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Freitag-Wolf, S.* ; Dommisch, H.* ; Graetz, C.* ; Jockel-Schneider, Y.* ; Harks, I.* ; Staufenbiel, I.* ; Meyle, J.* ; Eickholz, P.* ; Noack, B.* ; Bruckmann, C.* ; Gieger, C. ; Jepsen, S.* ; Lieb, W.* ; Schreiber, S.* ; König, I.R.* ; Schäfer, A.S.*

Genome-wide exploration identifies sex-specific genetic effects of alleles upstream NPY to increase the risk of severe periodontitis in men.

J. Clin. Periodontol. 41, 1115-1121 (2014)
Postprint DOI PMC
Open Access Green
AIM: Periodontitis (PD) is influenced by genetic as well as life-style and socio-economic factors. Epidemiological studies show that men are at greater risk of severe forms of PD, suggesting interplay between sex and genetic factors. We aimed to systematically analyze patients with aggressive periodontitis (AgP) for gene-sex interactions. MATERIALS AND METHODS: 329 German AgP cases and 983 controls were genotyped with Affymetrix 500K Arrays and were analyzed by logistic regression analysis. The most significant gene-sex interaction was replicated in an independent sample of 382 German/Austrian AgP cases and 489 controls. RESULTS: Ten single nucleotide polymorphisms (SNPs) in strong linkage disequilibrium (r(2) >0.85) upstream the gene neuropeptide Y (NPY) suggested gene-sex interaction (p<5x10(-5) ). SNP rs198712 showed the strongest association in interaction with sex (p=5.4x10(-6) ) with odds ratios in males and females of 1.63 and 0.69, respectively. In the replication, interaction of sex with rs198712 was verified with p=0.022 (pooled p=4.03x10(-6) ) and similar genetic effects. Analysis of chromatin elements from ENCODE data revealed tissue specific transcription at the associated non-coding region. CONCLUSION: The current study is the first to observe a sexually dimorphic role of alleles at NPY in humans and support previous genome-wide findings of a role of NPY in severe PD.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Npy ; Interaction ; Periodontitis ; Sex ; Genetic Association
Language english
Publication Year 2014
HGF-reported in Year 2014
ISSN (print) / ISBN 0303-6979
e-ISSN 1600-051X
Quellenangaben Volume: 41, Issue: 12, Pages: 1115-1121 Article Number: , Supplement: ,
Publisher Wiley
Reviewing status Peer reviewed
Institute(s) Institute of Epidemiology (EPI)
POF-Topic(s) 30202 - Environmental Health
Research field(s) Genetics and Epidemiology
PSP Element(s) G-504091-001
PubMed ID 25256105
Scopus ID 84914120923
Erfassungsdatum 2014-10-09