The interindividual variability of IgA, Igc, and IgM immunoglobulin levels
was studied using path analysis in a northeastern Brazilian sample (nuclear
families) to determine the genetic and/or environmental causes of their va
riation. The path analysis model decomposes the phenotype into genetic caus
es (autosomal and X-chromosome-linked genes) and environmental causes. A si
gnificant familial aggregation, mainly resulting from autosomal components,
was detected for the 3 immunoglobulin levels. The values of genetic herita
bility were h(2) = 0.410 +/- 0.030 for IgA, h(2) = 0.617 +/- 0.020 for IgG,
and h(2) = 0.540 +/- 0.023 for IgM, and the values for environmental-cultu
ral heritability were c(2) = 0.085 +/- 0.034 for IgA, c(2) = 0.084 +/- 0.02
7 for IgG, and c(2) = 0.023 + 0.023 for IgM. Our results did not show a her
itable component resulting from X-chromosome-linked genes on IgM levels, as
suggested by some studies (Wood et al. 1969; Grundbacher 1972; Purtilo and
Sullivan 1979). Some additional results were that (1) age and IgA concentr
ation were positively correlated, with IgA level increasing gradually from
childhood to adulthood (p < 0.001); (2) sex and the age x sex interaction a
ct on IgG concentration (p < 0.01); (3) age and IgM concentration are corre
lated (with children presenting lower levels than adults, especially in mal
es, p < 0.01); and (4) a significant association exists between sex and IgM
level (with females presenting higher levels than males, p < 0.001).