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Volume 17, Number 12—December 2011
Research

A Pilot Study of Host Genetic Variants Associated with Influenza-associated Deaths among Children and Young Adults1

Jill M. FerdinandsComments to Author , Amy M. Denison, Nicole F. Dowling, Heather A. Jost, Marta L. Gwinn, Lindy Liu, Sherif R. Zaki, and David K. Shay
Author affiliations: Centers for Disease Control and Prevention, Atlanta, Georgia, USA

Main Article

Table 4

Characteristics of 8 children and young adults who died of influenza and had invasive methicillin-resistant Staphylococcus aureus co-infection, United States, 1998–99 through 2007–08 influenza seasons

Patient age, y/sex Season Influenza type Previous conditions Sudden
death* MBL2 haplotype† MBL production haplotype‡ MBL2 structural
variant
29/M 2004–05 A None Yes YA/O Intermediate rs1800450 A/G
14/M 2006–07 A None No XA/YA High None
11/F 2006–07 B None Yes YA/YA High None
13/M 2006–07 B None Yes XA/O Low rs1800450 A/G
12/F 2006–07 B None No O/O Low rs1800450 A/A
8/F 2007–08 A Asthma Yes XA/O Low rs1800450 A/G
18/M 2007–08 A Asthma Yes XA/O Low rs1800450 A/G
32/M 2007–08 B Asthma No XA/YA High None

*Sudden death is defined as death occurring less than 3 days after symptom onset. MBL2, mannose-binding lectin gene.
†Per common designation for MBL2, A refers to the wild-type structural allele, O refers to any of the 3 variant structural alleles, and O/O refers to any combination of structural variant alleles. Y refers to the wild-type allele and X to the variant allele at promoter locus rs7096206 (the X/Y variant).
‡Low mannose-binding lectin (MBL) producers included MBL2 haplotypes O/O and XA/O. Intermediate producers included MBL2 haplotypes XA/XA and YA/O. High producers included MBL2 haplotypes XA/YA and YA/YA.

Main Article

1Portions of this study were presented at the Options for the Control of Influenza VII meeting, September 3–7, 2010, Hong Kong.

Page created: December 01, 2011
Page updated: December 01, 2011
Page reviewed: December 01, 2011
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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