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  1. AU="Duan, Jiasong"
  2. AU="He, Ruiying"
  3. AU="Auricchio, Salvatore"
  4. AU="Farnesini, L"
  5. AU="Gerald Berger"
  6. AU="Lenning, Ole Bernt"
  7. AU="Voetsch, Barbara"
  8. AU="Jakielska, Ewelina"
  9. AU="Sholl, Lynette"
  10. AU="Izquierdo, Inmaculada"
  11. AU="Miller, Andrew S"
  12. AU="Vincent-Levy-Frebault, V"
  13. AU="Willis, Zachary I"
  14. AU="Kruger, Eric S"
  15. AU="Ge, Shiyu"
  16. AU="Srivastava, Rajat"
  17. AU="Nemanja Vuksanovic"

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  1. Artikel ; Online: Distinctive trajectories of the COVID-19 epidemic by age and gender: A retrospective modeling of the epidemic in South Korea.

    Yu, Xinhua / Duan, Jiasong / Jiang, Yu / Zhang, Hongmei

    International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases

    2020  Band 98, Seite(n) 200–205

    Abstract: Objectives: Elderly people had suffered a disproportionate burden of COVID-19. We hypothesized that males and females in different age groups might have different epidemic trajectories.: Methods: Using publicly available data from South Korea, daily ... ...

    Abstract Objectives: Elderly people had suffered a disproportionate burden of COVID-19. We hypothesized that males and females in different age groups might have different epidemic trajectories.
    Methods: Using publicly available data from South Korea, daily new COVID-19 cases were assessed using generalized additive models, assuming Poisson and negative binomial distributions. Epidemic dynamics by age and gender groups were explored using interactions between smoothed time terms and age and gender.
    Results: A negative binomial distribution fitted the daily case counts best. The relationship between the dynamic patterns of daily new cases and age groups was statistically significant (p<0.001), but this was not the case with gender groups. People aged 20-39 years led the epidemic processes in South Korean society with two peaks - one major peak around March 1 and a smaller peak around April 7, 2020. The epidemic process among people aged 60 or above trailed behind that of the younger age group, and with smaller magnitude. After March 15, there was a consistent decline of daily new cases among elderly people, despite large fluctuations in case counts among young adults.
    Conclusions: Although young people drove the COVID-19 epidemic throughout society, with multiple rebounds, elderly people could still be protected from infection after the peak of the epidemic.
    Mesh-Begriff(e) Adolescent ; Adult ; Age Distribution ; Betacoronavirus ; COVID-19 ; Child ; Child, Preschool ; Coronavirus Infections/epidemiology ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Middle Aged ; Pandemics ; Pneumonia, Viral/epidemiology ; Republic of Korea/epidemiology ; Retrospective Studies ; SARS-CoV-2 ; Sex Characteristics ; Young Adult
    Schlagwörter covid19
    Sprache Englisch
    Erscheinungsdatum 2020-07-02
    Erscheinungsland Canada
    Dokumenttyp Journal Article
    ZDB-ID 1331197-9
    ISSN 1878-3511 ; 1201-9712
    ISSN (online) 1878-3511
    ISSN 1201-9712
    DOI 10.1016/j.ijid.2020.06.101
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Distinctive trajectories of the COVID-19 epidemic by age and gender

    Yu, Xinhua / Duan, Jiasong / Jiang, Yu / Zhang, Hongmei

    International Journal of Infectious Diseases

    A retrospective modeling of the epidemic in South Korea

    2020  Band 98, Seite(n) 200–205

    Schlagwörter Microbiology (medical) ; Infectious Diseases ; General Medicine ; covid19
    Sprache Englisch
    Verlag Elsevier BV
    Erscheinungsland us
    Dokumenttyp Artikel ; Online
    ZDB-ID 1331197-9
    ISSN 1878-3511 ; 1201-9712
    ISSN (online) 1878-3511
    ISSN 1201-9712
    DOI 10.1016/j.ijid.2020.06.101
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  3. Artikel: Distinctive trajectories of the COVID-19 epidemic by age and gender: A retrospective modeling of the epidemic in South Korea

    Yu, Xinhua / Duan, Jiasong / Jiang, Yu / Zhang, Hongmei

    Int J Infect Dis

    Abstract: OBJECTIVES: Elderly people had suffered a disproportionate burden of COVID-19. We hypothesized that males and females in different age groups might have different epidemic trajectories. METHODS: Using publicly available data from South Korea, daily new ... ...

    Abstract OBJECTIVES: Elderly people had suffered a disproportionate burden of COVID-19. We hypothesized that males and females in different age groups might have different epidemic trajectories. METHODS: Using publicly available data from South Korea, daily new COVID-19 cases were assessed using generalized additive models, assuming Poisson and negative binomial distributions. Epidemic dynamics by age and gender groups were explored using interactions between smoothed time terms and age and gender. RESULTS: A negative binomial distribution fitted the daily case counts best. The relationship between the dynamic patterns of daily new cases and age groups was statistically significant (p<0.001), but this was not the case with gender groups. People aged 20-39 years led the epidemic processes in South Korean society with two peaks - one major peak around March 1 and a smaller peak around April 7, 2020. The epidemic process among people aged 60 or above trailed behind that of the younger age group, and with smaller magnitude. After March 15, there was a consistent decline of daily new cases among elderly people, despite large fluctuations in case counts among young adults. CONCLUSIONS: Although young people drove the COVID-19 epidemic throughout society, with multiple rebounds, elderly people could still be protected from infection after the peak of the epidemic.
    Schlagwörter covid19
    Verlag WHO
    Dokumenttyp Artikel
    Anmerkung WHO #Covidence: #624019
    Datenquelle COVID19

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  4. Artikel: Methylation of Host Genes Associated with Coronavirus Infection from Birth to 26 Years

    Rathod, Rutu / Rathod, Aniruddha / Rahimabad, Parnian Kheirkhah / Duan, Jiasong / Zhang, Hongmei / Arshad, S. Hasan / Karmaus, Wilfried

    Genes. 2021 July 31, v. 12, no. 8

    2021  

    Abstract: DNA methylation (DNAm) patterns over time at 1146 CpGs on coronavirus-related genes were assessed to understand whether the varying differences in susceptibility, symptoms, and the outcomes of the SARS-CoV-2 infection in children and young adults could ... ...

    Abstract DNA methylation (DNAm) patterns over time at 1146 CpGs on coronavirus-related genes were assessed to understand whether the varying differences in susceptibility, symptoms, and the outcomes of the SARS-CoV-2 infection in children and young adults could be explained through epigenetic alterations in a host cell’s transcriptional apparatus to coronaviruses. DNAm data from the Isle of Wight birth cohort (IOWBC) at birth, 10, 18, and 26 years of age were included. Linear mixed models with repeated measurements stratified by sex were used to examine temporal patterns, and cluster analysis was performed to identify CpGs following similar patterns. CpGs on autosomes and sex chromosomes were analyzed separately. The association of identified CpGs and expression of their genes were evaluated. Pathway enrichment analyses of the genes was conducted at FDR = 0.05. DNAm at 635 of the 1146 CpGs on autosomes showed statistically significant time effects (FDR = 0.05). The 635 CpGs were classified into five clusters with each representing a unique temporal pattern of DNAm. Of the 29 CpGs on sex chromosomes, DNAm at seven CpGs in males and eight CpGs in females showed time effects (FDR = 0.05). Sex-specific and non-specific associations of DNAm with gene expression were found at 24 and 93 CpGs, respectively. Genes which mapped the 643 CpGs represent 460 biological processes. We suggest that the observed variability in DNAm with advancing age may partially explain differing susceptibility, disease severity, and mortality of coronavirus infections among different age groups.
    Schlagwörter Coronavirus infections ; DNA methylation ; Severe acute respiratory syndrome coronavirus 2 ; autosomes ; cluster analysis ; disease severity ; epigenetics ; gene expression ; mortality ; transcription (genetics)
    Sprache Englisch
    Erscheinungsverlauf 2021-0731
    Erscheinungsort Multidisciplinary Digital Publishing Institute
    Dokumenttyp Artikel
    ZDB-ID 2527218-4
    ISSN 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes12081198
    Datenquelle NAL Katalog (AGRICOLA)

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  5. Artikel ; Online: Methylation of Host Genes Associated with Coronavirus Infection from Birth to 26 Years.

    Rathod, Rutu / Rathod, Aniruddha / Rahimabad, Parnian Kheirkhah / Duan, Jiasong / Zhang, Hongmei / Arshad, S Hasan / Karmaus, Wilfried

    Genes

    2021  Band 12, Heft 8

    Abstract: DNA methylation (DNAm) patterns over time at 1146 CpGs on coronavirus-related genes were assessed to understand whether the varying differences in susceptibility, symptoms, and the outcomes of the SARS-CoV-2 infection in children and young adults could ... ...

    Abstract DNA methylation (DNAm) patterns over time at 1146 CpGs on coronavirus-related genes were assessed to understand whether the varying differences in susceptibility, symptoms, and the outcomes of the SARS-CoV-2 infection in children and young adults could be explained through epigenetic alterations in a host cell's transcriptional apparatus to coronaviruses. DNAm data from the Isle of Wight birth cohort (IOWBC) at birth, 10, 18, and 26 years of age were included. Linear mixed models with repeated measurements stratified by sex were used to examine temporal patterns, and cluster analysis was performed to identify CpGs following similar patterns. CpGs on autosomes and sex chromosomes were analyzed separately. The association of identified CpGs and expression of their genes were evaluated. Pathway enrichment analyses of the genes was conducted at FDR = 0.05. DNAm at 635 of the 1146 CpGs on autosomes showed statistically significant time effects (FDR = 0.05). The 635 CpGs were classified into five clusters with each representing a unique temporal pattern of DNAm. Of the 29 CpGs on sex chromosomes, DNAm at seven CpGs in males and eight CpGs in females showed time effects (FDR = 0.05). Sex-specific and non-specific associations of DNAm with gene expression were found at 24 and 93 CpGs, respectively. Genes which mapped the 643 CpGs represent 460 biological processes. We suggest that the observed variability in DNAm with advancing age may partially explain differing susceptibility, disease severity, and mortality of coronavirus infections among different age groups.
    Mesh-Begriff(e) Adolescent ; Adult ; COVID-19/genetics ; Child ; CpG Islands ; DNA Methylation ; Epigenome ; Female ; Humans ; Male
    Sprache Englisch
    Erscheinungsdatum 2021-07-31
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2527218-4
    ISSN 2073-4425 ; 2073-4425
    ISSN (online) 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes12081198
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Interweaving Between Genetic and Epigenetic Studies on Childhood Asthma.

    Rathod, Aniruddha / Duan, Jiasong / Zhang, Hongmei / Holloway, John W / Ewart, Susan / Arshad, S Hasan / Karmaus, Wilfried

    Epigenetics insights

    2020  Band 13, Seite(n) 2516865720923395

    Abstract: The cause and underlying mechanisms that contribute to asthma pathogenesis are not well known. Both genome- and epigenome-wide association studies have identified genes associated with asthma risk. It is unknown to what extent genes identified in these ... ...

    Abstract The cause and underlying mechanisms that contribute to asthma pathogenesis are not well known. Both genome- and epigenome-wide association studies have identified genes associated with asthma risk. It is unknown to what extent genes identified in these two types of studies overlap. Based on existing literature and the DisGeNET database, we extracted overlapping genes identified in genetic and epigenetic studies of childhood asthma. Through analyses of variance, we assessed whether DNA methylation (DNAm) at 5'-C-phosphate-G-3' (CpGs) on the overlapping genes was associated with neighboring single-nucleotide polymorphisms (SNPs) within 1M base pairs (bps) and with low linkage disequilibrium (
    Sprache Englisch
    Erscheinungsdatum 2020-07-22
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 2516-8657
    ISSN (online) 2516-8657
    DOI 10.1177/2516865720923395
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: DNA Methylation at Birth is Associated with Childhood Serum Immunoglobulin E Levels.

    Han, Luhang / Kaushal, Akhilesh / Zhang, Hongmei / Kadalayil, Latha / Duan, Jiasong / Holloway, John W / Karmaus, Wilfried / Banerjee, Pratik / Tsai, Shih-Fen / Wen, Hui-Ju / Arshad, Syed Hasan / Wang, Shu-Li

    Epigenetics insights

    2021  Band 14, Seite(n) 25168657211008108

    Abstract: Immunoglobulin E (IgE) is known to play an important role in allergic diseases. Epigenetic traits acquired due to modification of deoxyribonucleic acid (DNA) methylation (DNAm) in early life may have phenotypic consequences through their role in ... ...

    Abstract Immunoglobulin E (IgE) is known to play an important role in allergic diseases. Epigenetic traits acquired due to modification of deoxyribonucleic acid (DNA) methylation (DNAm) in early life may have phenotypic consequences through their role in transcriptional regulation with relevance to the developmental origins of diseases including allergy. However, epigenome-scale studies on the longitudinal association of cord blood DNAm with IgE over time are lacking. Our study aimed to examine the association of DNAm at birth with childhood serum IgE levels during early life. Genome-scale DNAm and total serum IgE measured at birth, 5, 8, and 11 years of children in the Taiwan Maternal and Infant Cohort Study were included in the study in the discovery stage. Linear mixed models were implemented to assess the association between cord blood DNAm at ~310K 5'-cytosine-phosphate-guanine-3' (CpG) sites with repeated IgE measurements, adjusting for cord blood IgE. Identified statistically significant CpGs (at a false discovery rate, FDR, of 0.05) were further tested in an independent replication cohort, the Isle of Wight (IoW) birth cohort. We mapped replicated CpGs to genes and conducted gene ontology analysis using ToppFun to identify significantly enriched pathways and biological processes of the genes. Cord blood DNAm of 273 CpG sites were significantly (FDR = 0.05) associated with IgE levels longitudinally. Among the identified CpGs available in both cohorts (184 CpGs), 92 CpGs (50%) were replicated in the IoW in terms of consistency in direction of associations between DNA methylation and IgE levels later in life, and 16 of the 92 CpGs showed statistically significant associations (
    Sprache Englisch
    Erscheinungsdatum 2021-04-05
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 2516-8657
    ISSN (online) 2516-8657
    DOI 10.1177/25168657211008108
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.

    Budu-Aggrey, Ashley / Kilanowski, Anna / Sobczyk, Maria K / Shringarpure, Suyash S / Mitchell, Ruth / Reis, Kadri / Reigo, Anu / Mägi, Reedik / Nelis, Mari / Tanaka, Nao / Brumpton, Ben M / Thomas, Laurent F / Sole-Navais, Pol / Flatley, Christopher / Espuela-Ortiz, Antonio / Herrera-Luis, Esther / Lominchar, Jesus V T / Bork-Jensen, Jette / Marenholz, Ingo /
    Arnau-Soler, Aleix / Jeong, Ayoung / Fawcett, Katherine A / Baurecht, Hansjorg / Rodriguez, Elke / Alves, Alexessander Couto / Kumar, Ashish / Sleiman, Patrick M / Chang, Xiao / Medina-Gomez, Carolina / Hu, Chen / Xu, Cheng-Jian / Qi, Cancan / El-Heis, Sarah / Titcombe, Philip / Antoun, Elie / Fadista, João / Wang, Carol A / Thiering, Elisabeth / Wu, Baojun / Kress, Sara / Kothalawala, Dilini M / Kadalayil, Latha / Duan, Jiasong / Zhang, Hongmei / Hadebe, Sabelo / Hoffmann, Thomas / Jorgenson, Eric / Choquet, Hélène / Risch, Neil / Njølstad, Pål / Andreassen, Ole A / Johansson, Stefan / Almqvist, Catarina / Gong, Tong / Ullemar, Vilhelmina / Karlsson, Robert / Magnusson, Patrik K E / Szwajda, Agnieszka / Burchard, Esteban G / Thyssen, Jacob P / Hansen, Torben / Kårhus, Line L / Dantoft, Thomas M / Jeanrenaud, Alexander C S N / Ghauri, Ahla / Arnold, Andreas / Homuth, Georg / Lau, Susanne / Nöthen, Markus M / Hübner, Norbert / Imboden, Medea / Visconti, Alessia / Falchi, Mario / Bataille, Veronique / Hysi, Pirro / Ballardini, Natalia / Boomsma, Dorret I / Hottenga, Jouke J / Müller-Nurasyid, Martina / Ahluwalia, Tarunveer S / Stokholm, Jakob / Chawes, Bo / Schoos, Ann-Marie M / Esplugues, Ana / Bustamante, Mariona / Raby, Benjamin / Arshad, Syed / German, Chris / Esko, Tõnu / Milani, Lili A / Metspalu, Andres / Terao, Chikashi / Abuabara, Katrina / Løset, Mari / Hveem, Kristian / Jacobsson, Bo / Pino-Yanes, Maria / Strachan, David P / Grarup, Niels / Linneberg, Allan / Lee, Young-Ae / Probst-Hensch, Nicole / Weidinger, Stephan / Jarvelin, Marjo-Riitta / Melén, Erik / Hakonarson, Hakon / Irvine, Alan D / Jarvis, Deborah / Nijsten, Tamar / Duijts, Liesbeth / Vonk, Judith M / Koppelmann, Gerard H / Godfrey, Keith M / Barton, Sheila J / Feenstra, Bjarke / Pennell, Craig E / Sly, Peter D / Holt, Patrick G / Williams, L Keoki / Bisgaard, Hans / Bønnelykke, Klaus / Curtin, John / Simpson, Angela / Murray, Clare / Schikowski, Tamara / Bunyavanich, Supinda / Weiss, Scott T / Holloway, John W / Min, Josine L / Brown, Sara J / Standl, Marie / Paternoster, Lavinia

    Nature communications

    2023  Band 14, Heft 1, Seite(n) 6172

    Abstract: Atopic dermatitis (AD) is a common inflammatory skin condition and prior genome-wide association studies (GWAS) have identified 71 associated loci. In the current study we conducted the largest AD GWAS to date (discovery N = 1,086,394, replication N = 3, ... ...

    Abstract Atopic dermatitis (AD) is a common inflammatory skin condition and prior genome-wide association studies (GWAS) have identified 71 associated loci. In the current study we conducted the largest AD GWAS to date (discovery N = 1,086,394, replication N = 3,604,027), combining previously reported cohorts with additional available data. We identified 81 loci (29 novel) in the European-only analysis (which all replicated in a separate European analysis) and 10 additional loci in the multi-ancestry analysis (3 novel). Eight variants from the multi-ancestry analysis replicated in at least one of the populations tested (European, Latino or African), while two may be specific to individuals of Japanese ancestry. AD loci showed enrichment for DNAse I hypersensitivity and eQTL associations in blood. At each locus we prioritised candidate genes by integrating multi-omic data. The implicated genes are predominantly in immune pathways of relevance to atopic inflammation and some offer drug repurposing opportunities.
    Mesh-Begriff(e) Humans ; Genome-Wide Association Study ; Dermatitis, Atopic/genetics ; Genetic Predisposition to Disease/genetics ; Hispanic or Latino/genetics ; Black People ; Polymorphism, Single Nucleotide
    Sprache Englisch
    Erscheinungsdatum 2023-10-04
    Erscheinungsland England
    Dokumenttyp Meta-Analysis ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-41180-2
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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