Genetic differences influence calcium absorption
Genetic variations in a gene that helps regulate the body's response
to vitamin D has given researchers new insight into why some children
have higher bone densities.
"We found that variations in the receptor gene for vitamin D could
predict differences in calcium absorption and bone density in healthy
children," said Dr. Steven Abrams, a professor of pediatrics at
Baylor College of Medicine who studies mineral metabolism in children
at the CNRC. A major function of vitamin D is to promote the absorption
of calcium from the intestines.
Abrams studied the relationship between three genetic variations
of the vitamin D receptor gene at a site called Fok1 and markers
of calcium status in 72 healthy, 7- to 12-year-old European-, African-
and Mexican-American children. Abrams was interested in Fok1 because
one variation, called the ff genotype, has been associated with
lower bone mass in adults and children. The other two variations
are known as FF and Ff genotypes.
The study found that children who had the FF genotype absorbed
over 40 percent more calcium from their diets than those with the
ff genotype, and 17 percent more than those whose genotype was Ff.
The children with the FF genotype also had significantly greater
bone density measurements.
A child's bone density is important because peak bone mass, which
occurs in early adulthood, is considered a significant determinant
of osteoporosis risk later in life.
Abrams cautioned that many factors, including diet and exercise,
affect bone density. "Further studies are needed to determine
how the gene-related differences in calcium absorption and bone
density found in this study affect osteoporosis risk," he said.
"This study provides evidence that genetic factors can lead to
identifiable changes in the way the body uses calcium, which is
a step towards understanding why some groups appear more likely
to develop osteoporosis," he said.
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