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  1. Article ; Online: In-field detection and characterization of B/Victoria lineage deletion variant viruses causing early influenza activity and an outbreak in Louisiana, 2019.

    Shu, Bo / Wilson, Malania M / Keller, Matthew W / Tran, Ha / Sokol, Theresa / Lee, Grace / Rambo-Martin, Benjamin L / Kirby, Marie K / Hassell, Norman / Haydel, Danielle / Hand, Julie / Wentworth, David E / Barnes, John R

    Influenza and other respiratory viruses

    2024  Volume 18, Issue 1, Page(s) e13246

    Abstract: Background: In 2019, the Louisiana Department of Health reported an early influenza B/Victoria (B ... to investigate it using genomics and a triplex real-time RT-PCR assay to detect three antigenically distinct B ... VIC lineage variant viruses.: Results: The investigation indicated that B/VIC V1A.3 subclade ...

    Abstract Background: In 2019, the Louisiana Department of Health reported an early influenza B/Victoria (B/VIC) virus outbreak.
    Method: As it was an atypically large outbreak, we deployed to Louisiana to investigate it using genomics and a triplex real-time RT-PCR assay to detect three antigenically distinct B/VIC lineage variant viruses.
    Results: The investigation indicated that B/VIC V1A.3 subclade, containing a three amino acid deletion in the hemagglutinin and known to be antigenically distinct to the B/Colorado/06/2017 vaccine virus, was the most prevalent circulating virus within the specimens evaluated (86/88 in real-time RT-PCR).
    Conclusion: This work underscores the value of portable platforms for rapid, onsite pathogen characterization.
    MeSH term(s) Humans ; Influenza, Human/epidemiology ; Influenza Vaccines ; Disease Outbreaks ; Louisiana/epidemiology
    Chemical Substances Influenza Vaccines ; L 644711 (SC0Y88002K)
    Language English
    Publishing date 2024-01-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 2274538-5
    ISSN 1750-2659 ; 1750-2640
    ISSN (online) 1750-2659
    ISSN 1750-2640
    DOI 10.1111/irv.13246
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Enhanced fitness of SARS-CoV-2 B.1.617.2 Delta variant in ferrets.

    Sun, Xiangjie / Belser, Jessica A / Kieran, Troy J / Brock, Nicole / Pulit-Penaloza, Joanna A / Pappas, Claudia / Basu Thakur, Poulami / Jones, Joyce / Wentworth, David E / Zhou, Bin / Tumpey, Terrence M / Maines, Taronna R

    Virology

    2023  Volume 582, Page(s) 57–61

    Abstract: Competition assays were conducted in vitro and in vivo to examine how the Delta (B.1.617.2) variant ...

    Abstract Competition assays were conducted in vitro and in vivo to examine how the Delta (B.1.617.2) variant displaced the prototype Washington/1/2020 (WA/1) strain. While WA/1 virus exhibited a moderately increased proportion compared to that in the inoculum following co-infection in human respiratory cells, Delta variant possessed a substantial in vivo fitness advantage as this virus becoming predominant in both inoculated and contact animals. This work identifies critical traits of the Delta variant that likely played a role in it becoming a dominant variant and highlights the necessities of employing multiple model systems to assess the fitness of newly emerged SARS-CoV-2 variants.
    MeSH term(s) Animals ; Humans ; Ferrets ; COVID-19 ; SARS-CoV-2/genetics ; Biological Assay
    Language English
    Publishing date 2023-04-05
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 200425-2
    ISSN 1096-0341 ; 0042-6822
    ISSN (online) 1096-0341
    ISSN 0042-6822
    DOI 10.1016/j.virol.2023.03.014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Differential interferon responses to influenza A and B viruses in primary ferret respiratory epithelial cells.

    Rowe, Thomas / Davis, William / Wentworth, David E / Ross, Ted

    Journal of virology

    2024  Volume 98, Issue 2, Page(s) e0149423

    Abstract: Influenza B viruses (IBV) cocirculate with influenza A viruses (IAV) and cause periodic ... and H3N2 subtypes) or IBV (B/Victoria and B/Yamagata lineages) and assessed for 72 h. Cells were ...

    Abstract Influenza B viruses (IBV) cocirculate with influenza A viruses (IAV) and cause periodic epidemics of disease, yet antibody and cellular responses following IBV infection are less well understood. Using the ferret model for antisera generation for influenza surveillance purposes, IAV resulted in robust antibody responses following infection, whereas IBV required an additional booster dose, over 85% of the time, to generate equivalent antibody titers. In this study, we utilized primary differentiated ferret nasal epithelial cells (FNECs) which were inoculated with IAV and IBV to study differences in innate immune responses which may result in differences in adaptive immune responses in the host. FNECs were inoculated with IAV (H1N1pdm09 and H3N2 subtypes) or IBV (B/Victoria and B/Yamagata lineages) and assessed for 72 h. Cells were analyzed for gene expression by quantitative real-time PCR, and apical and basolateral supernatants were assessed for virus kinetics and interferon (IFN), respectively. Similar virus kinetics were observed with IAV and IBV in FNECs. A comparison of gene expression and protein secretion profiles demonstrated that IBV-inoculated FNEC expressed delayed type-I/II IFN responses and reduced type-III IFN secretion compared to IAV-inoculated cells. Concurrently, gene expression of Thymic Stromal Lymphopoietin (
    MeSH term(s) Animals ; Child ; Humans ; Adaptive Immunity ; Antibodies, Viral/analysis ; Antibodies, Viral/biosynthesis ; Antibodies, Viral/immunology ; Disease Models, Animal ; Epithelial Cells/cytology ; Epithelial Cells/immunology ; Epithelial Cells/virology ; Ferrets/immunology ; Ferrets/virology ; Immunity, Innate ; Influenza A virus/classification ; Influenza A virus/growth & development ; Influenza A virus/immunology ; Influenza A Virus, H1N1 Subtype/immunology ; Influenza A Virus, H3N2 Subtype/immunology ; Influenza B virus/classification ; Influenza B virus/growth & development ; Influenza B virus/immunology ; Influenza Vaccines ; Influenza, Human/virology ; Interferons/immunology ; Nasal Mucosa/cytology ; Nasal Mucosa/immunology ; Nasal Mucosa/virology ; Thymic Stromal Lymphopoietin/genetics ; Thymic Stromal Lymphopoietin/immunology ; Cells, Cultured
    Chemical Substances Antibodies, Viral ; Influenza Vaccines ; Interferons (9008-11-1) ; Thymic Stromal Lymphopoietin (GT0IL38SP4)
    Language English
    Publishing date 2024-01-31
    Publishing country United States
    Document type Comparative Study ; Journal Article
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/jvi.01494-23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Genomic Surveillance for SARS-CoV-2 Variants: Predominance of the Delta (B.1.617.2) and Omicron (B.1.1.529) Variants - United States, June 2021-January 2022.

    Lambrou, Anastasia S / Shirk, Philip / Steele, Molly K / Paul, Prabasaj / Paden, Clinton R / Cadwell, Betsy / Reese, Heather E / Aoki, Yutaka / Hassell, Norman / Zheng, Xiao-Yu / Talarico, Sarah / Chen, Jessica C / Oberste, M Steven / Batra, Dhwani / McMullan, Laura K / Halpin, Alison Laufer / Galloway, Summer E / MacCannell, Duncan R / Kondor, Rebecca /
    Barnes, John / MacNeil, Adam / Silk, Benjamin J / Dugan, Vivien G / Scobie, Heather M / Wentworth, David E / Caravas, Jason / Kovacs, Nicholas A / Gerhart, Jonathan G / Jia Ng, Han / Beck, Andrew / Chau, Reina / Cintron, Roxana / Cook, Peter W / Gulvik, Christopher A / Howard, Dakota / Jang, Yunho / Knipe, Kristen / Lacek, Kristine A / Moser, Kara A / Paskey, Adrian C / Rambo-Martin, Benjamin L / Nagilla, Roopa R / Retchless, Adam C / Schmerer, Matthew W / Seby, Sandra / Shepard, Samuel S / Stanton, Richard A / Stark, Thomas J / Uehara, Anna / Unoarumhi, Yvette / Bentz, Meghan L / Burgin, Alex / Burroughs, Mark / Davis, Morgan L / Keller, Matthew W / Keong, Lisa M / Le, Shoshona S / Lee, Justin S / Madden Jr, Joseph C / Nobles, Sarah / Owuor, D. Collins / Padilla, Jasmine / Sheth, Mili / Wilson, Malania M

    MMWR. Morbidity and mortality weekly report

    2022  Volume 71, Issue 6, Page(s) 206–211

    Abstract: Genomic surveillance is a critical tool for tracking emerging variants of SARS-CoV-2 (the virus that causes COVID-19), which can exhibit characteristics that potentially affect public health and clinical interventions, including increased ... ...

    Abstract Genomic surveillance is a critical tool for tracking emerging variants of SARS-CoV-2 (the virus that causes COVID-19), which can exhibit characteristics that potentially affect public health and clinical interventions, including increased transmissibility, illness severity, and capacity for immune escape. During June 2021-January 2022, CDC expanded genomic surveillance data sources to incorporate sequence data from public repositories to produce weighted estimates of variant proportions at the jurisdiction level and refined analytic methods to enhance the timeliness and accuracy of national and regional variant proportion estimates. These changes also allowed for more comprehensive variant proportion estimation at the jurisdictional level (i.e., U.S. state, district, territory, and freely associated state). The data in this report are a summary of findings of recent proportions of circulating variants that are updated weekly on CDC's COVID Data Tracker website to enable timely public health action.
    MeSH term(s) COVID-19/epidemiology ; COVID-19/virology ; Centers for Disease Control and Prevention, U.S. ; Genomics ; Humans ; Prevalence ; Public Health Surveillance/methods ; SARS-CoV-2/genetics ; United States/epidemiology
    Language English
    Publishing date 2022-02-11
    Publishing country United States
    Document type Technical Report
    ZDB-ID 412775-4
    ISSN 1545-861X ; 0149-2195
    ISSN (online) 1545-861X
    ISSN 0149-2195
    DOI 10.15585/mmwr.mm7106a4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Detection and discrimination of influenza B Victoria lineage deletion variant viruses by real-time RT-PCR.

    Shu, Bo / Kirby, Marie K / Warnes, Christine / Sessions, Wendy M / Davis, William G / Liu, Ji / Wilson, Malania M / Lindstrom, Stephen / Wentworth, David E / Barnes, John R

    Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin

    2020  Volume 25, Issue 41

    Abstract: BackgroundDuring the 2016/17 influenza season, influenza B/VIC lineage variant viruses emerged ...

    Abstract BackgroundDuring the 2016/17 influenza season, influenza B/VIC lineage variant viruses emerged with two (K
    MeSH term(s) Hemagglutinin Glycoproteins, Influenza Virus/genetics ; Humans ; Influenza B virus/classification ; Influenza B virus/genetics ; Influenza B virus/isolation & purification ; Influenza, Human/epidemiology ; Molecular Epidemiology/methods ; Reverse Transcriptase Polymerase Chain Reaction/methods
    Chemical Substances Hemagglutinin Glycoproteins, Influenza Virus
    Language English
    Publishing date 2020-10-01
    Publishing country Sweden
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 1338803-4
    ISSN 1560-7917 ; 1025-496X
    ISSN (online) 1560-7917
    ISSN 1025-496X
    DOI 10.2807/1560-7917.ES.2020.25.41.1900652
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Multiplex Real-Time Reverse Transcription PCR for Influenza A Virus, Influenza B Virus, and Severe Acute Respiratory Syndrome Coronavirus 2.

    Shu, Bo / Kirby, Marie K / Davis, William G / Warnes, Christine / Liddell, Jimma / Liu, Ji / Wu, Kai-Hui / Hassell, Norman / Benitez, Alvaro J / Wilson, Malania M / Keller, Matthew W / Rambo-Martin, Benjamin L / Camara, Yamundow / Winter, Jörn / Kondor, Rebecca J / Zhou, Bin / Spies, Stacey / Rose, Laura E / Winchell, Jonas M /
    Limbago, Brandi M / Wentworth, David E / Barnes, John R

    Emerging infectious diseases

    2021  Volume 27, Issue 7, Page(s) 1821–1830

    Abstract: ... that causes symptoms similar to those caused by influenza A and B viruses. On July 2, 2020 ...

    Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in late 2019, and the outbreak rapidly evolved into the current coronavirus disease pandemic. SARS-CoV-2 is a respiratory virus that causes symptoms similar to those caused by influenza A and B viruses. On July 2, 2020, the US Food and Drug Administration granted emergency use authorization for in vitro diagnostic use of the Influenza SARS-CoV-2 Multiplex Assay. This assay detects influenza A virus at 10
    MeSH term(s) COVID-19 ; Humans ; Influenza A virus/genetics ; Influenza B virus/genetics ; Multiplex Polymerase Chain Reaction ; Reverse Transcription ; SARS-CoV-2
    Language English
    Publishing date 2021-06-21
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1380686-5
    ISSN 1080-6059 ; 1080-6040
    ISSN (online) 1080-6059
    ISSN 1080-6040
    DOI 10.3201/eid2707.210462
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Multiplex Reverse Transcription-PCR for Simultaneous Surveillance of Influenza A and B Viruses.

    Zhou, Bin / Deng, Yi-Mo / Barnes, John R / Sessions, October M / Chou, Tsui-Wen / Wilson, Malania / Stark, Thomas J / Volk, Michelle / Spirason, Natalie / Halpin, Rebecca A / Kamaraj, Uma Sangumathi / Ding, Tao / Stockwell, Timothy B / Salvatore, Mirella / Ghedin, Elodie / Barr, Ian G / Wentworth, David E

    Journal of clinical microbiology

    2017  Volume 55, Issue 12, Page(s) 3492–3501

    Abstract: Influenza A and B viruses are the causative agents of annual influenza epidemics that can be severe ... throughput sequencing of influenza viruses remains a challenge. We developed a single-reaction influenza A/B ... virus (FluA/B) multiplex reverse transcription-PCR (RT-PCR) method that amplifies the most critical ...

    Abstract Influenza A and B viruses are the causative agents of annual influenza epidemics that can be severe, and influenza A viruses intermittently cause pandemics. Sequence information from influenza virus genomes is instrumental in determining mechanisms underpinning antigenic evolution and antiviral resistance. However, due to sequence diversity and the dynamics of influenza virus evolution, rapid and high-throughput sequencing of influenza viruses remains a challenge. We developed a single-reaction influenza A/B virus (FluA/B) multiplex reverse transcription-PCR (RT-PCR) method that amplifies the most critical genomic segments (hemagglutinin [HA], neuraminidase [NA], and matrix [M]) of seasonal influenza A and B viruses for next-generation sequencing, regardless of viral type, subtype, or lineage. Herein, we demonstrate that the strategy is highly sensitive and robust. The strategy was validated on thousands of seasonal influenza A and B virus-positive specimens using multiple next-generation sequencing platforms.
    MeSH term(s) Epidemiological Monitoring ; High-Throughput Nucleotide Sequencing/methods ; Humans ; Influenza A virus/classification ; Influenza A virus/genetics ; Influenza A virus/isolation & purification ; Influenza B virus/classification ; Influenza B virus/genetics ; Influenza B virus/isolation & purification ; Influenza, Human/virology ; Molecular Epidemiology/methods ; Multiplex Polymerase Chain Reaction/methods ; Reverse Transcriptase Polymerase Chain Reaction/methods
    Language English
    Publishing date 2017-10-04
    Publishing country United States
    Document type Journal Article ; Validation Studies ; Research Support, Non-U.S. Gov't
    ZDB-ID 390499-4
    ISSN 1098-660X ; 0095-1137
    ISSN (online) 1098-660X
    ISSN 0095-1137
    DOI 10.1128/JCM.00957-17
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: (with research data) The contrasting phylodynamics of human influenza B viruses.

    Vijaykrishna, Dhanasekaran / Holmes, Edward C / Joseph, Udayan / Fourment, Mathieu / Su, Yvonne C F / Halpin, Rebecca / Lee, Raphael T C / Deng, Yi-Mo / Gunalan, Vithiagaran / Lin, Xudong / Stockwell, Timothy B / Fedorova, Nadia B / Zhou, Bin / Spirason, Natalie / Kühnert, Denise / Bošková, Veronika / Stadler, Tanja / Costa, Anna-Maria / Dwyer, Dominic E /
    Huang, Q Sue / Jennings, Lance C / Rawlinson, William / Sullivan, Sheena G / Hurt, Aeron C / Maurer-Stroh, Sebastian / Wentworth, David E / Smith, Gavin J D / Barr, Ian G

    eLife

    2015  Volume 4, Page(s) e05055

    Abstract: ... until now not been available for influenza B viruses, despite their significant disease burden ... lineages of influenza B virus (Victoria and Yamagata), showing that their individual dynamics are ... preference. In sum, this work identifies new factors that are important determinants of influenza B evolution ...

    Abstract A complex interplay of viral, host, and ecological factors shapes the spatio-temporal incidence and evolution of human influenza viruses. Although considerable attention has been paid to influenza A viruses, a lack of equivalent data means that an integrated evolutionary and epidemiological framework has until now not been available for influenza B viruses, despite their significant disease burden. Through the analysis of over 900 full genomes from an epidemiological collection of more than 26,000 strains from Australia and New Zealand, we reveal fundamental differences in the phylodynamics of the two co-circulating lineages of influenza B virus (Victoria and Yamagata), showing that their individual dynamics are determined by a complex relationship between virus transmission, age of infection, and receptor binding preference. In sum, this work identifies new factors that are important determinants of influenza B evolution and epidemiology.
    MeSH term(s) Age Distribution ; Animals ; Antigens, Viral/immunology ; Asparagine/metabolism ; Dogs ; Evolution, Molecular ; Genetic Variation ; Genome, Viral/genetics ; Glycosylation ; Hemagglutinin Glycoproteins, Influenza Virus/genetics ; Humans ; Influenza A virus/genetics ; Influenza A virus/immunology ; Influenza B virus/genetics ; Influenza B virus/immunology ; Influenza, Human/epidemiology ; Influenza, Human/transmission ; Influenza, Human/virology ; Madin Darby Canine Kidney Cells ; Models, Molecular ; New Zealand ; Phylogeny ; Reassortant Viruses/genetics ; Selection, Genetic ; Time Factors ; Victoria
    Chemical Substances Antigens, Viral ; Hemagglutinin Glycoproteins, Influenza Virus ; Asparagine (7006-34-0)
    Language English
    Publishing date 2015-01-16
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.05055
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  9. Article ; Online: Enhanced fitness of SARS-CoV-2 B.1.617.2 Delta variant in ferrets

    Sun, Xiangjie / Belser, Jessica A. / Kieran, Troy J. / Brock, Nicole / Pulit-Penaloza, Joanna A. / Pappas, Claudia / Basu Thakur, Poulami / Jones, Joyce / Wentworth, David E. / Zhou, Bin / Tumpey, Terrence M. / Maines, Taronna R.

    Virology. 2023 May, v. 582 p.57-61

    2023  

    Abstract: Competition assays were conducted in vitro and in vivo to examine how the Delta (B.1.617.2) variant ...

    Abstract Competition assays were conducted in vitro and in vivo to examine how the Delta (B.1.617.2) variant displaced the prototype Washington/1/2020 (WA/1) strain. While WA/1 virus exhibited a moderately increased proportion compared to that in the inoculum following co-infection in human respiratory cells, Delta variant possessed a substantial in vivo fitness advantage as this virus becoming predominant in both inoculated and contact animals. This work identifies critical traits of the Delta variant that likely played a role in it becoming a dominant variant and highlights the necessities of employing multiple model systems to assess the fitness of newly emerged SARS-CoV-2 variants.
    Keywords Severe acute respiratory syndrome coronavirus 2 ; humans ; inoculum ; mixed infection ; prototypes ; virology ; viruses ; SARS-CoV-2 ; Delta variant ; Ferrets ; Viral fitness
    Language English
    Dates of publication 2023-05
    Size p. 57-61.
    Publishing place Elsevier Inc.
    Document type Article ; Online
    ZDB-ID 200425-2
    ISSN 1096-0341 ; 0042-6822
    ISSN (online) 1096-0341
    ISSN 0042-6822
    DOI 10.1016/j.virol.2023.03.014
    Database NAL-Catalogue (AGRICOLA)

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  10. Article ; Online: HOMA2-B enhances assessment of type 1 diabetes risk among TrialNet Pathway to Prevention participants.

    Felton, Jamie L / Cuthbertson, David / Warnock, Megan / Lohano, Kuldeep / Meah, Farah / Wentworth, John M / Sosenko, Jay / Evans-Molina, Carmella

    Diabetologia

    2021  Volume 65, Issue 1, Page(s) 88–100

    Abstract: ... stratify autoantibody-positive (Aab+) individuals who are at risk of developing type 1 diabetes. HOMA2-B is ... glucose and insulin. The utility of HOMA2-B in association with type 1 diabetes progression has not been ... tested.: Methods: Baseline HOMA2-B values from single-Aab+ (n = 2652; mean age, 21.1 ± 14.0 years) and ...

    Abstract Aims/hypothesis: Methods to identify individuals at highest risk for type 1 diabetes are essential for the successful implementation of disease-modifying interventions. Simple metabolic measures are needed to help stratify autoantibody-positive (Aab+) individuals who are at risk of developing type 1 diabetes. HOMA2-B is a validated mathematical tool commonly used to estimate beta cell function in type 2 diabetes using fasting glucose and insulin. The utility of HOMA2-B in association with type 1 diabetes progression has not been tested.
    Methods: Baseline HOMA2-B values from single-Aab+ (n = 2652; mean age, 21.1 ± 14.0 years) and multiple-Aab+ (n = 3794; mean age, 14.5 ± 11.2 years) individuals enrolled in the TrialNet Pathway to Prevention study were compared. Cox proportional hazard models were used to determine associations between HOMA2-B tertiles and time to progression to type 1 diabetes, with adjustments for age, sex, HLA status and BMI z score. Receiver operating characteristic (ROC) analysis was used to test the association of HOMA2-B with type 1 diabetes development in 1, 2, 5 and 10 years.
    Results: At study entry, HOMA2-B values were higher in single- compared with multiple-Aab+ Pathway to Prevention participants (91.1 ± 44.5 vs 83.9 ± 38.9; p < 0.001). Single- and multiple-Aab+ individuals in the lowest HOMA2-B tertile had a higher risk and faster rate of progression to type 1 diabetes. For progression to type 1 diabetes within 1 year, area under the ROC curve (AUC-ROC) was 0.685, 0.666 and 0.680 for all Aab+, single-Aab+ and multiple-Aab+ individuals, respectively. When correlation between HOMA2-B and type 1 diabetes risk was assessed in combination with additional factors known to influence type 1 diabetes progression (insulin sensitivity, age and HLA status), AUC-ROC was highest for the single-Aab+ group's risk of progression at 2 years (AUC-ROC 0.723 [95% CI 0.652, 0.794]).
    Conclusions/interpretation: These data suggest that HOMA2-B may have utility as a single-time-point measurement to stratify risk of type 1 diabetes development in Aab+ individuals.
    MeSH term(s) Adolescent ; Adult ; Autoantibodies ; Blood Glucose/metabolism ; Child ; Child, Preschool ; Diabetes Mellitus, Type 1 ; Diabetes Mellitus, Type 2 ; Humans ; Insulin ; Insulin Resistance/physiology ; Young Adult
    Chemical Substances Autoantibodies ; Blood Glucose ; Insulin
    Language English
    Publishing date 2021-10-12
    Publishing country Germany
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1694-9
    ISSN 1432-0428 ; 0012-186X
    ISSN (online) 1432-0428
    ISSN 0012-186X
    DOI 10.1007/s00125-021-05573-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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