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Fard, D.* ; Läer, K.* ; Rothämel, T.* ; Schürmann, P.* ; Arnold, M. ; Cohen, M.* ; Vennemann, M.* ; Pfeiffer, H.* ; Bajanowski, T.* ; Pfeufer, A. ; Dörk, T.* ; Klintschar, M.*

Candidate gene variants of the immune system and sudden infant death syndrome.

Int. J. Legal Med. 130, 1025-1033 (2016)
DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
BACKGROUND: Sudden infant death syndrome (SIDS) causes early infant death with an incidence between 0.5 and 2.5 cases among 1000 live births. Besides central sleep apnea and thermal dysregulation, infections have been repeatedly suggested to be implicated in SIDS etiology. METHODS: To test the risk contribution of common genetic variants related to infection, we genotyped 40 single-nucleotide polymorphisms (SNPs) from 15 candidate genes for association with SIDS in a total of 579 cases and 1124 controls from Germany and the UK in a two-stage case control design. RESULTS: The discovery-stage series (267 SIDS cases and 303 controls) revealed nominally significant associations for variants in interleukin 6 (IL6) (rs1880243), interleukin 10 (IL10) (rs1800871, rs1800872), and mannose-binding lectin 2 (MBL2) (rs930506), and for several other variants in subgroups. Meta-analyses were then performed in adding genotype information from a genome-wide association study of another 312 European SIDS cases and 821 controls. Overall associations were observed for two independent variants in MBL2: rs930506 in a co-dominant model (odds ratio (OR) = 0.82, p = 0.04) and rs1838065 in a dominant model (OR = 1.27, p = 0.03). CONCLUSION: Our study did not replicate published associations of IL10 variants with SIDS. However, the evidence for two independent MBL2 variants in the combined analysis of two large series seems consistent with the hypothesis that infection may play a role in SIDS pathogenesis.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Association Study ; Genetic Predisposition ; Infection ; Mannose-binding Lectin ; Polymorphism ; Sids; Cerebrospinal-fluid; Increasing Protein; Il-10 Genotype; Binding Lectin; Syndrome Sids; Infection; Risk; Polymorphisms; Interleukin-6; Association
ISSN (print) / ISBN 0044-3433
e-ISSN 1437-1596
Quellenangaben Band: 130, Heft: 4, Seiten: 1025-1033 Artikelnummer: , Supplement: ,
Verlag Springer
Verlagsort New York
Begutachtungsstatus Peer reviewed