TY - JOUR
T1 - Family resemblance for fasting blood glucose
T2 - the Jerusalem Lipid Research Clinic
AU - Friedlander, Y.
AU - Kark, J. D.
AU - Bar‐On, H.
PY - 1987/10
Y1 - 1987/10
N2 - Familial aggregation of fasting plasma glucose was studied in a sample of families examined at the Jerusalem Lipid Research Clinic. We first examined homogeneity of familial correlations across major origin groups in the Israeli sample. Correlations were generally homogeneous across origin groups, except for mother‐son pairs. The pooled familial correlations were relatively low for unadjusted blood glucose values, and somewhat higher upon adjustment for sex, age, ethnicity, education, seasonality, body mass, cigarette smoking, alcohol consumption and dietary intake. Genetic and cultural determinants of blood glucose were estimated utilizing a path model with 10 parameters to be estimated from a total of 16 correlations. Under a reduced model genetic heritability (h2) was estimated to be 0.18±0.08 and cultural heritability (c2) was 0.10 4±0.02. However, within this population the additive variation could be explained by a cultural model of inheritance without introducing genetic parameters, and most of the variance is due to “random” unmeasured environmental factors. Commingling analysis was also performed, and our findings imply that there is no evidence for admixture in the distribution of fasting blood glucose in this Israeli population sample.
AB - Familial aggregation of fasting plasma glucose was studied in a sample of families examined at the Jerusalem Lipid Research Clinic. We first examined homogeneity of familial correlations across major origin groups in the Israeli sample. Correlations were generally homogeneous across origin groups, except for mother‐son pairs. The pooled familial correlations were relatively low for unadjusted blood glucose values, and somewhat higher upon adjustment for sex, age, ethnicity, education, seasonality, body mass, cigarette smoking, alcohol consumption and dietary intake. Genetic and cultural determinants of blood glucose were estimated utilizing a path model with 10 parameters to be estimated from a total of 16 correlations. Under a reduced model genetic heritability (h2) was estimated to be 0.18±0.08 and cultural heritability (c2) was 0.10 4±0.02. However, within this population the additive variation could be explained by a cultural model of inheritance without introducing genetic parameters, and most of the variance is due to “random” unmeasured environmental factors. Commingling analysis was also performed, and our findings imply that there is no evidence for admixture in the distribution of fasting blood glucose in this Israeli population sample.
KW - commingling analysis
KW - cultural
KW - family resemblance
KW - fasting blood glucose
KW - genetic
KW - path analysis
UR - http://www.scopus.com/inward/record.url?scp=0023239785&partnerID=8YFLogxK
U2 - 10.1111/j.1399-0004.1987.tb03305.x
DO - 10.1111/j.1399-0004.1987.tb03305.x
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C2 - 3677461
AN - SCOPUS:0023239785
SN - 0009-9163
VL - 32
SP - 222
EP - 234
JO - Clinical Genetics
JF - Clinical Genetics
IS - 4
ER -