Expression of the filaggrin gene in umbilical cord blood predicts eczema risk in infancy: A birth cohort study

被引:10
作者
Ziyab, A. H. [1 ]
Ewart, S. [2 ]
Lockett, G. A. [3 ]
Zhang, H. [4 ]
Arshad, H. [5 ,6 ]
Holloway, J. W. [3 ,6 ]
Karmaus, W. [4 ]
机构
[1] Kuwait Univ, Fac Med, Dept Community Med & Behav Sci, Safat, Kuwait
[2] Michigan State Univ, Coll Vet Med, E Lansing, MI 48824 USA
[3] Univ Southampton, Fac Med, Human Dev & Hlth, Southampton, Hants, England
[4] Univ Memphis, Sch Publ Hlth, Div Epidemiol Biostat & Environm Hlth, Memphis, TN USA
[5] St Marys Hosp, David Hide Asthma & Allergy Res Ctr, Newport, Shrops, England
[6] Univ Southampton, Fac Med, Clin & Expt Sci, Southampton, Hants, England
基金
美国国家卫生研究院;
关键词
atopic dermatitis; epidemiology; filaggrin; gene expression; genetics; POISSON REGRESSION APPROACH; TRANSEPIDERMAL WATER-LOSS; OF-FUNCTION MUTATIONS; ATOPIC-DERMATITIS; SKIN BARRIER; FAMILY-HISTORY; DISEASE; CHILDHOOD; ASTHMA; IGE;
D O I
10.1111/cea.12956
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Filaggrin gene (FLG) expression, particularly in the skin, has been linked to the development of the skin barrier and is associated with eczema risk. However, knowledge as to whether FLG expression in umbilical cord blood (UCB) is associated with eczema development and prediction is lacking. Objective: This study sought to assess whether FLG expression in UCB associates with and predicts the development of eczema in infancy. Methods: Infants enrolled in a birth cohort study (n=94) were assessed for eczema at ages 3, 6, and 12 months. Five probes measuring FLG transcripts expression in UCB were available from genomewide gene expression profiling. FLG genetic variants R501X, 2282del4, and S3247X were genotyped. Associations were assessed using Poisson regression with robust variance estimation. Area under the curve (AUC), describing the discriminatory/predictive performance of fitted models, was estimated from logistic regression. Results: Increased level of FLG expression measured by probe A_24_P51322 was associated with reduced risk of eczema during the first year of life (RR=0.60, 95% CI: 0.38-0.95). In contrast, increased level of FLG antisense transcripts measured by probe A_21_P0014075 was associated with increased risk of eczema (RR=2.02, 95% CI: 1.10-3.72). In prediction models including FLG expression, FLG genetic variants, and sex, discrimination between children who will and will not develop eczema at 3 months of age was high (AUC: 0.91, 95% CI: 0.84-0.98). Conclusions and Clinical Relevance: This study demonstrated, for the first time, that FLG expression in UCB is associated with eczema development in infancy. Moreover, our analysis provided prediction models that were capable of discriminating, to a great extent, between those who will and will not develop eczema in infancy. Therefore, early identification of infants at increased risk of developing eczema is possible and such high-risk newborns may benefit from early stratification and intervention.
引用
收藏
页码:1185 / 1192
页数:8
相关论文
共 48 条
  • [1] In search for predictive factors for atopy in human cord blood
    Allam, JP
    Zivanovic, O
    Berg, C
    Gembruch, U
    Bieber, T
    Novak, N
    [J]. ALLERGY, 2005, 60 (06) : 743 - 750
  • [2] [Anonymous], 2009, ALLERGY
  • [3] The Role of Filaggrin in the Skin Barrier and Disease Development
    Armengot-Carbo, M.
    Hernandez-Martin, A.
    Torrelo, A.
    [J]. ACTAS DERMO-SIFILIOGRAFICAS, 2015, 106 (02): : 86 - 95
  • [4] Armengot-Carbo M, 2015, PLOS GENET, V106, P86
  • [5] INTERNATIONAL STUDY OF ASTHMA AND ALLERGIES IN CHILDHOOD (ISAAC) - RATIONALE AND METHODS
    ASHER, MI
    KEIL, U
    ANDERSON, HR
    BEASLEY, R
    CRANE, J
    MARTINEZ, F
    MITCHELL, EA
    PEARCE, N
    SIBBALD, B
    STEWART, AW
    STRACHAN, D
    WEILAND, SK
    WILLIAMS, HC
    [J]. EUROPEAN RESPIRATORY JOURNAL, 1995, 8 (03) : 483 - 491
  • [6] NCBI GEO: archive for functional genomics data sets-update
    Barrett, Tanya
    Wilhite, Stephen E.
    Ledoux, Pierre
    Evangelista, Carlos
    Kim, Irene F.
    Tomashevsky, Maxim
    Marshall, Kimberly A.
    Phillippy, Katherine H.
    Sherman, Patti M.
    Holko, Michelle
    Yefanov, Andrey
    Lee, Hyeseung
    Zhang, Naigong
    Robertson, Cynthia L.
    Serova, Nadezhda
    Davis, Sean
    Soboleva, Alexandra
    [J]. NUCLEIC ACIDS RESEARCH, 2013, 41 (D1) : D991 - D995
  • [7] Profile of skin barrier proteins (filaggrin, claudins 1 and 4) and Th1/Th2/Th17 cytokines in adults with atopic dermatitis
    Batista, D. I. S.
    Perez, L.
    Orfali, R. L.
    Zaniboni, M. C.
    Samorano, L. P.
    Pereira, N. V.
    Sotto, M. N.
    Ishizaki, A. S.
    Oliveira, L. M. S.
    Sato, M. N.
    Aoki, V.
    [J]. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2015, 29 (06) : 1091 - 1095
  • [8] Atopic dermatitis: a candidate for disease-modifying strategy
    Bieber, T.
    Cork, M.
    Reitamo, S.
    [J]. ALLERGY, 2012, 67 (08) : 969 - 975
  • [9] Mechanisms of disease: Atopic dermatitis
    Bieber, Thomas
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (14) : 1483 - 1494
  • [10] Atopic dermatitis: a disease of altered skin barrier and immune dysregulation
    Boguniewicz, Mark
    Leung, Donald Y. M.
    [J]. IMMUNOLOGICAL REVIEWS, 2011, 242 : 233 - 246