez-Rozadilla, C., Via, M., et al. (2012). Development of a panel of genome-wide ancestry informative markers to study admixture throughout theAmericas.  PLoS Genet.  8:e1002554. doi: 10.1371/journal.pgen.1002554Hu, P., Wang, X., Haitsma, J. J., Furmli, S., Masoom, H., Liu, M., et al. (2012).Microarraymeta-analysisidentifiesacutelunginjurybiomarkersindonorlungsthat predict development of primary graft failure in recipients.  PLoS ONE  7:e45506. doi: 10.1371/journal.pone.0045506  February 2014 | Volume 5 | Article 20  |  5
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