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  1. Article: Measurement of glycosylated ferritin with Concanavalin A: Assay design, optimization and validation

    Raynor, Alexandre / Peoc'h, Katell / Boutten, Anne

    Journal of chromatography. 2022 Apr. 01, v. 1194

    2022  

    Abstract: Ferritin is the major iron-storage glycoprotein found in all tissues. Ferritin glycosylation can be assessed by the differential affinities of ferritin glycoforms for Concanavalin A (ConA), a lectin. The fraction of serum ferritin bound to ConA is called ...

    Abstract Ferritin is the major iron-storage glycoprotein found in all tissues. Ferritin glycosylation can be assessed by the differential affinities of ferritin glycoforms for Concanavalin A (ConA), a lectin. The fraction of serum ferritin bound to ConA is called “glycosylated ferritin” (GF). Low GF reflects macrophagic activation and is an essential biomarker used in adult-onset Still's disease (AOSD), macrophage activation syndrome (MAS) and Gaucher disease diagnosis and therapeutic management. To date, no complete assay description and method validation according to the ISO 15189 standard has been published. This study aimed to describe and validate our method used for GF measurement and describe GF values observed in patients. Ferritin glycoforms were separated based on their affinities for ConA using commercially available TRIS-barbital buffer, Sepharose and ConA/Sepharose 4B gels. Ferritin concentrations were measured on the Siemens Dimension Vista 1500®. We analysed 16,843 GF values obtained between 2000 and 2021 from our database of patients. Optimal separation of ferritin glycoforms was obtained by 15-min incubation of serum with ConA/Sepharose at pH 8. The optimized volume were 0.4 mL for total serum ferritin (TSF) 30–1000 µg/L and 0.5 mL for TSF 1000–2500 µg/L. Serum with higher TSF should be pre-diluted in the TRIS-barbital buffer. Reproducibility of ferritin measurement in the TRIS-barbital buffer matrix was excellent (intra-assay CV < 1%; inter-assay CV < 4%). Reproducibility of GF assay was good (intra-assay CV < 10% for low and high ferritin samples, respectively; and inter-assay CV < 10%). Inter-operator variability was 21.6% for GF < 20%. Ferritin was stable for up to 3 days in the TRIS-barbital buffer. An inter-laboratory exchange program conducted with another French hospital showed good agreement between results. In our database, <20% GF levels were scarce, compatible with the low prevalence of Still's disease, MAS, and Gaucher disease. The 95% confidence interval for GF was [26–58]%, lower than values described in the literature for healthy individuals. Thanks to good performances, this technique can become readily available for laboratories servicing patients with AOSD, MAS (including severe COVID-19 patients) and Gaucher disease patients.
    Keywords COVID-19 infection ; agarose ; biomarkers ; blood serum ; chromatography ; concanavalin A ; confidence interval ; databases ; disease diagnosis ; ferritin ; genetic disorders ; glycoproteins ; glycosylation ; hospitals ; macrophage activation ; pH ; therapeutics
    Language English
    Dates of publication 2022-0401
    Publishing place Elsevier B.V.
    Document type Article
    ISSN 1570-0232
    DOI 10.1016/j.jchromb.2022.123184
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Measurement of glycosylated ferritin with Concanavalin A: Assay design, optimization and validation.

    Raynor, Alexandre / Peoc'h, Katell / Boutten, Anne

    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences

    2022  Volume 1194, Page(s) 123184

    Abstract: Introduction: Ferritin is the major iron-storage glycoprotein found in all tissues. Ferritin glycosylation can be assessed by the differential affinities of ferritin glycoforms for Concanavalin A (ConA), a lectin. The fraction of serum ferritin bound to ...

    Abstract Introduction: Ferritin is the major iron-storage glycoprotein found in all tissues. Ferritin glycosylation can be assessed by the differential affinities of ferritin glycoforms for Concanavalin A (ConA), a lectin. The fraction of serum ferritin bound to ConA is called "glycosylated ferritin" (GF). Low GF reflects macrophagic activation and is an essential biomarker used in adult-onset Still's disease (AOSD), macrophage activation syndrome (MAS) and Gaucher disease diagnosis and therapeutic management. To date, no complete assay description and method validation according to the ISO 15189 standard has been published. This study aimed to describe and validate our method used for GF measurement and describe GF values observed in patients.
    Materials and methods: Ferritin glycoforms were separated based on their affinities for ConA using commercially available TRIS-barbital buffer, Sepharose and ConA/Sepharose 4B gels. Ferritin concentrations were measured on the Siemens Dimension Vista 1500®. We analysed 16,843 GF values obtained between 2000 and 2021 from our database of patients.
    Results: Optimal separation of ferritin glycoforms was obtained by 15-min incubation of serum with ConA/Sepharose at pH 8. The optimized volume were 0.4 mL for total serum ferritin (TSF) 30-1000 µg/L and 0.5 mL for TSF 1000-2500 µg/L. Serum with higher TSF should be pre-diluted in the TRIS-barbital buffer. Reproducibility of ferritin measurement in the TRIS-barbital buffer matrix was excellent (intra-assay CV < 1%; inter-assay CV < 4%). Reproducibility of GF assay was good (intra-assay CV < 10% for low and high ferritin samples, respectively; and inter-assay CV < 10%). Inter-operator variability was 21.6% for GF < 20%. Ferritin was stable for up to 3 days in the TRIS-barbital buffer. An inter-laboratory exchange program conducted with another French hospital showed good agreement between results. In our database, <20% GF levels were scarce, compatible with the low prevalence of Still's disease, MAS, and Gaucher disease. The 95% confidence interval for GF was [26-58]%, lower than values described in the literature for healthy individuals.
    Conclusion: Thanks to good performances, this technique can become readily available for laboratories servicing patients with AOSD, MAS (including severe COVID-19 patients) and Gaucher disease patients.
    MeSH term(s) Biomarkers/blood ; Biomarkers/metabolism ; Chemistry Techniques, Analytical/methods ; Concanavalin A/metabolism ; Ferritins/blood ; Ferritins/metabolism ; Gaucher Disease/blood ; Gaucher Disease/metabolism ; Humans ; Macrophage Activation Syndrome/blood ; Macrophage Activation Syndrome/metabolism ; Protein Binding ; Still's Disease, Adult-Onset/blood ; Still's Disease, Adult-Onset/metabolism
    Chemical Substances Biomarkers ; glycosylated ferritin ; Concanavalin A (11028-71-0) ; Ferritins (9007-73-2)
    Language English
    Publishing date 2022-02-26
    Publishing country Netherlands
    Document type Evaluation Study ; Journal Article
    ZDB-ID 1180823-8
    ISSN 1873-376X ; 0378-4347 ; 1570-0232 ; 1387-2273
    ISSN (online) 1873-376X
    ISSN 0378-4347 ; 1570-0232 ; 1387-2273
    DOI 10.1016/j.jchromb.2022.123184
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Stability of Rivaroxaban and Apixaban Anti-Xa Activities in Whole Blood Samples: A French Bicentric Study.

    Raynor, Alexandre / Lunte, Klara / Gaaloul, Mayssa / Caillault, Amandine / Zouiti, Fouzia / Desconclois, Céline / Planche, Virginie

    Thrombosis and haemostasis

    2023  Volume 123, Issue 5, Page(s) 565–567

    MeSH term(s) Humans ; Rivaroxaban/therapeutic use ; Pyridones/pharmacology ; Pyrazoles ; Heparin, Low-Molecular-Weight ; Factor Xa Inhibitors ; Anticoagulants/pharmacology
    Chemical Substances Rivaroxaban (9NDF7JZ4M3) ; apixaban (3Z9Y7UWC1J) ; Pyridones ; Pyrazoles ; Heparin, Low-Molecular-Weight ; Factor Xa Inhibitors ; Anticoagulants
    Language English
    Publishing date 2023-02-15
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 518294-3
    ISSN 2567-689X ; 0340-6245
    ISSN (online) 2567-689X
    ISSN 0340-6245
    DOI 10.1055/s-0043-1763254
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: High CDT without clinical context: Beware of the variant.

    Lebredonchel, Elodie / Raynor, Alexandre / Bruneel, Arnaud / Peoc'h, Katell / Klein, André

    Clinica chimica acta; international journal of clinical chemistry

    2023  Volume 544, Page(s) 117333

    Abstract: Carbohydrate-deficient transferrin (CDT) is a performant biomarker used for the diagnosis of chronic alcohol abuse. Here, we describe the case of a 39-year-old male of Tamil ethnicity who had extremely elevated (20%) CDT using capillary electrophoresis ( ... ...

    Abstract Carbohydrate-deficient transferrin (CDT) is a performant biomarker used for the diagnosis of chronic alcohol abuse. Here, we describe the case of a 39-year-old male of Tamil ethnicity who had extremely elevated (20%) CDT using capillary electrophoresis (but without glycoforms profile analysis), putting his driving license regranting at risk. However, the patient had no symptoms of chronic alcohol abuse, normal mean corpuscular volume and gamma-glutamyl transferase, and did not admit to any alcohol consumption. Re-analysis by N-Latex CDT immunoassay revealed a CDT at 1.7%. Further investigation by whole-exome sequencing revealed a c.1295A>G missense variant at the heterozygous state on the TFgene. This variant is characterized by an amino-acid change at a consensus sequence forN-glycosylation. Therefore, half of the patient transferrin proteins were lacking a completeN-glycan chain out of two, despite no alcohol consumption. This also explains the discrepancies between the techniques, as the NLatex antibodies did not recognize the mutated sequence. In conclusion, this case highlights the importance of comparing laboratory results between themselves and the clinical description, the absolute requirement for glycoforms profile analysis before delivering results, and the necessity to confirm intriguing results by another technique in a specialized laboratory.
    MeSH term(s) Male ; Humans ; Adult ; Alcoholism/diagnosis ; Alcoholism/genetics ; India ; Alcohol Drinking ; Transferrin/analysis ; Biomarkers/analysis
    Chemical Substances carbohydrate-deficient transferrin ; Transferrin ; Biomarkers
    Language English
    Publishing date 2023-04-06
    Publishing country Netherlands
    Document type Case Reports
    ZDB-ID 80228-1
    ISSN 1873-3492 ; 0009-8981
    ISSN (online) 1873-3492
    ISSN 0009-8981
    DOI 10.1016/j.cca.2023.117333
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Reversible atransferrinemia in a patient with chronic enteropathy: is transferrin mandatory for iron transport?

    Raynor, Alexandre / Stefanescu, Carmen / Bruneel, Arnaud / Puy, Hervé / Peoc'h, Katell / Manceau, Hana

    Biochemia medica

    2022  Volume 33, Issue 1, Page(s) 10801

    Abstract: Herein, we report the case of a 42-year-old woman, hospitalized in a French tertiary hospital for a relapse of a chronic enteropathy, who was found on admission to have no detectable serum transferrin. Surprisingly, she only exhibited mild anaemia. This ... ...

    Abstract Herein, we report the case of a 42-year-old woman, hospitalized in a French tertiary hospital for a relapse of a chronic enteropathy, who was found on admission to have no detectable serum transferrin. Surprisingly, she only exhibited mild anaemia. This atransferrinemia persisted for two months throughout her hospitalization, during which her haemoglobin concentration remained broadly stable. Based on her clinical history and evolution, we concluded to an acquired atransferrinemia secondary to chronic undernutrition, inflammation and liver failure. We discuss the investigations performed in this patient, and hypotheses regarding the relative stability of her haemoglobin concentration despite the absence of detectable transferrin.
    MeSH term(s) Humans ; Female ; Adult ; Transferrin ; Metal Metabolism, Inborn Errors ; Iron ; Hemoglobins
    Chemical Substances Transferrin ; Iron (E1UOL152H7) ; Hemoglobins
    Language English
    Publishing date 2022-12-15
    Publishing country Croatia
    Document type Case Reports
    ZDB-ID 1208725-7
    ISSN 1846-7482 ; 1330-0962
    ISSN (online) 1846-7482
    ISSN 1330-0962
    DOI 10.11613/BM.2023.010801
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Stability of Rivaroxaban and Apixaban Anti-Xa Activities in Whole Blood Samples: A French Bicentric Study

    Raynor, Alexandre / Lunte, Klara / Gaaloul, Mayssa / Caillault, Amandine / Zouiti, Fouzia / Desconclois, Céline / Planche, Virginie

    Thrombosis and Haemostasis

    2023  Volume 123, Issue 05, Page(s) 565–567

    Language English
    Publishing date 2023-02-15
    Publisher Georg Thieme Verlag KG
    Publishing place Stuttgart ; New York
    Document type Article
    ZDB-ID 518294-3
    ISSN 2567-689X ; 0340-6245
    ISSN (online) 2567-689X
    ISSN 0340-6245
    DOI 10.1055/s-0043-1763254
    Database Thieme publisher's database

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  7. Article ; Online: Capillary zone electrophoresis of transferrin and EDTA samples in congenital disorders of glycosylation screening: CaNOt do, really?

    Raynor, Alexandre / Raulet-Bussian, Célia / Verel, Léa / Plouviez, Grégory / Bruneel, Arnaud

    Clinica chimica acta; international journal of clinical chemistry

    2021  Volume 519, Page(s) 92–93

    MeSH term(s) Congenital Disorders of Glycosylation/diagnosis ; Congenital Disorders of Glycosylation/genetics ; Edetic Acid ; Electrophoresis, Capillary ; Humans ; Isoelectric Focusing ; Transferrin
    Chemical Substances Transferrin ; Edetic Acid (9G34HU7RV0)
    Language English
    Publishing date 2021-04-20
    Publishing country Netherlands
    Document type Letter
    ZDB-ID 80228-1
    ISSN 1873-3492 ; 0009-8981
    ISSN (online) 1873-3492
    ISSN 0009-8981
    DOI 10.1016/j.cca.2021.04.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Usual transaminase values: should they be reviewed and adjusted?

    Raynor, Alexandre / Soavelomandroso, Anna / Robert-Mercier, Tiphaine / Valla, Dominique / Peoc'h, Katell / Raulet-Bussian, Célia

    Annales de biologie clinique

    2022  Volume 80, Issue 3, Page(s) 213–222

    Abstract: Alanine (ALT) and aspartate aminotransferases (AST) are intracellular enzymes involved in the metabolism of amino acids. The measurements of their activities are two of the most ordered tests in clinical laboratories, used to screen, diagnose and follow ... ...

    Title translation Valeurs usuelles des transaminases : faut-il les réexaminer et les adapter ?
    Abstract Alanine (ALT) and aspartate aminotransferases (AST) are intracellular enzymes involved in the metabolism of amino acids. The measurements of their activities are two of the most ordered tests in clinical laboratories, used to screen, diagnose and follow diseases affecting the liver. Recent works highlighted that reference values for ALT and AST vary according to the analytical method and the individual’s characteristics, like with many other biomarkers. Reference values for ALT show clinically significant differences according to the analytical method (higher when supplementing samples with phosphate pyridoxal), gender (higher in males than in females), body mass index (positive correlation), and age (higher in infants and the elderly), but not according to ethnicity or employed analyzer. According to the analytical method and age, reported reference values for AST show clinically significant differences, similar to ALT. These observations prove clinical laboratories’ interest in updating their reference values according to sex, body mass index, age (especially when providing testing to pediatric or elderly populations), and the analytical method employed. If possible, a standardized method should be used, including sample supplementation with pyridoxal phosphate, to ensure the comparability of results between laboratories.
    MeSH term(s) Aged ; Alanine Transaminase/metabolism ; Aspartate Aminotransferases/metabolism ; Biomarkers ; Child ; Female ; Humans ; Liver/metabolism ; Male ; Reference Values
    Chemical Substances Biomarkers ; Aspartate Aminotransferases (EC 2.6.1.1) ; Alanine Transaminase (EC 2.6.1.2)
    Language French
    Publishing date 2022-07-07
    Publishing country France
    Document type Journal Article
    ZDB-ID 418098-7
    ISSN 1950-6112 ; 0003-3898
    ISSN (online) 1950-6112
    ISSN 0003-3898
    DOI 10.1684/abc.2022.1734
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Clinically relevant urine creatinine underestimation in the low concentration range on the Siemens Dimension Vista®.

    Raynor, Alexandre / Raulet-Bussian, Célia / Robert-Mercier, Tiphaine / Bruneel, Arnaud / Vidal-Petiot, Emmanuelle / Flamant, Martin / Boutten, Anne

    Clinical biochemistry

    2022  

    Abstract: While considerable efforts have been accomplished to standardize the measurement of plasma creatinine (PCr), urine creatinine (UCr) has not been subject to the same scrutiny. UCr is importantly used when measuring biomarkers in spot urines, to assess ... ...

    Abstract While considerable efforts have been accomplished to standardize the measurement of plasma creatinine (PCr), urine creatinine (UCr) has not been subject to the same scrutiny. UCr is importantly used when measuring biomarkers in spot urines, to assess urine output and variable dilution of urine samples. Here, we report underestimation of Jaffe UCr measurements on the Siemens Dimension Vista® analyzer, critically affecting samples with UCr ≤2 mmol/L. We demonstrate that this error is caused by automatic urine pre-dilution by the Vista's «urine mode», and that UCr measured in «plasma mode» without pre-dilution does not present this error. In the absence of a comprehensive solution proposed by Siemens, we propose simple formulae that can be easily implemented in a laboratory to correct these low UCr measurements. Importantly, the observed UCr underestimation can significantly influence reported results for biomarkers/UCr ratios measured in spot urine. Indeed, these results can be overestimated up to +84.4 % before correction using our formulae. This can sometimes lead to misclassification according to clinical thresholds, e.g. Kidney disease: improving global outcomes (KDIGO) guidelines for urine albumin/creatinine. This highlights the need for every clinical laboratory to assess the detection limits of their assays, including for lesser-discussed parameters such as UCr. Indeed, the error we reported here may affect other urine assays performing systematic urine pre-dilution and could have significant repercussions on the clinical management of patients.
    Language English
    Publishing date 2022-11-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 390372-2
    ISSN 1873-2933 ; 0009-9120
    ISSN (online) 1873-2933
    ISSN 0009-9120
    DOI 10.1016/j.clinbiochem.2022.10.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Breast milk in neonate oral care: oropharyngeal effects in extremely preterm infants.

    Bourgeois-Nicolaos, Nadège / Raynor, Alexandre / Shankar-Aguilera, Shivani / Schwartz, Eden / Doucet-Populaire, Florence / De Luca, Daniele

    European journal of pediatrics

    2022  

    Abstract: Ventilator-associated pneumonia (VAP) is a frequent nosocomial infection in neonatal intensive care units (NICU). Extremely preterm infants are at highest risk of developing VAP. Several studies indicate that oral care included in a preventive protocol ... ...

    Abstract Ventilator-associated pneumonia (VAP) is a frequent nosocomial infection in neonatal intensive care units (NICU). Extremely preterm infants are at highest risk of developing VAP. Several studies indicate that oral care included in a preventive protocol effectively reduces neonatal VAP incidence. We investigated the effects of oral care with breast milk on oral immune defenses and microbiota in extremely preterm infants. Thirty infants born ≤ 30 weeks gestation hospitalized at our NICU were selected and divided into three groups: oral care with breast milk, formula, or sterile water. Effects on oral immune defenses in vivo were studied using ELISA to measure lactoferrin (LF) and secretory immunoglobulin A (sIgA) in pharyngeal aspirates before and after oral care. Different LF concentrations were tested in vitro to assess their effects on loads of selected bacterial species by culture. Effects on selected bacteria potentially responsible for VAP in vivo were studied by real-time PCR detection in pharyngeal aspirates before and after oral care. Oral care with breast milk significantly increases LF concentrations to 69.8 × 10
    Conclusion: In extremely preterm infants, oral care with breast milk increases local immune defense markers (LF, sIgA), which combat bacterial infections. Further clinical trials should be conducted to evaluate their effects on VAP prevention in neonates.
    What is known: • The population at higher risk to develop VAP are preterm infants. • Several studies indicate oral care within a preventive bundle is effective in reducing neonatal VAP incidence.
    What is new: • In extremely premature infants, oral care with breast milk causes a significant increase in local immune defences in terms of lactoferrin (LF) and secretory immunoglobulin A (sIgA). • LF concentrations obtained after oral care with breast milk decreased loads of bacteria most commonly responsible for VAP in premature infants under experimental in-vitro.
    Language English
    Publishing date 2022-11-14
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 194196-3
    ISSN 1432-1076 ; 0340-6199 ; 0943-9676
    ISSN (online) 1432-1076
    ISSN 0340-6199 ; 0943-9676
    DOI 10.1007/s00431-022-04692-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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