Effect of hypogonadism and deficient calcium intake on bone density in patients with galactosemia

Forty children and adults with classic galactosemia had vertebral bone density determined by standard quantitative computed tomography at 3.4 to 44.2 years of age. Compared with age- and sex-matched control subjects, patients with galactosemia had diminished bone density ( p=<0.001). Prepubertal...

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Published inThe Journal of pediatrics Vol. 123; no. 3; pp. 365 - 370
Main Authors Kaufman, Francine Ratner, Loro, Maria Luiza, Azen, Colleen, Wenz, Elizabeth, Gilsanz, Vicente
Format Journal Article Conference Proceeding
LanguageEnglish
Published New York, NY Mosby, Inc 01.09.1993
Elsevier
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ISSN0022-3476
1097-6833
DOI10.1016/S0022-3476(05)81733-0

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Summary:Forty children and adults with classic galactosemia had vertebral bone density determined by standard quantitative computed tomography at 3.4 to 44.2 years of age. Compared with age- and sex-matched control subjects, patients with galactosemia had diminished bone density ( p=<0.001). Prepubertal patients of both sexes had bone density determinations below those of the control group ( p=0.008); similar findings were seen in postpubertal patients as well (women, p=0.001; men, p=0.008). Women receiving replacement estrogen-progestin therapy for premature ovarian failure had abnormal bone density (136.3±17.3 mg/cm 3 vs 166.0±17.5 mg/cm 3 for control subjects; p=0.002); patients with evidence of ovarian insufficiency not receiving replacement sex steroids had even lower bone density (92.4±14.3 mg/cm 3 vs 160.2±20.2 mg/cm 3 for control subjects; p<0.001). Calcium intake for the entire galactosemia group was 540±344 mg/day. Calcium intake correlated positively with bone density in women given exogenous estrogen ( r=0.87; p=0.002) and in men ( r=0.74; p=0.009). Thus the diminished mineralization of bones appears to be another abnormality associated with galactosemia. The results of our study suggest that this is likely secondary to abnormal levels of sex steroids in female patients, low calcium intake, and perhaps an intrinsic defect in the normal galactosylation of the collagen matrix of bone caused by the enzyme defect. Strategies to improve bone formation should be considered to diminish morbidity in patients with this inborn error of metabolism.
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ISSN:0022-3476
1097-6833
DOI:10.1016/S0022-3476(05)81733-0