The aim of this study was to determine whether there was evidence for
a genetic component in the immune response as measured by IgG2 levels.
The study was motivated by our studies of early-onset periodontitis (
EOP), a group of disorders characterized by rapid destruction of the s
upporting tissues of the teeth in otherwise healthy individuals. EOP h
as two subforms, localized juvenile periodontitis (LJP) and a generali
zed form (G-EOP). IgG2 Levels are elevated in LJP but not G-EOP indivi
duals; and African-American IgG2 levels are higher than Caucasian leve
ls regardless of EOP status. IgG2 levels were determined in 123 EOP fa
milies and in 508 unrelated non-EOP control individuals. Segregation a
nalysis under the regressive model approach of Bonney was used to anal
yze IgG2 levels for evidence of major locus segregation. After adjusti
ng for LJP status, race, sex, and age, the best-fitting model was an a
utosomal codominant major locus model (accounting for similar to 62% o
f the variance in IgG2), plus residual parent/offspring and spousal co
rrelations. Smoking and GM23 are also known to affect IgG2 levels. If
additional adjustments are made for smoking and GM23, the best-fitting
model is still a codominant major Locus but with no significant resid
ual correlations.