Cargando…

Characterization of sepsis inflammatory endotypes using circulatory proteins in patients with severe infection: a prospective cohort study

BACKGROUND: Sepsis is a heterogeneous syndrome due to a variable range of dysregulated processes in the host immune response. Efforts are made to stratify patients for personalized immune-based treatments and better prognostic prediction. Using gene expression data, different inflammatory profiles h...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ricaño-Ponce, Isis, Riza, Anca-Lelia, de Nooijer, Aline H., Pirvu, Andrei, Dorobantu, Stefania, Dragos, Adina, Streata, Ioana, Roskanovic, Mihaela, Grondman, Inge, Dumitrescu, Florentina, Kumar, Vinod, Netea, Mihai G., Ioana, Mihai
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2022
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9547371/ https://www.ncbi.nlm.nih.gov/pubmed/36209073 http://dx.doi.org/10.1186/s12879-022-07761-0

Ejemplares similares

Genetic Testing for Familial Hypercholesterolemia in a Pediatric Group: A Romanian Showcase
por: Constantin, Andreea Teodora, et al.
Publicado: (2023)

Phenotype Heterogeneity in 3q29 Microduplication Syndrome
por: STREATA, IOANA, et al.
Publicado: (2020)

Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies—Data from a Romanian Cohort
por: Riza, Anca-Lelia, et al.
Publicado: (2022)

Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability—Data from a Romanian Cohort
por: Streață, Ioana, et al.
Publicado: (2022)

Cytogenetic Analysis of Sporadic First-Trimester Miscarriage Specimens Using Karyotyping and QF-PCR: A Retrospective Romanian Cohort Study
por: Popescu-Hobeanu, Gabriela, et al.
Publicado: (2022)

Association between genetic variants and depression in a Romanian cohort
por: Costache, Andrei, et al.
Publicado: (2021)

PAH Pathogenic Variants and Clinical Correlations in a Group of Hyperphenylalaninemia Patients from North-Western Romania
por: Iuhas, Alin, et al.
Publicado: (2023)

Analysis of inflammatory protein profiles in the circulation of COVID-19 patients identifies patients with severe disease phenotypes
por: Keur, Nick, et al.
Publicado: (2023)

Impact of Human Genetic Variation on C-Reactive Protein Concentrations and Acute Appendicitis
por: Ricaño-Ponce, Isis, et al.
Publicado: (2022)

Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome
por: Papuc, Sorina Mihaela, et al.
Publicado: (2023)

THE ROLE OF OBESITY AND PLASMA ADIPOCYTOKINES IN IMMUNE DYSREGULATION IN SEPSIS PATIENTS
por: de Nooijer, Aline H., et al.
Publicado: (2023)

The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients
por: Budisteanu, Magdalena, et al.
Publicado: (2021)

604. IL-17C as an early diagnostic biomarker for invasive fungal infection or just a marker of any infection in at-risk haematology patients
por: Aerts, Robina, et al.
Publicado: (2023)

Serum Amino Acid Profiling in Children with Autistic Spectrum Disorder: Insights from a Single-Center Study in Southern Romania
por: Anastasescu, Cătălina Mihaela, et al.
Publicado: (2023)

Linking minimum inhibitory concentrations to whole genome sequence-predicted drug resistance in Mycobacterium tuberculosis strains from Romania
por: Ruesen, Carolien, et al.
Publicado: (2018)

TSH and T4 Levels in a Cohort of Depressive Patients
por: COSTACHE, ANDREI, et al.
Publicado: (2020)

Circulating Cortisol in a Cohort of Depressive Patients
por: COSTACHE, ANDREI, et al.
Publicado: (2020)

Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency
por: Chirita-Emandi, Adela, et al.
Publicado: (2021)

Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene
por: Riza, Anca-Lelia, et al.
Publicado: (2022)

Determination of VEGFR-2 (KDR) 604A>G Polymorphism in Pancreatic Disorders
por: Pădureanu, Vlad, et al.
Publicado: (2017)

Heart function assessment during aging in apolipoprotein E knock-out mice
por: Liehn, Elisa A., et al.
Publicado: (2021)

Array CGH - A Powerful Tool in Molecular Diagnostic of Pathogenic Microdeletions - Williams-Beuren Syndrome - A Case Report
por: STREAȚĂ, I., et al.
Publicado: (2016)

Some Information Measures Properties of the GOS-Concomitants from the FGM Family
por: Suter, Florentina, et al.
Publicado: (2022)

A systematic review of analytical methods used in genetic association analysis of the X-chromosome
por: Keur, Nick, et al.
Publicado: (2022)

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
por: Kozma, Kinga, et al.
Publicado: (2021)

Correction: The CARD9 Polymorphisms rs4077515, rs10870077 and rs10781499 Are Uncoupled from Susceptibility to and Severity of Pulmonary Tuberculosis
por: Streata, Ioana, et al.
Publicado: (2016)

The CARD9 Polymorphisms rs4077515, rs10870077 and rs10781499 Are Uncoupled from Susceptibility to and Severity of Pulmonary Tuberculosis
por: Streata, Ioana, et al.
Publicado: (2016)

Complement Activation in the Disease Course of Coronavirus Disease 2019 and Its Effects on Clinical Outcomes
por: de Nooijer, Aline H, et al.
Publicado: (2020)

Abnormal Thyroid Function Is Associated With Lymphopenia in Bacterial Sepsis and COVID-19
por: Grondman, Inge, et al.
Publicado: (2021)

Prevalence and Predictors of Renal Disease in a National Representative Sample of the Romanian Adult Population: Data from the SEPHAR IV Survey
por: Pop, Călin, et al.
Publicado: (2022)

A higher BMI is not associated with a different immune response and disease course in critically ill COVID-19 patients
por: Kooistra, Emma J., et al.
Publicado: (2021)

The genetics of East African populations: a Nilo-Saharan component in the African genetic landscape
por: Dobon, Begoña, et al.
Publicado: (2015)

Gene expression signatures identify biologically and clinically distinct tuberculosis endotypes
por: DiNardo, Andrew R., et al.
Publicado: (2022)

Increased sTREM-1 plasma concentrations are associated with poor clinical outcomes in patients with COVID-19
por: de Nooijer, Aline H., et al.
Publicado: (2021)

Human Monocytic Suppressive Cells Promote Replication of Mycobacterium tuberculosis and Alter Stability of in vitro Generated Granulomas
por: Agrawal, Neha, et al.
Publicado: (2018)

Characterization and Detection of ϵ-Berge-Zhukovskii Equilibria
por: Lung, Rodica Ioana, et al.
Publicado: (2015)

Anakinra treatment in critically ill COVID-19 patients: a prospective cohort study
por: Kooistra, Emma J., et al.
Publicado: (2020)

Developmental Abnormalities of the Skull Base in Patients with Turner Syndrome
por: TECUTA-BUSOI, ADINA-IOANA, et al.
Publicado: (2020)

The Carpathian range represents a weak genetic barrier in South-East Europe
por: Hervella, Montserrat, et al.
Publicado: (2014)

Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature
por: Shelby, Elena-Silvia, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_dpvlhqrrvmq9c3470e7fu5c4b3