Partitioning the variability of fasting plasma glucose levels in pedigrees: genetic and environmental factors

M BOEHNKE, PP MOLL, BA KOTTKE… - American journal of …, 1987 - academic.oup.com
M BOEHNKE, PP MOLL, BA KOTTKE, WH WEIDMAN
American journal of epidemiology, 1987academic.oup.com
Fasting plasma glucose measurements made in 1972–1977 on normoglycemic individuals
in three-generation Caucasian pedigrees from Rochester, Minnesota were analyzed. The
authors determined the contributions of polygenic loci and environmental factors to fasting
plasma glucose variability in these pedigrees. To that end, fasting plasma glucose
measurements were normalized by an inverse normal scores transformation and then
regressed separately for males and females on measured concomitants including age, body …
Abstract
Fasting plasma glucose measurements made in 1972–1977 on normoglycemic individuals in three-generation Caucasian pedigrees from Rochester, Minnesota were analyzed. The authors determined the contributions of polygenic loci and environmental factors to fasting plasma glucose variability in these pedigrees. To that end, fasting plasma glucose measurements were normalized by an inverse normal scores transformation and then regressed separately for males and females on measured concomitants including age, body mass index (weight/ heightM2), season of measurement, sex hormone use, and diuretic use. The authors found that 27.7% of the variability in normalized fasting plasma glucose in these pedigrees is explained by these measured concomitants. Subsequent variance components analysis suggested that unmeasured polygenic loci and unmeasured shared environmental factors together account for at least an additional 36.7% of the variability in normalized fasting plasma glucose, with genes alone accounting for at least 27.3%. These results are consistent with the known familiality of diabetes, for which fasting plasma glucose level is an important predictor. Further, these familial factors provide an explanation for at least half the variability in normalized fasting plasma glucose which remains after regression on known concomitants.
Oxford University Press