Evidence of a Substantial Genetic Basis for IgG2 Levels in Families with Aggressive Periodontitis

IgG2 is elevated in localized but not in generalized aggressive periodontitis (AgP). Exposure to pathogenic bacteria is essential for disease. Immune responses are dominated by IgG2 reactive with bacterial surface carbohydrates. We used variance component analyses to assess IgG2 heritability and det...

Full description

Saved in:
Bibliographic Details
Published inJournal of dental research Vol. 82; no. 9; pp. 708 - 712
Main Authors Diehl, S.R., Wu, T., Burmeister, J.A., Califano, J.V., Brooks, C.N., Tew, J.G., Schenkein, H.A.
Format Journal Article
LanguageEnglish
Published United States SAGE Publications 01.09.2003
SAGE PUBLICATIONS, INC
Subjects
Online AccessGet full text
ISSN0022-0345
1544-0591
DOI10.1177/154405910308200910

Cover

More Information
Summary:IgG2 is elevated in localized but not in generalized aggressive periodontitis (AgP). Exposure to pathogenic bacteria is essential for disease. Immune responses are dominated by IgG2 reactive with bacterial surface carbohydrates. We used variance component analyses to assess IgG2 heritability and determine whether genes that influence IgG2 are the same genes that influence disease susceptibility. We studied 17 Caucasian and 43 African American families with two or more localized or generalized AgP-affected members (274 subjects with IgG2 measurements). Only 16% of the variance in IgG2 was attributable to age, race, and smoking. Even with the addition of localized AgP, the model still explained only 19% of IgG2 variance. By contrast, heritability of IgG2 levels was estimated to be 38% and highly significant (P = 0.0006), demonstrating a substantial genetic basis. Bi-trait variance component analyses of IgG2 and quantitative measures of AgP indicate that different genes appear to control IgG2 levels and disease susceptibility.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:0022-0345
1544-0591
DOI:10.1177/154405910308200910